24199563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 5 prime UTR variant
orthologous variants: 135394826-A-G

24199695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 135394722-T-C

http://identifiers.org/hco/1/GRCh38#24199888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135394529-C-A

24199893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135394524-A-G

24201223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135394095-A-G

24201892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135393853-G-A

24202090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135393654-G-C

http://identifiers.org/hco/1/GRCh38#24202322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135393457-C-A

24202356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135393429-A-G

http://identifiers.org/hco/1/GRCh38#24202370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135393415-C-A

24202370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135393415-C-T

24202646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135393209-G-A

24202676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135393196-T-C

24202682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135393192-G-A

24202686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135393188-C-G

http://identifiers.org/hco/1/GRCh38#24202724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135393157-C-A

http://identifiers.org/hco/1/GRCh38#24202937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135392805-A-C

24202937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135392805-A-G

24202992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135392674-C-T

24203017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135392649-T-C

http://identifiers.org/hco/1/GRCh38#24203187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135392396-A-C

24203476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135392209-C-G

24203568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135392102-T-C

http://identifiers.org/hco/1/GRCh38#24205571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135389657-C-A

24205631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135389595-T-C

24205658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135389569-G-C

24205820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135389409-C-T

http://identifiers.org/hco/1/GRCh38#24205848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135389378-A-C

24206023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135389206-C-T

24206991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135388271-G-A

24206991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135388271-G-C

24207022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135388237-T-C

24207022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135388237-T-G

24207044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135388198-G-A

http://identifiers.org/hco/1/GRCh38#24207117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135388076-C-A

24207133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135388060-G-A

24207182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387854-G-A

24207216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387817-T-A

24207238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387795-G-C

24207406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387644-A-T

24207416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387634-G-T

24207417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387633-A-G

24207417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387633-A-T

24207466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387584-C-G

24207466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387584-C-T

24207497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387563-C-T

24207503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387557-A-G

24207532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387529-G-A

24207635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387422-G-A

24207681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387371-A-G

24207813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387226-A-T

http://identifiers.org/hco/1/GRCh38#24207848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135387193-A-C

24207848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387193-A-G

24207901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135387157-C-T

24209123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135385846-G-C

24209130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135385839-G-A

http://identifiers.org/hco/1/GRCh38#24209161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135385814-A-C

24209218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135385758-A-G

24209218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135385758-A-T

24216185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135384179-C-G

24216198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135384165-G-A

24216206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135384154-A-G

24216220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135384138-G-A

24216220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135384138-G-T

24216291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135384062-G-A

24216334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135384021-T-C

24216368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135383985-C-T

24216555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135383816-G-A

24216859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135383568-C-G

24216881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135383535-C-T

24222309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135380696-G-A

24222392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135380579-A-G

24222392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135380579-A-T

24222439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135380540-G-A

24222715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135380043-A-G

24222745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135380016-G-A

24222797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135379924-T-A

24222821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135379900-T-C

24223161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135379537-G-A

24223161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135379537-G-C

24224228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135378433-C-T

24224299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135378383-C-T

24224364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135378314-C-G

24224431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135378266-T-C

24225628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135377210-G-A

24225628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135377210-G-C

24234435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135373934-C-G

24234435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135373934-C-T

24235775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135373052-G-C

24235942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135372925-T-C

24236045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135372810-C-G

24236045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135372810-C-T

24236046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135372809-G-A

http://identifiers.org/hco/1/GRCh38#24236047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135372808-C-A

24236047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135372808-C-G

24236135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135372726-T-C

http://identifiers.org/hco/1/GRCh38#24236195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135372676-A-C

24236239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135372657-G-A

24236239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135372657-G-T

24236700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135372232-G-A

24237119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135371817-G-T

24240553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135365982-A-G

24245640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135362305-G-A

24245656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135362289-G-A

24245658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135362287-A-G

http://identifiers.org/hco/1/GRCh38#24245659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135362286-C-A

24245659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135362286-C-T

24245709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135362261-G-C

24246147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135362148-G-A

http://identifiers.org/hco/1/GRCh38#24249200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135359754-C-A

24249331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135359635-G-A

24249332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135359634-A-G

http://identifiers.org/hco/1/GRCh38#24249531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135359435-A-C

24249560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135359405-A-G

24249662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135359349-C-T

24249914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135358963-T-C

24252156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135356411-T-C

24252317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135356248-G-A

24252782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135355817-G-C

24253149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135355476-C-G

24253355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135355316-C-T

24253399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135355274-G-C

24253781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135354966-G-T

24253816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135354932-G-A

24254070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135354688-G-A

24254570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135354316-A-T

24254572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135354314-G-C

24254958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135353959-T-C

24254961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135353956-T-C

24255058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135353860-G-A

24255099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135353823-G-T

24256374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135353575-G-A

24256488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135353390-T-G

24256625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135353284-G-T

24256637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135353271-G-A

http://identifiers.org/hco/1/GRCh38#24257391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135352269-A-C

24257470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135352190-G-A

24257733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135351939-C-G

24257733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135351939-C-T

24257772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135351900-G-A

24257772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135351900-G-C

24257995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135351668-C-T

24258167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135351514-C-G

24258167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135351514-C-T

24258235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135351445-G-A

24258373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135351311-T-C

24258474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135351212-T-A

24258739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135350966-A-G

24259081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135350692-G-A

24259094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135350679-G-A

24259285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135350472-T-C

24259650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135350397-C-G

24259669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135350378-G-C

24259854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135350177-C-G

24259854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135350177-C-T

24260034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135349958-C-T

24260081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135349913-C-T

24260283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135349841-G-A

24260283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135349841-G-C

24260283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135349841-G-T

24260425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135349809-A-G

24260653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135349673-T-A

24260752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135349596-G-T

24261004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135349358-G-A

24261261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135349143-A-G

24262832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135345894-T-A

24262905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135345827-G-A

24262949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135345789-A-T

http://identifiers.org/hco/1/GRCh38#24263290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135345440-A-C

24263296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135345434-A-T

http://identifiers.org/hco/1/GRCh38#24263632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135345220-C-A

24264059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135345020-T-C

24264925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135342312-C-T

http://identifiers.org/hco/1/GRCh38#24265016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135342227-C-A

24265058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135342184-T-C

24265126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135342128-C-G

24265136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135342118-A-G

24265260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135341857-C-G

24265378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135341734-T-A

http://identifiers.org/hco/1/GRCh38#24265401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135341711-C-A

24265711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135341339-A-G

24266037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135340981-G-A

24266050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135340968-A-G

24266066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135340952-T-A

24266066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135340952-T-G

24266088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135340903-G-A

24266184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135340794-G-A

24266197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135340781-G-T

24266247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135340701-T-A

24266291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135340603-T-G

24266301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135340593-C-T

24266344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135340551-C-T

24266372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135340524-G-T

24266499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135340425-C-G

24266809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135340149-T-C

24266813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135340145-A-G

24266848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135340108-G-A

24276709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135335696-C-G

24276844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135335574-A-G

24276870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135335549-T-C

24276946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135335481-T-C

http://identifiers.org/hco/1/GRCh38#24277042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135335385-A-C

24277175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135335252-A-G

24277275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135335144-G-A

24277286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135335133-C-T

24277323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135335097-G-T

24277624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135334874-A-G

24277624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135334874-A-T

24277790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135334720-T-C

24278585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135333309-C-T

24278615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135333279-G-C

24278630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135333264-T-A

24278674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135333220-A-G

24278729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135333166-G-T

24278751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135333144-C-G

24278751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135333144-C-T

24278765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135333130-G-T

24278908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135333002-G-A

24280855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135329546-G-A

24280960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135329442-C-T

24281852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135328847-G-A

24282458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135327939-T-C

24282676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135327694-T-G

24282851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135327504-T-C

24282851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135327504-T-G

24282853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135327502-G-A

24283059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135327347-T-C

24283117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135327295-C-T

24283171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135327243-C-T

24283205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135327209-A-G

24283835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135326651-G-A

24283835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135326651-G-T

24283899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135326583-A-T

24284385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135325740-G-C

24284451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135325669-C-T

24284476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135325644-C-G

24284476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135325644-C-T

24284582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135325629-C-G

24285139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135325316-G-A

24285269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135325176-T-C

24285711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135324883-G-T

24286040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135324573-G-A

24286405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135324095-C-T

24286486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135324026-C-T

24286782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135323755-G-A

24286824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135323696-T-A

24286989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135323509-A-G

24287062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135323430-T-A

24287062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135323430-T-C

24287062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135323430-T-G

24287281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135323136-A-G

24290174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135319929-G-A

24293253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135318760-C-G

24294251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135317831-C-G

24294251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135317831-C-T

24294847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135317022-A-G

24294856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, undefined
orthologous variants: 135317013-G-T

24294883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135316993-A-G

24295311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135316679-G-A

24295566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135316417-T-C

24295643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135316352-G-A

24295748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135316244-C-T

24297210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135315538-G-A

24297258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135315494-G-A

24297259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135315493-G-T

24300827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135313320-A-G

24300853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135313290-G-T

24301165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135313011-G-T

24301805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135312497-G-T

24302032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135312334-G-A

24302134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135312238-T-A

24302445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135312015-G-T

24302475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135312007-G-A

24306004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135311476-G-A

24306018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135311462-G-A

24306333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135310800-G-A

24306354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135310779-G-A

24306924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135310258-C-T

http://identifiers.org/hco/1/GRCh38#24306929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135310253-C-A

24307013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135310180-G-C

24307246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135309973-T-C

24307422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135309843-T-C

24307422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135309843-T-G

24307608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135309697-G-A

http://identifiers.org/hco/1/GRCh38#24307823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135309648-C-A

24307823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135309648-C-T

http://identifiers.org/hco/1/GRCh38#24307864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135309616-C-A

24307864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135309616-C-T

24307884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135309597-G-A

24308095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135309492-A-G

24308381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135309183-G-A

24308381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135309183-G-T

http://identifiers.org/hco/1/GRCh38#24308429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135309136-C-A

24308449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135309117-G-T

24308792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135308855-G-A

24308856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135308796-G-A

24308856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135308796-G-C

24309740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135308092-C-G

http://identifiers.org/hco/1/GRCh38#24310180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135307666-C-A

24310180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135307666-C-T

24310345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135307506-C-T

24311736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135307148-G-C

24311736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135307148-G-T

24311738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135307146-G-A

24311738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135307146-G-T

24311825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135307066-G-T

http://identifiers.org/hco/1/GRCh38#24311911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135306961-C-A

24311971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135306908-T-C

24311994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 135306885-T-C

24312018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135306861-A-G

http://identifiers.org/hco/1/GRCh38#24312019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135306860-C-A

24312063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135306815-A-G

24312227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135306651-T-A

24312232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135306646-T-A

24312355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135306560-G-A

24312516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135306469-G-A

24312841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135306187-C-T

http://identifiers.org/hco/1/GRCh38#24313607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135305841-C-A

24315156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135304107-A-T

24315258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135303913-G-C

24315297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135303880-T-C

24315309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135303868-A-G

24316530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135303530-T-C

http://identifiers.org/hco/1/GRCh38#24316634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135303448-A-C

24316951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135303181-G-A

http://identifiers.org/hco/1/GRCh38#24317180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135303025-C-A

24317191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135303014-A-G

24317394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135302805-C-T

24317504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135302741-G-C

24317531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135302723-T-G

24317553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135302700-G-T

24317946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135302343-C-T

24318180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135302165-A-G

24318311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135302018-T-G

24318561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135301787-G-T

24318709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135301569-T-C

http://identifiers.org/hco/1/GRCh38#24318838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135301452-C-A

http://identifiers.org/hco/1/GRCh38#24318907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135301376-C-A

24318907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135301376-C-T

24319063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135301228-A-G

http://identifiers.org/hco/1/GRCh38#24319192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135301102-C-A

24319192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135301102-C-T

http://identifiers.org/hco/1/GRCh38#24319196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135301098-C-A

24319232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135301065-T-A

http://identifiers.org/hco/1/GRCh38#24319281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135301015-C-A

24319281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135301015-C-T

24319350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135300946-T-G

24319469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135300832-G-A

24319469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135300832-G-T

http://identifiers.org/hco/1/GRCh38#24319537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135300748-C-A

24319537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135300748-C-G

24319592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135300687-T-A

http://identifiers.org/hco/1/GRCh38#24319892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135300386-C-A

24319892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135300386-C-T

24320012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135300267-G-T

24320414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135299863-G-T

24320514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135299765-C-T

24320705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135299578-T-A

24321172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135299101-G-A

http://identifiers.org/hco/1/GRCh38#24321278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135299007-A-C

24321564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135298498-T-C

http://identifiers.org/hco/1/GRCh38#24321635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135298452-C-A

24321657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135298423-A-G

http://identifiers.org/hco/1/GRCh38#24321701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135298375-C-A

24321707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135298369-T-C

24321720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135298355-G-A

24321720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135298355-G-T

24321894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135298185-G-A

24321894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135298185-G-C

24322134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135297945-A-G

24322202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135297895-C-T

24323241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135296954-T-G

24323401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135296710-G-C

24323474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135296639-A-G

24323938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135296107-G-C

24324289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135295814-G-C

24324775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135295373-C-G

24324775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135295373-C-T

24324996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135295161-C-T

24325126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135295032-A-G

24325132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135295026-G-A

24325132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135295026-G-C

24325265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135294898-G-T

24325552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135294573-G-A

24325730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135294424-C-T

24325926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135294218-C-G

24325974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135294173-C-G

24325986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135294161-A-G

24326066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135294078-G-C

24326172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135293951-G-T

24326554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135293684-G-A

24326606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135293647-T-C

24326894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135293436-A-G

http://identifiers.org/hco/1/GRCh38#24326984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135293344-C-A

24327080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135293238-T-C

24327566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135292770-T-C

24327608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135292722-C-T

24328654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135291708-T-C

24328894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135291453-T-C

http://identifiers.org/hco/1/GRCh38#24328938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135291397-C-A

24328988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135291353-G-T

24329121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135291231-C-G

24329121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135291231-C-T

24329290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135291069-A-G

24329444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135290912-G-A

24329563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135290583-A-T

24329601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135290545-C-T

24329617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135290529-C-T

http://identifiers.org/hco/1/GRCh38#24329619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135290527-A-C

24329988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135290230-C-T

24330636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135289720-T-G

24330996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135289385-T-C

24331029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135289353-T-C

http://identifiers.org/hco/1/GRCh38#24331282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135289106-C-A

24331282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135289106-C-T

24331289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135289095-G-A

24331289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135289095-G-T

24331408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135288682-C-T

24331415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135288675-C-T

24331487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135288603-A-G

24331626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135288464-C-G

http://identifiers.org/hco/1/GRCh38#24331660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135288435-C-A

24331660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135288435-C-T

24331674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135288420-T-C

http://identifiers.org/hco/1/GRCh38#24331680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135288414-C-A

24331680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135288414-C-G

24331680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135288414-C-T

24331726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135288387-T-G

24331729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135288384-A-G

http://identifiers.org/hco/1/GRCh38#24331753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135288379-A-C

http://identifiers.org/hco/1/GRCh38#24331992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135288149-C-A

24332109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135288055-C-T

24332195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135288025-C-T

http://identifiers.org/hco/1/GRCh38#24332397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135287847-A-C

24332397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135287847-A-G

24332419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135287831-A-G

24332435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135287819-G-A

24332435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135287819-G-T

24332513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135287739-T-C

24332575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135287714-A-G

24332819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135287472-T-C

24332871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135287428-G-A

24332927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135287364-G-A

http://identifiers.org/hco/1/GRCh38#24334575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135286546-C-A

24334575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135286546-C-T

24334576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135286545-A-G

24334582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135286539-G-A

24334582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135286539-G-T

24334594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135286527-C-T

24334599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135286512-A-G

24334742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135286374-T-C

24334775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135286337-G-T

http://identifiers.org/hco/1/GRCh38#24334796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135286317-C-A

24334796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135286317-C-T

24335064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135285798-G-C

24335300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135285621-G-A

24335321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135285604-A-G

24336200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135285077-G-A

24336250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135285032-A-T

24336266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135285018-C-T

24336349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135284933-T-A

24336349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135284933-T-C

24336355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135284915-G-A

24336355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135284915-G-T

http://identifiers.org/hco/1/GRCh38#24336686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135284618-C-A

24336686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135284618-C-T

24336696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135284608-G-A

24336696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135284608-G-T

24336711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135284593-C-T

24336804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense variant
orthologous variants: 135284500-A-T

24336832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284472-G-A

24336832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284472-G-T

24336896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284403-T-C

24336978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284324-T-A

24336978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284324-T-C

24336992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284311-T-C

http://identifiers.org/hco/1/GRCh38#24336994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135284309-C-A

http://identifiers.org/hco/1/GRCh38#24337007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135284297-C-A

http://identifiers.org/hco/1/GRCh38#24337013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135284291-C-A

http://identifiers.org/hco/1/GRCh38#24337019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135284285-C-A

24337169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284136-G-A

24337169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284136-G-C

24337169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284136-G-T

http://identifiers.org/hco/1/GRCh38#24337171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135284134-C-A

24337171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284134-C-T

24337196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284123-G-A

24337197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284122-G-A

http://identifiers.org/hco/1/GRCh38#24337214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135284105-C-A

24337214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284105-C-T

http://identifiers.org/hco/1/GRCh38#24337225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135284043-C-A

24337236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135284032-G-T

http://identifiers.org/hco/1/GRCh38#24337274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135283973-C-A

24337274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135283973-C-T

24337429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135283709-G-A

24337456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135283683-T-C

24337512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135283662-A-G

24337519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135283655-T-A

http://identifiers.org/hco/1/GRCh38#24337530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135283644-C-A

24337530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 135283644-C-T

24337544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135283630-G-A

24337559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135283617-G-A

24337730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135283455-G-A

24337913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283323-A-G

24337958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283274-G-A

24337958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283274-G-T

24337962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283270-G-A

24337962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283270-G-C

24337962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283270-G-T

24338123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283099-T-C

http://identifiers.org/hco/1/GRCh38#24338125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135283097-C-A

http://identifiers.org/hco/1/GRCh38#24338230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135283069-C-A

24338230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283069-C-G

24338230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283069-C-T

24338231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283068-G-A

24338231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283068-G-C

24338231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283068-G-T

24338242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283054-A-G

http://identifiers.org/hco/1/GRCh38#24338251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135283045-C-A

24338251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283045-C-T

24338255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135283041-T-C

http://identifiers.org/hco/1/GRCh38#24338439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135282697-A-C

http://identifiers.org/hco/1/GRCh38#24338444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135282692-A-C

24338542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135282516-G-A

24338542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135282516-G-C

24338542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135282516-G-T

24338611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135282425-C-T

24338869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135282231-T-C

24338929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135282177-C-T

24339016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135282084-T-C

24339607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135281971-T-C

24339615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135281963-T-A

http://identifiers.org/hco/1/GRCh38#24339631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135281949-C-A

http://identifiers.org/hco/1/GRCh38#24339909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135281724-C-A

24339910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135281723-T-C

24340145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135281596-C-G

24340233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135281531-G-A

24340284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135281503-C-T

24340305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135281476-C-G

24340610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135281218-A-G

24341033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135280843-G-C

24341034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135280842-G-A

24341225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135280683-G-C

24341408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135280507-G-A

http://identifiers.org/hco/1/GRCh38#24341616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135280336-C-A

24341723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135280258-C-T

24341997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135280078-A-T

http://identifiers.org/hco/1/GRCh38#24342091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135280027-C-A

24342091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135280027-C-G

24342118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135280000-T-C

24342121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135279997-A-G

24342253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense variant
orthologous variants: 135279865-A-G

http://identifiers.org/hco/1/GRCh38#24342292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135279788-C-A

24342292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135279788-C-T

http://identifiers.org/hco/1/GRCh38#24342330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135279759-C-A

24342330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135279759-C-G

24342330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135279759-C-T

http://identifiers.org/hco/1/GRCh38#24342373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135279703-C-A

24342373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135279703-C-T

24342384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135279692-T-C

24342384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135279692-T-G

24342399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135279644-T-C

24342407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135279636-T-C

http://identifiers.org/hco/1/GRCh38#24342558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135279501-C-A

24342558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135279501-C-G

24342558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135279501-C-T

http://identifiers.org/hco/1/GRCh38#24342564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135279495-A-C

24342609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135279469-C-T

http://identifiers.org/hco/1/GRCh38#24342656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135279422-C-A

24342712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense variant
orthologous variants: 135279369-C-T

24342932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense variant
orthologous variants: 135279148-G-C

24342969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense variant
orthologous variants: 135279111-C-G

24342969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense variant
orthologous variants: 135279111-C-T

http://identifiers.org/hco/1/GRCh38#24343005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135279075-A-C

24343005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: missense variant
orthologous variants: 135279075-A-T

24343048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, missense_variant
orthologous variants: 135279037-G-A

24343048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, missense_variant
orthologous variants: 135279037-G-C

24343078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, missense_variant
orthologous variants: 135279009-T-C

24343110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, stop_gained
orthologous variants: 135278979-G-T

24343158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135278887-G-A

24343187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135278850-G-T

24343202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135278835-T-C

24343202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135278835-T-G

http://identifiers.org/hco/1/GRCh38#24343302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135278773-A-C

24343302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135278773-A-G

http://identifiers.org/hco/1/GRCh38#24343401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135278695-C-A

24343401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135278695-C-T

24343495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135278628-T-C

24343601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135278517-C-G

24343601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135278517-C-T

24343620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135278496-G-T

24343892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135278265-C-T

24343983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135278199-A-T

24344253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135278020-G-A

24344388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135277973-A-G

24344397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135277968-C-T

24344683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135277789-T-C

http://identifiers.org/hco/1/GRCh38#24344781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135277713-A-C

24344781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135277713-A-T

24344962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135277572-C-T

24344973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135277561-C-G

24344973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135277561-C-T

http://identifiers.org/hco/1/GRCh38#24344980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135277554-C-A

24344980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135277554-C-T

24345004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135277532-G-A

24345004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135277532-G-C

24345004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135277532-G-T

http://identifiers.org/hco/1/GRCh38#24345015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135277517-A-C

24345015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135277517-A-T

24345866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135277176-T-C

24346368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135276795-G-C

http://identifiers.org/hco/1/GRCh38#24346419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135276738-C-A

24346419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135276738-C-G

24346419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135276738-C-T

24346423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135276734-T-C

24346472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135276696-G-T

24346477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135276691-T-C

24346976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135276243-C-G

24346976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135276243-C-T

24347207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135276028-A-G

24347406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135275843-G-A

24347424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135275837-T-C

24347430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135275831-T-C

24347436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135275825-T-C

24347689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135275663-G-A

http://identifiers.org/hco/1/GRCh38#24348104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135275311-A-C

24348104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135275311-A-G

24348106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135275309-C-T

24348205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135275234-G-A

24348269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135275168-T-G

24348753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135274873-T-C

24349524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135274118-A-T

24349625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135274006-T-C

24349831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135273814-C-T

24349981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135273688-A-G

24350406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135273294-C-T

http://identifiers.org/hco/1/GRCh38#24350562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135273155-A-C

http://identifiers.org/hco/1/GRCh38#24350574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135273143-C-A

24350605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135273113-G-A

24350605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135273113-G-C

24350634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135273084-A-T

24350839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135272922-T-C

24351142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135272848-G-A

24351162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135272828-C-T

http://identifiers.org/hco/1/GRCh38#24351317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135272767-C-A

24351518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135272552-C-G

24351520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135272550-C-T

24351573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135272510-C-T

24351771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135272333-C-G

24351815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135272289-G-A

24351815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135272289-G-C

http://identifiers.org/hco/1/GRCh38#24352707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135271597-A-C

24353223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135271089-T-A

24353439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135270900-G-T

24354225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135270207-T-G

24354244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135270188-G-A

24354244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135270188-G-T

24354319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135270139-G-T

24354423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, missense_variant
orthologous variants: 135270033-G-A

24354423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, missense_variant
orthologous variants: 135270033-G-T

24354453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, missense_variant
orthologous variants: 135270003-G-C

http://identifiers.org/hco/1/GRCh38#24354492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135269960-C-A

24354492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269960-C-T

24354498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269954-A-G

24354499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269953-G-A

http://identifiers.org/hco/1/GRCh38#24354550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135269925-C-A

24354550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269925-C-G

24354571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269907-G-T

http://identifiers.org/hco/1/GRCh38#24354600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135269879-C-A

http://identifiers.org/hco/1/GRCh38#24354615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135269863-C-A

24354615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269863-C-T

24354664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269814-T-A

24354664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269814-T-C

24354670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269808-G-A

24354670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269808-G-C

http://identifiers.org/hco/1/GRCh38#24354738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135269747-A-C

24354738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269747-A-G

24354771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269718-A-T

24354818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269677-A-G

24354833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269672-A-G

http://identifiers.org/hco/1/GRCh38#24354865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135269642-C-A

24354878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269629-G-A

http://identifiers.org/hco/1/GRCh38#24354919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135269578-A-C

http://identifiers.org/hco/1/GRCh38#24355314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135269194-C-A

24355314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135269194-C-T

24355375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135269125-T-C

24355487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135269033-C-G

24355501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135269019-C-T

24355569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135268964-G-C

24355590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135268945-G-A

24355909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135268627-T-G

24356225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135268368-C-T

24356238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135268361-T-A

24356238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135268361-T-C

24356441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135268235-G-A

http://identifiers.org/hco/1/GRCh38#24356453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135268223-A-C

24356461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron variant
orthologous variants: 135268215-G-A

24357254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267657-T-A

24357254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267657-T-C

24357284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267627-G-T

24357345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267592-A-G

http://identifiers.org/hco/1/GRCh38#24357361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267576-C-A

24357394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267534-G-A

24357394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267534-G-T

24357442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267494-G-A

24357442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267494-G-C

24357442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267494-G-T

http://identifiers.org/hco/1/GRCh38#24357451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267485-C-A

http://identifiers.org/hco/1/GRCh38#24357456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267480-C-A

24357456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267480-C-T

http://identifiers.org/hco/1/GRCh38#24357482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267467-C-A

24357527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267421-C-T

http://identifiers.org/hco/1/GRCh38#24357554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267394-C-A

24357554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267394-C-T

24357565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267383-T-C

http://identifiers.org/hco/1/GRCh38#24357638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267331-C-A

24357638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267331-C-T

24357685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267285-A-G

http://identifiers.org/hco/1/GRCh38#24357709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267269-C-A

24357709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267269-C-G

24357709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267269-C-T

24357713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267266-G-A

http://identifiers.org/hco/1/GRCh38#24357738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267240-C-A

24357738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267240-C-G

24357738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267240-C-T

24357936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267092-G-T

http://identifiers.org/hco/1/GRCh38#24357985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267053-A-C

http://identifiers.org/hco/1/GRCh38#24358169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135264251-C-A

24358215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135264202-C-T

http://identifiers.org/hco/1/GRCh38#24358406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135264061-C-A

24358406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135264061-C-T

24358507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135264003-G-T

24358638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135263873-G-T

24358670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135263837-T-G

24360772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135261204-A-T

24360789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135261187-C-G

24360812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135261164-A-G

24360813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135261163-G-T

24361117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260860-G-T

http://identifiers.org/hco/1/GRCh38#24361125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135260852-C-A

24361125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260852-C-G

24361125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260852-C-T

24361149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260835-A-T

24361167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260821-G-A

24361167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260821-G-C

24361167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25839
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260821-G-T