39252832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973540-A-T

http://identifiers.org/hco/17/GRCh38#39252859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97973567-C-A

39252859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973567-C-G

http://identifiers.org/hco/17/GRCh38#39252885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97973593-C-A

39252885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973593-C-T

http://identifiers.org/hco/17/GRCh38#39252927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97973633-C-A

39252927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973633-C-T

39252928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973634-T-C

39253026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973730-G-A

39253026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973730-G-T

39253080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973772-G-C

39253080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973772-G-T

39253167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973831-A-G

39253204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973866-G-A

39253204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973866-G-C

39253216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973876-A-G

39253217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97973877-G-T

39253372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97974025-A-G

39253373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97974026-A-G

39253373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97974026-A-T

39253530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97974131-C-T

39253586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97974167-T-A

39254409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97974577-T-C

http://identifiers.org/hco/17/GRCh38#39254461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97974608-C-A

http://identifiers.org/hco/17/GRCh38#39254502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97974648-C-A

39254875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97974884-T-C

39255003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97975010-G-T

39256793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97975830-G-A

39256793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97975830-G-T

39256819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 97975850-T-C

39256850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 97975864-A-G

39256881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 97975896-A-G

39257348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976068-G-T

39257351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976071-T-A

39257453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976163-G-T

39257502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976212-A-G

39257527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976242-A-G

39257584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976303-T-C

39257652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976368-A-G

39257692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976408-C-G

39257765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976485-A-T

39257852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976533-A-G

39257890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976556-T-C

39257909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976575-G-T

39257940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976592-C-T

39258054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976691-G-C

39258166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97976844-A-G

39258532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97977579-T-C

39258677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97977724-T-A

39258899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97977945-C-G

39258899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97977945-C-T

39258967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97978191-G-A

39259153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3 prime UTR variant
orthologous variants: 97978373-G-T

http://identifiers.org/hco/17/GRCh38#39259488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97978514-A-C

39259488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97978514-A-G

39259573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97978590-T-C

39259598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97978622-G-A

39259598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97978622-G-C

39259598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97978622-G-T

http://identifiers.org/hco/17/GRCh38#39259620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97978642-C-A

39259620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97978642-C-T

39260088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97978999-A-G

39260101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97979012-T-C

39260124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97979032-G-T

http://identifiers.org/hco/17/GRCh38#39260192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97979097-C-A

http://identifiers.org/hco/17/GRCh38#39260239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97979154-C-A

http://identifiers.org/hco/17/GRCh38#39260277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97979207-C-A

39260493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97979422-G-T

39260509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97979446-T-C

39260686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97979620-A-G

39260713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97979647-T-C

http://identifiers.org/hco/17/GRCh38#39260758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97979686-A-C

39260758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97979686-A-G

39260771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97979699-G-A

39260771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97979699-G-T

http://identifiers.org/hco/17/GRCh38#39260777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97979705-C-A

39260792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97979723-G-T

http://identifiers.org/hco/17/GRCh38#39260868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97979839-C-A

39261030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97979994-C-T

39261083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980046-G-A

39261083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980046-G-T

39261171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980137-C-T

39261172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980138-T-C

39261175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980141-G-C

39261175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980141-G-T

39261180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980146-T-G

http://identifiers.org/hco/17/GRCh38#39261261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97980224-C-A

39261261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980224-C-G

39261285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980248-T-A

39261285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980248-T-C

39261285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980248-T-G

39261311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980273-T-A

39261311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980273-T-C

39261311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97980273-T-G

39261466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: missense variant
orthologous variants: 97980423-G-C

39261617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97980569-A-G

39261624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97980580-T-C

39261657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97980610-A-G

39261672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97980622-G-A

39261672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97980622-G-C

39261672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97980622-G-T

39261703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97980649-G-A

http://identifiers.org/hco/17/GRCh38#39261719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97980664-C-A

39261719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97980664-C-T

http://identifiers.org/hco/17/GRCh38#39263844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97981231-C-A

39263873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97981260-G-T

http://identifiers.org/hco/17/GRCh38#39263998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97981364-C-A

39263998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97981364-C-T

39264055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97981397-C-T

39264134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97981458-C-T

39264431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97981740-G-A

39264454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97981763-T-A

39264467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97981777-G-T

http://identifiers.org/hco/17/GRCh38#39264472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97981782-C-A

39264472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97981782-C-T

39264586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97981909-G-A

39264614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97981937-C-T

39265382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97982956-C-T

39265406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: synonymous variant
orthologous variants: 97982980-A-G

39265473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97983050-T-C

39268749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97983868-G-A

39268749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97983868-G-T

39268753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97983872-T-A

39268753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97983872-T-C

39268753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97983872-T-G

39268773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97983884-T-C

39268773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97983884-T-G

39268796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97983911-T-C

39268817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97983929-A-G

http://identifiers.org/hco/17/GRCh38#39268887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97983999-A-C

39269673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97984929-T-C

39269705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97984961-T-C

39269738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97985014-T-C

39269740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97985016-C-T

39269778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97985053-A-G

39269797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97985072-C-T

39270270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97985708-G-A

39270281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97985733-C-T

39270743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97985910-G-C

39270743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97985910-G-T

39270856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 97986019-T-A

39270856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 97986019-T-C

39270926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron_variant, undefined
orthologous variants: 97986087-G-A

39270926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron_variant, undefined
orthologous variants: 97986087-G-T

39271148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97986286-G-C

39271201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97986338-C-G

39274832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97987642-G-A

39274832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97987642-G-C

39274832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97987642-G-T

http://identifiers.org/hco/17/GRCh38#39274921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97987704-A-C

39274922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97987705-G-A

39274922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97987705-G-C

39275155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97987941-A-T

http://identifiers.org/hco/17/GRCh38#39281024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97989005-A-C

39281043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989023-C-T

39281044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989024-A-G

39281059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989039-C-G

39281059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989039-C-T

39281155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989090-G-C

39281155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989090-G-T

39281253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989147-T-C

39281262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989156-A-G

39281262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989156-A-T

39281275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989169-G-T

39281281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989175-G-A

39281281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989175-G-T

39281311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989180-G-A

39281339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989200-T-C

39281355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989212-C-T

39281357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989214-A-G

39281367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989224-A-G

39281373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989230-G-A

http://identifiers.org/hco/17/GRCh38#39281377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97989234-A-C

39281910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97989821-T-C

39282593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97990686-G-A

39282593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97990686-G-T

39282600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97990692-A-T

http://identifiers.org/hco/17/GRCh38#39282641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97990732-C-A

39282641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97990732-C-T

39282652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97990743-T-A

39282652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97990743-T-C

http://identifiers.org/hco/17/GRCh38#39283050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97991041-A-C

39283864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97991439-T-C

39284285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97991834-C-T

39284350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97991882-C-T

39284384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97991904-T-C

39285366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97992426-T-C

http://identifiers.org/hco/17/GRCh38#39285688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97992946-C-A

39286391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97993872-T-G

39286393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97993874-T-C

39286458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97993959-G-A

39296783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 97999947-G-T

39296898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000010-C-T

39296946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000055-G-T

39297113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000309-C-T

39297265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000458-A-T

39297280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000459-G-A

39297280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000459-G-T

39297301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000480-T-G

39297302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000481-G-A

39297302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000481-G-T

39297304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000483-G-C

39297304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000483-G-T

39297365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000539-T-C

39297365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000539-T-G

39297374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000548-T-A

39297374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000548-T-C

39297374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000548-T-G

http://identifiers.org/hco/17/GRCh38#39297375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98000549-C-A

39297380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000554-T-A

39297380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000554-T-C

39297385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98000559-T-G

39298847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98001607-A-T

39298919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98001685-A-G

39298919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98001685-A-T

39298936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98001702-A-G

http://identifiers.org/hco/17/GRCh38#39299144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98001910-C-A

39299144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98001910-C-T

39299182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98001955-G-A

39299182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98001955-G-T

39299448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98002195-G-A

39301083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 98004129-A-G

39301101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98004147-T-C

http://identifiers.org/hco/17/GRCh38#39301105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98004151-C-A

39301105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98004151-C-T

39301125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98004171-A-G

http://identifiers.org/hco/17/GRCh38#39301126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98004172-A-C

http://identifiers.org/hco/17/GRCh38#39303560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98006195-C-A

39303560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98006195-C-G

39303560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98006195-C-T

39303570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98006205-G-A

39303570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98006205-G-T

http://identifiers.org/hco/17/GRCh38#39303692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98006319-C-A

39303812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98006415-G-A

39304034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98006847-A-G

39306808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98009514-C-G

39306913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98009602-T-C

39342437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98018341-T-C

39342450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98018354-T-G

39342475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98018378-G-A

http://identifiers.org/hco/17/GRCh38#39342480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98018383-C-A

http://identifiers.org/hco/17/GRCh38#39342520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98018410-C-A

39342541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98018431-C-T

39342724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98018585-C-T

39342791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98018644-A-G

39342792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98018645-G-A

39342807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98018651-G-A

39342830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98018674-C-T

39342835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98018680-T-C

39342863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98018705-C-T

39342906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98018761-C-T

39343079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98019044-A-G

39343094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98019057-G-A

39343094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98019057-G-T

39343135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98019097-T-C

39343150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98019114-A-G

39343311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98019261-T-A

39343311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98019261-T-C

39343311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98019261-T-G

http://identifiers.org/hco/17/GRCh38#39343331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98019281-A-C

39343333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98019283-G-A

39343333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98019283-G-C

39343333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98019283-G-T

39365047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98026388-T-C

39365198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98026713-T-A

39365546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98027043-T-C

39389193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98030306-A-G

39389399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98030506-G-A

39390042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98030772-A-G

39390919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98031483-C-G

39390950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98031532-G-A

39391297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98031857-G-A

39391384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98031936-C-T

http://identifiers.org/hco/17/GRCh38#39391557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98032087-C-A

39391557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98032087-C-T

39392507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98033496-T-G

39392549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98033543-G-A

39394157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98034464-C-T

39394163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98034470-G-A

39394279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98034587-T-C

http://identifiers.org/hco/17/GRCh38#39397334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98035844-A-C

39397362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98035870-C-G

39397756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98036198-A-G

39397814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98036257-T-G

39398867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98037365-G-A

39398868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98037366-T-G

39398986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98037495-T-C

http://identifiers.org/hco/17/GRCh38#39399007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98037511-A-C

39399072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98037576-T-C

39399280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98038184-G-A

39399280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98038184-G-C

39401030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98039819-G-A

39401135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98039930-G-A

http://identifiers.org/hco/17/GRCh38#39401216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98040008-A-C

39401216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98040008-A-G

39401258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98040046-T-C

39401295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98040082-G-A

39401295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98040082-G-C

39401295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98040082-G-T

39401415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98040196-T-C

39401415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98040196-T-G

39401716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98040498-G-A

39401716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98040498-G-C

39401716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98040498-G-T

http://identifiers.org/hco/17/GRCh38#39401717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98040499-C-A

39401754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98040524-G-A

39401772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98040542-C-T

39401776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98040546-T-A

39401776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98040546-T-C

39401776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: 98040546-T-G

http://identifiers.org/hco/17/GRCh38#39401782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#98040552-A-C

http://identifiers.org/hco/17/GRCh38#39401819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#98040589-C-A

39401819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron_variant, undefined
orthologous variants: 98040589-C-G

39401819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron_variant, undefined
orthologous variants: 98040589-C-T

39401944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron_variant, undefined
orthologous variants: 98040732-G-A

39401944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron_variant, undefined
orthologous variants: 98040732-G-T

39401993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron_variant, undefined
orthologous variants: 98040780-G-A

39401993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron_variant, undefined
orthologous variants: 98040780-G-C

39401993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron_variant, undefined
orthologous variants: 98040780-G-T

39402096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron_variant, undefined
orthologous variants: 98040868-T-A

39402096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: intron_variant, undefined
orthologous variants: 98040868-T-C

39402401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98041157-G-A

39402414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98041171-C-G

39402414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98041171-C-T

http://identifiers.org/hco/17/GRCh38#39402428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#98041185-C-A

39402428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98041185-C-T

39402534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98041286-G-T

39402548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98041300-G-A

39402548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24679
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98041300-G-T