43650284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118037056-G-T

43650316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, undefined
orthologous variants: 118037022-T-G

43650384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118036956-G-T

43650572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118036770-A-G

43650622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118036724-A-G

http://identifiers.org/hco/1/GRCh38#43650788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118036564-C-A

43651298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118036057-T-A

43651298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118036057-T-C

43651329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118036026-A-G

43651573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118035798-C-T

43651843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118035566-C-T

43652089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118035361-G-A

43653151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 5 prime UTR variant
orthologous variants: 118034756-A-G

43653169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 5 prime UTR variant
orthologous variants: 118034734-A-G

43653171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 5 prime UTR variant
orthologous variants: 118034732-G-A

http://identifiers.org/hco/1/GRCh38#43653443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118034391-C-A

43653558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118034272-T-C

43653558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118034272-T-G

43653594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118034260-G-T

43653597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118034257-T-A

43653597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118034257-T-C

43653710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 118034157-T-C

43653766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 118034103-T-C

43653921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033951-G-A

43653955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033919-T-G

43653957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033917-T-C

43653989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033889-A-G

43655277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033186-T-A

43655285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033178-G-A

43655304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033167-A-G

43655458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033048-G-A

43655461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033045-A-T

http://identifiers.org/hco/1/GRCh38#43655462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118033044-A-C

43655467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033039-G-A

43655467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033039-G-T

43655481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118033025-A-G

http://identifiers.org/hco/1/GRCh38#43655511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118032995-C-A

43655511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032995-C-T

43655543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032962-G-A

43655877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032205-G-A

43655877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032205-G-T

43655889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032193-G-A

43655889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032193-G-T

http://identifiers.org/hco/1/GRCh38#43655890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118032192-C-A

43655890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032192-C-G

43655890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032192-C-T

43655892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032190-G-A

43655892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032190-G-C

43655892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032190-G-T

43655895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032187-T-A

43655895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032187-T-C

43655895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032187-T-G

http://identifiers.org/hco/1/GRCh38#43655896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118032186-C-A

43655896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032186-C-G

43655896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032186-C-T

http://identifiers.org/hco/1/GRCh38#43655918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118032164-A-C

43655929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118032154-C-T

43655964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118031317-G-C

http://identifiers.org/hco/1/GRCh38#43657562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118029862-A-C

43657616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118029814-C-G

43659902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118028984-T-C

43659911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118028975-C-G

http://identifiers.org/hco/1/GRCh38#43660200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118027562-C-A

43660200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118027562-C-T

43660308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 118027221-C-G

http://identifiers.org/hco/1/GRCh38#43660543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118027018-C-A

43660543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118027018-C-T

43660564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118026998-A-G

43660827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118026727-T-C

43660827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118026727-T-G

43662878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118025788-G-A

43662878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118025788-G-C

43662933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 118025734-C-G

43662933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 118025734-C-T

http://identifiers.org/hco/1/GRCh38#43665612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118023710-C-A

43665612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118023710-C-T

http://identifiers.org/hco/1/GRCh38#43665655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118023669-C-A

43665655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118023669-C-G

43665655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118023669-C-T

43665683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118023642-C-T

43665844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118023487-G-T

43665913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118023401-T-C

43666049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118023262-A-G

43666216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118023034-G-A

43666353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118022249-T-A

43666353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118022249-T-G

43666418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118022177-C-T

43666421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118022174-T-C

43666424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118022171-G-A

43666432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118022162-G-A

43666432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118022162-G-T

43666566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118022028-G-A

43666646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118021937-G-T

43666648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118021935-G-T

43666822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118021849-G-T

43666823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118021848-A-G

http://identifiers.org/hco/1/GRCh38#43666858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118021815-C-A

43666858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118021815-C-T

http://identifiers.org/hco/1/GRCh38#43666872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118021801-C-A

43666872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118021801-C-T

43666882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118021791-G-A

43666899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118021769-A-G

http://identifiers.org/hco/1/GRCh38#43666903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118021765-C-A

43666903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118021765-C-G

43666914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118021751-T-C

43667117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118021559-A-G

43667176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118021511-T-C

43667176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118021511-T-G

43667709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118019906-G-A

43667709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118019906-G-T

43667856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: missense variant
orthologous variants: 118019753-G-A

43667988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: missense variant
orthologous variants: 118019621-G-C

http://identifiers.org/hco/1/GRCh38#43669005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118019146-C-A

43669005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118019146-C-T

43669022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118019129-T-G

43669023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118019128-G-A

43669023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118019128-G-T

43669266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: missense variant
orthologous variants: 118018883-G-C

43669266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: missense variant
orthologous variants: 118018883-G-T

43669340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118018808-A-G

http://identifiers.org/hco/1/GRCh38#43669361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118018787-C-A

43669409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118018759-G-A

43669409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118018759-G-T

43669937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118018304-G-A

43670283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118018073-G-A

43671360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017834-T-C

43671372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017820-T-C

43671372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017820-T-G

43671381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017813-G-A

43671381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017813-G-T

http://identifiers.org/hco/1/GRCh38#43671404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118017789-C-A

43671404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017789-C-T

http://identifiers.org/hco/1/GRCh38#43671405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118017788-C-A

43671405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017788-C-T

http://identifiers.org/hco/1/GRCh38#43671411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118017782-C-A

43671411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017782-C-G

43671411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017782-C-T

43671419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017774-G-A

43671618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: missense variant
orthologous variants: 118017586-G-A

43671621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: missense variant
orthologous variants: 118017583-T-C

43671636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: missense variant
orthologous variants: 118017568-C-T

43671793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: missense variant
orthologous variants: 118017411-A-G

43671880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017324-G-A

43671938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017295-G-A

43671938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017295-G-C

43671947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118017286-T-A

43672881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118016616-G-A

43673071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118016424-G-T

43673151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118016348-G-T

http://identifiers.org/hco/1/GRCh38#43673614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118014672-C-A

43673766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118014547-C-T

43679500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118012970-A-G

43683188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118011233-C-T

43683544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118010933-G-A

43683544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118010933-G-C

43683544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118010933-G-T

43683553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118010924-T-G

43683738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: missense variant
orthologous variants: 118010451-C-T

43683829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118010360-G-A

http://identifiers.org/hco/1/GRCh38#43683855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118010333-C-A

43683856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118010332-T-C

43683909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118010286-G-A

43683909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118010286-G-T

http://identifiers.org/hco/1/GRCh38#43683934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118010272-A-C

43683934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118010272-A-G

43684419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118010011-C-G

43684570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118009976-G-A

43684629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118009941-G-A

43684629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118009941-G-C

43684681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118009912-C-T

http://identifiers.org/hco/1/GRCh38#43684913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118009747-A-C

43684913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118009747-A-G

43684949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118009711-G-A

43685061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron variant
orthologous variants: 118009592-T-C

43685151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118009512-A-T

43685475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118009086-A-G

43685519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118009042-A-G

43685541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118009021-G-T

43685542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118009020-G-A

43685577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118008992-G-A

43686427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118008270-C-T

43686584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118008085-G-A

43687641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118007233-C-T

43687792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118007086-G-A

43687798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118007080-A-T

43687813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118007065-C-T

43688199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118006755-A-G

http://identifiers.org/hco/1/GRCh38#43688780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118006187-C-A

43688780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118006187-C-T

http://identifiers.org/hco/1/GRCh38#43688817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118006156-C-A

43688817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118006156-C-G

43688829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118006144-G-A

43688829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118006144-G-T

43689165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118005811-T-C

43689170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118005806-A-G

43689440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118005583-T-C

43690001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118005023-C-T

43690815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118004434-C-T

43690980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118004262-C-G

43690983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118004259-T-C

43691120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118004149-C-T

43691166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118004097-G-T

43691175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118004088-G-C

43691175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118004088-G-T

http://identifiers.org/hco/1/GRCh38#43691180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118004083-C-A

43691887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003506-T-C

http://identifiers.org/hco/1/GRCh38#43692105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118003459-C-A

http://identifiers.org/hco/1/GRCh38#43692175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118003405-C-A

43692175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003405-C-G

43692175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003405-C-T

43692221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003361-T-C

43692351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003241-G-A

43692399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003198-A-G

43692432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003165-G-A

43692432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003165-G-T

43692818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118002500-T-C

43692870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118002449-T-C

43692982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118002339-A-G

43692993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118002328-C-T

43693086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118002255-T-G

http://identifiers.org/hco/1/GRCh38#43693097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118002219-A-C

43693193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118002126-T-G

http://identifiers.org/hco/1/GRCh38#43693945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118001711-C-A

43693945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001711-C-G

43693945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001711-C-T

http://identifiers.org/hco/1/GRCh38#43694133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118001531-C-A

43694133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001531-C-G

43694133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001531-C-T

43694141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001523-A-G

43694176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001500-A-G

43694566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001428-T-C

43694591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001400-T-A

43694591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001400-T-C

http://identifiers.org/hco/1/GRCh38#43694651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118001337-C-A

43694651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001337-C-G

43694651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001337-C-T

http://identifiers.org/hco/1/GRCh38#43694674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118001314-C-A

43694674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001314-C-G

43694743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 118001245-C-G

43694871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 118001117-C-T

43694921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001069-C-T

43694982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001010-T-C

http://identifiers.org/hco/1/GRCh38#43695631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118000507-C-A

43697433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000172-C-G

43697440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000167-T-C

http://identifiers.org/hco/1/GRCh38#43697453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#118000154-A-C

43697679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117999866-G-A

43697740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117999813-T-C

43697740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117999813-T-G

http://identifiers.org/hco/1/GRCh38#43697800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#117999782-C-A

43697800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117999782-C-T

43698064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117999526-T-C

43698085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117999502-T-C

43703261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996519-T-C

43703261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996519-T-G

43703413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117996376-T-A

43703413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117996376-T-C

43703413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117996376-T-G

43703521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117996280-T-C

43703756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996038-T-A

43704204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117995591-C-T

43704314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117995481-T-C

43704457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 117995326-T-A

43704457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 117995326-T-C

http://identifiers.org/hco/1/GRCh38#43704501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#117995282-C-A

43704501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117995282-C-T

http://identifiers.org/hco/1/GRCh38#43704554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#117995231-C-A

43704554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117995231-C-T

43704581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117995204-T-A

43704581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117995204-T-C

http://identifiers.org/hco/1/GRCh38#43704666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#117995122-C-A

43704698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117995096-T-C

43704698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117995096-T-G

43704791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117994881-G-A

43704791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117994881-G-T

43704864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117994806-T-C

43704959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117994713-T-C

http://identifiers.org/hco/1/GRCh38#43704965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#117994707-C-A

43704965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117994707-C-T

43704973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117994699-G-T

43704979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117994693-G-T

43705211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117994469-A-G

43705293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117994362-G-A

43705293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117994362-G-C

43705293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22978
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117994362-G-T