42892740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: 5 prime UTR variant
orthologous variants: 68188724-A-T

42892758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: 5 prime UTR variant
orthologous variants: 68188734-T-A

42892875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: 5 prime UTR variant
orthologous variants: 68188872-A-G

42892934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: 5 prime UTR variant
orthologous variants: 68188929-A-G

42893123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: 5 prime UTR variant
orthologous variants: 68189114-G-A

42893123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: 5 prime UTR variant
orthologous variants: 68189114-G-T

42893129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: 5 prime UTR variant
orthologous variants: 68189120-T-G

42893187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: 5 prime UTR variant
orthologous variants: 68189173-T-C

42893413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: missense variant
orthologous variants: 68189395-C-G

42893422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: missense variant
orthologous variants: 68189404-A-G

42893479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: synonymous variant
orthologous variants: 68189461-T-C

42893482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: missense variant
orthologous variants: 68189464-G-T

42893488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: missense variant
orthologous variants: 68189470-G-T

http://identifiers.org/hco/4/GRCh38#42893680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68189663-C-A

42893725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68189709-A-G

42893770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68189745-G-A

42893770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68189745-G-C

42893770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68189745-G-T

http://identifiers.org/hco/4/GRCh38#42893776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68189750-C-A

42893776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68189750-C-T

http://identifiers.org/hco/4/GRCh38#42893792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68189766-C-A

42893792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68189766-C-T

42893799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68189773-G-A

42893799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68189773-G-T

42893994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68189948-G-A

42894950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68190003-A-T

42895073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68190127-G-A

42895079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68190133-A-T

42895895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68190809-A-T

42896099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68191025-G-A

42896099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68191025-G-T

42896137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68191060-G-A

42896137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68191060-G-T

42896203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68191127-T-C

42896430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68191349-G-A

42896430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68191349-G-T

42896445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68191364-C-G

42896523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68191448-C-T

http://identifiers.org/hco/4/GRCh38#42896806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68191767-A-C

42896806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68191767-A-G

42897049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68191985-T-C

42897050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68191986-C-T

http://identifiers.org/hco/4/GRCh38#42897118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68192067-C-A

42897118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68192067-C-G

42897299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68192242-A-G

42897749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68192533-T-G

42897967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68192651-G-T

42898256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68192798-C-T

42898596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68193096-C-G

42898685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68193205-C-G

42898788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68193299-T-G

42898828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68193324-T-C

42898911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68193402-C-T

42898951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68193445-G-T

42898983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68193477-T-A

42898983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68193477-T-C

42898989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68193483-T-C

42899037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68193526-C-T

42899203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68193952-A-G

42900311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68197847-T-C

42900357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68197892-C-T

42900427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68197948-C-G

42900427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68197948-C-T

42900567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68198081-C-T

42900618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68198132-G-A

42900630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68198144-T-C

42900899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68198359-G-T

42900917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68198377-G-A

42900947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68198402-A-G

http://identifiers.org/hco/4/GRCh38#42900989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68198451-A-C

http://identifiers.org/hco/4/GRCh38#42901005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68198467-A-C

42901132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68198601-G-A

42901132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68198601-G-T

42901135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68198604-T-A

42901204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68198673-A-G

42901229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68198699-A-G

42901464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68198916-T-C

42902163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68201276-A-G

42902225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68201337-A-G

42902261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68201374-A-T

42903294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68203799-C-T

42903308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68203813-A-T

42903887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68204815-T-G

42904082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68204982-C-T

http://identifiers.org/hco/4/GRCh38#42904083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68204983-A-C

42904083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68204983-A-G

42904083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68204983-A-T

42904343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68205236-T-C

42904588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68205520-T-C

42904610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68205548-T-C

42904791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68205997-A-G

42904791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68205997-A-T

42904812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68206019-T-A

42904903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68206108-T-A

42905311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68206451-C-T

42905406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68206531-G-A

http://identifiers.org/hco/4/GRCh38#42906355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68208520-C-A

42906355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68208520-C-T

42906421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68208577-T-A

42906472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68208614-T-G

42906564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68208688-G-A

http://identifiers.org/hco/4/GRCh38#42907215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68210753-C-A

42907789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68211583-G-A

42907945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68211727-G-A

42907945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68211727-G-T

42908154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68211938-C-T

42908188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68211967-G-T

42908189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68211968-C-G

42908190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68211969-T-G

42908314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68212101-G-A

42908339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68212125-C-G

42908339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68212125-C-T

42909656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68214117-C-T

42909797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68214243-A-G

42909931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68214311-C-T

42909935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68214315-T-A

42909988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68214329-A-G

42910516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68214624-G-A

42910548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68214656-A-G

http://identifiers.org/hco/4/GRCh38#42910583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68214690-A-C

42910632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68214750-C-T

42910729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68215137-C-T

http://identifiers.org/hco/4/GRCh38#42910883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68216164-C-A

42910883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68216164-C-T

http://identifiers.org/hco/4/GRCh38#42910997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68216260-C-A

42911013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68216276-A-G

42911076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68216337-T-G

42911088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68216349-T-C

42911259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68216523-T-C

42911320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68216582-A-T

42911568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68216801-T-C

42912057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68219147-A-G

42912121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68219196-G-A

http://identifiers.org/hco/4/GRCh38#42912347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68219357-C-A

42912358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68219368-C-T

42912362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68219372-C-T

http://identifiers.org/hco/4/GRCh38#42917837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68226773-C-A

42917873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68226809-T-C

http://identifiers.org/hco/4/GRCh38#42917957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68226893-A-C

42918198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68227421-G-A

42918204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68227427-T-G

http://identifiers.org/hco/4/GRCh38#42918315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68227539-C-A

http://identifiers.org/hco/4/GRCh38#42918426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68227616-C-A

42918426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68227616-C-T

42918572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68227757-T-G

42918604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68227781-A-G

42918609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68227786-G-T

42918722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68227897-C-T

42920029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68228904-C-T

http://identifiers.org/hco/4/GRCh38#42920155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68229044-A-C

42920404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68229271-T-C

42920498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68229364-G-A

42920719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68229716-A-T

42921695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68230709-C-T

42921702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68230713-A-G

42921726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68230741-C-T

42921866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68230844-C-T

42921916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68230876-C-T

http://identifiers.org/hco/4/GRCh38#42921939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68230897-C-A

42921939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68230897-C-T

42922183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68231132-G-T

42922208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68231157-G-A

42922208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68231157-G-T

42922258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68231207-C-T

42922320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68231262-C-T

http://identifiers.org/hco/4/GRCh38#42922409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68231345-C-A

42922490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68231430-G-A

42922515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68231455-T-C

42922515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68231455-T-G

42923746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68232313-T-A

42923860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68232424-C-T

http://identifiers.org/hco/4/GRCh38#42923883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68232446-A-C

http://identifiers.org/hco/4/GRCh38#42924133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68232658-C-A

42925276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68233065-G-A

42925283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68233072-G-T

42925285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68233074-G-T

42925313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68233098-A-G

42925389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68233171-T-C

42925505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68233283-T-C

42925619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68233385-C-T

42925620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68233386-T-C

42925637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68233406-G-A

42925637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68233406-G-T

42930796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68234833-C-T

42930805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68234842-T-C

42930823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68234855-T-C

42931005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68235018-T-C

42931274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68236082-A-G

42931340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68236147-G-A

42931361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68236168-G-C

42931398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68236208-C-T

42931445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68236254-G-C

42932273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68240040-C-T

42932299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68240066-C-G

42932447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68240218-C-T

http://identifiers.org/hco/4/GRCh38#42932462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68240243-C-A

42932488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68240271-G-A

42932532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68240316-A-T

http://identifiers.org/hco/4/GRCh38#42932540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68240323-C-A

42932575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68240343-T-A

42932575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68240343-T-C

42932575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68240343-T-G

http://identifiers.org/hco/4/GRCh38#42932578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68240346-A-C

42932670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68242427-T-A

42932670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68242427-T-C

42932670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68242427-T-G

42932674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68242431-T-G

http://identifiers.org/hco/4/GRCh38#42932675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68242432-A-C

42932696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68242453-G-A

42932697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68242454-G-A

42932728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68242488-A-G

42932851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68242611-T-C

42932970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68242749-G-A

42932981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68242760-C-T

42941904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68244070-A-T

42941925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68244091-T-C

42942138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68244303-T-C

42942191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68244356-T-C

42942330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68244486-T-C

42942473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68244664-C-G

42942717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68244889-T-C

http://identifiers.org/hco/4/GRCh38#42943053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68245310-C-A

42943055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68245312-C-T

42943166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68245425-T-C

42943493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68245665-T-C

42943693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68245813-T-A

42943797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68245913-C-T

http://identifiers.org/hco/4/GRCh38#42943831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68245942-A-C

42943842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68245953-G-T

42943881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68245986-T-C

42944338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68246570-G-C

42944338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68246570-G-T

42944761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68246989-G-C

42944812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68247050-C-T

42944926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68247188-G-T

42949534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68249845-C-T

http://identifiers.org/hco/4/GRCh38#42949642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68249942-C-A

42949642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68249942-C-T

42949774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68250093-T-A

42949817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68250137-G-A

42949841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68250161-T-C

42949849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68250169-T-C

42949874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68250194-C-T

42949972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68250283-C-T

42949986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68250291-C-G

42949986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68250291-C-T

42950257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68250822-A-G

42950294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68250853-T-C

42950340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68250901-G-T

42950494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68251053-C-T

42950525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68251084-A-G

42950753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68251302-C-G

42950753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68251302-C-T

42950904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68251597-T-C

42950963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68251734-A-G

42950977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68251747-T-C

42951227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68251956-A-G

42951259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68251988-C-T

42951326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68252039-C-T

http://identifiers.org/hco/4/GRCh38#42951376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68252093-C-A

42951391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68252099-C-T

42951881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68252730-G-C

42953720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253073-T-A

42953821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253176-A-G

42953951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253311-A-T

42953985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253323-T-C

42954027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253357-T-C

42954062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253389-C-T

42954064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253392-A-G

42954067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253395-T-A

http://identifiers.org/hco/4/GRCh38#42954110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68253437-C-A

42954110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253437-C-T

http://identifiers.org/hco/4/GRCh38#42954152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68253478-A-C

42954155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253481-G-C

42954161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253487-G-A

42954441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253779-C-T

42954543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253858-A-G

42954676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68253981-T-C

42955177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68254286-G-A

42955285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68254419-T-C

42955302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68254444-G-A

http://identifiers.org/hco/4/GRCh38#42955320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68254462-A-C

42955658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68254791-A-G

42955999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68255141-C-T

42956034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68255171-C-T

42956160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68255273-G-C

http://identifiers.org/hco/4/GRCh38#42956188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68255301-A-C

42956195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68255308-T-C

42956214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68255327-G-A

http://identifiers.org/hco/4/GRCh38#42956315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68255422-C-A

42956329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68255442-C-T

42956374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68255492-G-T

http://identifiers.org/hco/4/GRCh38#42956636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68255666-A-C

42956636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68255666-A-G

42956743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68255771-G-T

42956799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68255827-T-C

42956909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68255920-C-T

42956916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68255927-G-T

42957036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68256037-C-G

42957077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68256072-T-C

http://identifiers.org/hco/4/GRCh38#42957080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68256075-C-A

42957080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68256075-C-G

42957101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68256090-G-A

42957211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68256179-G-A

42957217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68256185-A-G

42957244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68256211-T-A

42957330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68256288-C-T

42961390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68265557-A-G

42961570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68265713-T-C

42961662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68265802-T-C

42961727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68266087-T-C

42961731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68266091-G-A

http://identifiers.org/hco/4/GRCh38#42961785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68266145-C-A

42961785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68266145-C-T

42961904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68266276-G-A

42961929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68266299-C-T

42962148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68266435-A-T

42962291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68266578-A-T

http://identifiers.org/hco/4/GRCh38#42962298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68266585-A-C

42962361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68266645-C-T

42962436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68266719-G-A

42962668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68266928-G-A

42962786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68267527-A-T

42962861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68267624-A-G

42962867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68267630-T-C

42962870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68267633-C-T

42962906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: missense variant
orthologous variants: 68267669-T-G

42962939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: synonymous variant
orthologous variants: 68267702-C-G

42963071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: synonymous variant
orthologous variants: 68267834-A-T

42963086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: synonymous variant
orthologous variants: 68267849-T-C

42963101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: synonymous variant
orthologous variants: 68267864-C-T

http://identifiers.org/hco/4/GRCh38#42963165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68267930-A-C

42963165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68267930-A-G

http://identifiers.org/hco/4/GRCh38#42963172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68267937-C-A

42963224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68267978-A-G

42963266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68268018-A-T

http://identifiers.org/hco/4/GRCh38#42963292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68268042-C-A

42963370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68268120-A-G

42963391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68268140-G-A

42963514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68268260-A-G

42963543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68268290-A-G

42963668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68268402-G-A

http://identifiers.org/hco/4/GRCh38#42963675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68268409-C-A

42963698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68268436-G-A

42964049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68268771-A-G

42964256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68268971-A-G

42964395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68269109-T-C

42964883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68269659-T-A

42965022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68269793-C-T

42965432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68270156-A-G

42965435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68270159-G-A

http://identifiers.org/hco/4/GRCh38#42965453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68270176-C-A

42965453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68270176-C-T

42965479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68270203-T-C

42965700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68270433-C-G

42965706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68270434-A-G

42965921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68270632-C-T

42965922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68270633-G-A

42966019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68270721-G-A

42966019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68270721-G-T

42966036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68270738-A-T

42966041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68270743-T-A

42976016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68277663-T-C

42976051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68277708-C-G

42976051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68277708-C-T

42985552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68278368-G-A

42985628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68278442-A-G

42985928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68278735-T-C

42985974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68278780-A-G

42986006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68278812-A-G

42986081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68278885-T-A

http://identifiers.org/hco/4/GRCh38#42986275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68279086-A-C

42986454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68279250-C-T

42986640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68279430-A-G

42986642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68279432-G-A

42987096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68279840-C-T

42987593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68279983-G-A

42987667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68280052-C-G

http://identifiers.org/hco/4/GRCh38#42987847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68280221-A-C

42988062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68280407-G-T

42988183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68280523-T-C

42988231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68280566-G-A

42988231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68280566-G-C

42988733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68281015-A-G

42989877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68283504-T-A

42989893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68283525-C-G

42990166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68283787-A-T

http://identifiers.org/hco/4/GRCh38#42990788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68284125-A-C

42990845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68284178-A-G

42990905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68284384-T-C

42990940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68284494-A-G

42991019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68284669-G-T

42991063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68284738-A-G

42991428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68285118-A-G

42991755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68285493-G-A

42995920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68286338-G-A

42995972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68286392-C-T

42996027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68286449-C-T

42996087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68286538-G-A

42996143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68286592-G-A

42996341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68286784-T-C

42997039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68287477-G-T

42997154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68287564-T-C

42997229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68287629-G-A

42997257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68287649-G-C

42997261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68287653-G-A

43001546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68292278-C-T

43005358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68292775-G-A

43005358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68292775-G-T

43005385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68292810-A-G

43005458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68292873-T-G

43005554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68292980-C-T

43005571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68292997-G-A

43005572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68292998-G-A

43005574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68293000-A-G

43005602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68293018-A-G

http://identifiers.org/hco/4/GRCh38#43005739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68293152-C-A

http://identifiers.org/hco/4/GRCh38#43007639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68293186-C-A

43007747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68293288-G-A

43007747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68293288-G-T

43007990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68293540-A-T

43008012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68293563-C-T

43008014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68293565-C-T

43008069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68293615-A-G

43008103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68293646-T-A

43008244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68293780-C-T

43008589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68301723-A-T

43008833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68301979-T-C

43009015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68302149-T-A

43009015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68302149-T-C

43009059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68302192-T-C

43009480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68302587-T-A

43009755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68302879-C-T

43009917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68303072-G-A

43011631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68304086-G-A

43012179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68304649-G-A

43013726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68306802-A-G

43013857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68306972-G-A

43013938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307049-G-A

43014039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307150-T-A

43014214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307277-C-T

43014316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307382-T-C

43014338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307404-A-G

43014393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307459-C-T

http://identifiers.org/hco/4/GRCh38#43014461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68307527-C-A

43014670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307669-C-G

43014670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307669-C-T

43014690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307689-G-T

43014702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307701-T-C

43014745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307745-T-G

http://identifiers.org/hco/4/GRCh38#43014861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68307853-A-C

http://identifiers.org/hco/4/GRCh38#43014864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68307856-C-A

43014894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307886-C-T

43014980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307953-G-A

43015004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307976-C-T

43015007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68307979-G-A

43015181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68308124-T-C

43015343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68308250-A-T

43015460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68308362-A-G

43015763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68308673-A-G

43015764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68308674-A-G

43015792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68308711-T-C

43015800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68308719-C-T

43017077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68308775-G-A

43017077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68308775-G-T

43017157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68308858-C-T

43017282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68308973-T-A

http://identifiers.org/hco/4/GRCh38#43017485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68309255-A-C

43017536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68309289-T-C

http://identifiers.org/hco/4/GRCh38#43017690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68309438-A-C

43017825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68309569-T-G

http://identifiers.org/hco/4/GRCh38#43017961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68309703-C-A

43018312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68310023-C-T

43018322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68310033-T-A

43018468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68310196-G-A

43018604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68310326-T-A

43018721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68310442-A-T

43018837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68310558-A-G

43018878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68310597-C-T

43018879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68310598-G-A

43018908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68310636-A-G

43018956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68310683-C-T

43019045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68310766-A-T

43019193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68310929-C-T

43019506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68311184-A-G

43019548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68311226-C-G

43019548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68311226-C-T

43019714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68312590-G-T

43020045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68312893-C-G

43020129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68312959-G-A

43020145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68312975-T-A

43020232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68313047-A-T

http://identifiers.org/hco/4/GRCh38#43020311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68313125-C-A

http://identifiers.org/hco/4/GRCh38#43020336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68313153-A-C

http://identifiers.org/hco/4/GRCh38#43020492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68313306-C-A

43020492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68313306-C-T

43020498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68313312-G-A

43020498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68313312-G-T

43020612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68313424-C-T

43020714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68313520-C-G

43021152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68313877-C-T

43021208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68313933-G-A

43021312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68314031-A-G

43021315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68314034-T-C

43021595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68314311-C-G

43021615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68314331-T-C

43021688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68314399-G-A

43021747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68314458-T-A

43021977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68314629-T-C

http://identifiers.org/hco/4/GRCh38#43022053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68314702-A-C

http://identifiers.org/hco/4/GRCh38#43022147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68314801-A-C

43022147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68314801-A-G

http://identifiers.org/hco/4/GRCh38#43022347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68315742-C-A

43022489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68315876-T-G

43022491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68315878-A-G

43022545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68315931-T-C

43023259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68319728-T-C

43023433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68319896-A-G

43026975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68320117-T-G

43027029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68320168-A-G

43027070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68320203-G-A

43027070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68320203-G-T

43027562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68320688-G-C

43027643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68320772-T-C

43028159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68320969-G-T

43028319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68321132-C-T

43028325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68321138-C-T

43028374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68321183-G-C

http://identifiers.org/hco/4/GRCh38#43028575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#68321572-C-A

43028722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68321695-T-C

43029067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68322100-T-C

43029091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68322164-G-A

43029091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68322164-G-C

43029156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68322258-G-A

43029287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68322383-A-G

43029391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68322478-G-A

43029753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68322824-G-A

43029806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68322875-G-A

43029806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68322875-G-T

43029877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68322950-A-G

43030000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: intron variant
orthologous variants: 68323074-T-A

43030378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: missense variant
orthologous variants: 68323452-T-A

43030378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: synonymous variant
orthologous variants: 68323452-T-C

43030378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: missense variant
orthologous variants: 68323452-T-G

43030612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: 3 prime UTR variant
orthologous variants: 68323695-T-A

43030614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: 3 prime UTR variant
orthologous variants: 68323697-A-G

43030632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: 3 prime UTR variant
orthologous variants: 68323715-T-C

43030632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: 3 prime UTR variant
orthologous variants: 68323715-T-G

43030648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31673
most severe consequence: 3 prime UTR variant
orthologous variants: 68323731-G-A