http://identifiers.org/hco/17/GRCh38#60041322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83674549-A-C

60041365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83674507-C-T

60041474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83674409-G-A

60041485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83674398-G-C

60041606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83674298-G-A

60041656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83674253-G-C

http://identifiers.org/hco/17/GRCh38#60041707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83674201-C-A

60041809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83674083-C-G

60041971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83673417-C-T

60042275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83673180-G-A

http://identifiers.org/hco/17/GRCh38#60042313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83673149-C-A

60042313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83673149-C-T

60043261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83672822-A-G

60043276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83672807-G-A

60043276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83672807-G-C

60043276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83672807-G-T

http://identifiers.org/hco/17/GRCh38#60043287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83672796-C-A

60043287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83672796-C-T

60043405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83672699-G-A

60043405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83672699-G-C

60043405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83672699-G-T

60043486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83672620-G-T

60043493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83672613-C-T

60043495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83672611-C-T

60043546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3 prime UTR variant
orthologous variants: 83672563-A-G

60043582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83672527-G-A

60043587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 83672522-T-G

60043595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 83672514-G-A

60043595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83672514-G-T

60043709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83672400-T-C

60043709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83672400-T-G

60043789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83672320-A-G

60044017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83672092-T-A

60044017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83672092-T-C

60044095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83672014-G-A

60044131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83671978-G-C

60044177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83671932-A-G

60044220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83671892-A-G

60044225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83671886-T-A

60044445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83671491-C-T

http://identifiers.org/hco/17/GRCh38#60044533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83671417-C-A

http://identifiers.org/hco/17/GRCh38#60044643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83671308-C-A

60044840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83671144-T-C

60044911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83671108-C-T

60045651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83670744-A-G

60045664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83670731-T-A

60045736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83670662-T-C

60045876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83670558-T-G

http://identifiers.org/hco/17/GRCh38#60045939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83670518-C-A

60045939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83670518-C-T

60045941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83670516-T-A

60045941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83670516-T-C

60045948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83670509-A-G

60046015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83670439-A-G

60046126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83670328-T-C

60046180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83670274-T-C

60046238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83670215-A-T

60046239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83670214-A-T

60047456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83669619-T-C

60047464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83669611-T-C

60047506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83669566-A-G

60047553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83669525-T-C

60047775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83669141-C-T

60048147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83668301-G-T

60048186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83668262-T-C

60048194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83668254-G-T

60048207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83668241-T-A

60048207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83668241-T-C

60048207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83668241-T-G

60048229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83668224-G-A

60048229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83668224-G-T

60048427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83668028-G-A

http://identifiers.org/hco/17/GRCh38#60048429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83668026-C-A

60048429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83668026-C-G

http://identifiers.org/hco/17/GRCh38#60048707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83667874-C-A

60048707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667874-C-G

60048707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667874-C-T

http://identifiers.org/hco/17/GRCh38#60048736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83667846-A-C

60048736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667846-A-G

60048915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667754-T-C

60049520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667612-A-G

60049530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667600-G-A

60049530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667600-G-T

60049563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667577-A-G

60049716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667423-G-A

60049777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667360-A-G

http://identifiers.org/hco/17/GRCh38#60049779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83667358-A-C

60049779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667358-A-G

60049801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667350-T-C

60049818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667333-T-C

60049822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667329-G-A

60049822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667329-G-C

60049822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667329-G-T

60049830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667321-G-A

60049865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667290-C-T

60050150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83667035-G-A

60050643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83666828-G-T

60050646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83666825-G-A

60050692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83666794-T-C

60050693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83666793-G-A

60050693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83666793-G-C

60050693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83666793-G-T

60050707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83666789-T-C

60050722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83666775-G-A

60050722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83666775-G-T

60050734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83666763-C-T

60050735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83666762-C-G

60050735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83666762-C-T

http://identifiers.org/hco/17/GRCh38#60050761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83666737-C-A

60050886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83666616-T-A

60050886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83666616-T-G

60050898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83666604-G-A

60050898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83666604-G-T

http://identifiers.org/hco/17/GRCh38#60050984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83666518-C-A

60050984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 83666518-C-T

60051198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83665948-C-T

60055416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83665415-G-T

http://identifiers.org/hco/17/GRCh38#60055424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83665407-C-A

http://identifiers.org/hco/17/GRCh38#60055425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83665406-A-C

60055425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83665406-A-G

60055430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83665401-A-G

60055436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83665395-T-C

60055540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83665307-G-A

60055540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83665307-G-C

60055541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83665306-G-C

60055581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 83665266-T-C

60055581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 83665266-T-G

http://identifiers.org/hco/17/GRCh38#60055606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83665241-C-A

60055620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83665226-A-G

http://identifiers.org/hco/17/GRCh38#60055635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83665207-C-A

60055635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83665207-C-T

60055637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83665205-G-A

60055637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83665205-G-T

60056122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83664809-C-G

60056122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83664809-C-T

60056252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83664681-T-C

http://identifiers.org/hco/17/GRCh38#60056287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83664649-C-A

60056287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83664649-C-T

60056288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83664648-A-G

60056310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83664628-T-C

http://identifiers.org/hco/17/GRCh38#60056315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83664623-C-A

60056366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83664577-A-T

60056415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83664546-T-C

60056822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83663582-A-G

60056830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83663574-C-G

60057122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83663350-A-G

60057122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83663350-A-T

60057203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83663269-T-C

60057298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83663174-C-G

60057298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83663174-C-T

60057474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83663001-G-C

60057507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83662969-T-C

http://identifiers.org/hco/17/GRCh38#60057551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83662936-C-A

60057551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83662936-C-T

60058512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83661741-T-C

60058657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83661610-C-T

60058771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83661483-C-G

60058912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83661347-G-C

60059055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83661193-C-T

60059056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83661192-G-A

60059071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83661177-T-C

http://identifiers.org/hco/17/GRCh38#60059273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83660904-C-A

60059273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83660904-C-G

60059273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83660904-C-T

60059282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83660895-A-G

60059288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83660889-G-T

60059316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83660868-T-G

http://identifiers.org/hco/17/GRCh38#60059834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83660132-A-C

60059834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83660132-A-T

60059851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83660109-C-T

60060121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83659855-T-C

60060129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83659847-T-A

60060186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83659792-A-G

60060221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83659759-A-T

60060302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83659731-C-G

60060302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83659731-C-T

60060515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83659650-C-T

60060538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83659628-G-C

60060538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83659628-G-T

http://identifiers.org/hco/17/GRCh38#60065340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83658858-A-C

60065503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83658702-T-C

60065829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83658398-T-C

60065845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83658385-A-G

60066402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 83657893-G-A

60066404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 83657891-A-G

60066429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83657866-A-G

60066691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83657641-G-A

60066691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83657641-G-T

60066785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83657557-G-A

60067320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83657092-T-A

60067320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83657092-T-C

60067321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83657091-G-A

60067321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83657091-G-T

http://identifiers.org/hco/17/GRCh38#60067323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83657089-C-A

60067323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83657089-C-G

http://identifiers.org/hco/17/GRCh38#60067324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83657088-C-A

60067357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83657057-T-G

60067394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83657024-T-C

60067414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83657004-A-G

60067581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 83656837-A-T

60067599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 83656819-G-A

http://identifiers.org/hco/17/GRCh38#60067660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83656758-C-A

60067743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83656666-G-A

60067743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83656666-G-C

60067772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83656563-T-A

60067842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83656490-T-C

60067856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83656476-A-G

60067891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83656443-C-T

60069221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83656275-G-A

60069272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83656244-C-T

http://identifiers.org/hco/17/GRCh38#60069483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83656073-A-C

60069580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83655983-G-A

60069580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83655983-G-T

60069597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83655966-G-T

60069615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83655948-G-T

60069652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83655911-A-G

60069677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83655881-G-T

60069730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 83655828-C-T

60069757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 83655801-G-A

60069856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 83655702-T-C

60069856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 83655702-T-G

http://identifiers.org/hco/17/GRCh38#60069873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83655685-C-A

60069909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83655672-A-G

http://identifiers.org/hco/17/GRCh38#60069950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83655656-C-A

60069963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83655643-G-A

60070022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83655517-G-A

60070022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83655517-G-C

60070655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83651873-T-A

60070687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83651842-A-G

60070687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83651842-A-T

60070690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83651840-T-C

60070715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 83651815-A-G

60070854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83651672-T-C

60070896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83651644-G-A

60070896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83651644-G-T

http://identifiers.org/hco/17/GRCh38#60070952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83651605-C-A

60071087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83651468-G-A

60071315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83651102-G-A

60071352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83651066-T-C

60071668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650759-A-G

60071942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650548-T-C

60071942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650548-T-G

60072028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650456-A-G

60072082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650402-G-T

http://identifiers.org/hco/17/GRCh38#60072176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83650282-C-A

60072244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83650213-A-G

60072343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650113-G-A

60072343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650113-G-C

60072343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650113-G-T

http://identifiers.org/hco/17/GRCh38#60072375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83650087-A-C

60072375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650087-A-G

60072375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650087-A-T

60072382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650080-T-A

60072382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650080-T-C

60072382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650080-T-G

60072405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650057-G-A

60072405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650057-G-T

http://identifiers.org/hco/17/GRCh38#60072450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83650013-C-A

60072451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650012-T-A

60072451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83650012-T-C

60072739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83649716-T-C

60072897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83649591-A-G

60073026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 83649489-T-C

60073055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 83649463-A-T

60073132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83649256-T-C

60073253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 83649139-G-A

http://identifiers.org/hco/17/GRCh38#60073297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83649095-C-A

60073297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83649095-C-T

60073361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83649040-T-C

60073399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83649002-G-A

60073399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83649002-G-T

http://identifiers.org/hco/17/GRCh38#60073415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83648987-C-A

60073415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83648987-C-T

60073579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83648848-C-T

60073658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83648757-A-T

60073668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83648747-T-C

60073780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83648240-G-A

60073780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83648240-G-C

60073834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83648186-G-C

http://identifiers.org/hco/17/GRCh38#60073895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83648125-A-C

60073895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 83648125-A-G

60074099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 83648021-A-G

60074112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 83648002-T-C

60074159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 83647957-G-A

60074159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 83647957-G-T

http://identifiers.org/hco/17/GRCh38#60074208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83647903-A-C

60074210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83647901-T-C

http://identifiers.org/hco/17/GRCh38#60074237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83647874-A-C

60074383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83647725-T-A

60074384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83647724-A-T

http://identifiers.org/hco/17/GRCh38#60074513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83647590-C-A

60075419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83647427-T-C

60075488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83647342-A-T

60075508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83647321-G-C

60075863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83647138-T-A

60075863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83647138-T-G

60075885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83647115-T-A

60075900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83647100-G-A

60075900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83647100-G-T

60076000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83647014-T-C

60076053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83646691-A-G

60076053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83646691-A-T

60076253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83646518-A-G

60076253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83646518-A-T

http://identifiers.org/hco/17/GRCh38#60076266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83646501-A-C

60076266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83646501-A-G

60076287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83646480-G-A

60076287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83646480-G-C

60076287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83646480-G-T

http://identifiers.org/hco/17/GRCh38#60076398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83646409-C-A

60076398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83646409-C-T

60076475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83646374-A-G

http://identifiers.org/hco/17/GRCh38#60076725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83646339-A-C

http://identifiers.org/hco/17/GRCh38#60076910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83646206-C-A

http://identifiers.org/hco/17/GRCh38#60076927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83646188-C-A

60076929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83646186-T-A

60076933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83646182-T-A

60077054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83646037-G-C

60077061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83646014-G-C

60077248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83645932-G-A

60077283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83645893-C-T

60077431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83645734-C-T

60077523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83645662-G-A

60077737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83645485-A-G

60078084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83645227-T-G

http://identifiers.org/hco/17/GRCh38#60078145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83645208-A-C

60078145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83645208-A-G

60078159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83645193-G-C

60078178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83645170-T-C

60078418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83644957-G-C

60078546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83644891-G-T

60078561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83644875-G-T

http://identifiers.org/hco/17/GRCh38#60078578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#83644858-C-A

60078578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83644858-C-T

60078602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83644834-G-T

60078607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83644829-G-T

60078618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83644822-G-A

60078618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83644822-G-C

http://identifiers.org/hco/17/GRCh38#60078641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#83644799-C-A

60078641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83644799-C-G

60078720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 83644741-G-A

60078720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24076
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 83644741-G-T