18507180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45730692-G-A

18507427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45730453-A-G

18513414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 45725516-A-G

http://identifiers.org/hco/16/GRCh38#18513443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45725487-A-C

18513477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45725463-T-G

18513570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45725374-A-G

18513745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45725232-T-C

18514193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45722181-C-G

18514245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45722130-G-A

18520405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45716142-T-C

18520439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45716107-C-G

18520450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45716096-A-T

18520515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45716039-C-T

18520530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45716023-T-C

18520574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45715987-T-C

18520720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45715837-C-T

18520777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45715790-G-C

18520819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45715748-T-C

18520819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45715748-T-G

18520998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45715570-T-C

18521016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45715552-G-A

18521016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45715552-G-T

18521028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45715542-T-C

18521041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45715529-G-A

18521041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45715529-G-C

18521043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45715527-A-G

18521135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45715436-T-C

http://identifiers.org/hco/16/GRCh38#18522233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45713900-C-A

18522343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45713791-C-T

18522488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45713639-G-T

18522542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45713610-T-C

18522551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45713601-T-G

18522640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45713508-C-T

18522674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45713471-T-C

18523254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45712897-A-G

http://identifiers.org/hco/16/GRCh38#18523343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45712829-C-A

18523574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45712646-G-A

http://identifiers.org/hco/16/GRCh38#18523588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45712632-A-C

18523721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45712542-T-G

18523724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45712539-G-A

18523832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45712496-C-T

18524152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711720-C-T

18524193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711760-T-C

18524362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711393-G-A

18524362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711393-G-T

18524417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711323-T-A

http://identifiers.org/hco/16/GRCh38#18524418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45711322-C-A

18524418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711322-C-T

18524421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711319-T-A

18524421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711319-T-C

18524421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711319-T-G

http://identifiers.org/hco/16/GRCh38#18524444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45711296-C-A

18524444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711296-C-T

http://identifiers.org/hco/16/GRCh38#18524465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45711278-A-C

18524475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711268-A-G

http://identifiers.org/hco/16/GRCh38#18524617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45711140-A-C

18524617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711140-A-G

http://identifiers.org/hco/16/GRCh38#18524619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45711138-C-A

http://identifiers.org/hco/16/GRCh38#18524636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45711117-C-A

18524636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711117-C-T

18524646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711106-G-A

18524646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711106-G-T

http://identifiers.org/hco/16/GRCh38#18524659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45711093-C-A

18524659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711093-C-T

http://identifiers.org/hco/16/GRCh38#18524686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45711066-C-A

18524697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711055-G-A

18524698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711054-G-A

18524698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711054-G-C

18524698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45711054-G-T

18527560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45710365-T-A

http://identifiers.org/hco/16/GRCh38#18527608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, stop_gained
orthologous variants: http://identifiers.org/mco/7/GRCm39#45710317-C-A

18527659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45710266-G-A

18527659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45710266-G-C

18527659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45710266-G-T

18527673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45710226-C-T

18527693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45710062-T-G

18527838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45709918-T-A

18527915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45709888-G-C

http://identifiers.org/hco/16/GRCh38#18528005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45709803-A-C

18528026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 45709779-G-T

http://identifiers.org/hco/16/GRCh38#18528048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45709752-C-A

18528048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 45709752-C-G

18528048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 45709752-C-T

18528123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45709702-C-T

http://identifiers.org/hco/16/GRCh38#18528125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45709700-C-A

18528125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45709700-C-T

http://identifiers.org/hco/16/GRCh38#18528130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45709695-C-A

18528130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45709695-C-T

18528169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45709653-G-C

18528179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45709644-T-C

18528189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45709634-G-C

http://identifiers.org/hco/16/GRCh38#18528210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45709615-C-A

18528383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45709476-T-C

18528399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45709460-C-G

18529429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 45708041-G-A

18529438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 45708032-T-A

18529439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 45708031-C-T

18529693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45707803-G-A

18529693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45707803-G-C

18529693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45707803-G-T

http://identifiers.org/hco/16/GRCh38#18529696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45707797-C-A

18529696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45707797-C-G

18529696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45707797-C-T

18529740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45707743-A-G

18529925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45707610-G-A

18529933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45707602-T-A

18529933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45707602-T-C

18530259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45707318-A-G

18530560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45707003-G-A

18530632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45706940-G-A

18530632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45706940-G-C

18530644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45706931-C-T

18530718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45706870-T-C

http://identifiers.org/hco/16/GRCh38#18530757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45706829-C-A

18530789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45706800-A-G

18531111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45706556-C-T

http://identifiers.org/hco/16/GRCh38#18531201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45706466-C-A

18531223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45706424-G-A

18531223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45706424-G-T

18531248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45706396-A-T

18531395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45706227-T-C

18531409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45706213-C-T

18531440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45706184-G-A

18531448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45706176-T-C

18531498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45706126-A-G

18531498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 45706126-A-T

18531522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45706102-A-G

18531576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45706048-C-T

18531602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45706022-C-T

18531618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45706006-G-A

18531654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45705767-T-A

http://identifiers.org/hco/16/GRCh38#18531658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45705763-C-A

18531658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45705763-C-T

18531672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45705749-G-A

18531685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45705736-C-T

18531711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45705710-T-C

18531723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45705698-G-A

18531723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45705698-G-T

18531829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45705560-G-A

18532209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45705024-T-C

18532311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45704970-A-G

18532334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45704949-G-A

18532424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45704875-C-G

18532424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45704875-C-T

18532480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45704817-G-A

18532481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45704816-T-C

18532787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45704571-C-T

18532825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45704474-G-A

18533118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45703985-T-C

18533138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45703965-T-G

18533155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 45703948-T-A

18533155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 45703948-T-G

18533200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45703903-A-G

http://identifiers.org/hco/16/GRCh38#18533245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45703862-C-A

18533245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45703862-C-G

18533305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45703845-G-A

18533305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45703845-G-C

18533452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45703745-G-A

http://identifiers.org/hco/16/GRCh38#18533460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45703737-C-A

http://identifiers.org/hco/16/GRCh38#18533472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45703721-C-A

18533472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45703721-C-G

18533472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45703721-C-T

18533535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45703678-C-T

18533757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45703547-A-G

18535621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 45702072-T-C

18535658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 45702032-C-T

18535732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45701956-A-G

18535779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 45701906-C-T

18538556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45700088-G-A

http://identifiers.org/hco/16/GRCh38#18538658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45699986-C-A

18538658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45699986-C-G

18538708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699936-A-G

18538769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699876-G-A

18538769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699876-G-T

18538770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699875-T-C

18538795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699861-C-T

18538829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699828-C-T

18538838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699818-G-A

18538845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699811-C-T

http://identifiers.org/hco/16/GRCh38#18538948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45699708-A-C

18538948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45699708-A-G

18538972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45699683-A-G

18539006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699666-C-T

18539012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699660-C-T

18539065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699620-C-G

http://identifiers.org/hco/16/GRCh38#18539066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45699619-C-A

18539066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699619-C-T

18539193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699513-A-G

18539416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699358-C-G

18539416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699358-C-T

18539621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699255-G-A

18539710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699233-C-T

http://identifiers.org/hco/16/GRCh38#18539986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45699041-C-A

18539986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45699041-C-T

http://identifiers.org/hco/16/GRCh38#18540059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45698962-A-C

18540081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45698940-A-G

http://identifiers.org/hco/16/GRCh38#18540744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45697679-A-C

18540746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45697677-T-C

18540995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45697493-C-T

18541127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45697422-G-A

18541127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45697422-G-T

http://identifiers.org/hco/16/GRCh38#18541446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45697191-C-A

18541446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45697191-C-T

18542095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45696493-T-A

18542115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45696473-T-C

18542254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45696338-A-G

18542333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45696276-G-A

18542369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45696243-G-C

http://identifiers.org/hco/16/GRCh38#18542374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45696238-A-C

18542412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45696203-C-G

18542607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45695395-C-G

18542805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45695213-T-A

18542830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45695190-T-C

18542830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45695190-T-G

18542897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45695126-T-C

18542921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45695104-G-A

18542921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45695104-G-T

18542940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45695085-G-T

18543012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 45695037-T-C

http://identifiers.org/hco/16/GRCh38#18543047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#45695005-A-C

18543063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45694989-A-T

http://identifiers.org/hco/16/GRCh38#18543079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45694974-A-C

18543117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45694948-C-T

18543820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45694635-G-A

18543820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45694635-G-C

18543820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45694635-G-T

18547201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45693753-A-G

18547244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45693709-G-A

18547314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45693639-A-G

18548439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45692740-T-C

18548847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45692345-G-A

18548908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45692296-C-T

http://identifiers.org/hco/16/GRCh38#18549383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45692159-C-A

http://identifiers.org/hco/16/GRCh38#18549420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45692128-C-A

18549420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45692128-C-T

18549481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45692080-C-T

http://identifiers.org/hco/16/GRCh38#18549482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45692079-C-A

18549482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45692079-C-G

18549482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45692079-C-T

18549490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45692071-A-G

18549596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 45691985-G-A

18549596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 45691985-G-T

http://identifiers.org/hco/16/GRCh38#18549632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45691949-C-A

http://identifiers.org/hco/16/GRCh38#18549642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45691940-A-C

http://identifiers.org/hco/16/GRCh38#18551458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45690972-C-A

18551518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45690912-T-C

http://identifiers.org/hco/16/GRCh38#18551548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45690878-C-A

18551548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45690878-C-T

18551593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45690836-A-G

18554918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45687905-T-A

18554918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45687905-T-C

18554936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45687887-T-C

18554971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45687860-G-A

18554971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45687860-G-C

http://identifiers.org/hco/16/GRCh38#18555081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45687752-C-A

18557387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45687371-C-G

18557387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45687371-C-T

18557529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45687227-G-A

18557529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45687227-G-C

18557536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45687222-C-T

18557733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 45687039-T-C

http://identifiers.org/hco/16/GRCh38#18557844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45686924-C-A

18557844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45686924-C-G

18557844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45686924-C-T

18557853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45686916-T-C

18557853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45686916-T-G

18557912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45686857-T-G

18558098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45686681-T-C

18558098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45686681-T-G

18560427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45684445-C-G

18560504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45684419-G-C

18560504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45684419-G-T

18560528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45684396-G-A

18560663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45684189-G-T

18560810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45684075-A-G

18561011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45683945-G-T

18561934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 45683336-A-G

18561943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 45683327-T-A

18561943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 45683327-T-C

18561946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 45683324-G-A

18561946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, stop_gained, undefined
orthologous variants: 45683324-G-T

18561973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 45683297-A-G

18562091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 45683204-T-C

http://identifiers.org/hco/16/GRCh38#18562103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#45683192-C-A

18562103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 45683192-C-T

18562124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 45683171-T-G

http://identifiers.org/hco/16/GRCh38#18562129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45683166-C-A

18562129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 45683166-C-G

18562129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 45683166-C-T

18562183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45683121-G-A

18562183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45683121-G-T

18562186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22652
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45683118-C-T