131949948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 110918468-C-T

131950021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: 5 prime UTR variant
orthologous variants: 110918397-A-G

131950049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, undefined
orthologous variants: 110918369-G-A

131950049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, undefined
orthologous variants: 110918369-G-T

131950112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110918326-G-C

131950112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110918326-G-T

131950143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110918295-C-T

131954393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: -G-C

131957484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110907421-C-T

131957770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110907160-A-G

131960507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110904728-G-A

131960507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110904728-G-T

131960821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110904397-A-G

131961079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110904139-G-A

131961131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110904087-T-C

http://identifiers.org/hco/12/GRCh38#131961157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110904061-A-C

131961394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110903824-A-G

131961529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110903686-G-A

http://identifiers.org/hco/12/GRCh38#131961601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110903614-C-A

131961601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110903614-C-T

http://identifiers.org/hco/12/GRCh38#131961603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110903612-C-A

131961603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: synonymous variant
orthologous variants: 110903612-C-T

131961988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110903227-T-C

131962453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110902769-T-C

131963281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110902020-A-G

131969957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110896155-A-G

http://identifiers.org/hco/12/GRCh38#131970531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110895631-A-C

131979350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110890331-A-G

131979635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110890005-G-A

131979635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110890005-G-C

131979667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110889951-A-G

131979756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: synonymous variant
orthologous variants: 110889862-T-C

http://identifiers.org/hco/12/GRCh38#131979812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110889814-C-A

131979812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110889814-C-T

131979863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110889790-A-G

131980925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110888696-A-G

131980956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110888667-A-G

131981027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110888595-A-G

131981348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110888280-A-G

131981670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110887980-G-T

131981753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110887892-A-G

http://identifiers.org/hco/12/GRCh38#131982002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110887636-A-C

131982002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110887636-A-G

http://identifiers.org/hco/12/GRCh38#131982081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110887557-C-A

131982326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110887312-C-G

131982574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110887040-G-A

131986368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110883651-T-C

131986395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110883615-T-C

131986395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110883615-T-G

131986517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110883507-G-T

131986720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: synonymous variant
orthologous variants: 110883301-T-C

131986888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110883088-G-A

131986888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110883088-G-C

131986902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110883066-C-G

131986902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110883066-C-T

131986986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110882912-G-T

131987568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110881883-T-A

131987568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110881883-T-C

131987617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110881838-A-G

131987617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110881838-A-T

http://identifiers.org/hco/12/GRCh38#131987679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110881795-C-A

131987679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110881795-C-T

http://identifiers.org/hco/12/GRCh38#131987686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110881785-C-A

131987686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110881785-C-T

131987852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110881621-G-A

131988541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110881223-T-C

131988969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110880850-G-A

131988984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110880835-A-G

131989613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110878566-G-A

131989917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110877865-G-A

131989917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110877865-G-C

http://identifiers.org/hco/12/GRCh38#131990161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110877628-C-A

http://identifiers.org/hco/12/GRCh38#131990175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110877613-C-A

http://identifiers.org/hco/12/GRCh38#131990213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110877582-C-A

131990350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110877474-G-A

131990907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, undefined
orthologous variants: 110876127-G-A

131990907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, undefined
orthologous variants: 110876127-G-T

131990919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110876115-C-G

131991193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110875855-A-G

131991312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110875556-G-A

131991312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110875556-G-T

http://identifiers.org/hco/12/GRCh38#131991326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110875539-C-A

131991326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110875539-C-T

131991330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110875535-A-G

131991558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110875316-T-A

131991558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110875316-T-C

131992070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110874910-T-G

http://identifiers.org/hco/12/GRCh38#131992072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110874908-C-A

131992072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110874908-C-T

131992116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110874860-T-C

131992116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110874860-T-G

131992131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110874846-G-T

http://identifiers.org/hco/12/GRCh38#131992511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110874247-A-C

131992574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110874184-C-G

131994231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110872967-T-C

131995107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110872138-T-A

131995107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110872138-T-C

131995107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110872138-T-G

131995109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110872136-A-G

131995181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110872070-G-A

131995181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110872070-G-T

132005162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: synonymous variant
orthologous variants: 110868622-G-A

132005162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: synonymous variant
orthologous variants: 110868622-G-T

132005199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110868585-T-A

132005288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110868428-T-A

132005401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110868176-A-G

132005401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110868176-A-T

132005645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110867906-C-T

132006153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: synonymous variant
orthologous variants: 110867446-T-C

132006153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110867446-T-G

132006291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110867308-G-A

132006297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110867302-A-G

132006760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: synonymous variant
orthologous variants: 110867068-C-T

132006891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110866937-A-G

132012905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110856866-G-A

132012905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110856866-G-T

132013129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110856687-G-A

132013129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110856687-G-C

132013202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110856610-T-C

132013204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110856608-G-T

132020286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110849427-T-C

http://identifiers.org/hco/12/GRCh38#132020316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110849397-C-A

132020316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110849397-C-T

132021851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110847925-T-G

132022522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110847348-A-G

132023590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110846939-T-C

132024096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110846459-C-T

http://identifiers.org/hco/12/GRCh38#132025498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110845390-C-A

132025498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110845390-C-T

132025507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110845381-T-G

132025850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110845029-T-A

132025875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110844995-A-G

132027457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110843891-G-A

132027474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: synonymous variant
orthologous variants: 110843874-T-C

http://identifiers.org/hco/12/GRCh38#132027897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110843542-C-A

132027897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110843542-C-T

http://identifiers.org/hco/12/GRCh38#132029574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110841613-C-A

132029574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110841613-C-T

132029759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110841428-C-T

132030170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110841009-A-G

132030170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110841009-A-T

132030183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110840992-T-A

132030231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110840947-T-A

132030377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110840829-C-T

132030825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110840452-C-T

132031091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110840160-G-A

132031147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110840106-G-T

132031319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110839953-G-A

132031324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110839948-T-C

132032121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110839511-G-A

132032232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110839455-A-G

132032318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110839368-T-C

132032318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110839368-T-G

132032476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110839216-G-A

132032476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110839216-G-T

132037288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110836490-G-A

132037362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110836428-G-T

132037430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110836367-C-T

132037652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110836219-G-C

132037652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110836219-G-T

http://identifiers.org/hco/12/GRCh38#132037828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110835969-C-A

132037828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110835969-C-T

132037842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110835957-C-G

132037842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110835957-C-T

http://identifiers.org/hco/12/GRCh38#132037867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110835918-C-A

132038028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110835730-G-T

132038146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110835600-G-A

132038146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110835600-G-C

132038152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110835594-C-T

132038213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110835518-T-C

132038256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110835477-T-G

132043131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110833505-T-G

http://identifiers.org/hco/12/GRCh38#132043253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110833424-A-C

132043253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110833424-A-G

132043262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110833415-T-G

http://identifiers.org/hco/12/GRCh38#132043547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110833125-C-A

132043547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110833125-C-T

132044282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110832426-A-G

132044533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110832122-A-T

132044608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110832053-T-C

http://identifiers.org/hco/12/GRCh38#132044627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110832034-C-A

132044722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110831944-G-T

132044824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110831839-C-G

132044864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110831799-T-G

132045235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110831323-G-A

132045235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110831323-G-T

132045266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110831293-C-T

132045306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110831252-C-T

132045441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110831119-A-G

132045441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110831119-A-T

132045555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110831005-C-T

http://identifiers.org/hco/12/GRCh38#132045584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110830973-C-A

132045584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110830973-C-G

132045679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110830890-C-T

132045689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110830874-G-A

132046478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110830322-C-G

132046572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110830248-G-A

132049068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110829268-C-T

132049156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110829203-C-T

132049184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110829181-G-C

132049202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110829163-A-G

132049444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110828925-G-A

http://identifiers.org/hco/12/GRCh38#132049900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110828569-C-A

132050661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110827822-T-A

http://identifiers.org/hco/12/GRCh38#132050701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110827777-C-A

132050701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110827777-C-T

132050742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110827747-T-C

132050857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110827608-T-A

132050896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110827565-G-A

132050907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110827554-A-G

132050907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110827554-A-T

132053244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110824685-C-T

132053349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110824605-G-A

132053521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110824391-A-G

132053538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110824374-G-A

132053538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110824374-G-T

132054104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110823874-C-T

132054147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110823837-C-T

132054350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110823657-C-G

132054661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110823315-A-G

132062382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110821222-C-T

132062837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110820876-G-A

132062843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110820870-T-A

132062843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110820870-T-C

http://identifiers.org/hco/12/GRCh38#132062876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110820839-A-C

http://identifiers.org/hco/12/GRCh38#132062888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110820828-A-C

132062888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron variant
orthologous variants: 110820828-A-G

132064725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense variant
orthologous variants: 110818903-C-T

http://identifiers.org/hco/12/GRCh38#132065007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110818607-C-A

132065117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110818461-T-A

132065117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110818461-T-C

132065169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110818402-T-C

132065191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110818381-T-A

132065191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110818381-T-C

132065219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110818353-G-A

132065219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110818353-G-T

http://identifiers.org/hco/12/GRCh38#132065242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110818331-C-A

132065242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110818331-C-T

132065300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110818285-G-C

132065362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110818225-T-C

132065362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110818225-T-G

http://identifiers.org/hco/12/GRCh38#132065382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110818208-C-A

132065382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110818208-C-T

132065383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110818207-G-A

http://identifiers.org/hco/12/GRCh38#132066226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110817127-C-A

132066226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110817127-C-T

http://identifiers.org/hco/12/GRCh38#132066576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#110816804-C-A

http://identifiers.org/hco/12/GRCh38#132066626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110816763-C-A

132067343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110816073-G-A

132067409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 110816007-C-T

132067569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110815860-A-G

132067591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110815838-T-C

132067591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110815838-T-G

132076665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110814328-A-G

132076667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110814326-G-A

132077369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110813967-G-C

132077369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110813967-G-T

132077384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110813952-T-C

132077394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110813945-G-A

132077422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 11958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110813917-C-T