45981783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: 5 prime UTR variant
orthologous variants: 76561818-G-A

45981783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: 5 prime UTR variant
orthologous variants: 76561818-G-C

45981783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: 5 prime UTR variant
orthologous variants: 76561818-G-T

http://identifiers.org/hco/21/GRCh38#45981837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#76561763-C-A

45981837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 76561763-C-T

http://identifiers.org/hco/21/GRCh38#45981903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76561693-C-A

45981903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76561693-C-T

45981952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, undefined
orthologous variants: 76561647-G-T

45982014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76561561-G-A

45982014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76561561-G-T

http://identifiers.org/hco/21/GRCh38#45982015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76561560-C-A

45982015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76561560-C-T

http://identifiers.org/hco/21/GRCh38#45982027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76561542-C-A

45982027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76561542-C-G

45982027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76561542-C-T

http://identifiers.org/hco/21/GRCh38#45982028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76561541-C-A

45982055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76561498-T-A

45982055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76561498-T-C

45982057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76561496-G-A

45982110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76561427-C-T

45982548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76561011-G-A

45982548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76561011-G-T

45982556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560997-G-A

45982556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560997-G-C

45982601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560938-G-A

http://identifiers.org/hco/21/GRCh38#45982706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76560828-C-A

45982753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76560781-C-G

45982767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560767-G-A

45982806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560730-C-T

45982909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560620-T-A

45982909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560620-T-C

45982913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560613-G-C

45982913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560613-G-T

45982925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560601-G-A

http://identifiers.org/hco/21/GRCh38#45982999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76560563-A-C

45983014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560557-G-T

45983088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560482-G-A

http://identifiers.org/hco/21/GRCh38#45983161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76560411-C-A

45983234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560358-G-A

45983338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560291-G-A

http://identifiers.org/hco/21/GRCh38#45983474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76560161-C-A

45983510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560122-C-T

45983570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76560071-C-T

45983731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76559961-G-A

45983880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76559831-C-T

45983964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76559760-T-C

http://identifiers.org/hco/21/GRCh38#45984123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#76559577-C-A

45984124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, undefined
orthologous variants: 76559576-T-G

http://identifiers.org/hco/21/GRCh38#45984233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76559443-C-A

45984233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76559443-C-T

45984378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76559299-C-G

http://identifiers.org/hco/21/GRCh38#45984387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76559290-A-C

45984408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76559269-T-A

http://identifiers.org/hco/21/GRCh38#45984488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#76559189-C-A

45984497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, undefined
orthologous variants: 76559180-G-A

45984497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, undefined
orthologous variants: 76559180-G-T

http://identifiers.org/hco/21/GRCh38#45984510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#76559166-C-A

45984510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, undefined
orthologous variants: 76559166-C-T

45984525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, undefined
orthologous variants: 76559154-G-A

45984525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, undefined
orthologous variants: 76559154-G-C

45984525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, undefined
orthologous variants: 76559154-G-T

45984531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76559148-G-A

45984531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76559148-G-C

45984621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76559066-G-A

45984621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76559066-G-T

45986272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76558059-G-A

45986353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557983-C-T

http://identifiers.org/hco/21/GRCh38#45986400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76557951-C-A

45986400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557951-C-T

http://identifiers.org/hco/21/GRCh38#45986401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76557950-C-A

45986402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557949-A-G

45986408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557943-A-G

45986409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557942-G-A

45986409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557942-G-T

http://identifiers.org/hco/21/GRCh38#45986428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76557927-C-A

45986428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557927-C-T

45986447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557904-G-A

45986447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557904-G-C

45986447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557904-G-T

45986497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557836-G-A

45986497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557836-G-T

http://identifiers.org/hco/21/GRCh38#45986513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76557820-C-A

45986513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557820-C-T

45986514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557819-T-C

http://identifiers.org/hco/21/GRCh38#45986515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76557818-C-A

45986515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557818-C-T

45986527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 76557806-G-A

45986527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 76557806-G-C

45986527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 76557806-G-T

45986566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76557767-A-G

45986566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76557767-A-T

45986569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76557764-G-A

45986569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76557764-G-T

45986693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76557640-C-G

45986693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76557640-C-T

45986719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557619-A-G

45986723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557614-C-T

45986753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557578-G-A

45986753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557578-G-T

45986797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557494-C-G

45986808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557483-T-C

45986856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557451-G-A

45986856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557451-G-T

45986885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557419-G-A

45986885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557419-G-T

45986887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557417-G-A

45986887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557417-G-T

45986888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557416-G-A

http://identifiers.org/hco/21/GRCh38#45986891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76557411-C-A

45986893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557409-G-A

45986893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557409-G-T

45986995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76557312-A-G

45986995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76557312-A-T

http://identifiers.org/hco/21/GRCh38#45987019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76557288-C-A

45987019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76557288-C-T

http://identifiers.org/hco/21/GRCh38#45987081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76557217-C-A

45987081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557217-C-G

45987081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76557217-C-T

45987291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76557047-T-C

45987291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76557047-T-G

http://identifiers.org/hco/21/GRCh38#45987545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76556907-C-A

45987545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76556907-C-T

http://identifiers.org/hco/21/GRCh38#45987594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76556853-C-A

45987657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76556790-G-T

http://identifiers.org/hco/21/GRCh38#45989016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76555602-C-A

45989016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76555602-C-G

45989099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76555493-C-G

45989099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76555493-C-T

45989187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76555394-A-G

45989206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76555375-T-A

45989206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76555375-T-G

http://identifiers.org/hco/21/GRCh38#45989274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76555291-C-A

http://identifiers.org/hco/21/GRCh38#45989307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76555260-C-A

45989331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76555227-C-T

45989335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76555223-C-G

45989335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76555223-C-T

45989657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554952-G-A

45989662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554947-C-T

45989678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554924-G-A

45989678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554924-G-C

45989678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554924-G-T

45989742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554847-G-A

45989761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76554828-G-A

45989761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76554828-G-C

45989767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76554822-C-T

45989797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554792-C-T

http://identifiers.org/hco/21/GRCh38#45989811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76554778-C-A

45989811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554778-C-T

45989823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554767-G-A

45989823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554767-G-T

45990297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554336-T-C

45990305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554328-G-A

45990305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554328-G-C

45990305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554328-G-T

45990306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554327-G-A

45990306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554327-G-C

45990306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554327-G-T

45990370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76554257-C-T

45990393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76554234-C-G

45990393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76554234-C-T

45990402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76554225-G-A

45990402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76554225-G-T

45990664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554034-G-A

45990664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554034-G-T

45990666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554032-T-C

45990666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554032-T-G

45990674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554024-G-C

45990674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554024-G-T

45990685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554013-G-T

45990687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554011-G-A

45990687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76554011-G-T

http://identifiers.org/hco/21/GRCh38#45990732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76553977-C-A

45990797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76553920-C-T

45990831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553886-G-A

45990831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553886-G-T

45990887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553830-A-G

45990910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553766-G-A

45990910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553766-G-T

45990938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553732-T-G

45990963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553707-G-A

http://identifiers.org/hco/21/GRCh38#45991045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76553623-A-C

45991752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553544-C-T

45991759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553537-G-A

http://identifiers.org/hco/21/GRCh38#45991765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76553531-C-A

45991823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553471-G-A

45991905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553392-G-A

45991905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553392-G-T

45991912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553385-C-T

45991942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553342-G-A

45991960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553324-C-T

45992104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553219-G-C

45992105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553218-G-A

45992123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553200-T-C

45992212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76553099-G-A

45992212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76553099-G-C

45992244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76553076-T-A

45992434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552925-C-G

45992434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552925-C-T

45992604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552759-G-A

45992604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552759-G-T

45992646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552715-G-A

45992646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552715-G-T

http://identifiers.org/hco/21/GRCh38#45992712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76552650-A-C

45992713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552649-G-A

45992713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552649-G-T

http://identifiers.org/hco/21/GRCh38#45992714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76552648-C-A

45992714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552648-C-T

45992718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552644-G-T

45992790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76552571-C-G

45992790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76552571-C-T

http://identifiers.org/hco/21/GRCh38#45992840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76552530-A-C

45992840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552530-A-G

45992853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552521-G-A

45992853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552521-G-T

45992888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552489-G-A

45992907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552470-A-G

45992907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76552470-A-T

http://identifiers.org/hco/21/GRCh38#45994149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76552173-C-A

45994149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76552173-C-G

45994149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76552173-C-T

45994212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76552110-G-C

http://identifiers.org/hco/21/GRCh38#45994218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76552104-C-A

45997379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76551199-G-A

45997379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76551199-G-T

45997486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76551100-G-C

http://identifiers.org/hco/21/GRCh38#45997558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76551041-C-A

45997558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76551041-C-T

45997560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76551039-G-A

45997560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76551039-G-T

http://identifiers.org/hco/21/GRCh38#45997605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76550991-C-A

http://identifiers.org/hco/21/GRCh38#45997606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76550990-C-A

45997606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76550990-C-T

http://identifiers.org/hco/21/GRCh38#45997694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76550895-C-A

http://identifiers.org/hco/21/GRCh38#45997991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76550650-C-A

45997991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76550650-C-T

http://identifiers.org/hco/21/GRCh38#45997992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76550649-C-A

45997992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76550649-C-G

45998015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76550628-G-T

45998095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76550568-C-G

45998095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76550568-C-T

45998116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76550545-C-T

http://identifiers.org/hco/21/GRCh38#45998285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76550392-C-A

45998302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76550376-G-A

45998302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76550376-G-T

45998332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76550341-T-C

45998350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76550323-C-T

45998380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76550298-C-T

45998601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76550147-G-A

45998609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76550137-C-G

45998641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76550117-C-T

45998663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76550100-G-A

45998720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76550087-G-A

45998811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76550051-T-C

45998939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76549966-G-A

45998939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76549966-G-C

45998939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense variant
orthologous variants: 76549966-G-T

45998992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549908-A-G

45999009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549895-G-A

45999009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549895-G-C

45999018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549886-C-T

45999043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549862-C-T

45999067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549843-C-T

45999073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549837-C-G

45999073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549837-C-T

45999130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549793-G-T

45999363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549618-G-A

45999363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549618-G-C

45999363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549618-G-T

45999383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549603-G-A

45999383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron variant
orthologous variants: 76549603-G-T

45999701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549449-G-A

45999701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549449-G-T

45999727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549420-C-T

http://identifiers.org/hco/21/GRCh38#45999728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76549419-C-A

45999728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549419-C-T

45999793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549372-G-A

45999793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549372-G-C

45999793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549372-G-T

45999804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549359-T-A

45999804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549359-T-C

45999804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549359-T-G

http://identifiers.org/hco/21/GRCh38#45999811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76549352-C-A

45999811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549352-C-G

45999811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549352-C-T

45999823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549344-G-A

45999823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549344-G-T

45999891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549299-C-T

46000115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549233-G-A

46000147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549201-C-T

46000179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549181-G-T

http://identifiers.org/hco/21/GRCh38#46000184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76549176-C-A

46000184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549176-C-T

http://identifiers.org/hco/21/GRCh38#46000218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76549137-C-A

46000218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549137-C-G

46000226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549129-G-A

46000226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549129-G-C

46000226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549129-G-T

46000299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76549074-T-C

46000388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76548994-G-A

46000388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76548994-G-T

46000613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76548775-G-T

46000692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76548730-A-G

46000810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76548669-G-A

46000810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76548669-G-T

http://identifiers.org/hco/21/GRCh38#46000819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76548660-C-A

46000819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76548660-C-G

46000819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76548660-C-T

46000822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76548657-G-C

46000838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76548618-A-G

http://identifiers.org/hco/21/GRCh38#46000868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#76548590-C-A

46000868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76548590-C-G

46000870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76548588-C-T

http://identifiers.org/hco/21/GRCh38#46000883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76548580-C-A

http://identifiers.org/hco/21/GRCh38#46000920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76548530-C-A

46000983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76548484-G-A

46000983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76548484-G-C

46000983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76548484-G-T

46000992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76548475-T-A

46000992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76548475-T-C

46001075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76548370-G-T

46001126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76548337-G-T

46001198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76548276-G-A

46001198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76548276-G-T

46001900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547581-T-A

46001900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547581-T-G

46001930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547549-T-G

http://identifiers.org/hco/21/GRCh38#46001941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76547538-C-A

46001948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547529-G-T

46001979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76547498-T-A

46001979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76547498-T-G

46002018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76547459-G-A

http://identifiers.org/hco/21/GRCh38#46002110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76547374-C-A

46002110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547374-C-T

46002115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547369-C-T

46002133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547359-G-T

http://identifiers.org/hco/21/GRCh38#46002170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76547323-C-A

46002170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547323-C-G

46002170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547323-C-T

46002219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 76547297-G-A

46002219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 76547297-G-T

46002267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76547249-G-T

46002288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 76547228-C-T

http://identifiers.org/hco/21/GRCh38#46002291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76547225-C-A

46002291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76547225-C-T

46002303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76547213-A-G

http://identifiers.org/hco/21/GRCh38#46002372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76547144-C-A

46002372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76547144-C-T

46002421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547093-G-C

http://identifiers.org/hco/21/GRCh38#46002431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76547083-C-A

46002431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547083-C-T

46002436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547078-C-T

46002441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547073-G-A

46002469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547027-C-G

46002469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76547027-C-T

46002507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76546988-G-A

46002539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76546959-G-A

46002720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546774-G-T

46002732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546762-C-T

46002944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546540-C-G

46003002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546413-G-A

46003002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546413-G-T

46003016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546376-G-T

http://identifiers.org/hco/21/GRCh38#46003025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76546367-C-A

46003025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546367-C-T

http://identifiers.org/hco/21/GRCh38#46003066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76546297-C-A

46003066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546297-C-T

46003098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546250-G-A

46003186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546139-G-A

46003271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546099-T-C

46003271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546099-T-G

46003278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546092-G-A

46003278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76546092-G-T

46003459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76545945-T-C

46003540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76545864-C-T

46003657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76545747-A-G

46003660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76545744-G-A

46003759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76545645-G-T

46003969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76545435-G-A

46003993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76545411-A-G

46004026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76545378-G-A

46004026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76545378-G-T

46004029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2211
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76545362-G-A