http://identifiers.org/hco/6/GRCh38#40391731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49404474-A-C

40391731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: 3 prime UTR variant
orthologous variants: 49404474-A-G

40391731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: 3 prime UTR variant
orthologous variants: 49404474-A-T

40391924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: 3 prime UTR variant
orthologous variants: 49404261-G-A

40392088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49404098-T-C

http://identifiers.org/hco/6/GRCh38#40392151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49404041-C-A

40392208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49403984-G-A

40392211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49403981-G-C

40392211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49403981-G-T

40392226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49403966-T-C

40392238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49403954-T-G

40392325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49403867-A-G

http://identifiers.org/hco/6/GRCh38#40392403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49403789-C-A

40392403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49403789-C-T

40392404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49403788-G-A

http://identifiers.org/hco/6/GRCh38#40392424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49403768-C-A

40392465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: synonymous variant
orthologous variants: 49403727-G-A

40392465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: synonymous variant
orthologous variants: 49403727-G-T

40392606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: synonymous variant
orthologous variants: 49403583-T-A

40392645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: synonymous variant
orthologous variants: 49403544-G-A

40392916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 49403273-G-A

40392916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 49403273-G-C

40392965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49403237-G-T

40392995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49403207-G-C

40392995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49403207-G-T

http://identifiers.org/hco/6/GRCh38#40393039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49403192-A-C

40393039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49403192-A-T

http://identifiers.org/hco/6/GRCh38#40393048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49403183-C-A

40393048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49403183-C-T

40393062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49403169-G-A

40393062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49403169-G-T

40393073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49403158-A-T

40393113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49403118-A-G

40393241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49403007-A-G

40394250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49402738-G-A

40394518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49402463-C-T

40397731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49398470-G-A

40397733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49398468-C-T

40397884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49398329-G-A

http://identifiers.org/hco/6/GRCh38#40398030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49398189-A-C

40398113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49398106-C-T

40398298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49397951-G-A

40398411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49397854-C-T

http://identifiers.org/hco/6/GRCh38#40398439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49397827-C-A

40398439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49397827-C-T

40398469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49397800-G-A

40398493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49397776-G-A

40398523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49397748-G-A

40398771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49397318-G-A

40398815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49397269-T-C

http://identifiers.org/hco/6/GRCh38#40401243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49397051-A-C

40401417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49396912-G-T

http://identifiers.org/hco/6/GRCh38#40401807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49396578-C-A

40401807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49396578-C-G

40401873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49396522-C-T

40401882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49396513-C-T

40401942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49396457-T-C

40402178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49396234-C-T

40402234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49396191-G-A

40402235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49396190-T-C

http://identifiers.org/hco/6/GRCh38#40402329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49396108-C-A

40410474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49393748-T-C

40413022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49393112-G-A

40413135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49393013-C-T

40413337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49392822-G-A

40413615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49392530-A-G

40413632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49392512-A-T

40413743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49392423-A-G

http://identifiers.org/hco/6/GRCh38#40413839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49392339-A-C

40413839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49392339-A-T

40414003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49392161-C-T

40416406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49391819-G-A

40416426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49391799-G-A

40416786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49391502-C-T

40416901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49391391-A-G

40416909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49391383-A-G

40417560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49390720-G-A

40417560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49390720-G-C

40417607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49390463-G-C

40417607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49390463-G-T

40417729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49390337-G-A

40417729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49390337-G-C

40417854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49390268-G-A

40418098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49390070-T-C

40418110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49390058-C-G

40418110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49390058-C-T

40418157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49390003-C-T

40418358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49389803-G-A

40422072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49388853-G-A

40422107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49388833-C-T

40422499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49388486-G-A

40422809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49388276-T-A

40422985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49388137-G-A

40423147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49387996-T-A

40423147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49387996-T-G

40423150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49387993-G-A

40423179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49387969-A-T

40423237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49387909-T-C

40423318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49387836-G-C

40423380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49387716-C-T

40423390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49387700-A-G

40423517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49387371-A-G

40423817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49387106-T-C

http://identifiers.org/hco/6/GRCh38#40423841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49387083-C-A

40423841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49387083-C-G

http://identifiers.org/hco/6/GRCh38#40424034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49386939-A-C

http://identifiers.org/hco/6/GRCh38#40424043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49386930-C-A

40424257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49386703-G-A

40424257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49386703-G-C

40424257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49386703-G-T

40424310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49386672-T-G

40424343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49386652-C-T

40424651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49386442-C-T

40424683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49386419-C-G

40424842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49386264-C-T

40425247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49385587-C-G

40425247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49385587-C-T

40425262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49385572-C-T

http://identifiers.org/hco/6/GRCh38#40425345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49385480-C-A

40425345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49385480-C-G

40425436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49385388-G-A

40425505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49385319-T-G

40425597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49385244-T-G

40425671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49385171-C-G

40425671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49385171-C-T

40425766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49385076-A-G

40425923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49384937-C-T

40426031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49384841-A-T

40426301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49384626-G-A

40426508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49384434-C-T

40426651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49384192-G-A

40426765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49384071-C-T

40426781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49384055-C-T

40426798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49384032-T-G

http://identifiers.org/hco/6/GRCh38#40426871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49383975-C-A

http://identifiers.org/hco/6/GRCh38#40428635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49382343-C-A

40428635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49382343-C-T

40428752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49382232-A-T

40428821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49382163-G-A

40428853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49382131-G-T

40429265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49380907-C-T

40429554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49380594-T-C

40429604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49380541-C-T

40429731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49380390-G-A

http://identifiers.org/hco/6/GRCh38#40429766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49380350-A-C

40429873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49380241-G-A

40429873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49380241-G-C

40430050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49380046-C-T

40430201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49379882-G-T

40430325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49379771-A-G

40430504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49379624-C-T

40430516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49379612-G-A

40430542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49379586-T-C

40430721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49379240-G-A

40430762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49379201-C-T

40430832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49379136-C-T

40430883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49379085-C-T

40430960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49379020-C-T

40431377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49378644-A-T

40431446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49378580-C-T

40431629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49378396-G-A

40431629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49378396-G-T

http://identifiers.org/hco/6/GRCh38#40431648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49378381-C-A

40431648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49378381-C-T

40431673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49378363-G-A

40431673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49378363-G-C

40431673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49378363-G-T

http://identifiers.org/hco/6/GRCh38#40431674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49378362-C-A

40431674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49378362-C-G

40431674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49378362-C-T

40431677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49378359-G-T

http://identifiers.org/hco/6/GRCh38#40431698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49378339-A-C

40431819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49378213-G-A

40431921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49378111-T-C

40432032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49378000-G-A

40432176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49377856-A-G

40432476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49377556-G-A

40432476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49377556-G-T

40432608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49377424-A-G

40432797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49377235-T-C

http://identifiers.org/hco/6/GRCh38#40433094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49376938-C-A

40433094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: missense variant
orthologous variants: 49376938-C-T

40433119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: 5 prime UTR variant
orthologous variants: 49376913-G-T

http://identifiers.org/hco/6/GRCh38#40433136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49376890-A-C

40433136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 49376890-A-G

40433207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49376827-T-A

http://identifiers.org/hco/6/GRCh38#40433216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49376817-A-C

40433216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49376817-A-G

40433414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49376622-G-A

40434793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49375244-T-G

40435015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49375043-A-T

40435016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49375042-T-C

40435037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49375021-A-G

40435038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49375020-T-G

http://identifiers.org/hco/6/GRCh38#40435473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49374701-A-C

40435933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49373982-G-T

40435950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49373965-G-C

40435994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49373909-G-A

40436359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49373589-C-T

http://identifiers.org/hco/6/GRCh38#40436589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49373370-C-A

40436589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49373370-C-G

40437208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49373094-C-T

40437276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49373031-A-G

40437324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49372990-T-C

40437828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49372467-A-T

40438071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49372287-C-T

40438145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49372228-T-C

40438145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49372228-T-G

40438250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49372142-T-C

http://identifiers.org/hco/6/GRCh38#40438614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49371777-C-A

40438732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49371661-G-T

40438802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49371593-G-A

40438809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49371586-T-C

40439357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49370761-C-G

40439639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49370476-A-G

40439821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49370114-G-A

40439836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49370063-G-A

40439836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49370063-G-T

40439981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49369850-G-A

40439982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49369849-G-A

40440228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49369682-A-G

40440319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49369597-T-C

40440404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49369523-C-T

40440453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49369474-C-T

40440548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49369405-T-C

40440592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49369361-A-G

40440691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49369282-C-T

40440721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49369249-C-T

40440797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49369175-C-T

40440817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49369155-G-A

40440821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49369151-C-T

40441092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49368859-C-T

40441199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49368611-G-A

40441220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49368575-C-T

40441240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49368547-T-C

40441369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49368400-A-G

40441375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49368392-C-T

40441588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49368179-C-T

40441843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49367950-G-A

http://identifiers.org/hco/6/GRCh38#40441880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49367921-C-A

40441887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49367913-A-G

40441988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49367850-G-A

40442074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49367764-C-G

40442074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49367764-C-T

40442185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49367662-T-C

40442198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49367649-T-G

40442514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49367330-C-G

40443686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49367135-G-T

40443731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49367087-T-A

40443778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49367040-C-T

40444111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49366777-C-T

40444122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49366766-A-G

40444274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49366618-G-T

40444393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49366526-T-C

40445062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49365645-G-C

40445371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49365392-C-T

http://identifiers.org/hco/6/GRCh38#40445372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49365391-C-A

40445558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49365206-C-T

40445597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49365133-T-C

40445813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49364878-C-G

40446143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49364559-C-T

40446176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49364519-G-A

40446455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49364310-A-G

40446641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49364171-A-G

40447012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49363784-G-T

http://identifiers.org/hco/6/GRCh38#40447078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49363707-C-A

40447103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49363682-C-G

40447999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49363444-G-A

40448244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49363199-G-A

40448245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49363198-T-C

40448392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49363057-G-T

40448412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49363037-G-A

40448545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49362889-G-T

http://identifiers.org/hco/6/GRCh38#40449180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49362351-A-C

40449180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49362351-A-G

40449649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49361363-C-T

40449823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49361201-T-C

40449823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49361201-T-G

40450121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49360916-G-A

40450162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49360880-C-T

http://identifiers.org/hco/6/GRCh38#40450182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49360860-C-A

40450182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49360860-C-T

40450318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49360723-A-G

40450406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49360647-G-A

40450406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49360647-G-C

40450467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49360595-G-T

40450548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49360510-T-C

http://identifiers.org/hco/6/GRCh38#40450713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49360363-A-C

40450903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49360182-G-A

40450971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49360118-C-T

40451084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49360008-C-T

40451099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49359993-C-T

40451179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49359911-G-A

40451261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49359830-C-T

40451484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49359283-G-A

40451484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49359283-G-C

40451513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49359255-C-G

40451596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49359173-G-T

40451631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49359138-A-T

40451640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49359129-G-A

40451659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49359110-C-T

40451751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49359018-C-G

40451886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49358900-G-A

40451963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49358834-A-G

40452137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49358668-G-A

40452303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49358526-A-T

40452316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49358513-A-G

40452373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49358456-C-T

40452436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49358393-T-C

40452445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49358384-T-A

40452445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49358384-T-G

40452627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49358219-T-C

40452746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49358151-T-C

40457129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49353955-T-C

40457337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49353758-A-G

40457347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49353753-G-A

40457559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49353602-A-G

40457719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49353580-C-T

40457903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49353429-T-A

40457909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49353423-G-A

40460645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49351288-A-G

40461929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49350112-G-A

40461929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49350112-G-C

40461929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49350112-G-T

40461981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49350061-C-G

40462325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49349712-A-G

40462458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49349596-C-T

40462478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49349576-C-T

40462694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49349459-G-C

40463081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49349339-C-T

40463130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49349294-G-T

40463231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49349194-T-C

40463265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49349159-G-A

40463403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49349007-T-G

40467905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49347309-T-C

40472321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49345798-G-A

40472356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49345753-T-C

40472746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49344795-G-T

40473057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49344566-G-C

40473216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49344451-G-A

http://identifiers.org/hco/6/GRCh38#40473571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49344142-C-A

http://identifiers.org/hco/6/GRCh38#40473591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49344135-A-C

40474216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49343548-C-G

http://identifiers.org/hco/6/GRCh38#40474383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49343411-C-A

40474383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49343411-C-G

40474419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49343364-C-T

40474913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49342867-T-G

http://identifiers.org/hco/6/GRCh38#40475008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49342799-C-A

40475215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49342616-A-G

40475275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49342564-C-T

http://identifiers.org/hco/6/GRCh38#40475353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49342483-C-A

40475441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49342361-G-A

40475491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49342323-G-A

40475584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49342223-G-A

40475772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49342050-T-A

40475815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49342009-A-G

40475848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49341975-G-C

40475885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49341939-G-A

http://identifiers.org/hco/6/GRCh38#40476082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49341698-C-A

40476777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49341110-T-A

40476826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49341078-T-G

40477156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49340784-A-G

40477170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49340770-A-G

40477401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49340544-A-G

http://identifiers.org/hco/6/GRCh38#40477479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49340477-C-A

http://identifiers.org/hco/6/GRCh38#40477545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49340438-C-A

40477591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49340382-C-G

40477813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49340217-T-C

40477948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49340111-G-A

40478127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49339977-G-C

40478376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49339788-A-G

40478442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49339728-G-A

40478474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49339699-G-A

40479719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49339094-G-T

40479721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49339092-G-A

http://identifiers.org/hco/6/GRCh38#40479843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49338976-C-A

40480013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49338821-A-G

40480704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49338491-G-A

40480704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49338491-G-T

40481546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49338201-G-A

40481631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49338104-G-A

40481829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49337932-G-A

40482782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49336931-C-G

40482782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49336931-C-T

40483115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49336581-C-T

40483233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49336533-T-C

40483526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49336237-C-T

40483563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49336199-C-G

40484441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49335182-G-A

40485276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49334511-C-T

40485380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49334405-T-A

http://identifiers.org/hco/6/GRCh38#40485464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49334321-C-A

40485540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49334246-A-G

40485570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49334216-A-G

40485647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49334152-G-C

40485725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49334074-C-T

40486010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49333814-G-T

40486057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49333764-G-A

40486451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49333552-A-T

40486499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49333496-G-A

40486550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49333458-G-T

40486746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49333297-C-T

40489778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49331769-A-G

40489883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49331675-C-T

40490091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49331493-C-G

40490111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49331474-C-G

40490134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49331455-G-A

40490448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49331150-A-G

40490494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49331104-G-A

40490515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49331083-T-C

40490617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49330979-G-A

40490799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49330826-A-G

40490832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49330802-C-T

http://identifiers.org/hco/6/GRCh38#40490836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49330796-C-A

http://identifiers.org/hco/6/GRCh38#40490895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49330749-C-A

40490895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49330749-C-T

40491069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49330650-T-C

40491176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49330544-G-A

40491184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49330536-G-A

40491263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49330483-G-A

40491357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49330387-A-G

40492139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49330193-A-G

40492251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49330079-C-T

http://identifiers.org/hco/6/GRCh38#40492394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49330022-C-A

40492395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49330021-C-G

40492515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49329901-T-C

40492521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49329895-C-T

40492595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49329820-A-G

40492710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49329718-C-T

40492738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49329696-C-T

40493039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49329520-C-G

40493141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49329443-C-T

40493317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49329273-G-C

40493471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49329127-C-T

40493589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49329018-T-C

40493722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328932-T-C

40493722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328932-T-G

40493732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328922-G-A

40493736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328918-A-G

40493842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328841-T-G

40493951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328737-T-C

40493982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328706-G-A

40494086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328602-G-C

40494119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328572-G-T

40494162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328523-G-C

40494221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328468-A-T

40497526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328387-A-G

40497739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328163-C-G

40497873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49328060-T-C

40497941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49327992-G-A

40497941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49327992-G-C

40498029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49327916-G-A

40498207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49327752-A-G

40498229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49327732-G-A

40498274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49327690-A-G

http://identifiers.org/hco/6/GRCh38#40498523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49327471-A-C

40498523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49327471-A-T

http://identifiers.org/hco/6/GRCh38#40498624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49327296-C-A

40498741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49326942-C-G

40498826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49326862-T-C

40498836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49326852-A-G

40498862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49326826-T-C

40498904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49326780-G-C

40498912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49326772-G-T

40498991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49326682-C-T

40498993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49326680-G-A

40499131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49326506-T-C

40499195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49326477-C-T

http://identifiers.org/hco/6/GRCh38#40499372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49326299-C-A

40499386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49326285-A-G

40499572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49326074-G-A

40499623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49326024-T-G

40499651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49325996-A-G

40505149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49324743-C-T

40505257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49324848-C-G

40505295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49324886-G-C

40505303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49324898-G-A

40505652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49325229-T-C

40505921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49325427-C-T

40506655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49323965-G-A

40506669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49323951-G-A

40507039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49323579-T-C

40507089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49323525-G-A

40507152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49323462-T-C

40507261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49323353-A-G

40507262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49323352-T-C

40507282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49323332-A-T

40507389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49323220-T-C

40507405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49323204-A-G

40507413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49323196-G-A

40512962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49320755-C-T

40513244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49319009-T-A

40513346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49318912-G-A

40513454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49318847-G-A

40513454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49318847-G-C

40513454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49318847-G-T

http://identifiers.org/hco/6/GRCh38#40513581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49318720-C-A

40513729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49318580-G-C

40513823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49318499-C-T

40514085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49317917-T-C

40514784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49317526-T-A

40514827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49317483-C-T

40515919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49317100-T-A

40515919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49317100-T-C

40515919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49317100-T-G

40515931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49317088-G-A

40516056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49316950-G-T

40516152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49316888-A-G

40516236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49316800-T-G

http://identifiers.org/hco/6/GRCh38#40516264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49316772-C-A

40516264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49316772-C-T

40516454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49316607-A-G

40516569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49316528-G-A

40516673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49316369-C-T

40516831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315981-C-G

40516831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315981-C-T

http://identifiers.org/hco/6/GRCh38#40516952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49315846-A-C

40517005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315800-G-A

40517100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315716-C-G

http://identifiers.org/hco/6/GRCh38#40517139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49315672-A-C

40517149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315662-G-T

http://identifiers.org/hco/6/GRCh38#40517159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49315653-C-A

40517159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315653-C-T

http://identifiers.org/hco/6/GRCh38#40517161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49315651-C-A

40517161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315651-C-T

40517192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315598-G-A

40517192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315598-G-T

40517193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315597-C-G

40517194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315596-C-T

40517319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315457-G-T

40517326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315450-G-A

40517326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315450-G-T

40517349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315431-A-G

40517350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315430-G-A

40517350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315430-G-T

40517359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315420-G-T

40517373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315405-G-A

40517373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315405-G-T

40517427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315354-A-G

40517428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315353-T-C

40517559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315247-G-T

http://identifiers.org/hco/6/GRCh38#40517565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49315241-C-A

40517606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315201-A-G

http://identifiers.org/hco/6/GRCh38#40517651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49315159-A-C

40517651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315159-A-T

40517660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315150-T-C

40517809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49315043-T-A

40517874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49314999-G-A

40517948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49314957-C-T

40517949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49314956-T-C

40518067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -G-A

http://identifiers.org/hco/6/GRCh38#40518098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -C-A

40518117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -T-G

40518120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -C-T

40518125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -G-A

40518138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -T-C

40518140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -A-G

40518430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -A-T

40518597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -C-T

40518729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -T-C

40518759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -G-A

40518759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -G-T

40518825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -G-T

40518843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -G-A

40518843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: -G-C

40519973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49313270-G-A

40520099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49313187-T-C

40520170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49313118-G-A

40520181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49313107-T-C

40520250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49313037-C-T

http://identifiers.org/hco/6/GRCh38#40520282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49313005-A-C

40520286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49313001-G-T

40520314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49312973-G-A

40520357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49312937-T-C

40520438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49312865-G-A

40520519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49312798-T-C

40520546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49312772-A-G

40520731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49312591-G-A

40520731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49312591-G-T

40520836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49312504-G-T

40521117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49312379-A-G

40521131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49312365-G-A

40521305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49312237-G-A

40521808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49311762-T-C

http://identifiers.org/hco/6/GRCh38#40521815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49311755-A-C

40521913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49311681-A-G

40521995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49311600-A-G

http://identifiers.org/hco/6/GRCh38#40523787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49309312-C-A

40523789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49309310-G-C

40523789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49309310-G-T

40523883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49309207-G-C

40523884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49309204-A-G

40523900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49309189-C-T

40523946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49309144-T-A

40524033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49309074-T-C

http://identifiers.org/hco/6/GRCh38#40524041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49309066-C-A

40524041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49309066-C-G

40524097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49309007-G-A

40524097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49309007-G-C

40524110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49308994-G-A

40524309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49308541-C-T

http://identifiers.org/hco/6/GRCh38#40524415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49308421-A-C

40524415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49308421-A-T

40525232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49307148-G-A

40525535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49306831-T-C

40525588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49306778-T-C

40525640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49306727-C-T

http://identifiers.org/hco/6/GRCh38#40525647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49306720-A-C

40525693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49306670-C-T

http://identifiers.org/hco/6/GRCh38#40525704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#49306659-C-A

40525704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49306659-C-T

40527600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49304840-T-A

40527600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49304840-T-C

40527979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49304512-T-A

40532346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49302321-A-G

40532498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49302116-T-C

40532530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49302084-G-T

40532571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49302043-C-T

40532669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49301944-T-C

40532694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49301919-C-T

40532819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49301804-A-G

40532954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49301698-T-A

40532975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49301678-C-T

40533180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49301545-G-T

40533295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49301435-T-C

http://identifiers.org/hco/6/GRCh38#40533376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49301352-C-A

40533415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49301313-T-A

40533704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49301051-G-A

40535042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49300544-A-G

40535318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49300281-T-C

40535498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49300069-T-C

40535593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49299974-T-C

40535604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49299960-G-T

40535611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49299952-A-T

40535619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49299944-C-T

http://identifiers.org/hco/6/GRCh38#40535706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49299868-C-A

40536085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49299507-G-A

40536133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49299457-G-C

40536148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49299444-G-A

40536218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49299390-G-A

40537428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49289597-C-T

40537540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49289500-C-T

40537670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49289388-T-A

40537931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49289174-G-C

40538042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49289086-C-G

40538057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49289071-C-T

40538065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49289063-G-A

40538065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49289063-G-T

40538066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49289062-C-T

http://identifiers.org/hco/6/GRCh38#40538088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49289058-C-A

40538263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49288902-C-T

http://identifiers.org/hco/6/GRCh38#40538458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49288730-C-A

40538522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49288669-C-T

40538749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49288463-G-A

40538801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49288411-G-A

40538884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49288342-A-G

40539258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49287115-C-T

40539779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49286451-G-A

http://identifiers.org/hco/6/GRCh38#40540063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49286213-C-A

40540197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49286103-T-G

40540218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49286081-G-T

40540221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49286078-T-A

40540285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285833-T-C

40540312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285795-C-T

40540319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285788-T-G

40540373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285733-C-T

40540416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285690-T-C

40540424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285686-C-G

40540592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285516-G-A

40540716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285385-C-T

40540721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285380-T-C

40540832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285274-G-A

40540949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285166-G-A

40540963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285152-C-T

40540983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285128-T-C

40541083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49285026-G-T

40541371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49284828-G-A

40541606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49284604-C-G

40541835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49284151-C-G

http://identifiers.org/hco/6/GRCh38#40541897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49284035-A-C

40542153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49283884-G-T

40542310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49283731-C-T

40542445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49283347-C-T

40542542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49283256-C-T

40542581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49283216-G-A

40542647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49283150-T-C

40542783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49283029-T-G

http://identifiers.org/hco/6/GRCh38#40542916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49282746-A-C

40542916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49282746-A-G

40543090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49282593-G-A

40543136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49282542-C-T

40543174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49282516-A-G

40543176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49282514-T-C

40543213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49282476-A-T

http://identifiers.org/hco/6/GRCh38#40543305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49282389-C-A

40543688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49282006-C-T

40543891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49281813-G-C

40543891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49281813-G-T

40544238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49280774-A-G

40544521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49280485-G-T

40544719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49280303-C-G

40545684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49278070-C-G

40545782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49277992-C-G

40545918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49277769-G-T

40545954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49277733-C-T

http://identifiers.org/hco/6/GRCh38#40546001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49277685-A-C

40547434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49276444-C-T

40547764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49276199-T-C

40547873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49276092-C-T

40547911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49276054-C-T

40548702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49275566-A-G

40548703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49275565-T-C

http://identifiers.org/hco/6/GRCh38#40549007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49275065-A-C

http://identifiers.org/hco/6/GRCh38#40549388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49274691-C-A

40549433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49274664-G-A

40550214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49273830-G-A

40550268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49273775-G-C

40550699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49273405-C-T

40550948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49273161-G-C

40552535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49270599-A-G

40552733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49270335-G-A

40552885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49270128-T-C

40552886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49270127-G-A

40552920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49270093-T-C

40554009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49269192-A-T

40554051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49269157-C-G

40554051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49269157-C-T

40554419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49268742-G-C

http://identifiers.org/hco/6/GRCh38#40554516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49268605-A-C

40554560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49268333-A-G

40554701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49268210-C-T

40554745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49268154-T-C

40555155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49267733-T-C

40555175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49267713-C-T

40555181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49267707-G-A

40555563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49267295-A-G

40555735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49267167-A-G

40555844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49267097-T-C

40555877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49267066-A-G

40556006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49266952-G-A

http://identifiers.org/hco/6/GRCh38#40556428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49266579-C-A

40557134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49265875-G-C

40557202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49265798-C-T

40557494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49265540-C-T

40558311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49265324-C-T

40558445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49265241-G-A

40558615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49265104-T-A

40558624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49265095-A-T

40559146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49264906-G-T

40559148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49264904-T-G

40559188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49264854-G-A

40559293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49264749-A-G

http://identifiers.org/hco/6/GRCh38#40559347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49264694-C-A

40559460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49264590-G-A

40559493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49264548-G-A

40559516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49264522-G-A

40559581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49264360-G-A

40559598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49264343-C-T

40559612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49264315-G-A

http://identifiers.org/hco/6/GRCh38#40559699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49264224-C-A

40559709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49264214-C-G

http://identifiers.org/hco/6/GRCh38#40559725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49264161-C-A

http://identifiers.org/hco/6/GRCh38#40559768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49264119-C-A

40559842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49264031-T-A

40560329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49263564-C-T

40560456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49263435-C-T

40560616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49263269-G-T

40562565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49262398-G-T

40562683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49262306-C-T

40562869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49262158-A-T

40562873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49262154-T-C

40563142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49261923-G-A

40563142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49261923-G-C

40563241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49261809-G-A

40563253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49261797-C-T

http://identifiers.org/hco/6/GRCh38#40563324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49261736-C-A

40563428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49261646-A-T

40563465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49261610-T-C

40563492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49261585-G-A

40564825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49260400-C-G

40564834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49260391-C-G

40564862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49260349-C-T

http://identifiers.org/hco/6/GRCh38#40565076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49260184-A-C

40567159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49259725-C-T

40567242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49259684-G-A

40567242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49259684-G-T

http://identifiers.org/hco/6/GRCh38#40567453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49259482-A-C

40567453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49259482-A-T

40569268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49257442-C-G

40569292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49257408-A-G

40569653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49257114-C-T

40569916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49256873-A-T

40570157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49256615-C-T

40570398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49256378-A-G

40570406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49256370-C-T

http://identifiers.org/hco/6/GRCh38#40570475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49256320-C-A

40570583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49256226-C-G

40570716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49256145-G-A

40570891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49255946-C-T

40571183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49255663-G-T

40572288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49254130-T-A

40572288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49254130-T-C

40572473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49253944-G-A

40572473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49253944-G-C

40572519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49253897-G-A

40572519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49253897-G-C

40572579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49253856-C-G

http://identifiers.org/hco/6/GRCh38#40572967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49253492-C-A

40572967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49253492-C-T

40573213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49253275-A-G

40573221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49253267-T-C

40573229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49253255-C-T

40573233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49253253-T-G

40573498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49253036-G-A

40573534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49253001-A-G

40576008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49250824-C-T

40576073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49250767-G-A

40576088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49250752-C-T

40576089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49250751-G-A

40576361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49250518-G-A

40576543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49250349-C-T

40577918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49249577-C-T

40577926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49249566-G-A

http://identifiers.org/hco/6/GRCh38#40577957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49249535-C-A

40578015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49249469-T-C

http://identifiers.org/hco/6/GRCh38#40578089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49249408-C-A

http://identifiers.org/hco/6/GRCh38#40578157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49249342-C-A

40578218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49249270-T-C

http://identifiers.org/hco/6/GRCh38#40578364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49249165-A-C

40578416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49249086-C-T

40578451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49249054-G-A

40578451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49249054-G-T

40578459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49249046-T-A

40578495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49249005-A-G

40578616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49248879-T-C

40578656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49248854-A-T

http://identifiers.org/hco/6/GRCh38#40578878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49248647-C-A

40578950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49248577-G-A

40579111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49248424-G-A

http://identifiers.org/hco/6/GRCh38#40579118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49248417-C-A

40579125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49248410-A-G

http://identifiers.org/hco/6/GRCh38#40579187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49248353-C-A

40579594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49247354-A-G

40579597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49247351-C-T

40579635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49247293-C-G

40579676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49247252-A-G

40579889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49247063-G-C

40580296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49246606-C-T

40580453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49246459-C-T

40580492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49246417-G-A

40580637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49246299-G-A

40580651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49246285-A-G

40580897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49246158-G-A

http://identifiers.org/hco/6/GRCh38#40580921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49246131-A-C

40581081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49246013-G-A

40581264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49245856-C-G

40581264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49245856-C-T

40581411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49245597-G-T

40581530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49245488-C-T

40581544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49245474-C-T

40581624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49245399-A-G

40581624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49245399-A-T

40581851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49245001-A-G

40581862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49244995-T-G

40582009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49244877-A-G

40582433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49244337-C-T

40582757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49244033-G-A

40583059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49243696-T-G

40583065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49243690-A-T

40583066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49243689-C-T

40583180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49243574-T-C

http://identifiers.org/hco/6/GRCh38#40583361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49243360-C-A

40583411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49243315-C-T

40583889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49242687-G-T

40583940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49242636-T-C

40584026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49242552-G-T

http://identifiers.org/hco/6/GRCh38#40584181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49242447-C-A

40584534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49242156-C-T

40584680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49242008-C-T

40584701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49241977-G-A

40584956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49241743-T-C

http://identifiers.org/hco/6/GRCh38#40585081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49241639-C-A

40585359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49241356-T-A

40585375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49241328-G-C

40585449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49241267-A-G

40585549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49241183-C-T

40585921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron_variant, undefined
orthologous variants: 49240847-G-C

40586214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49240542-T-G

40586282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49240471-C-G

40586572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49240208-T-C

40586691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49240075-C-T

40586702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: 49240064-C-T

http://identifiers.org/hco/6/GRCh38#40586716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#49240050-C-A