http://identifiers.org/hco/16/GRCh38#22206373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#120442128-C-A

22206373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 120442128-C-T

http://identifiers.org/hco/16/GRCh38#22206375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#120442130-C-A

22206375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 120442130-C-T

http://identifiers.org/hco/16/GRCh38#22206381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#120442136-C-A

22206381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 120442136-C-T

http://identifiers.org/hco/16/GRCh38#22206405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#120442141-C-A

22206405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 120442141-C-T

22206513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 120442185-G-A

22206513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 120442185-G-T

22206518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 120442190-T-C

http://identifiers.org/hco/16/GRCh38#22206621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120442265-A-C

22206621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 120442265-A-G

http://identifiers.org/hco/16/GRCh38#22206622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120442266-C-A

22206650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 120442294-G-A

22206754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120442365-G-T

22206819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120442382-T-C

22206856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120442418-G-A

22207094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120442621-C-T

22207241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120442773-C-G

22207323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120442859-T-A

22207348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120442883-G-C

22207930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120443126-A-G

22216403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 120448292-A-G

22220030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120450715-A-G

22220057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120450742-A-G

22225140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120457067-G-C

22225152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120457079-G-C

22225363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120457286-A-G

22225440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120457348-A-G

22225501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120457425-G-A

22225644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120457557-T-C

22225644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120457557-T-G

22225645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120457558-T-A

22225724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 120457637-A-G

22225825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 120457738-C-T

22225887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 120457800-A-G

22225887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 120457800-A-T

http://identifiers.org/hco/16/GRCh38#22225996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120457899-A-C

22225996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120457899-A-G

22226060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120457959-T-C

22227623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120459094-A-G

22227655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120459118-A-G

22228133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120459173-G-C

22228365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120459447-C-T

22229868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120460845-T-C

22229946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120460946-T-G

http://identifiers.org/hco/16/GRCh38#22230063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120461084-A-C

22232762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120462549-A-G

22232878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120462631-G-A

22233046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120462787-G-A

22233046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120462787-G-T

22234182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120465094-G-A

22234235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120465140-C-T

http://identifiers.org/hco/16/GRCh38#22234256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120465158-A-C

22234266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120465168-C-T

http://identifiers.org/hco/16/GRCh38#22244550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120472467-C-A

22244550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120472467-C-G

22244550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120472467-C-T

22244553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120472470-G-A

22244553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120472470-G-T

22244559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120472476-A-G

http://identifiers.org/hco/16/GRCh38#22248605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120475531-A-C

22248605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120475531-A-G

22248651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120475569-G-T

22248663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120475581-G-A

22248663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120475581-G-T

22248677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120475595-A-G

22248696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120475606-C-T

22248707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120475617-A-G

22248853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120475753-G-A

http://identifiers.org/hco/16/GRCh38#22248888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120475782-C-A

22248948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120475834-G-A

22248948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120475834-G-T

22248977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120475856-T-C

22249068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120475933-C-T

http://identifiers.org/hco/16/GRCh38#22250403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120478807-C-A

http://identifiers.org/hco/16/GRCh38#22250557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120478962-C-A

22250557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120478962-C-T

22250611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120478997-G-A

22250740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479106-G-A

22250790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479157-G-A

22250793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479160-G-A

22250793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479160-G-C

22250793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479160-G-T

http://identifiers.org/hco/16/GRCh38#22250811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120479178-C-A

http://identifiers.org/hco/16/GRCh38#22250825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120479192-C-A

22250825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479192-C-T

22250831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479198-G-A

22250877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479258-G-C

22250942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479318-G-C

22251004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479367-G-A

22251004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479367-G-T

22251021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479402-T-C

22251076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479453-G-T

22251089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120479467-G-C

22251205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 120479582-C-T

22251242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 120479619-G-A

22251295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 120479672-G-T

22254221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120481931-C-T

22254265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120481966-C-T

22254465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120482155-G-A

22254466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120482156-T-C

22254607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120482481-A-G

http://identifiers.org/hco/16/GRCh38#22254665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -A-C

22255331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120483467-G-A

22255331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120483467-G-T

22255376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120483508-C-T

22255483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120483615-A-G

22256598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120483786-T-G

http://identifiers.org/hco/16/GRCh38#22256653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120483816-C-A

22256721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120483851-G-A

22256721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120483851-G-T

22256725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120483855-G-A

22256927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120484073-C-T

http://identifiers.org/hco/16/GRCh38#22256931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120484090-C-A

http://identifiers.org/hco/16/GRCh38#22256933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120484092-C-A

http://identifiers.org/hco/16/GRCh38#22256956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120484172-C-A

22256956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120484172-C-T

22257306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 120484698-C-T

22257455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120484843-C-G

22257455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120484843-C-T

http://identifiers.org/hco/16/GRCh38#22257459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120484847-C-A

22257459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120484847-C-T

22257464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120484852-A-G

http://identifiers.org/hco/16/GRCh38#22257477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120484865-C-A

22257477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120484865-C-T

22257505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120484890-A-G

22257513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120484898-G-T

22257590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120484978-G-A

22257590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120484978-G-T

22257625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120485015-C-G

22257625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 120485015-C-T

22257695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120485085-C-T

22257746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120485136-A-G

22257797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120485187-G-A

22257797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120485187-G-T

22257802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120485191-G-A

22257802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120485191-G-T

22258070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120485424-T-C

22258070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120485424-T-G

22258191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120485537-C-T

22258625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120485940-C-T

22260310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120486868-G-C

22260310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120486868-G-T

22260349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120486906-T-C

22262978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120488282-G-T

22263066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120488370-G-A

22263133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120488436-C-T

22263145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120488448-T-G

22263245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120488547-G-A

http://identifiers.org/hco/16/GRCh38#22263269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120488563-A-C

22263269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120488563-A-G

22263290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120488584-T-A

22263290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120488584-T-C

http://identifiers.org/hco/16/GRCh38#22263307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120488600-A-C

22263307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120488600-A-G

22264850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 120488944-T-C

22264941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489018-C-G

22264953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489030-T-A

http://identifiers.org/hco/16/GRCh38#22264959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120489036-A-C

22264959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489036-A-G

22264960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489037-T-C

22264962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489039-T-A

22264968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489044-G-T

22265071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489124-T-C

22265075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489128-G-A

22265075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489128-G-T

22265080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489133-G-A

22265080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489133-G-T

http://identifiers.org/hco/16/GRCh38#22265132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120489169-C-A

22265142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489179-C-T

http://identifiers.org/hco/16/GRCh38#22265159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120489197-A-C

http://identifiers.org/hco/16/GRCh38#22265187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120489223-C-A

22265208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489246-A-G

22265212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 120489250-T-C

22265267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120489301-T-G

http://identifiers.org/hco/16/GRCh38#22265296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120489911-A-C

http://identifiers.org/hco/16/GRCh38#22265302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120489917-C-A

22265311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120489929-G-T

22265317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120489935-G-A

22265317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120489935-G-T

http://identifiers.org/hco/16/GRCh38#22265323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120489941-C-A

22265323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120489941-C-T

22265339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120489946-C-T

22265356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120489968-T-G

http://identifiers.org/hco/16/GRCh38#22265379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120489991-C-A

22265477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490053-C-G

22265477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490053-C-T

22265480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490056-G-A

22265880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490302-T-A

22266067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490489-G-T

22266079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490512-G-A

22266149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490581-G-A

22266153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490585-T-C

22266247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490663-G-T

22266288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490700-A-T

http://identifiers.org/hco/16/GRCh38#22266343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120490755-C-A

22266343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490755-C-T

22266368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490780-C-G

22266368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490780-C-T

22266374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490803-G-A

22266374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490803-G-T

22266401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: missense variant
orthologous variants: 120490830-G-T

http://identifiers.org/hco/16/GRCh38#22266402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120490831-A-C

22266402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: missense variant
orthologous variants: 120490831-A-G

22266550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120490979-C-G

22266694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: missense variant
orthologous variants: 120491094-C-G

22266694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: synonymous variant
orthologous variants: 120491094-C-T

22267037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120491932-C-T

22267070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120491952-C-T

22267611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120492188-T-A

22267611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120492188-T-G

22267667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120492213-G-C

22267887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120492464-C-T

http://identifiers.org/hco/16/GRCh38#22273501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120494276-C-A

22273501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120494276-C-T

22273588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120494371-T-C

http://identifiers.org/hco/16/GRCh38#22273591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120494374-A-C

22273591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120494374-A-G

22278422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120496940-T-G

22278488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120496998-G-A

22278547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120497049-A-G

http://identifiers.org/hco/16/GRCh38#22278563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120497073-C-A

22278666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120497144-C-T

22278764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120497238-G-A

22279717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120498047-G-A

http://identifiers.org/hco/16/GRCh38#22279778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120498106-C-A

22279779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120498107-G-A

22279793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120498142-G-A

22280073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron_variant, undefined
orthologous variants: 120498450-A-G

22280096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120498473-C-T

22280100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120498477-G-A

22280100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120498477-G-T

22280126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120498520-G-A

22280126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120498520-G-T

22280155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron_variant, undefined
orthologous variants: 120498550-T-C

22280161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron_variant, undefined
orthologous variants: 120498556-G-T

22280300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: synonymous_variant, undefined
orthologous variants: 120498693-G-A

22280349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: missense variant
orthologous variants: 120498742-G-A

22280349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: missense variant
orthologous variants: 120498742-G-C

22280349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: missense variant
orthologous variants: 120498742-G-T

22280544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120498927-A-G

22283808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: intron variant
orthologous variants: 120502432-G-A

http://identifiers.org/hco/16/GRCh38#22283891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120502509-C-A

22283891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: synonymous variant
orthologous variants: 120502509-C-T

22283966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: synonymous variant
orthologous variants: 120502584-T-C

22284040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120502654-A-G

http://identifiers.org/hco/16/GRCh38#22284140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120502735-C-A

22284215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120502799-G-A

22284215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120502799-G-T

22284219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120502803-G-T

22284274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120502838-T-C

22284274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120502838-T-G

http://identifiers.org/hco/16/GRCh38#22284366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120502848-C-A

22284366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120502848-C-T

22284367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120502849-G-A

22284374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120502856-G-A

22284374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120502856-G-T

http://identifiers.org/hco/16/GRCh38#22284715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120502966-C-A

22284849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120503046-G-A

22284849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120503046-G-T

22284862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120503070-G-T

http://identifiers.org/hco/16/GRCh38#22285070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120503262-C-A

http://identifiers.org/hco/16/GRCh38#22285110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120503301-C-A

22285110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120503301-C-T

22285187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120503375-A-G

22285188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120503376-G-A

22285234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120503429-G-T

22285697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3 prime UTR variant
orthologous variants: 120503734-A-G

http://identifiers.org/hco/16/GRCh38#22286851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#120504745-C-A

22286872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120504769-G-A

22286872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120504769-G-T

22286884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120504781-C-T

22286898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120504794-A-G

22286961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120504849-G-A

22286961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120504849-G-T

22287012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120504899-T-C

22287176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505263-G-A

22287176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505263-G-C

22287176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505263-G-T

22287221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120505295-G-T

22287233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120505311-T-A

22287233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120505311-T-C

22287241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505319-G-A

22287241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505319-G-T

22287257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505335-C-G

22287300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505385-C-G

22287300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505385-C-T

22287322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505407-T-C

22287399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505475-A-T

22287440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505535-A-G

22287491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505574-G-A

22287614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505676-G-A

22287614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505676-G-T

22287617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120505679-G-A

22288466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120505923-T-C

22288546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120506017-G-T

22288547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120506018-G-T

22288553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120506024-A-G

22288567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24615
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120506037-G-T