121712803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123214395-G-A

121712803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123214395-G-T

121712858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123214452-G-A

121712858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123214452-G-C

121712858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123214452-G-T

121712907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 123214501-G-A

121712907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 123214501-G-T

121713175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123214759-C-G

121714139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123215625-G-A

121714139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123215625-G-T

121715430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123215973-T-G

121715478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123216030-G-A

121716930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123218063-T-C

121717059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123218184-G-T

121717374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123218471-C-T

http://identifiers.org/hco/12/GRCh38#121718344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123220138-C-A

121718344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123220138-C-T

121718616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123220348-C-G

121720951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123221996-G-A

121720971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123222016-A-G

121720971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123222016-A-T

121721004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123222047-C-T

121721038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123222082-C-T

121721059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123222095-C-G

121721136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123222165-C-T

121721169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123222200-G-A

121721169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123222200-G-T

121725249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123224178-C-T

121726963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123225837-G-A

121726978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123225852-A-T

121727162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123226059-G-A

121728664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123226580-G-T

121728685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123226600-C-T

http://identifiers.org/hco/12/GRCh38#121728822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123226717-A-C

121728824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123226719-G-C

121728848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123226737-G-C

121728850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123226739-C-T

121728961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123226844-C-T

http://identifiers.org/hco/12/GRCh38#121729046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123226928-C-A

121729220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123227090-C-T

http://identifiers.org/hco/12/GRCh38#121738283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123231303-A-C

121738393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123231404-G-T

121738468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123231480-G-A

121741796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123233074-C-T

http://identifiers.org/hco/12/GRCh38#121742006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#123233268-C-A

121742040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123233302-T-C

http://identifiers.org/hco/12/GRCh38#121743604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123236213-C-A

121743797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123236582-T-C

121743797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123236582-T-G

121743861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123236654-T-C

121745188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123237011-C-G

121745188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123237011-C-T

121745208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123237031-C-T

121745212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123237035-G-A

121748355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 123237929-C-G

121748355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 123237929-C-T

121748359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 123237933-G-C

121748545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123238078-G-A

121748545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123238078-G-C

121748545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123238078-G-T

121748691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123238226-C-T

121749162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123238715-G-A

121749331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123238882-C-G

http://identifiers.org/hco/12/GRCh38#121749914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123239289-A-C

http://identifiers.org/hco/12/GRCh38#121749916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123239291-A-C

http://identifiers.org/hco/12/GRCh38#121749919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123239294-A-C

121750167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123239478-A-G

121751513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123239796-A-G

121752003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123240220-T-C

121752003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123240220-T-G

http://identifiers.org/hco/12/GRCh38#121752103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123240293-C-A

121752103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123240293-C-T

121752179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123240368-C-T

121752194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123240383-C-G

121752194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123240383-C-T

http://identifiers.org/hco/12/GRCh38#121752310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123240484-C-A

121752335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123240503-A-G

121752336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123240504-T-G

121752339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123240507-T-C

http://identifiers.org/hco/12/GRCh38#121752361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123240529-C-A

121752361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123240529-C-T

121752418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123240585-G-A

121753898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123241567-G-A

121754171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123241822-T-G

121754334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123241991-C-T

121754345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123242008-C-T

121754405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123242072-C-T

http://identifiers.org/hco/12/GRCh38#121754434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123242101-A-C

121761453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123242359-A-G

121761562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123242422-T-C

http://identifiers.org/hco/12/GRCh38#121761569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123242429-C-A

121761569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123242429-C-T

121761571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123242431-G-A

121761571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123242431-G-T

121761652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123242488-G-T

121761721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123242557-C-T

http://identifiers.org/hco/12/GRCh38#121761730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123242566-C-A

121761730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 123242566-C-G

121761730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123242566-C-T

http://identifiers.org/hco/12/GRCh38#121761750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123242586-C-A

121761754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123242590-G-A

http://identifiers.org/hco/12/GRCh38#121761769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123242605-C-A

http://identifiers.org/hco/12/GRCh38#121761868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123242639-C-A

121761868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123242639-C-G

121764857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123246213-G-A

121765001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123246317-C-T

121765090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123246389-A-G

121765182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123246496-T-A

http://identifiers.org/hco/12/GRCh38#121765818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#123247016-C-A

121765978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123247191-G-A

http://identifiers.org/hco/12/GRCh38#121766054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123247268-C-A

http://identifiers.org/hco/12/GRCh38#121766336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123247526-C-A

121766753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123247825-A-G

http://identifiers.org/hco/12/GRCh38#121766786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123247857-A-C

121766792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123247863-G-A

121767481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123248201-T-A

121767482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123248202-G-A

http://identifiers.org/hco/12/GRCh38#121767779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123248476-A-C

121767802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123248499-A-G

121768619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123249547-A-G

121768825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123249733-C-T

121769982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123251431-G-A

http://identifiers.org/hco/12/GRCh38#121770054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123251492-C-A

121770054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123251492-C-T

121770229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123251664-A-G

121770246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123251682-G-A

121770359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123251770-C-G

121770382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123251788-T-C

121770400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123251803-C-T

121770401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123251804-G-A

121770401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123251804-G-C

121770402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123251805-G-A

121770425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123251824-T-G

121770632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123251923-G-A

121770697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123251988-G-C

121770735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252026-C-T

121770755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252045-G-A

121770755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252045-G-T

121770757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252047-G-A

121770757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252047-G-T

http://identifiers.org/hco/12/GRCh38#121770767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123252050-A-C

121770767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252050-A-G

121770780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252062-G-A

121770780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252062-G-T

121770833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252097-G-A

121771014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252265-T-C

121771020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252271-C-G

121771046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252297-T-C

121771062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252315-G-A

121771062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252315-G-C

121771062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252315-G-T

http://identifiers.org/hco/12/GRCh38#121771340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123252514-A-C

121771431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252565-A-G

121771450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252584-G-A

121771594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123252735-T-A

http://identifiers.org/hco/12/GRCh38#121773315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#123253064-C-A

121773315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123253064-C-T

http://identifiers.org/hco/12/GRCh38#121773333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#123253088-C-A

121773333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123253088-C-G

121773357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123253109-G-A

121773357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123253109-G-C

121773357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123253109-G-T

121773406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123253148-G-A

http://identifiers.org/hco/12/GRCh38#121773586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#123253321-C-A

121773586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123253321-C-G

http://identifiers.org/hco/12/GRCh38#121773605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123253335-C-A

http://identifiers.org/hco/12/GRCh38#121773613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123253343-C-A

121773613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123253343-C-G

121773613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123253343-C-T

121773658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123253387-G-A

121773658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123253387-G-T

121774823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123253958-G-A

121774823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123253958-G-T

121774840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123253975-G-A

121774849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123254002-G-A

121774849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123254002-G-C

121774849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123254002-G-T

http://identifiers.org/hco/12/GRCh38#121774863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123254016-C-A

121774863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123254016-C-T

121774928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123254129-A-G

121774933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123254130-G-A

121774933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123254130-G-T

121775024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123254226-G-C

121775043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123254244-C-G

121775043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123254244-C-T

121775082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant, undefined
orthologous variants: 123254285-C-G

121775082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant, undefined
orthologous variants: 123254285-C-T

121775359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 123254459-G-A

121775416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123254507-C-T

121775417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123254508-G-A

121775518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123254605-G-A

121775518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123254605-G-T

121775529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 123254618-C-T

http://identifiers.org/hco/12/GRCh38#121775727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123254826-C-A

121775727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123254826-C-G

121775727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123254826-C-T

121775775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123254890-G-T

121775852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 123254974-A-G

121775859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123254981-T-A

121775859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 123254981-T-C

http://identifiers.org/hco/12/GRCh38#121775912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123255043-C-A

121775912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123255043-C-G

121775912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123255043-C-T

http://identifiers.org/hco/12/GRCh38#121775923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123255054-C-A

121775923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123255054-C-G

121775923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123255054-C-T

http://identifiers.org/hco/12/GRCh38#121775939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123255071-C-A

121775939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123255071-C-G

121775950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123255082-G-A

http://identifiers.org/hco/12/GRCh38#121775961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123255093-C-A

121775961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123255093-C-T

121775980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123255117-G-A

121775984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123255121-C-T

121775988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123255125-G-A

121776036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123255177-T-C

http://identifiers.org/hco/12/GRCh38#121776039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123255180-C-A

121776088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 123255228-G-C

121776088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 123255228-G-T

121776180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 123255323-T-C

http://identifiers.org/hco/12/GRCh38#121776217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#123255357-C-A

121776402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123255571-A-G

121776402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123255571-A-T

http://identifiers.org/hco/12/GRCh38#121776431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#123255590-C-A

121776431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123255590-C-T

121776481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123255654-T-C

121776481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123255654-T-G

121776530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123255707-G-A

121776530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123255707-G-T

121776551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123255733-G-A

121776686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123255821-T-A

121776757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123255867-T-C

121776758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123255868-G-A

121776758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123255868-G-T

http://identifiers.org/hco/12/GRCh38#121777554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123256052-C-A

121777554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123256052-C-T

http://identifiers.org/hco/12/GRCh38#121777558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123256056-C-A

121777558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123256056-C-T

http://identifiers.org/hco/12/GRCh38#121777590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123256109-C-A

121777590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123256109-C-T

121777616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123256139-G-T

121777735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 123256232-A-G

http://identifiers.org/hco/12/GRCh38#121777846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123256342-C-A

121777846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123256342-C-G

121777859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123256355-G-A

121778625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123256671-T-C

121778677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123256719-G-T

121778806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123256845-G-T

http://identifiers.org/hco/12/GRCh38#121778947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123256984-C-A

121778947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123256984-C-T

http://identifiers.org/hco/12/GRCh38#121779065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123257100-A-C

121779098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123257133-A-G

121779141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123257171-T-G

121779151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123257183-A-G

http://identifiers.org/hco/12/GRCh38#121779192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123257228-A-C

http://identifiers.org/hco/12/GRCh38#121779371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123257404-C-A

121779371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123257404-C-G

121779371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123257404-C-T

121779384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123257413-G-A

121779384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123257413-G-C

121779384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123257413-G-T

121779452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123257449-G-A

121779452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123257449-G-T

http://identifiers.org/hco/12/GRCh38#121779537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123257532-C-A

121779537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123257532-C-G

121779537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123257532-C-T

121779632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123257627-C-G

http://identifiers.org/hco/12/GRCh38#121779633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123257628-A-C

121779633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123257628-A-G

121779875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123257858-A-G

http://identifiers.org/hco/12/GRCh38#121779918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123257907-C-A

121779918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123257907-C-G

121779918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123257907-C-T

121780851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123258334-A-G

121780852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123258335-G-A

121780852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123258335-G-T

121780980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 123258467-G-T

121781054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123258544-G-T

121781101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123258592-G-A

121781163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123258654-G-T

121781227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123258721-C-T

121781252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123258758-G-A

121781252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123258758-G-T

121781253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123258759-T-G