126482209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: 3 prime UTR variant
orthologous variants: 90340332-A-G

126482209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: 3 prime UTR variant
orthologous variants: 90340332-A-T

126482640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90339960-C-T

126482951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90339642-G-A

126483304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90338594-G-A

126483304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90338594-G-C

126483313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90338585-G-T

126483492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90338407-A-T

126483504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90338400-G-T

126483506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90338398-G-A

126483506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90338398-G-T

126483525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90338380-A-G

126487441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron_variant, undefined
orthologous variants: -C-T

http://identifiers.org/hco/3/GRCh38#126487453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron_variant, undefined
orthologous variants: -C-A

126487453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron_variant, undefined
orthologous variants: -C-T

126488034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90336152-T-G

http://identifiers.org/hco/3/GRCh38#126488147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90336016-C-A

126488147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90336016-C-T

126488161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90336003-A-G

126488294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90335870-A-G

126488374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90335809-A-G

126488559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90335575-A-G

126488605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90335491-A-G

126489378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90334495-G-A

126489378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90334495-G-T

126489492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90334381-T-C

126489732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90334147-A-G

126491312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90333369-C-T

126491948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332781-T-G

126492035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332705-C-G

126492035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332705-C-T

126492142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332611-A-T

126492166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332586-G-A

126492228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332536-T-C

126492337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332434-G-A

126492337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332434-G-T

126492577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332198-G-T

126492586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332190-G-A

126492586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332190-G-T

126492635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332160-G-A

126492635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332160-G-T

http://identifiers.org/hco/3/GRCh38#126492647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90332148-C-A

126492647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90332148-C-T

http://identifiers.org/hco/3/GRCh38#126492777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90331999-C-A

126492777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90331999-C-T

126492860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90331917-C-T

126493053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90331727-T-G

http://identifiers.org/hco/3/GRCh38#126493189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90331631-A-C

126493191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90331629-C-T

126494545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90329883-C-T

126494966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90329619-T-A

126494977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90329608-G-C

126495461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90328591-T-C

126495479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90328573-C-T

126495521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90328546-A-G

126495676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90328424-T-C

126495758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90328392-A-G

126495828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90328331-C-G

126495944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90328247-T-C

http://identifiers.org/hco/3/GRCh38#126495948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90328243-C-A

126495957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90328234-G-A

126495957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90328234-G-T

http://identifiers.org/hco/3/GRCh38#126495958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90328233-C-A

126495958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90328233-C-T

126496016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90328155-T-C

126496104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: synonymous variant
orthologous variants: 90328068-C-T

http://identifiers.org/hco/3/GRCh38#126496125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90328045-A-C

126496125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90328045-A-G

126496344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90327830-C-G

126496417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90327761-G-A

126496792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90327438-G-A

126496792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90327438-G-T

126496860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90327337-C-T

126497071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90327123-C-T

126497769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90326392-C-G

126497996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90326240-G-A

126497996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90326240-G-T

126498013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90326223-G-A

126498029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90326208-G-A

http://identifiers.org/hco/3/GRCh38#126498074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90326161-A-C

126498534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90325708-C-G

126498534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90325708-C-T

126498921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90325329-C-G

126499042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron_variant, undefined
orthologous variants: 90325214-A-G

126499052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron_variant, undefined
orthologous variants: 90325185-G-A

126499052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron_variant, undefined
orthologous variants: 90325185-G-T

126499228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90325040-G-C

126499228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90325040-G-T

http://identifiers.org/hco/3/GRCh38#126499244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90325024-A-C

126499272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90325006-G-A

126499272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90325006-G-T

http://identifiers.org/hco/3/GRCh38#126499278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90325000-C-A

126499284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324994-C-T

126499316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324961-T-A

126499387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: synonymous variant
orthologous variants: 90324894-A-T

126499406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense variant
orthologous variants: 90324875-G-A

126499406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense variant
orthologous variants: 90324875-G-C

126499501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324791-G-A

126499613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324672-G-T

126499918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324459-A-G

126499918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324459-A-T

126499979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324394-G-A

126499979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324394-G-T

http://identifiers.org/hco/3/GRCh38#126499996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90324378-C-A

126499996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324378-C-T

126500043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324334-C-T

126500113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense variant
orthologous variants: 90324264-T-A

126500113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense variant
orthologous variants: 90324264-T-C

126500168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324209-T-A

126500168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324209-T-C

126500169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324208-G-T

126500191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324201-G-T

http://identifiers.org/hco/3/GRCh38#126500237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90324165-C-A

126500237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324165-C-T

http://identifiers.org/hco/3/GRCh38#126500243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90324159-A-C

126500243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324159-A-G

126500243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324159-A-T

http://identifiers.org/hco/3/GRCh38#126500295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90324097-A-C

126500295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90324097-A-G

126500508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90323907-C-T

126500587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90323831-T-A

126500587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90323831-T-C

126500752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense variant
orthologous variants: 90323742-T-C

http://identifiers.org/hco/3/GRCh38#126500858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#90323636-C-A

126500858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense variant
orthologous variants: 90323636-C-T

126500953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90323538-T-C

http://identifiers.org/hco/3/GRCh38#126500964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90323535-C-A

http://identifiers.org/hco/3/GRCh38#126500969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90323530-C-A

126500969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90323530-C-T

http://identifiers.org/hco/3/GRCh38#126500970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90323529-C-A

126500970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90323529-C-T

126501135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90323398-G-A

126501135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90323398-G-T

126501145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90323388-A-G

126501146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90323387-G-A

126501146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90323387-G-T

http://identifiers.org/hco/3/GRCh38#126501311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90323257-C-A

126501311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 90323257-C-T

126501327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90323241-A-G

126503878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90322475-A-G

126504011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense variant
orthologous variants: 90322361-A-T

126504412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90322167-G-A

126504412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90322167-G-T

http://identifiers.org/hco/3/GRCh38#126504421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90322158-A-C

126504595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321981-A-G

126505276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321724-C-T

126505304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321695-C-T

126505389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321596-A-G

126505584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321416-G-T

126505643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321310-G-C

126505646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321307-A-G

126505647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321306-G-A

126505647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321306-G-C

126505651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321302-G-A

126505651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321302-G-T

126505685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321252-G-A

http://identifiers.org/hco/3/GRCh38#126505877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90321059-A-C

http://identifiers.org/hco/3/GRCh38#126505880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90321056-C-A

126505880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321056-C-T

http://identifiers.org/hco/3/GRCh38#126505883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90321053-A-C

126505883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321053-A-G

126505894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321047-T-A

126505894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321047-T-C

126505894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321047-T-G

126505905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321041-T-A

126505905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321041-T-C

126505905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90321041-T-G

126506040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90320912-G-A

http://identifiers.org/hco/3/GRCh38#126506114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90320877-C-A

126506114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90320877-C-G

126506131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90320860-T-C

126506154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90320841-G-A

http://identifiers.org/hco/3/GRCh38#126506157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90320838-C-A

126506157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90320838-C-T

http://identifiers.org/hco/3/GRCh38#126506419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90319996-C-A

126506419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90319996-C-T

126507671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315902-A-G

http://identifiers.org/hco/3/GRCh38#126507870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90315746-A-C

126507910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315720-T-C

126507934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315691-G-A

126507954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315671-G-A

126507954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315671-G-C

126507954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315671-G-T

126508106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315519-A-G

126508118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315507-G-A

126508187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315430-C-T

126508212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315386-C-G

http://identifiers.org/hco/3/GRCh38#126508242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90315355-C-A

126508242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315355-C-T

126508290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315308-T-C

126508456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense variant
orthologous variants: 90315209-G-C

http://identifiers.org/hco/3/GRCh38#126508488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90315177-C-A

126508488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315177-C-G

126508488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90315177-C-T

http://identifiers.org/hco/3/GRCh38#126509564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90314750-C-A

126509564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90314750-C-T

126509676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 90314639-G-A

126509676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 90314639-G-T

http://identifiers.org/hco/3/GRCh38#126509715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90314580-C-A

126509715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90314580-C-T

http://identifiers.org/hco/3/GRCh38#126509721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90314574-A-C

http://identifiers.org/hco/3/GRCh38#126509757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90314555-C-A

126509757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90314555-C-T

126509761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90314551-T-C

126509962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90314300-G-T

126510607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90314027-C-T

126510653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90313981-A-G

126510760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense variant
orthologous variants: 90313873-G-A

126510760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense variant
orthologous variants: 90313873-G-T

http://identifiers.org/hco/3/GRCh38#126510772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90313861-C-A

126510772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: missense variant
orthologous variants: 90313861-C-T

126510849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90313797-T-C

126513572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90313136-G-A

126513644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90313077-C-T

126513667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90313053-G-A

126513822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312925-C-T

126513867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312705-C-G

126513867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312705-C-T

126513877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312695-C-T

126514001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312583-G-C

126514143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312463-C-T

126514213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312389-T-C

126514222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312382-G-A

126514222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312382-G-T

126514504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312092-C-G

126514504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312092-C-T

126514544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312051-C-T

126514554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312045-T-G

126514558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26444
most severe consequence: intron variant
orthologous variants: 90312041-T-C