http://identifiers.org/hco/2/GRCh38#23385204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5425693-C-A

23385204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5 prime UTR variant
orthologous variants: 5425693-C-T

23385575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5 prime UTR variant
orthologous variants: 5425306-G-A

23385575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5 prime UTR variant
orthologous variants: 5425306-G-T

http://identifiers.org/hco/2/GRCh38#23385614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5425267-C-A

23385614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5 prime UTR variant
orthologous variants: 5425267-C-T

http://identifiers.org/hco/2/GRCh38#23385648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#5425233-C-A

23385648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 5425233-C-T

23385826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5425049-G-A

23385826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5425049-G-C

23385826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5425049-G-T

http://identifiers.org/hco/2/GRCh38#23385831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5425032-C-A

23385872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: 5424998-G-A

23385872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: 5424998-G-T

23385879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: 5424991-C-G

23385879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: 5424991-C-T

23385934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5424932-A-G

23386023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5424842-C-G

http://identifiers.org/hco/2/GRCh38#23386117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5424750-C-A

23386307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5424560-C-T

23387062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5423848-C-G

23387062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5423848-C-T

23388286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5422654-C-T

23388424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5422508-C-G

23388627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5422297-G-C

23388627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5422297-G-T

23389101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5421853-G-C

23389150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5421794-G-A

23389150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5421794-G-T

23389659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5421353-T-C

23389829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5421263-A-G

23390342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5420777-A-G

23390380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5420743-G-A

23391852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5419744-A-G

23391873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5419731-T-A

23391876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5419728-G-A

23391887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5419721-C-G

23391887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5419721-C-T

23391897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5419707-T-C

23392114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5419520-T-C

23392274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5418982-C-T

23392432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5418829-G-C

23392773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5418378-G-A

23392773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5418378-G-T

23393020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5418030-A-G

23393261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5417766-A-G

23393285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5417742-G-A

23393305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5417722-G-C

23393517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5417502-A-T

23393666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5417347-G-A

23393782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5417211-C-T

23393901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5417056-C-T

23394090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5416785-G-C

23394334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5416586-G-T

23394642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5416324-T-C

23394683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5416280-A-G

23394791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5416164-G-A

23394878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5416076-A-G

23394893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5416065-G-A

23394893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5416065-G-T

23395067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5415898-G-C

23395248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5415803-T-C

23395276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5415775-G-A

23395572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5415602-C-G

23395572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5415602-C-T

23395743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5415484-T-A

23395743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5415484-T-C

23396003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5415188-G-A

23396003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5415188-G-C

23396389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5414815-G-A

23396587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5414640-A-G

23396587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5414640-A-T

23396723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5414510-C-T

23396925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5414306-G-A

23396952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5414284-T-C

23396961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5414275-A-G

23397001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5414236-C-G

23397001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5414236-C-T

23397228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5413996-C-G

23397844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5413346-T-C

23397959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5413232-C-T

23397976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5413215-G-A

23398187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5413002-A-G

23398267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5412843-G-A

23398272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5412838-T-G

23398280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5412798-T-C

23398489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5412616-G-A

23400165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5411747-G-C

23401789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5411374-T-C

23401789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5411374-T-G

23401817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5411348-C-G

23402248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5411001-A-G

23402513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5410795-C-G

23402513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5410795-C-T

23403263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5410153-G-A

23403284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5410138-G-C

23403380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5410043-C-T

23403415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5410005-C-G

23403415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5410005-C-T

23403481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5409939-G-C

23403711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5409694-A-G

23403723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5409682-G-A

23403751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5409654-G-A

23403751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5409654-G-T

23403771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5409634-G-A

23403771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5409634-G-T

23403772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5409633-C-T

23403894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5409354-T-G

23404318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5408930-A-T

23404719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5408523-G-A

23404719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5408523-G-C

23404854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5408386-A-G

23404947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5408258-T-C

23405312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5407808-G-A

23405318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5407802-T-C

http://identifiers.org/hco/2/GRCh38#23405413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5407713-A-C

23405437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5407706-C-G

http://identifiers.org/hco/2/GRCh38#23405438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5407705-C-A

23405608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5407531-A-G

23405643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5407476-A-G

http://identifiers.org/hco/2/GRCh38#23406293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5407016-A-C

23406293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5407016-A-T

http://identifiers.org/hco/2/GRCh38#23406321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5406977-C-A

23406321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5406977-C-G

23406321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5406977-C-T

23406478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5406816-T-C

23406556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5406722-C-T

23407028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5406121-C-G

23407028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5406121-C-T

23407332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5405715-T-C

23407336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5405711-T-C

23407364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5405683-C-T

23407405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5405641-G-A

23407766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5405281-T-C

23408305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5404932-A-G

23408305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5404932-A-T

23408320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5404910-T-A

23408320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5404910-T-G

23408502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5404743-C-T

23408660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5404376-G-A

23408946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5404087-C-T

23408967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5404066-G-C

23408974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5404059-C-T

23408994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5404043-G-A

23408994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5404043-G-C

23408994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5404043-G-T

23409174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5403872-T-G

23409396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5403651-G-A

23409687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5403359-G-C

23410647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5401970-G-A

23410647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5401970-G-T

23410684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5401955-G-A

23410831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5401829-G-A

23410848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5401813-T-C

23410917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5401757-G-A

23410926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5401748-C-T

23411157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5401522-T-C

23411240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5401440-T-C

23411318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5401364-G-A

23411347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5401338-C-T

23411419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5401264-G-A

23411622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5401066-C-T

23411787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5400895-G-A

23411787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5400895-G-C

23411810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5400872-T-C

23412233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5400634-A-G

23412293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5400577-A-G

23412644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5400343-C-T

23412685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5400302-G-C

23412959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5399927-A-G

23413054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5399831-A-G

23413080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5399806-G-A

23413189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5399697-G-A

23413420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5399451-T-A

23413563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5399078-A-G

23413625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5399030-G-A

23413625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5399030-G-C

23413629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5399026-C-T

23413914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5398606-G-A

23414122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5398399-A-G

23414158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5398363-A-G

23414294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5398243-T-G

23414345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5398191-T-G

23414364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5398172-G-A

23414385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5398150-A-G

23414662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5397917-A-G

http://identifiers.org/hco/2/GRCh38#23414993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#5397618-C-A

23414994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: 5397617-C-T

23415228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: 5397410-A-G

23415904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5397128-T-C

23416041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5396997-C-T

23416101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5396938-A-G

23416774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5396509-G-A

23416988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5396304-C-T

23417045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5396252-G-A

23417065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5396232-T-C

23417131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5396170-T-C

23417161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5396150-G-A

23417161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5396150-G-T

23417198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5396111-C-T

23417267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5396064-G-A

23417271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5396060-A-G

http://identifiers.org/hco/2/GRCh38#23417352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5395980-C-A

23417352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5395980-C-G

23417352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5395980-C-T

23417991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5395952-C-T

23418132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5395815-C-T

23418185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5395764-C-T

23418200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5395749-G-C

http://identifiers.org/hco/2/GRCh38#23418206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5395743-C-A

23418208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5395741-G-T

23418232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5395717-C-G

http://identifiers.org/hco/2/GRCh38#23418407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5395521-C-A

23418707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5395223-C-T

23418858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5394628-T-C

23419970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5392799-C-T

23420015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5392744-G-A

23420154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5392505-G-A

23420165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5392494-C-T

23420468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5392200-C-T

23420472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5392194-C-T

23420852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5391893-C-G

http://identifiers.org/hco/2/GRCh38#23420860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5391885-C-A

23420968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5391783-A-G

23420994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5391758-G-A

23420995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5391757-C-T

23421005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5391747-C-T

23422546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5390854-C-G

23423036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5390432-G-A

23423052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5390416-C-T

23423114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5390338-G-A

23423474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5389696-G-A

23423547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5389597-A-G

23424193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5389073-A-G

23424317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5388934-T-C

23424756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5388493-T-C

23425279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5387970-G-A

23425279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5387970-G-T

23425370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5387912-G-A

23425582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5387679-A-G

23425756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5387511-C-G

23426503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5386759-C-T

23426848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5386430-A-G

23426848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5386430-A-T

http://identifiers.org/hco/2/GRCh38#23426875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5386403-A-C

23426875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5386403-A-G

23427141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5386137-C-T

23427740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5385516-T-G

23427842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5385413-G-C

23429931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5384880-C-G

23429955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5384856-T-C

http://identifiers.org/hco/2/GRCh38#23430605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#5384094-C-A

23430605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: 5384094-C-T

23430749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5383968-G-A

http://identifiers.org/hco/2/GRCh38#23431021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5383645-A-C

23431032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5383640-C-T

23431034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5383638-T-C

23431040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5383632-G-A

23431040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5383632-G-C

23431040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5383632-G-T

23431075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5383580-T-A

23431075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5383580-T-G

23432009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5383026-C-T

23432093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5382964-G-A

23432117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5382940-G-A

23432679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5382363-G-A

23432751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5382306-G-T

23432789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5382289-G-A

23432838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5382229-A-G

23433319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5381555-G-T

23434530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5381020-C-G

23434588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5380962-A-G

http://identifiers.org/hco/2/GRCh38#23434820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#5380730-C-A

23434978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: 5380606-C-G

23434978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: 5380606-C-T

23435049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5380533-A-G

23435234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5380064-G-A

23435516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5379826-G-A

23435545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5379809-G-T

23435582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5379772-G-T

23435815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5379550-T-G

23435850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5379516-G-C

23435850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5379516-G-T

http://identifiers.org/hco/2/GRCh38#23435992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5379417-C-A

23435992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5379417-C-T

23436239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5379170-A-G

http://identifiers.org/hco/2/GRCh38#23436398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5379083-C-A

23436432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5379050-T-G

23436433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5379049-G-A

23436456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5379026-G-A

23436471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5379015-T-G

23436586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378912-A-G

http://identifiers.org/hco/2/GRCh38#23436618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5378880-C-A

23436621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378877-C-T

23436644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378854-C-T

23436695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378819-T-A

23436900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378628-T-C

23436928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378599-A-G

23436935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378592-A-T

23437009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378520-A-T

23437022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378504-A-G

23437096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378433-T-C

23437105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378424-C-T

23437120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378409-G-A

23437120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378409-G-T

23437153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378376-A-G

http://identifiers.org/hco/2/GRCh38#23437256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5378285-A-C

23437295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378253-T-C

23437309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378239-A-G

23437405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378146-G-C

23437487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378067-A-T

23437514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5378040-A-G

http://identifiers.org/hco/2/GRCh38#23442494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5377362-A-C

23442681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5377174-T-C

23442681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5377174-T-G

23442732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5377123-C-T

23442735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5377120-A-G

23442780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5377076-A-T

23442837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5377026-A-G

23442839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5377024-A-T

23443507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5376061-A-T

23443558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5376022-A-G

http://identifiers.org/hco/2/GRCh38#23443605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5375982-C-A

23443605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5375982-C-T

23443613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5375974-C-T

23443696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5375904-A-G

23444720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5374923-A-T

23444722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5374921-T-C

http://identifiers.org/hco/2/GRCh38#23444792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5374844-C-A

23445209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5374450-A-T

23445287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5374377-T-C

23445287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5374377-T-G

23445403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5374271-T-G

23445433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5374241-C-T

23446059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5373572-T-G

23446161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5373434-A-G

23446240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5373366-A-G

23446240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5373366-A-T

23446283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5373309-A-G

23446286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5373306-T-C

23446437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5373170-G-A

23446956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5372527-C-T

23446980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5372503-A-G

23447153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5372334-C-T

23447433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5372134-T-C

23447481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5372095-C-T

23447895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5371758-C-T

23448245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5371453-C-T

23448416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5371281-G-A

23448483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5371217-T-G

http://identifiers.org/hco/2/GRCh38#23448675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5371074-A-C

23448675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5371074-A-G

23448829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5370926-A-G

23448898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5370860-C-T

23448981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5370777-G-C

23449166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5370617-T-G

23449270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5370519-T-C

23449346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5370442-T-G

23449389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5370401-A-G

23449420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5370373-T-C

23449614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5370203-G-A

23449829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5370008-G-A

23449829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5370008-G-T

23450136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5369716-G-A

23450291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5369558-A-G

23450291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5369558-A-T

23450709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5369190-T-G

23450837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5369052-C-T

http://identifiers.org/hco/2/GRCh38#23452541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5366760-C-A

http://identifiers.org/hco/2/GRCh38#23452660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5366636-C-A

23452706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5366588-G-A

23452711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5366583-G-A

23452711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5366583-G-T

23452877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5366416-T-C

23452878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5366415-G-C

23453279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5366064-G-A

23453587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365819-C-G

http://identifiers.org/hco/2/GRCh38#23453622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5365785-C-A

23453622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365785-C-T

23454076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365330-T-C

23454155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365256-C-G

23454155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365256-C-T

http://identifiers.org/hco/2/GRCh38#23454169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5365242-C-A

23454172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365239-C-T

23454182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365229-C-T

23454245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365175-G-A

23454245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365175-G-C

23454245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365175-G-T

23454258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365162-A-T

23454274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365138-T-C

23454930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5364533-C-T

23455080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5364389-G-A

23455285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5364080-T-G

http://identifiers.org/hco/2/GRCh38#23455294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5364046-C-A

23455730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5363548-G-A

http://identifiers.org/hco/2/GRCh38#23456115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5363163-A-C

23456200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5363078-A-G

23456232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5363046-A-G

23456363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5362916-C-G

23456366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5362913-A-G

23456416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5362857-G-T

23456437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5362837-T-C

23456441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5362833-C-G

23456441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5362833-C-T

23456886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5362415-T-A

23456894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5362407-C-G

23456894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5362407-C-T

23457244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5362093-C-T

23457406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5361939-C-G

23457543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5361810-G-A

23457590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5361784-G-A

23457596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5361777-G-A

23458092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5361343-C-T

23458173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5361249-A-T

23458175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5361247-A-T

23458288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5361133-G-C

23458294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5361127-C-T

http://identifiers.org/hco/2/GRCh38#23458334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5361088-C-A

23458344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5361076-T-C

23458424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5360939-A-G

23458692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5360588-C-T

23458783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5360533-G-A

23458805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5360513-G-A

23458805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5360513-G-T

23458923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5360394-G-A

23458923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5360394-G-T

23459197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5360142-G-A

23459357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5359109-A-T

23459441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5359024-T-G

23459454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5359012-G-T

23459642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5358852-G-T

23459662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5358833-C-G

23459760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5358744-G-C

23460135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5358410-A-G

23460234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5358310-T-C

23460239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5358305-A-G

23460592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5357994-G-A

23460950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5357841-G-A

23461316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5357117-C-G

23461518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5356910-G-T

23461581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5356849-T-A

http://identifiers.org/hco/2/GRCh38#23461719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5356715-C-A

23461719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5356715-C-G

23461719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5356715-C-T

23462166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5356430-T-C

23462548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5356078-G-A

http://identifiers.org/hco/2/GRCh38#23462606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5356020-C-A

23462606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5356020-C-T

23462772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5355860-T-A

23463081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5355683-C-G

23463081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5355683-C-T

23463164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5355593-A-T

http://identifiers.org/hco/2/GRCh38#23463541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5354874-A-C

23463669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5354767-A-G

23463765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5354674-A-G

23464146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5354290-G-A

23464146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5354290-G-C

http://identifiers.org/hco/2/GRCh38#23464675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5353779-C-A

23464678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5353776-C-G

23464689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5353765-T-C

23464981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5353480-C-T

23465224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5353258-G-A

23465242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5353237-G-A

23465617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5352893-T-G

23465635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5352864-A-T

23465943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5352596-T-A

23466128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5352433-G-A

23466170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5352391-G-A

23466878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5351739-T-A

23466878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5351739-T-C

23466901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5351716-C-T

http://identifiers.org/hco/2/GRCh38#23467580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5350940-C-A

23467657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5350857-G-A

http://identifiers.org/hco/2/GRCh38#23467760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5350806-A-C

23468252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5350405-A-G

23468528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5350151-G-A

23468706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5350003-T-C

23468767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5349943-G-A

23468773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5349937-A-G

23468971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5349773-G-A

23469328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5349446-C-T

23469460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5349316-G-A

23469795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5348966-C-G

23469795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5348966-C-T

23469864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5348893-T-C

23469866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5348891-C-G

23469866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5348891-C-T

23469868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5348889-A-G

23469951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5348819-G-T

23470768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5346835-G-A

http://identifiers.org/hco/2/GRCh38#23470788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5346816-A-C

23471644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5345940-A-G

http://identifiers.org/hco/2/GRCh38#23471739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5345845-A-C

23471739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5345845-A-G

23472052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5344458-G-A

http://identifiers.org/hco/2/GRCh38#23472075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5344435-C-A

23472138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5344366-T-A

23472138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5344366-T-G

23473334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5343638-G-A

23473546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5343495-G-A

23473736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5343277-G-A

23473976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5343031-C-T

23474247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5342776-G-A

23474777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5342208-G-A

23474777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5342208-G-C

23474927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5342059-T-A

23474927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5342059-T-C

23475038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5341957-A-T

http://identifiers.org/hco/2/GRCh38#23475411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5341606-C-A

23475411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5341606-C-T

23475413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5341604-G-A

23475574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5 prime UTR variant
orthologous variants: 5341428-T-C

23475690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5341313-T-C

23475703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5341300-G-A

23475703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5341300-G-T

http://identifiers.org/hco/2/GRCh38#23475723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5341280-C-A

23475723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5341280-C-T

23475740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5341263-T-C

23475797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5341218-A-G

23475797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5341218-A-T

23477062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5340046-A-G

23477202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5340024-C-T

23477313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5339920-T-C

23477402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5339829-G-T

23477522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5339716-A-G

23477811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5339441-G-T

23477812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5339440-C-T

23477854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5339393-G-A

23477854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5339393-G-C

23478263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5339023-T-C

23478266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5339020-G-A

23478453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338863-C-T

23478518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338799-C-T

23478550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338769-G-A

23478624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338711-G-A

23478624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338711-G-C

23478699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338632-G-A

23478915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338545-G-A

23478915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338545-G-T

http://identifiers.org/hco/2/GRCh38#23478938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5338525-C-A

23478994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338511-G-A

23478994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338511-G-T

23479452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338171-G-A

23479497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338124-A-G

23479497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338124-A-T

23479515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5338117-G-A

23479758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5337719-C-T

23479914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5337582-C-T

23482060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5337223-G-A

23482060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5337223-G-C

23482079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5337202-T-C

23482097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5337189-T-A

23482097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5337189-T-C

23482251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5337057-G-A

23482251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5337057-G-T

23482260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5337048-C-G

23482947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5336085-C-T

23483135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5335931-C-T

23484159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5335863-A-G

23484351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5335646-C-T

23484525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5335468-G-A

23484797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5335189-C-T

23485530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5334782-T-C

23485589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5334723-G-A

http://identifiers.org/hco/2/GRCh38#23485936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5334447-A-C

23486144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5334233-G-A

23486784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5333833-T-G

23486919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5333703-T-C

23486948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5333675-G-A

23486948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5333675-G-C

23486948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5333675-G-T

23486961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5333660-A-T

23487002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5333634-C-T

23487018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5333618-G-A

23487079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5333554-C-T

23487409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5333222-C-T

http://identifiers.org/hco/2/GRCh38#23487951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#5332752-A-C

23488000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5332697-C-T

23488146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5332549-T-A

23488161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5332533-C-T

23488168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5332526-A-G

23488182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5332512-C-T

23488356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5332408-G-A

23488839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5332054-T-C

23488950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5331930-G-A

23489086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5331808-G-A

http://identifiers.org/hco/2/GRCh38#23489107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5331789-C-A

23489107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5331789-C-T

23489110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5331786-G-C

23489229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5331663-G-A

http://identifiers.org/hco/2/GRCh38#23489531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5331348-C-A

23489531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5331348-C-T

23489539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5331340-C-T

23489545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5331334-C-T

23489586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5331299-C-T

http://identifiers.org/hco/2/GRCh38#23489929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5331048-C-A

23490028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5330951-A-T

23490259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5330640-C-G

23490375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5330529-C-T

23490917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5330013-C-T

23494204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5326047-A-T

23494471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5325780-C-G

23494539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5325729-C-T

23494767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5325513-C-T

23494768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5325512-G-A

23494918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5325405-G-A

23494918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5325405-G-T

23495389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5325116-A-G

23495408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5325097-G-A

23495448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5325061-C-G

23495498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5325010-A-G

23495503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5325005-C-G

http://identifiers.org/hco/2/GRCh38#23495549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5324980-C-A

23495623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5324902-G-C

http://identifiers.org/hco/2/GRCh38#23496341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5324257-A-C

23496462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5324135-G-C

23496558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5324084-G-T

23496968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5323712-C-G

http://identifiers.org/hco/2/GRCh38#23497127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5323556-C-A

23497175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5323511-G-A

23497175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5323511-G-T

23497487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5323219-A-T

23497570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5323157-G-T

23497631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5323106-G-C

23497682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5323055-G-A

23498578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5322273-C-T

23498851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5322037-C-T

23499162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5321769-T-A

23499162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5321769-T-G

http://identifiers.org/hco/2/GRCh38#23499363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#5321565-A-C

23499363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: 5321565-A-G

23499880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5320895-A-G

23500264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5320350-C-T

23500983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5319574-C-T

http://identifiers.org/hco/2/GRCh38#23500986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5319571-C-A

23501159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5319432-C-T

23501456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5319173-C-T

23501502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5319127-C-G

23501702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5318939-C-G

23501766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5318877-G-C

23501785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5318858-C-T

23501854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5318791-C-T

23502142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5318542-A-G

23502424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5318277-C-T

23502495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5318208-G-A

23502495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5318208-G-C

23502495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5318208-G-T

23502511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5318192-A-G

23502514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5318189-G-A

23502643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5318117-C-T

23502726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5318056-T-C

23502886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5317828-G-C

http://identifiers.org/hco/2/GRCh38#23503116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5317573-C-A

23503495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5317227-T-C

23503661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5317057-G-A

23503688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5317030-C-G

23503778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5316979-G-A

23504242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5316577-G-T

23504643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5316287-G-A

23504643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5316287-G-T

23504644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5316286-G-A

23504644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5316286-G-T

23505184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5315909-G-T

23505230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5315864-T-A

23505387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5315704-T-G

23505388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5315700-G-T

23505549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5315554-G-T

http://identifiers.org/hco/2/GRCh38#23505901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5315313-A-C

23505901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5315313-A-G

23505995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5315215-C-G

23505997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5315213-T-C

23506012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5315199-G-A

23506012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5315199-G-C

23506018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5315193-G-A

23506296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5314722-A-G

23506296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5314722-A-T

23506525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5314510-G-A

23506620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5314434-C-T

23506666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5314388-G-A

23506721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5314336-G-A

23506972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5314095-G-A

23506972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5314095-G-T

23507020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5314049-G-A

23507020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5314049-G-T

http://identifiers.org/hco/2/GRCh38#23507053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5314016-C-A

23507053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5314016-C-G

23507053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5314016-C-T

23507174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5313954-A-G

23507175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5313953-T-C

http://identifiers.org/hco/2/GRCh38#23507206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5313925-C-A

23507206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5313925-C-T

http://identifiers.org/hco/2/GRCh38#23507207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5313924-C-A

23507207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5313924-C-G

23507256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5313878-T-G

http://identifiers.org/hco/2/GRCh38#23507318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5313805-C-A

23507500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5313694-A-G

23507501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5313693-C-G

http://identifiers.org/hco/2/GRCh38#23507525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5313668-C-A

23507525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5313668-C-T

23508442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5312423-T-C

23508603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5312264-G-A

23508603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5312264-G-C

23508697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5312175-C-G

23508745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5312115-G-T

23508857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5312056-G-T

23509746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5311133-G-A

23510104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5310792-G-A

23510152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5310744-A-G

23510240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5310659-G-A

23510664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5310247-A-G

23510782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5310137-G-A

23510782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5310137-G-C

23510931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5310019-A-G

23510981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5309972-T-A

23510981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5309972-T-C

23511186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5309775-G-A

23512459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5308570-G-T

23512758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5308298-A-G

23512778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5308278-C-T

23512783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5308273-C-G

23513203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5307919-G-A

23513203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5307919-G-C

23513494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5307624-A-G

23513522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5307571-C-G

23513534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5307559-C-G

23513593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5307494-A-G

http://identifiers.org/hco/2/GRCh38#23513854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5307279-A-C

23513994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5307138-C-T

23514002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5307130-G-C

23514290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5306801-C-T

23514318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5306776-G-A

23514325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5306769-G-A

23514466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5306635-T-C

23514498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5306602-C-T

23514523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5306579-G-A

http://identifiers.org/hco/2/GRCh38#23514906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5306155-A-C

23515061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5306000-C-T

23515090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5305970-T-C

23515188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5305869-G-C

23515188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5305869-G-T

23515454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5305648-G-A

23515454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5305648-G-C

23515665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5305440-C-G

23515665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5305440-C-T

23515710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5305395-G-A

23515736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5305369-T-C

23516080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5304934-C-T

http://identifiers.org/hco/2/GRCh38#23516151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5304863-C-A

23516151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5304863-C-T

http://identifiers.org/hco/2/GRCh38#23516491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5303968-C-A

23516570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5303913-C-T

23516703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5303781-G-T

23516777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5303706-A-G

23516876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5303615-C-G

23516876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5303615-C-T

23516887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5303604-G-C

23517238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5303279-G-A

23517903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5302468-G-A

23518050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5302290-C-T

23518189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5302081-G-A

23518497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5301756-C-T

23518582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5301639-C-T

23518751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5301452-C-G

23518906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5301343-T-C

23519227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5301129-G-A

23519227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5301129-G-C

23519346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5301036-T-A

23519346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5301036-T-C

23519493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5300909-C-T

23520204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5300707-C-T

23520236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5300477-G-A

23520236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5300477-G-T

23520430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5300307-C-G

23520430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5300307-C-T

23520482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5300261-T-A

23520640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5300115-T-G

23520719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5300049-T-C

23520947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5299813-C-T

23521073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5299721-C-T

23521182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5299621-A-G

23521183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5299620-C-G

23521183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5299620-C-T

23521349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5299472-G-A

http://identifiers.org/hco/2/GRCh38#23521351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5299470-A-C

23521451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5299377-C-T

23521504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5299325-T-C

23522089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5298549-A-G

23522112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5298527-C-T

23522901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5297794-G-A

23523012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5297695-A-G

23523012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5297695-A-T

23523227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5297447-G-A

23523282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5297404-T-C

23523368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5297321-A-G

23523523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5297171-G-A

23523578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5297116-C-T

23523910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5296792-T-C

http://identifiers.org/hco/2/GRCh38#23524132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5296557-C-A

23524264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5296450-G-A

23524264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5296450-G-C

23524264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5296450-G-T

23524411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 5296322-G-T

23524825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5295920-G-C

23524825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5295920-G-T

23524870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5295857-G-A

23524982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5295750-C-G

23525053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5295705-A-T

23525215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5295546-C-T

23525499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5295281-C-T

23525500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5295280-C-T

http://identifiers.org/hco/2/GRCh38#23525638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5295148-C-A

23526019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5294739-G-A

23526226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5294534-G-A

23526410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5294193-C-G

23526410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5294193-C-T

23526588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5293828-C-T

23526705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5293722-C-T

23527587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5293059-A-T

23527603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5293038-G-A

23527607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5293034-C-T

http://identifiers.org/hco/2/GRCh38#23527626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5293015-C-A

23527626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5293015-C-T

23527641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5293000-G-T

23528484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5292200-C-T

23528522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5292161-C-T

http://identifiers.org/hco/2/GRCh38#23528528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5292155-C-A

23528756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5291929-C-T

23528819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5291867-T-C

http://identifiers.org/hco/2/GRCh38#23528936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5291745-C-A

http://identifiers.org/hco/2/GRCh38#23528938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5291743-C-A

23528992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5291683-G-A

http://identifiers.org/hco/2/GRCh38#23529005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5291670-C-A

http://identifiers.org/hco/2/GRCh38#23529265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5291176-A-C

http://identifiers.org/hco/2/GRCh38#23529762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5290670-C-A

23529762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5290670-C-G

23529999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5290431-C-T

23530314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5290157-C-T

23530681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5289790-C-T

23530855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5289620-C-T

23531029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5289436-T-C

23531086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5289316-T-C

23531192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5289006-T-C

23531482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5288758-G-C

http://identifiers.org/hco/2/GRCh38#23531564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5288674-A-C

23531829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5288425-C-G

23531829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5288425-C-T

23531918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5288358-A-G

23532103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5288198-C-G

23532332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5287988-T-C

23532371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5287950-T-C

23532441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5287880-C-G

23532441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5287880-C-T

http://identifiers.org/hco/2/GRCh38#23532997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5287124-C-A

23532997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5287124-C-T

23533036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5287085-T-C

23533047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5287074-G-A

23533197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286948-A-G

23533627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286502-G-A

23533698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286426-G-C

23533790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286339-T-C

23533912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286219-G-A

23534013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286130-A-G

23534207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5285712-C-T

23534329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5285574-C-G

23534595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5285375-C-G

23534667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5285293-A-G

23534691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5285254-A-G

23535109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5284861-A-T

23535297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5284643-G-A

23535353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5284591-A-G

23535368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5284576-G-A

23535571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5284361-A-G

23535883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5283913-A-G

23536179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5283648-G-A

23536282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5283544-C-T

http://identifiers.org/hco/2/GRCh38#23536459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5283340-C-A

23536495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5283306-C-T

23536892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5282891-A-G

23537030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5282783-G-A

23537030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5282783-G-C

23537030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5282783-G-T

23537032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5282781-C-T

23537091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5282722-C-G

23537297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5282552-C-T

23537472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5282316-G-A

23537472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5282316-G-T

23537625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5282161-G-A

23537792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5281978-A-G

23538384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5281529-T-C

23538461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5281463-G-A

23538524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5281350-C-T

23538858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5281006-T-C

23538873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5280991-G-A

23538916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5280955-C-T

23538959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5280911-A-G

23539002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5280868-A-G

23539043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5280825-G-C

23540077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5279706-C-T

23540341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5279462-A-G

23540385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5279316-T-C

http://identifiers.org/hco/2/GRCh38#23540496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5279215-C-A

23540673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5279044-C-G

23540837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5278875-A-G

23540989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5278726-G-A

http://identifiers.org/hco/2/GRCh38#23541095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5278633-A-C

23541110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5278617-T-C

23541187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5278542-G-C

23541413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5278032-T-C

23542184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5277273-T-C

23542818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5276654-G-A

23543343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5276170-C-T

23543383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5276091-G-A

23543614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5275846-G-C

23544199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5275285-C-T

23544254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5275236-A-T

23544363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5275137-G-T

23544657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5274950-G-C

23544792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5274858-G-T

23544823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5274831-G-T

http://identifiers.org/hco/2/GRCh38#23545041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5274648-A-C

23545055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5274635-G-C

23545657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5274086-G-A

23545992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5273824-T-A

23545992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5273824-T-C

23548879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5271982-C-T

23549096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5271797-G-A

23549254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5271624-C-T

23549392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5271485-C-G

23549661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5271227-T-C

23549776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5271116-A-G

23550068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5270914-T-C

23550283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5270696-G-A

23550388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5270617-G-C

23550574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5270422-G-A

23550729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5270267-G-C

23550973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5270023-T-A

23550973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5270023-T-C

23551000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5269995-C-T

23551375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5269634-C-T

23551432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5269577-G-C

23551732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5269099-G-A

23551732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5269099-G-T

23551970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5268580-G-A

23552293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5268286-G-A

23552412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5268179-A-T

23552638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5267956-C-G

23553246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5267654-G-A

23553310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5267560-A-G

http://identifiers.org/hco/2/GRCh38#23553431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5267464-C-A

23553871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5267035-G-A

23553912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5266996-C-T

23554433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5266494-G-A

23554553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5266370-G-T

23554675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5266245-T-A

http://identifiers.org/hco/2/GRCh38#23554768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5266111-A-C

23554768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5266111-A-G

23554774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5266105-G-T

23554859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5266020-C-T

23554878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5265998-A-G

23555207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5265673-G-A

23555250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5265631-C-T

23555860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264994-T-C

23555947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264936-C-T

23555990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264892-G-A

23555990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264892-G-T

23556188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264751-G-A

23556304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264633-G-A

23556312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264625-C-T

23556752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264261-G-C

23556854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264170-G-A

23556854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264170-G-T

23556948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5264076-C-T

23557177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5263848-A-G

23557345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5263681-T-C

23557361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5263666-G-A

23557392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5263635-C-T

23557598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5263425-T-G

23561098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5261234-G-T

23561271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5261084-A-G

23561423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5260934-A-G

23561600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5260799-C-T

23561659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5260742-C-T

23561775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5260631-A-G

23561777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5260629-A-G

23561777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5260629-A-T

23562014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5260414-G-A

23562014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5260414-G-T

http://identifiers.org/hco/2/GRCh38#23562126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5260283-C-A

23562126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5260283-C-T

23562398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5260013-A-G

23562459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5259952-C-T

23562470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5259941-G-A

23562470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5259941-G-T

23562507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5259904-A-G

http://identifiers.org/hco/2/GRCh38#23562549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5259875-C-A

23562560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5259867-G-A

23562560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5259867-G-T

23563118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5259385-T-A

23563348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5259037-G-A

23563402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5258987-C-T

23563507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5258919-G-A

23563642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5258800-G-A

23563733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5258711-G-A

23563837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5258606-C-T

23563855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5258588-A-G

23563972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5258475-C-G

23564376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5258065-G-A

23564397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5258044-G-A

23564478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5257950-T-C

23564672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5257528-A-G

23564796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5257401-C-T

23564972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5257249-C-T

23565443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5256948-G-A

23565515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5256874-C-G

23565609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5256751-C-T

23565723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5256660-G-A

23566004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5256392-C-T

http://identifiers.org/hco/2/GRCh38#23566196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5256207-C-A

23567068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5255480-C-T

23567377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5255156-T-A

23567398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5255135-G-A

23567398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5255135-G-C

23567646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5254909-G-A

23567808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5254766-A-G

23567870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5254702-G-A

23567998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5254578-G-C

23567998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5254578-G-T

23568119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5254449-A-G

http://identifiers.org/hco/2/GRCh38#23568242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5254355-A-C

23568264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5254333-G-T

23569445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5253362-A-G

23570067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5252996-G-A

http://identifiers.org/hco/2/GRCh38#23570090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5252973-A-C

23570324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5252796-C-T

23570938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5252535-C-T

23571015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5252454-A-G

23571230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5252305-G-A

23571975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5251628-A-G

23572368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5251322-A-G

23572413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5251284-C-T

http://identifiers.org/hco/2/GRCh38#23572504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5251224-A-C

23572504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5251224-A-T

23572515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5251213-A-G

23573069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5250994-G-A

23573099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5250963-A-T

23575052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5249954-G-T

23575150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5249871-A-G

23575209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5249805-G-T

23575370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5249693-T-C

23575761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5249328-A-G

23576347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5249172-T-G

23576892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5248602-T-C

23576892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5248602-T-G

23576954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5248543-A-T

23577770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5248343-A-G

23577843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5248270-G-A

23577843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5248270-G-C

23578253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5247964-T-C

http://identifiers.org/hco/2/GRCh38#23578430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5247785-A-C

23578430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5247785-A-G

23578489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5247734-C-T

23578813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5247405-C-T

23579027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5247198-C-T

23579097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5247130-G-A

23579173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5247052-A-G

23579252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5246986-G-A

23579254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5246984-T-C

23579524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5246750-C-T

23579651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5246628-C-T

23579850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5246494-C-G

23579851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5246493-A-G

23579872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5246472-T-G

23579919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5246433-G-A

23582069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5245733-A-G

http://identifiers.org/hco/2/GRCh38#23582081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5245721-A-C

23582086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5245716-C-T

23583157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5244617-C-T

23583306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5244536-G-A

http://identifiers.org/hco/2/GRCh38#23583480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5244401-C-A

23583480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5244401-C-G

23583641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5244216-C-G

23583641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5244216-C-T

http://identifiers.org/hco/2/GRCh38#23583689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5244166-C-A

23583689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5244166-C-G

23583939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5243930-A-G

23584081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5243790-C-T

23584464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5243407-G-C

23585420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5242335-T-C

23585468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5242287-G-T

23585519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5242224-G-A

23585627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5242121-C-T

23585703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5242042-C-T

23585881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5241862-G-A

23585881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5241862-G-T

23585921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5241822-T-C

23585921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5241822-T-G

23586143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5241606-T-A

23586174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5241573-T-C

http://identifiers.org/hco/2/GRCh38#23586337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5241407-C-A

23586337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5241407-C-G

23586337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5241407-C-T

23587064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5240465-A-G

23587093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5240435-C-G

23587093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5240435-C-T

http://identifiers.org/hco/2/GRCh38#23587118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5240410-A-C

23587118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5240410-A-G

23587128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5240400-A-G

23587194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5240327-A-G

23587579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5239898-A-G

23587670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5239807-G-A

23587671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5239806-C-T

23588032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5239411-A-T

23588426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5239081-G-A

23588426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5239081-G-T

23588427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5239080-C-T

23588701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5238807-C-G

23588957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5238579-G-A

23589173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5238347-G-A

23589216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5238304-A-G

23589904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5237659-C-T

http://identifiers.org/hco/2/GRCh38#23590174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5237261-A-C

23590736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5236741-C-T

23590861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5236612-A-G

23593253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5235768-A-G

23593876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5234461-G-A

23593876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5234461-G-T

23594130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5234220-G-A

23594212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5234142-A-G

23594284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5234063-A-G

http://identifiers.org/hco/2/GRCh38#23594491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5233874-C-A

23594491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5233874-C-T

23595126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5233246-A-G

23595922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5232983-C-T

http://identifiers.org/hco/2/GRCh38#23595932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5232972-C-A

23595989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5232924-G-A

23596007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5232906-G-C

23596195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5232714-C-G

23596206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5232692-C-T

23596451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5232452-G-A

23597027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5231937-C-T

23597029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5231935-G-A

23597043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5231922-G-A

http://identifiers.org/hco/2/GRCh38#23597174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5231803-A-C

23597174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5231803-A-G

23598108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5231071-C-T

23598178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5231000-C-G

23598426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5230768-A-G

23598495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5230673-C-T

23598498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5230670-A-G

http://identifiers.org/hco/2/GRCh38#23598613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5230562-A-C

23598629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5230546-C-T

23598857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5230249-G-A

23598907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5230213-G-A

23598911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5230209-G-T

23598971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5230148-G-A

http://identifiers.org/hco/2/GRCh38#23599828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5229847-C-A

23600690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5229017-G-T

23600806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5228931-G-A

23600919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5228840-C-G

23601009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5228757-A-G

http://identifiers.org/hco/2/GRCh38#23601175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5228604-A-C

23601319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5228352-C-T

23601687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5227878-A-T

23601766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5227805-A-G

23601965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5227643-T-C

23602100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5227529-C-T

23602367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5227240-T-A

http://identifiers.org/hco/2/GRCh38#23602392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5227222-A-C

23602392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5227222-A-T

http://identifiers.org/hco/2/GRCh38#23602607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5227043-A-C

23602607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5227043-A-G

23602861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226925-C-G

23603001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226786-A-G

23603189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226605-G-A

23603190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226604-G-T

23603269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226526-G-A

23603269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226526-G-C

23603361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226428-C-T

23603368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226421-G-A

23603621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226184-G-A

23603855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225997-G-A

23604067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225791-C-T

23604082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225776-T-C

23604619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225519-G-A

23604674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225470-A-G

http://identifiers.org/hco/2/GRCh38#23604989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5225158-C-A

23604989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225158-C-G

23605448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225021-A-G

23605495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5224972-C-G

23605505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5224959-A-G

23605521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5224945-G-A

23605735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5224749-A-G

23605735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5224749-A-T

23606639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223772-G-A

23606773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223622-C-G

23606823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223566-C-G

23606867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223522-G-A

23607095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223329-G-A

23607254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5223218-G-A

23607254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5223218-G-T

23607300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5223173-C-T

23607309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5223164-C-G

23607340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5223133-C-T

23607389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223084-G-A

23607415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5222992-A-T

23607425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5222972-G-T

23607460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5222864-T-A

23607897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5222403-T-A

23607969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5222331-A-T

23608253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5222051-T-A

23608700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5221691-C-T

23608816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5221571-T-C

23609076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5220947-A-G

23609334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5220494-C-T

23609551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5220302-G-A

23609551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5220302-G-T

23609726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5220145-C-G

23609726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5220145-C-T

23614386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5217031-G-A

23614581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216837-T-G

23614845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216458-G-A

23614857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216438-G-A

23614857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216438-G-C

23614858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216437-G-A

23615174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216166-C-G

23615184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5216156-G-A

23615849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5215611-G-A

23615849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5215611-G-T

23616060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5215397-C-T

23616156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5215304-C-G

http://identifiers.org/hco/2/GRCh38#23616274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5215198-C-A

23616368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5215108-C-T

http://identifiers.org/hco/2/GRCh38#23616433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5215042-A-C

23616433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5215042-A-G

http://identifiers.org/hco/2/GRCh38#23616463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5215014-C-A

http://identifiers.org/hco/2/GRCh38#23616543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5214947-C-A

23616599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5214888-C-T

http://identifiers.org/hco/2/GRCh38#23616693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5214084-C-A

23616720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5214055-G-A

23616720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5214055-G-T

23616743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5214032-T-C

23616851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213942-C-T

23616899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213893-G-C

23616899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213893-G-T

http://identifiers.org/hco/2/GRCh38#23616987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5213810-C-A

23616987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213810-C-T

23617083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213716-T-C

23617129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213668-T-G

23617172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213607-T-C

23617201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213576-A-G

23617300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213504-G-T

23617487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213333-G-A

23617574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213249-T-C

23617702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5213130-C-T

23617708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5213124-T-A

23617708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5213124-T-C

23617718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213114-G-A

23617718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213114-G-T

23617725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213107-G-A

23617770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213062-A-G

23617782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5213050-G-C

23618022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5212806-C-G

23618022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5212806-C-T

23618339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5212296-G-C

23618349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5212286-G-A

23618349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5212286-G-T

23618373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5212262-A-G

23618569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5212034-G-A

23618911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5211768-C-T

23618952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5211727-G-A

23618952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5211727-G-T

23619055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5211603-G-A

23619221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5211291-T-C

23619802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210507-T-A

23619997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210327-A-G

23619997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210327-A-T

23620063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210288-A-G

23620099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210252-C-T

23620235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210144-A-T

23620339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210043-A-G

23620363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210019-G-C

23620446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5209918-C-T

23620634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5209767-G-C

23620636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5209765-G-A

23621257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5209357-C-G

23621284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5209333-C-G

23621284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5209333-C-T

http://identifiers.org/hco/2/GRCh38#23621332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5209270-C-A

23621382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5209217-C-G

23621406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5209193-A-G

23621428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5209167-C-G

23621526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5209057-T-G

23621542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5208647-G-A

23621562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5208625-G-A

23621562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5208625-G-T

23622042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5208075-C-T

23622563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5207626-A-G

23622839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5207349-G-A

23622909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5207285-C-T

23623033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5207158-C-G

23623056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5207145-G-A

23623097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5207110-C-G

23623180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5207024-T-A

23623300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5206905-G-A

23623366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5206856-G-A

23623602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5206626-C-T

23623606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5206625-G-A

23623951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5206411-A-T

23624033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5206333-G-A

http://identifiers.org/hco/2/GRCh38#23624239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5206144-C-A

23624239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5206144-C-G

23624369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5206070-A-G

23624553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5205898-G-A

23624589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5205857-A-G

23624733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5205721-C-T

23624795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5205663-A-G

23624796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5205662-A-T

23624868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5205600-G-T

23625104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5205130-T-C

23625828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5204403-C-T

23625846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5204389-T-C

23626476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5204118-A-T

http://identifiers.org/hco/2/GRCh38#23627346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5203282-A-C

23627346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5203282-A-G

23627584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5203114-C-T

23627750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5202944-G-C

23628817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5202409-A-G

23628958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5202260-G-C

http://identifiers.org/hco/2/GRCh38#23629102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5202137-C-A

23629137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5202103-C-T

23629138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5202102-G-A

23629166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5202072-G-A

23629417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5201830-A-T

23629731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5201517-G-A

23629808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5201442-C-G

23629839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5201411-G-A

23629932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5201311-A-G

23629949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5201298-C-G

23629949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5201298-C-T

23629950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5201297-G-A

23630867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5199912-A-G

23630960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5199812-G-C

23631042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5199746-A-G

23631095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5199682-A-G

23631101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5199677-G-A

23631112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5199668-G-A

23631426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5199373-C-T

23631730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5199081-C-T

23631792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5198825-A-G

23631860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5198757-G-C

23631889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5198726-T-G

http://identifiers.org/hco/2/GRCh38#23631938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5198672-C-A

23631938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5198672-C-G

23631938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5198672-C-T

23632039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5198582-A-G

23632065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5198555-G-A

23632105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5198527-G-A

23632298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5198357-A-G

23632635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5198037-A-G

23632934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5197777-G-A

23633035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5197671-C-T

23633064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5197645-C-G

23633380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5197355-C-T

23633505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5197224-T-C

23634136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5195821-G-A

23634230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5195629-T-C

23634309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5195558-C-T

23634491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5195418-G-A

http://identifiers.org/hco/2/GRCh38#23635162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5194827-C-A

23635290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5194704-T-C

23635489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5194542-C-T

23635866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5194190-G-A

23636366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5193633-G-A

23636523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5193431-C-G

23636722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5193223-G-A

23636798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5193167-C-T

23637117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5192941-C-T

23637584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5192406-G-A

23637584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5192406-G-T

http://identifiers.org/hco/2/GRCh38#23637838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5192180-C-A

23637932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5192120-T-A

http://identifiers.org/hco/2/GRCh38#23638081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5191970-A-C

23638081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191970-A-G

23638081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191970-A-T

23638112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191758-G-A

23638112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191758-G-C

23638112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191758-G-T

23638122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191748-G-A

23638168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191707-C-T

23638599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191330-G-A

23638599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191330-G-C

23638617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191310-A-T

23638637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191279-C-G

23638747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191158-A-G

23638760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191143-T-C

23638916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190986-G-A

http://identifiers.org/hco/2/GRCh38#23638971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5190932-A-C

23639090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190756-G-C

23639370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190504-A-T

http://identifiers.org/hco/2/GRCh38#23639401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5190473-C-A

23639401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190473-C-G

23639401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190473-C-T

23639623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190414-T-C

23639760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190310-A-G

23639797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190287-C-T

23639921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190203-G-C

23639921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190203-G-T

23640001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190123-C-T

http://identifiers.org/hco/2/GRCh38#23640562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5189489-C-A

23640791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189253-G-A

23640821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189226-C-T

23641243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5188838-A-G

23641371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5188712-C-T

http://identifiers.org/hco/2/GRCh38#23642206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5188070-A-C

23642206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5188070-A-G

23642206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5188070-A-T

http://identifiers.org/hco/2/GRCh38#23642241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5188035-C-A

23642241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5188035-C-T

23642251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5188024-T-C

23642298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187975-A-G

http://identifiers.org/hco/2/GRCh38#23642308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5187965-C-A

23642308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187965-C-T

http://identifiers.org/hco/2/GRCh38#23642451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5187820-C-A

23642451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5187820-C-G

23642451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5187820-C-T

http://identifiers.org/hco/2/GRCh38#23642688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5187583-C-A

23642688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5187583-C-T

23642748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5187523-G-A

23642748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5187523-G-T

23642760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5187511-C-G

http://identifiers.org/hco/2/GRCh38#23642911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5187379-C-A

23642911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5187379-C-G

23643026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5187225-G-A

23643026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5187225-G-C

23643026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5187225-G-T

23643031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5187207-G-A

23643031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5187207-G-T

23643095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5187130-A-G

http://identifiers.org/hco/2/GRCh38#23643112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5187114-C-A

23643112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5187114-C-T

23643216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5187047-G-A

23643216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5187047-G-T

23643286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5186979-T-G

23643287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5186978-G-A

23643287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5186978-G-T

23643307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5186958-T-C

http://identifiers.org/hco/2/GRCh38#23643451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5186831-C-A

23643451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5186831-C-T

23643493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5186791-G-A

23643493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5186791-G-C

23643942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5186443-G-A

23643942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5186443-G-T

23643949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5186436-T-C

23643971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5186418-A-G

23644350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5185831-G-A

23644350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5185831-G-T

23644858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5185360-G-A

http://identifiers.org/hco/2/GRCh38#23644986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5185249-C-A

23644986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5185249-C-T

23645232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5185013-A-G

23645232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5185013-A-T

23645302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5184940-G-A

23645302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5184940-G-C

23645493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5184729-C-G

23646287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5183925-G-A

23646546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5183794-T-G

23646621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5183716-G-A

23646627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5183710-G-A

23646627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5183710-G-T

23647085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5183136-G-C

http://identifiers.org/hco/2/GRCh38#23647220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5183022-A-C

23647220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5183022-A-G

23647225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5183017-T-G

23647374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5182933-C-T

23647642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5182801-C-G

23647648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5182795-T-C

23647665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5182777-G-T

23647744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5182673-A-G

23647923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5182490-C-T

23647953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5182459-C-T

23648044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5182392-T-C

23648064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5182378-C-T

23648444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5181993-G-A

23648481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5181958-G-A

23648861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5181612-C-T

23649338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5181278-C-G

23649342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5181274-C-T

23649346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5181270-G-A

23649612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5181014-G-A

23649835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5180809-G-A

23649835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5180809-G-T

23649966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5180674-G-C

23649979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5180661-C-T

23650113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, undefined
orthologous variants: 5180525-G-A

23650135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5180482-G-A

23650374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5180260-C-G

23650769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5180109-A-G

23650781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5180097-T-G

23650785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5180094-G-A

23650911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5179957-C-T

23651032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5179835-A-G

23651276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5179570-A-G

23651400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5179490-A-T

23651517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5179381-C-T

23651693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5179340-G-A

23652079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5178908-C-G

23652079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5178908-C-T

23653097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5178692-A-G

23653105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5178684-G-A

23653162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5178638-G-A

23653450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5178398-A-G

23653460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5178387-C-T

http://identifiers.org/hco/2/GRCh38#23654547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5177487-C-A

23654547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5177487-C-G

23654547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5177487-C-T

23654663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5177370-A-G

http://identifiers.org/hco/2/GRCh38#23654692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5177341-A-C

23654692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5177341-A-G

23654803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5177229-G-A

http://identifiers.org/hco/2/GRCh38#23654910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5177139-C-A

23655015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5177052-G-A

23655057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5177028-T-C

23655167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5176942-G-A

23655167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5176942-G-C

http://identifiers.org/hco/2/GRCh38#23655194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5176918-A-C

23655214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5176898-C-G

23655214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5176898-C-T

23655268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5176844-C-T

23655320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5176792-C-T

23655403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5176709-C-T

23655502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5176508-A-G

23655528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5176482-A-G

23655729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5176328-G-A

23655745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5176313-G-C

23656120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5176005-G-A

23657143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5174975-A-G

23657293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5174817-T-A

23657793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5174187-C-T

23657962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5174031-G-A

23658067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173967-C-G

23658182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173853-C-T

23658188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173847-C-G

23658231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173806-C-T

23658232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173805-G-A

23658232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173805-G-T

23658263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173778-G-T

23658472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173599-C-G

23658472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173599-C-T

23658474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173590-C-T

23658527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173532-C-T

23658653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173433-C-T

23658917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173222-C-T

23659071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5173068-C-T

23659251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5172889-G-A

23659404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5172747-A-G

23659502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5172658-T-G

23659590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5172604-T-G

23659889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5172358-T-C

23660170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5172078-T-C

23660356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5171918-G-A

23660431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5171840-C-T

http://identifiers.org/hco/2/GRCh38#23661445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5171485-C-A

23661445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5171485-C-T

23661460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5171470-C-T

23661591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5171363-C-T

23661699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5171302-T-G

23661863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5171131-C-G

23661863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5171131-C-T

23662174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5170921-A-G

23662199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5170902-A-T

23662362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5170786-G-C

23662379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5170769-G-T

23662534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5170652-C-T

23662579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5170615-C-T

23662588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5170606-C-T

23662630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5170567-G-T

23662911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5170242-A-G

23664872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5168557-T-G

23665031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5168338-C-G

http://identifiers.org/hco/2/GRCh38#23665465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5167919-C-A

23665465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5167919-C-G

23665479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5167905-G-A

23665541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5167834-T-A

23665978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5167421-A-G

http://identifiers.org/hco/2/GRCh38#23666132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5167276-C-A

23666132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5167276-C-T

23666152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5167258-C-G

23666982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron variant
orthologous variants: 5166640-G-A

23669578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5165577-T-C

http://identifiers.org/hco/2/GRCh38#23669706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5165482-C-A

http://identifiers.org/hco/2/GRCh38#23670092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#5165106-C-A

23670092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5165106-C-T

23670149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5165041-A-G

23670268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5164945-A-G

23670293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164923-G-A

23670293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164923-G-T

23670322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164893-G-A

23670322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164893-G-T

23670461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164768-G-A

23670497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164729-C-T

23670531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164708-A-T

23670812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164466-C-T

23670874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164422-C-T

23670910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164383-T-C

23670937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164356-T-A

23670937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164356-T-C

23670937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164356-T-G

23670945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164348-T-C

23670945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164348-T-G

23671156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164232-T-C

23671194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164194-T-G

23671223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164165-T-C

23671277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164111-C-T

23671346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5164049-C-G

23671440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5163970-G-A

23671440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5163970-G-T

23674002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5161985-C-T

23674219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5161774-T-C

23674239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5161752-G-A

23674239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5161752-G-C

23674239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5161752-G-T

23674402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5161600-T-C

23674579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5161418-C-T

http://identifiers.org/hco/2/GRCh38#23674808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5161223-A-C

23674958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5161080-C-T

23675593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5159746-C-T

http://identifiers.org/hco/2/GRCh38#23676057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5159314-A-C

23677752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5158777-T-C

23677755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5158774-G-A

23678094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5158437-G-A

23678125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5158406-T-A

23678254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5158279-C-T

http://identifiers.org/hco/2/GRCh38#23679085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5157530-A-C

23679156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5157462-G-T

23679176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5157441-C-T

23679362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5157303-A-T

23679437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5157268-G-C

23679439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5157266-G-C

23679911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5156835-G-A

23679927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5156819-G-A

23679967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5156784-G-C

23680469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5156528-T-A

23680621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5156460-G-T

23680984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5156262-C-G

http://identifiers.org/hco/2/GRCh38#23681396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5155859-C-A

23681449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5155806-G-A

23681689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5155599-G-A

23681689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5155599-G-T

23682011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5155202-G-C

23682107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5155112-T-C

23682107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5155112-T-G

23682114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5155101-C-T

23682180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5155021-G-C

23682477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5154724-G-A

23682547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5154655-G-A

23682599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5154619-C-G

23682999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5154353-G-A

23683012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5154334-T-C

23683104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5154190-A-G

23683686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5153562-G-A

23683776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5153463-T-C

23683776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5153463-T-G

23683825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5153414-A-G

http://identifiers.org/hco/2/GRCh38#23684683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5152542-C-A

23684810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5152378-G-A

23684893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5152297-G-C

http://identifiers.org/hco/2/GRCh38#23685183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5152039-C-A

23685595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5151606-G-T

23685845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5151372-A-G

23685871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5151346-G-A

23685871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5151346-G-C

23686544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5150795-G-A

23687032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5150333-T-C

23687188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5150221-G-A

23688670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147972-G-A

23688670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147972-G-T

23688689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147953-T-C

http://identifiers.org/hco/2/GRCh38#23688709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5147946-C-A

23688709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147946-C-T

23688810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147854-T-C

23688972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147702-G-A

23688972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147702-G-T

http://identifiers.org/hco/2/GRCh38#23689020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5147659-C-A

23689020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147659-C-T

23689022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147657-A-G

23689084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147586-G-A

23689135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147544-G-T

23689166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147516-G-A

23689166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147516-G-T

http://identifiers.org/hco/2/GRCh38#23689170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5147512-C-A

23689170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147512-C-T

23689187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147480-G-A

23689223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147448-G-A

23689223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147448-G-T

23689238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147433-G-A

23689255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147426-G-T

http://identifiers.org/hco/2/GRCh38#23689370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5147287-C-A

http://identifiers.org/hco/2/GRCh38#23689397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5147260-C-A

http://identifiers.org/hco/2/GRCh38#23689441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5147216-C-A

23689441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147216-C-T

23689532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147127-G-A

23689532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147127-G-C

http://identifiers.org/hco/2/GRCh38#23689628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5147034-A-C

23689628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147034-A-G

23689628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5147034-A-T

http://identifiers.org/hco/2/GRCh38#23689822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5146812-C-A

23689822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146812-C-G

23689822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146812-C-T

23689850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146785-A-G

23689972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146663-T-C

http://identifiers.org/hco/2/GRCh38#23690087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5146571-C-A

23690087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146571-C-T

23690279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146405-T-C

23690336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146362-A-G

23690396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146306-T-C

http://identifiers.org/hco/2/GRCh38#23690465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5146239-C-A

23690465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146239-C-T

23690531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146174-G-A

23690531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146174-G-T

23690558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146147-A-G

23690640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146078-G-A

23690640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146078-G-C

23690640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146078-G-T

23690659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5146060-A-G

23690956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5145740-G-A

23690956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5145740-G-C

http://identifiers.org/hco/2/GRCh38#23691089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5145605-A-C

23691142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5145551-T-G

23691157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5145534-G-A

23691157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5145534-G-T

23691280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5145412-G-A

23691280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5145412-G-C

23691280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5145412-G-T

23691527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5145163-G-T

23691599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5145091-G-T

23691854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5144837-C-G

http://identifiers.org/hco/2/GRCh38#23691991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5144793-C-A

23692008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5144776-G-A

23692008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5144776-G-T

23692078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5144745-A-G

23692186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5144656-G-C

23692212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5144625-G-A

23692383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5144470-C-T

23692463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5144386-G-A

23692539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5144314-G-C

http://identifiers.org/hco/2/GRCh38#23693150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5143859-C-A

23693150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5143859-C-G

23693150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5143859-C-T

23693159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5143850-G-C

23693159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5143850-G-T

http://identifiers.org/hco/2/GRCh38#23693163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5143846-C-A

23693163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5143846-C-G

23693163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5143846-C-T

http://identifiers.org/hco/2/GRCh38#23693167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5143842-C-A

23693167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5143842-C-G

23693167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5143842-C-T

23693254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5143758-C-G

23693254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5143758-C-T

http://identifiers.org/hco/2/GRCh38#23693263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5143749-C-A

23693334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5143678-G-A

23693870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5143124-G-A

23693870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5143124-G-T

http://identifiers.org/hco/2/GRCh38#23694937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5142048-A-C

23694943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5142042-G-A

23695294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5141692-A-G

23695491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5141547-G-C

23695491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5141547-G-T

http://identifiers.org/hco/2/GRCh38#23695542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5141493-C-A

23695542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5141493-C-T

23695644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5141417-G-A

23695644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5141417-G-T

23695798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5141263-G-A

23695830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5141231-G-A

23695830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5141231-G-C

23695830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5141231-G-T

23695838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5141223-C-T

23695874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5141189-G-A

23695874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5141189-G-C

23695904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5141146-G-A

23695904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5141146-G-T

http://identifiers.org/hco/2/GRCh38#23695937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5141113-C-A

23696169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5140882-G-A

23696169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5140882-G-T

http://identifiers.org/hco/2/GRCh38#23696219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5140831-C-A

23696219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5140831-C-T

http://identifiers.org/hco/2/GRCh38#23696470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5140577-C-A

23696470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5140577-C-G

23696525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5140522-A-G

23696569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5140498-T-C

23697017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5140238-A-G

23697075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5140181-G-A

23697146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5140103-T-C

23697222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5140010-G-A

23697222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5140010-G-T

23697295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139934-C-T

23697322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139901-T-C

23697379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139831-G-A

23697379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139831-G-C

23697393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139816-A-G

23697527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139680-G-A

23697601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139600-G-A

23697601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139600-G-T

23697630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139571-C-T

23697685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139520-G-A

http://identifiers.org/hco/2/GRCh38#23697762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5139442-C-A

23697762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139442-C-G

23697762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139442-C-T

23697766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139438-A-T

23697773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139431-G-A

23697773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139431-G-T

23697804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139399-T-C

23697897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5139302-A-G

23698053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5139147-C-G

23698241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5138936-G-A

23698247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5138930-C-T

23698487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5138707-G-A

23703040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134616-C-T

23703089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134575-G-A

23703089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134575-G-C

23703089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134575-G-T

23703126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134528-T-G

http://identifiers.org/hco/2/GRCh38#23703229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5134442-C-A

23703250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5134421-G-A

23703290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5134381-G-C

23703290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5134381-G-T

23703316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5134355-G-A

23703316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5134355-G-C

http://identifiers.org/hco/2/GRCh38#23703322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5134349-C-A

http://identifiers.org/hco/2/GRCh38#23703411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5134262-C-A

23703411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134262-C-G

23703431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134242-G-A

23703431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134242-G-C

23703431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134242-G-T

23703433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134240-T-C

23703513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134202-T-C

23703513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134202-T-G

http://identifiers.org/hco/2/GRCh38#23703571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5134159-C-A

23703571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134159-C-G

23703571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134159-C-T

23703578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134152-G-T

http://identifiers.org/hco/2/GRCh38#23703594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5134137-C-A

23703594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134137-C-G

http://identifiers.org/hco/2/GRCh38#23703595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5134136-A-C

http://identifiers.org/hco/2/GRCh38#23703707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5134046-C-A

23703707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5134046-C-T

http://identifiers.org/hco/2/GRCh38#23703714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5134039-C-A

23703877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5133882-G-A

http://identifiers.org/hco/2/GRCh38#23703958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5133790-C-A

23703966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5133783-A-G

23703966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5133783-A-T

23703980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5133769-G-A

23704029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5133718-G-C

23705533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5133032-G-C

23706278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5132092-T-C

http://identifiers.org/hco/2/GRCh38#23706407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5131410-C-A

23706407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5131410-C-G

23706407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5131410-C-T

23706518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5131295-G-A

http://identifiers.org/hco/2/GRCh38#23706846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5130968-A-C

23706882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5130915-T-G

http://identifiers.org/hco/2/GRCh38#23707008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5130791-C-A

23707008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5130791-C-G

23707083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5130716-T-A

23707083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5130716-T-C

23707083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5130716-T-G

23707448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5130279-G-T

23707633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5130079-G-A

23707633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5130079-G-T

http://identifiers.org/hco/2/GRCh38#23707932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5129758-C-A

23707932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5129758-C-T

23707998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5129691-G-A

23707998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5129691-G-C

23708235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5129459-A-G

http://identifiers.org/hco/2/GRCh38#23708401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29404
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5129292-C-A