http://identifiers.org/hco/6/GRCh38#69900313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24598758-A-C

69900314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24598757-G-A

69900314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24598757-G-T

69900315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: synonymous variant
orthologous variants: 24598756-T-C

69900315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24598756-T-G

69900316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24598755-G-A

69900316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24598755-G-T

69900367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24598699-T-A

69900367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24598699-T-C

69900367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24598699-T-G

69900443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24598627-A-G

69900561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24598544-C-T

69900572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24598533-G-T

69900593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24598518-C-T

69900796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24598316-T-C

69900889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24598283-T-C

http://identifiers.org/hco/6/GRCh38#69901108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24598244-C-A

69901108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24598244-C-T

69901212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24598131-T-C

69901602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24597889-G-A

http://identifiers.org/hco/6/GRCh38#69901694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24597735-A-C

http://identifiers.org/hco/6/GRCh38#69901859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24597569-C-A

69901896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24597529-G-A

69906235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24596099-C-T

69906313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24596032-G-A

69906407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24595925-A-T

69906536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24595788-G-A

69906666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24595655-A-G

http://identifiers.org/hco/6/GRCh38#69907463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24594442-C-A

69907728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24594182-A-G

69907735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24594175-T-A

69907735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24594175-T-G

69907823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24594098-A-G

69907894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24594036-T-A

69908386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24592740-G-A

69908428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, undefined
orthologous variants: 24592707-G-T

69908521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24592499-C-T

69908799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24592260-G-A

http://identifiers.org/hco/6/GRCh38#69908908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24592150-A-C

69908931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24592120-A-T

69909144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24591260-A-G

69909144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24591260-A-T

69909156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24591247-A-G

69909304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24591122-T-A

69909304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24591122-T-C

69909332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24591090-G-A

http://identifiers.org/hco/6/GRCh38#69913191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24590470-C-A

http://identifiers.org/hco/6/GRCh38#69913316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#24590349-A-C

69913554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24590126-G-T

69913588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24590078-A-G

69913791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24589870-G-A

69913811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24589845-C-T

69913883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, undefined
orthologous variants: 24589774-T-C

http://identifiers.org/hco/6/GRCh38#69913917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#24589737-A-C

69914014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24589651-G-A

69914021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24589644-C-T

69914783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24588875-T-G

69914808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24588850-T-C

69914955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24588640-A-G

69915400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24588377-A-G

http://identifiers.org/hco/6/GRCh38#69915407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24588368-C-A

69915593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24588189-A-G

69915593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24588189-A-T

http://identifiers.org/hco/6/GRCh38#69915601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24588181-A-C

69915654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24588139-G-A

69915713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24588079-C-G

69915714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24588078-A-G

69915957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24587892-T-A

69915957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24587892-T-C

69916275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24587531-A-G

69916644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24587216-T-C

69916668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24587189-T-G

69917068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24586769-G-A

69917069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24586768-G-A

69917069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24586768-G-T

69917312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24586504-G-A

69917399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24586446-A-G

http://identifiers.org/hco/6/GRCh38#69917417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24586431-C-A

69917639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24586247-G-A

69917648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24586238-G-A

69917997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, undefined
orthologous variants: 24586108-T-A

69918115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, undefined
orthologous variants: 24585990-G-A

69918115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, undefined
orthologous variants: 24585990-G-C

69919006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24584147-G-T

69919156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24583805-T-C

http://identifiers.org/hco/6/GRCh38#69919252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24583708-A-C

69919252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24583708-A-G

http://identifiers.org/hco/6/GRCh38#69919551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24583351-A-C

69919551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24583351-A-T

69919613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24583286-A-G

69919644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24583255-A-G

69919703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24583194-C-G

69919906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24583025-G-T

69920057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24582670-A-G

69920251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24582483-A-G

69920421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24582320-T-C

http://identifiers.org/hco/6/GRCh38#69920458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24582283-A-C

69920458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24582283-A-G

69920478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24582263-G-T

69920574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24582186-C-T

69920603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24582155-T-A

69920603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24582155-T-C

69920669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24582102-G-T

69920680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24582091-G-A

69920787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24581991-G-A

69922056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24581667-G-C

69922093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24581630-G-C

69922104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24581619-G-A

69922125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24581598-T-A

69922353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24581360-T-A

69922353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24581360-T-C

http://identifiers.org/hco/6/GRCh38#69922509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24581230-C-A

69922509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24581230-C-G

69922509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24581230-C-T

69927428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24576572-T-C

69927507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24576503-G-C

69927835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24576154-G-A

69927863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24576127-G-A

69927863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24576127-G-T

http://identifiers.org/hco/6/GRCh38#69928084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24575929-A-C

69928128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24575885-G-A

69928211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24575804-C-T

69928343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24575447-A-G

69928483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24575313-C-T

http://identifiers.org/hco/6/GRCh38#69928855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24573970-C-A

69928879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24573946-G-A

69928881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24573944-T-C

69928993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24573825-G-A

69929299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24573504-G-C

69929340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24573483-A-G

69929349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24573474-G-A

69929349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24573474-G-T

69929399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24573424-T-C

69929412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24573411-T-C

69929445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: synonymous variant
orthologous variants: 24573367-T-C

69929623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24573189-A-G

69929716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24573096-A-G

69929896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24572371-C-G

69929898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24572369-C-G

69930011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24572240-T-C

69930022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24572230-A-G

69931530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24570645-A-G

69931716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24570471-T-C

69931740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24570445-C-G

69931980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24570206-C-G

69932243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24569628-A-G

69932319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24569548-G-A

69932319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24569548-G-C

69932319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24569548-G-T

69932328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24569539-T-G

69932331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24569536-A-T

69932650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24569214-A-T

69932733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24569135-A-T

69932813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24569057-A-G

69932943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24568924-A-G

69932944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24568923-G-T

http://identifiers.org/hco/6/GRCh38#69933014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24568854-C-A

69933084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24568797-C-G

69933084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24568797-C-T

69933899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24568434-G-A

69934297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24568064-C-T

69934626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24567760-G-A

69934666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24567708-G-C

69934885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24567499-A-G

69934917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24567466-A-T

69935485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24566870-G-A

69935537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24566828-T-G

69935557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24566809-G-A

69935589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24566774-G-C

69935595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24566768-G-A

69935649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24566714-G-A

69935649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24566714-G-C

69936203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24566106-C-T

69936270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24566066-C-G

69936275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24566061-G-A

69936538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24565812-T-C

http://identifiers.org/hco/6/GRCh38#69936817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#24565557-A-C

69936817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 24565557-A-G

69936841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 24565533-C-T

69936900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24565474-T-C

http://identifiers.org/hco/6/GRCh38#69936958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24565415-A-C

69936958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24565415-A-T

69937000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24565372-T-C

69937043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24565332-G-C

69937043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24565332-G-T

http://identifiers.org/hco/6/GRCh38#69937234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24565175-C-A

69937426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564988-A-G

69937999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564786-A-G

69937999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564786-A-T

69938069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24564714-C-T

69938135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564647-G-T

69938151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564631-G-C

69938151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564631-G-T

69938173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564607-A-G

69938200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564592-G-A

69938200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564592-G-T

69938250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564540-T-C

69938252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564538-G-A

69938288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564511-A-G

69938295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564504-G-A

69938307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564490-C-T

69938387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564413-C-G

69938387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564413-C-T

69938649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564179-G-T

69938774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564068-G-A

69940589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563726-T-C

69940590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563723-T-C

69940622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563691-T-C

69940915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563424-G-T

69940950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563393-C-T

69941057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563290-G-A

69941135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563210-T-C

69941312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563054-T-C

http://identifiers.org/hco/6/GRCh38#69941711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24562699-C-A

69941711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24562699-C-T

69942051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24562651-A-G

69942175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24562529-T-A

69942176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24562528-C-T

69945792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24561964-T-A

http://identifiers.org/hco/6/GRCh38#69945837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24561928-C-A

69945879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24561887-T-C

69946646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24561763-T-G

69946730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24561685-G-T

69946883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24561535-A-G

69947190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24561218-A-G

69947192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24561205-T-G

http://identifiers.org/hco/6/GRCh38#69947196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24561201-C-A

69947231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24561131-G-T

http://identifiers.org/hco/6/GRCh38#69947310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24561055-A-C

69947333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24561032-T-C

69947337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24561028-A-G

http://identifiers.org/hco/6/GRCh38#69947343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24561022-C-A

http://identifiers.org/hco/6/GRCh38#69947365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24561001-A-C

69947439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24560836-T-C

69947439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24560836-T-G

69948635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24560080-T-C

http://identifiers.org/hco/6/GRCh38#69949247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24559837-C-A

69949450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24559649-A-G

69950068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24558656-A-G

69950246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24558470-C-T

69950370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24558350-G-T

69950383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24558337-A-G

69950410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24558323-G-T

69950445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24558288-C-T

69950683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24558010-C-T

http://identifiers.org/hco/6/GRCh38#69950688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24558005-A-C

69950716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24557977-A-T

69950803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557890-C-T

69950806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557887-A-G

69950817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557876-C-G

69950837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557856-T-G

69950853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557841-A-G

http://identifiers.org/hco/6/GRCh38#69951255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24557363-A-C

69951853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24556823-G-T

http://identifiers.org/hco/6/GRCh38#69952085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24556611-C-A

69952131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24556577-T-C

69952345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24556370-C-T

69952351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24556364-C-T

69952855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555908-G-C

69953258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555004-T-A

69953258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555004-T-C

69953401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554890-T-C

69953432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554861-A-G

69953436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554857-T-C

http://identifiers.org/hco/6/GRCh38#69953496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24554802-C-A

69953496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554802-C-T

69953497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554801-A-T

http://identifiers.org/hco/6/GRCh38#69953816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24554485-C-A

69953816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554485-C-T

69953984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554315-A-T

69954023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554276-G-A

69954070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554230-G-C

69954263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554053-C-G

69954287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554038-C-T

69954304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554021-C-T

69954368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553951-G-A

69955059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553384-A-T

69955088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553354-G-T

69955114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553331-T-C

69955116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553329-T-C

69955275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553177-G-A

69955288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553161-C-T

69955326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553136-T-C

69955364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553102-T-C

69955526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552943-T-A

69955636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552864-T-C

69955688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552823-G-A

69955788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552734-T-C

69955792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552730-A-G

69957644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552328-G-A

69957719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552255-A-T

69957786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552133-A-G

69957937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551934-G-A

69957964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551872-C-T

69958013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551824-A-T

69958052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551788-C-G

69958238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551704-C-T

69958261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551681-G-A

69958268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551672-G-A

69958268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551672-G-T

69958421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551516-T-C

69958510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551428-G-C

69958510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551428-G-T

69958515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551423-G-T

69958545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551395-T-C

69958845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24551105-A-G

69959294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24550687-T-G

69959502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24550516-A-T

69959738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24550226-A-G

http://identifiers.org/hco/6/GRCh38#69959901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24550050-C-A

69959914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24550040-A-G

69960140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24549881-T-G

http://identifiers.org/hco/6/GRCh38#69960143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24549878-C-A

69960143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24549878-C-T

69960146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24549875-A-G

http://identifiers.org/hco/6/GRCh38#69960216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24549831-C-A

http://identifiers.org/hco/6/GRCh38#69960436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24549634-C-A

69960968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24549153-C-T

69961078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24549044-G-A

69961098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24549024-T-C

69961169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548954-G-C

69961170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548953-G-A

69961345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548776-T-G

69961420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548701-A-G

69961420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548701-A-T

69961597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548520-A-G

69961803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548334-G-A

69961815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548327-T-A

69961824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548318-T-A

69961844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548286-A-G

69961844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548286-A-T

69962023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548062-T-A

69962120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547968-C-T

69962198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547876-G-A

69962202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547872-A-G

69962219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547856-T-C

69962373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547718-C-T

69962553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547561-A-G

69962554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547560-T-C

http://identifiers.org/hco/6/GRCh38#69962721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24547409-C-A

69962761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547369-G-A

69962761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547369-G-C

69962761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547369-G-T

69962850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24547283-A-G

69962965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547179-T-C

69963210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546949-A-G

69963520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546646-C-T

69963543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546623-A-G

69963572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546607-C-T

69963586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546595-T-C

69963602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546590-A-G

69963638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546558-A-G

http://identifiers.org/hco/6/GRCh38#69963837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24546361-A-C

69963837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546361-A-G

69964113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546258-T-G

69964147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546224-C-T

69964284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546094-G-A

69964382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24545974-G-A

69964382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24545974-G-C

http://identifiers.org/hco/6/GRCh38#69964496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24545864-A-C

69967369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24544879-T-G

69967402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24544852-G-T

69967422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24544832-T-C

69967530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24544723-T-C

69967848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24544410-A-T

69967992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24544252-A-G

69968126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24544069-T-G

69968132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24544063-A-G

69968261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24543937-C-T

http://identifiers.org/hco/6/GRCh38#69968332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24543875-C-A

69968333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24543874-A-G

69968343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24543865-T-A

69968343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24543865-T-C

69968662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24543565-A-T

69968735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24543491-A-G

69969453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542522-T-C

69970338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24535270-A-G

69970435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24535184-T-C

http://identifiers.org/hco/6/GRCh38#69970678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24534936-C-A

69970678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24534936-C-T

http://identifiers.org/hco/6/GRCh38#69970769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24534850-A-C

69971210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24534456-A-G

69971279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24534386-T-C

69971337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24534346-G-A

69971462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24534241-A-G

69971629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24534078-C-T

69971645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24534062-A-T

69971657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24534051-C-T

69971805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24533869-T-A

69972029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24533676-C-T

69972283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24533184-T-C

69972364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24533101-A-G

69972438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24533030-T-C

69972451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24533017-A-G

69972526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24532951-C-G

http://identifiers.org/hco/6/GRCh38#69972831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24532624-C-A

69973005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24532450-A-G

69973427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24532085-C-T

http://identifiers.org/hco/6/GRCh38#69973769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24531663-C-A

69973918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24531517-T-C

69974009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24531437-G-A

69974009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24531437-G-T

69974118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24531333-A-G

69974118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24531333-A-T

69974140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24531318-A-G

69974163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24531300-G-T

69974355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24531103-C-T

69974569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24530899-G-A

69975735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24528701-G-T

69975881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24528575-C-T

http://identifiers.org/hco/6/GRCh38#69975900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24528556-C-A

69976179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24528305-A-G

69976261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24528228-G-A

69976291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24528202-T-C

69976358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24528157-A-G

69976582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24527935-G-A

69976763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24527763-C-T

http://identifiers.org/hco/6/GRCh38#69976800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24527726-A-C

69976845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24527567-A-T

69976871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24527541-G-A

69977685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: -C-T

69977738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: -G-T

http://identifiers.org/hco/6/GRCh38#69977950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24526921-A-C

69977953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24526918-T-A

69977955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24526916-T-A

69978212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24526690-G-A

69978212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24526690-G-T

69978327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24526519-A-G

69978486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24526068-C-T

69978490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24526064-A-G

69978641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24525885-A-T

69978823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24525684-A-G

69978864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24525653-G-T

69978978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24525543-C-T

69979069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24525472-T-C

69979473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24525079-A-G

69979685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24524895-T-C

69979702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24524883-T-C

69979751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24524837-G-A

69979771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24524812-G-T

69979800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24524778-A-G

69979955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24524640-A-G

69980388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523961-A-G

69980453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523894-A-G

69980479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523868-T-C

69980479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523868-T-G

69980580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523770-A-G

69980679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523693-G-A

69980751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523617-G-A

69980830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523543-C-T

69981030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523348-G-A

69981053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523324-T-C

69981095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523283-C-G

69981165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523225-T-C

http://identifiers.org/hco/6/GRCh38#69981242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24523136-C-A

69981289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523093-T-C

69981308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523074-A-G

69981310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523072-T-A

69981324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24523055-T-G

69981372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24522775-T-C

http://identifiers.org/hco/6/GRCh38#69981669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24522426-A-C

69981891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24522291-A-G

69981904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24522278-G-A

69981904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24522278-G-C

69981981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24522113-A-G

69982048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24522064-A-G

69982135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24521994-G-A

69982184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24521945-C-G

69982184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24521945-C-T

69985147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24520640-C-G

69985242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24520547-A-G

69985281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24520514-G-C

69985377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24520457-C-T

69985425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24520411-G-C

69985955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24519895-C-G

http://identifiers.org/hco/6/GRCh38#69986189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24519666-C-A

69986641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24519298-G-A

69986641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24519298-G-C

69986804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24519134-T-C

69987122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24519025-A-G

http://identifiers.org/hco/6/GRCh38#69987155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24518995-A-C

69987349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24518823-A-G

http://identifiers.org/hco/6/GRCh38#69987394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24518775-A-C

69987417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24518752-G-A

69988311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24518667-T-C

69988391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24518608-G-C

69988508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24518497-G-A

69988551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24518457-G-A

69988650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24518362-G-A

69988688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24518331-A-G

69994127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24510995-A-G

69994129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24510993-A-G

69994242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24510884-G-A

69994628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24510479-G-A

69994628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24510479-G-T

69994656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24510451-A-G

69994925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24510181-T-G

69995040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24510072-A-G

69995354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24509750-A-T

69995358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24509746-T-C

69995424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24509684-T-A

70019583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24507983-T-G

70019624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24507942-C-T

70019711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24507832-G-C

70020005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24507538-A-G

70020015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24507526-T-G

70020171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24507368-G-A

70020344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24507223-A-T

70020385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24507188-A-G

70020386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24507187-G-C

70020557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24507035-T-C

70020693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24506889-C-T

70020697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24506886-G-A

70020728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24506852-A-G

70020791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24506791-T-C

70020810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24506772-G-C

70020845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24506744-G-C

70022377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24504099-T-G

70022706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24501234-T-C

70022857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24501035-A-G

70022986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24500952-G-T

70023020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24500918-T-C

70023021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24500917-G-C

http://identifiers.org/hco/6/GRCh38#70023505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24500738-C-A

70023505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24500738-C-G

70023505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24500738-C-T

http://identifiers.org/hco/6/GRCh38#70023522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24500721-A-C

70023553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24500688-A-T

70023577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24500661-A-G

70023592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24500646-T-C

70023777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24500460-G-A

70023777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24500460-G-T

70023807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24500430-A-G

70024127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24500095-T-C

70024262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24499955-G-C

70024262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24499955-G-T

70024371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24499843-T-G

70024445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24499772-A-G

70024527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24499647-A-T

http://identifiers.org/hco/6/GRCh38#70024834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24499310-A-C

70024845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24499299-G-C

70024925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24499224-T-C

70024926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24499223-T-G

70027014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24498641-C-T

70027230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24498418-T-C

70027308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24498343-C-T

70027361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24498305-T-C

http://identifiers.org/hco/6/GRCh38#70027534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24497989-A-C

70027579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24497897-G-A

70027674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24497813-A-G

70027674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24497813-A-T

http://identifiers.org/hco/6/GRCh38#70027682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24497805-C-A

70027878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24497702-A-T

70028855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24497518-A-G

70028957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24497425-T-C

70029023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24497364-C-T

70029025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24497362-C-G

http://identifiers.org/hco/6/GRCh38#70029206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24497183-A-C

70029321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24497080-C-G

70029343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24497069-T-C

70029480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24496946-G-A

70029520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24496910-C-T

70029754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24496096-G-A

http://identifiers.org/hco/6/GRCh38#70029768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24496082-C-A

70029791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24496059-G-A

70029810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24496040-A-G

70029997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24495852-A-G

70030008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24495841-A-G

70032434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24494590-C-T

70032534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24494500-A-G

70032773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24494307-G-A

70032791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24494289-T-C

70032983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24494119-A-G

70032986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24494116-C-T

70032994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24494103-C-T

70033246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24493917-C-T

70033258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24493905-T-C

70033303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24493857-T-C

70033309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24493851-G-A

70033478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24493691-T-A

70033714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24493481-A-G

70033778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24493417-G-A

70033778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24493417-G-T

70033872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24493322-C-G

70033872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24493322-C-T

70034005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24493189-A-G

70034192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24492939-G-A

70034192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24492939-G-C

http://identifiers.org/hco/6/GRCh38#70034693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24492287-C-A

70034899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24492102-T-G

http://identifiers.org/hco/6/GRCh38#70035022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24492006-C-A

70035461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24491447-G-A

70035765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24491129-G-A

70035765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24491129-G-T

70035809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24490967-T-C

70035809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24490967-T-G

70035894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24490886-T-C

70035981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24490803-A-G

70036009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24490775-G-A

http://identifiers.org/hco/6/GRCh38#70036017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24490767-C-A

70036059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24490728-G-A

70036059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24490728-G-T

http://identifiers.org/hco/6/GRCh38#70036320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24490457-A-C

70036328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24490449-A-G

70036352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24490206-T-G

70036504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24490005-C-T

70036774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24489764-A-G

70036774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24489764-A-T

70036927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24489658-T-C

http://identifiers.org/hco/6/GRCh38#70036941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24489644-C-A

70037625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24488119-T-C

70037652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24488087-T-C

70037891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24487841-A-G

70038233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24487540-T-C

http://identifiers.org/hco/6/GRCh38#70038315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24487459-A-C

70038326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24487448-G-A

70038328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24487446-C-T

70039626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24486766-T-C

70039657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24486736-A-G

70040309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24486185-A-G

70040341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24486152-G-A

70040372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24486126-T-C

70040485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24486045-A-G

70040848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24485577-T-C

70040914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24485501-T-G

70040964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24485458-A-G

70046045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24479184-C-G

70046191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24479045-A-G

70046402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24478764-C-G

70046648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24477817-G-T

70046687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24477781-T-A

70046794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24477674-T-C

70047063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24477429-C-T

70047270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24477231-C-T

70047824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476968-T-G

70047849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476943-C-G

70047855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476937-T-C

70047987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476766-T-C

70048168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476582-C-G

70048261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476489-A-G

70048282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476468-T-A

70048290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476460-T-C

70048449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476323-C-T

http://identifiers.org/hco/6/GRCh38#70048470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24476302-C-A

70048471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476301-A-G

70048529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476262-G-A

70048529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476262-G-T

70048552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476239-A-G

70048642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24476156-A-G

70052313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24472410-A-G

70052726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24472025-C-T

70052814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24471937-T-C

70053170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24462482-A-G

70053208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24462446-T-C

70053713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24461951-T-A

http://identifiers.org/hco/6/GRCh38#70053786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24461874-C-A

70053786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24461874-C-T

70053831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24461833-T-G

http://identifiers.org/hco/6/GRCh38#70053964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24461718-C-A

70054025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24461657-A-T

70057717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24458063-T-C

70057739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24458033-G-A

70057739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24458033-G-T

70057852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457910-G-A

70057852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457910-G-T

70057931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457833-T-C

70058146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457624-G-A

70058153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457617-T-C

70058165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457605-A-T

70058273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457500-C-T

70058279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457494-T-G

70058297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457478-G-A

70058335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457441-T-A

70058430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457348-G-A

70058544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457229-A-G

70058658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457118-A-G

70058668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24457108-G-C

http://identifiers.org/hco/6/GRCh38#70058746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24457042-A-C

70058954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24456928-G-A

http://identifiers.org/hco/6/GRCh38#70058965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24456917-A-C

70059895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24456000-G-A

70059895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24456000-G-C

70059895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24456000-G-T

70059953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24455952-T-C

70060121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24455810-C-T

70060201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24453533-G-A

70060348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24453389-A-G

70061100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24453172-T-C

70061315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24452839-A-T

70061464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24452697-G-A

70061856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24452270-C-G

70061954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24452176-G-A

http://identifiers.org/hco/6/GRCh38#70062049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24452093-C-A

70062049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24452093-C-T

70062060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24452077-T-C

70062061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24452076-A-T

70062081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24452056-G-A

70062229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24451925-T-C

70062336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24451803-C-T

70066651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450988-G-T

70066674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450965-A-G

70066712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450930-C-T

70066822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450783-T-G

70066920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450704-A-G

70067008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450613-G-T

70067079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450593-C-T

70067240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450525-A-G

70067251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450515-C-T

70067272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450487-G-A

70067360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450411-A-T

70067384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450389-G-C

70067384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450389-G-T

70067486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450305-G-T

70067584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450204-G-C

70067669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450116-G-T

70067702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24450078-T-C

70067820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449933-G-A

70067848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449889-T-A

http://identifiers.org/hco/6/GRCh38#70067888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24449850-A-C

70068046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449706-A-G

70068108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449646-A-G

70068108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449646-A-T

70068247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449500-G-A

70068368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449381-G-A

70068368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449381-G-T

70068411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449340-T-C

70068459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24449292-G-A

http://identifiers.org/hco/6/GRCh38#70068494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24449257-A-C

70068494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449257-A-G

70068500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449251-T-A

http://identifiers.org/hco/6/GRCh38#70068536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24449215-C-A

http://identifiers.org/hco/6/GRCh38#70068547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24449204-A-C

70068547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449204-A-G

70068614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449142-A-G

70068620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449136-G-A

70068685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24449071-T-C

70068872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24448883-T-C

70068958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24448800-G-A

70068958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24448800-G-C

70068958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24448800-G-T

70069180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24448599-A-G

70069274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24448508-C-T

70069275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24448507-G-A

70069646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24448156-C-T

70069724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24448075-C-T

70069813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24447999-T-C

http://identifiers.org/hco/6/GRCh38#70069963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24447873-C-A

70069963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24447873-C-T

70070015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24447823-C-G

70070015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24447823-C-T

70070337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24447521-A-G

70070363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24447495-C-T

http://identifiers.org/hco/6/GRCh38#70070584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24447293-C-A

70070593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24447284-C-T

70070611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24447266-T-C

http://identifiers.org/hco/6/GRCh38#70070768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24447091-C-A

70070768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24447091-C-T

70071346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24446393-T-C

70071362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24446377-T-C

70071458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24446291-A-T

70071509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24446261-G-A

70071555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24446226-A-G

70071555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24446226-A-T

70072054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24445282-G-A

70072156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24445180-A-T

70072298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24445054-T-A

70072300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24445052-A-G

70072410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24444937-A-G

70072464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24444888-T-C

70072484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24444868-C-G

70072484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24444868-C-T

70073851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24444716-G-T

70075509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24444258-T-C

http://identifiers.org/hco/6/GRCh38#70075723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24444034-C-A

70076009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24443751-A-G

70076058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24443711-G-C

70076130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24443636-G-T

70076451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24443169-A-G

70076466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24443162-C-T

70076573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24443048-G-T

70076637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24442988-A-G

70076959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24442681-G-A

70076974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24442666-G-A

70077068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24442594-G-A

70077068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24442594-G-C

70077683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24442060-G-A

70077689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24442053-T-A

70078005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24441775-A-G

http://identifiers.org/hco/6/GRCh38#70078123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24441656-C-A

70078346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24441523-G-A

70078346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24441523-G-T

70078386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24441487-C-T

70078561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24441309-A-G

http://identifiers.org/hco/6/GRCh38#70078583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24441287-C-A

70079219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24440764-A-G

70079219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24440764-A-T

70079346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24440639-C-T

70079895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24439685-C-T

70080324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24439058-T-C

70080346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24439036-G-A

70080448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438945-C-T

http://identifiers.org/hco/6/GRCh38#70080709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24438649-A-C

70080709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438649-A-T

70080796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438572-T-C

70080820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438548-C-T

70080822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438546-T-A

70080822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438546-T-G

70080897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438470-A-G

70080897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438470-A-T

70080957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438412-G-C

70081052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438331-G-A

70081095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438288-C-T

70081103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438280-C-T

70081127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438256-A-G

70081134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438249-G-A

70081188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438221-C-T

70081318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438097-G-A

70081380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438053-A-G

70081413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24438018-G-C

70081508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24437926-C-G

70083790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24432472-A-G

70083802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24432463-G-A

70083889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24432372-A-G

70083966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24432296-C-T

70083970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24432294-T-A

70084295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24431782-A-G

70084330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24431746-C-G

70084539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24431551-G-A

70084913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24430924-G-A

70084913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24430924-G-T

70084958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24430872-C-G

70084976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24430854-G-C

70084976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24430854-G-T

70085065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24430700-C-T

70085073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24430691-A-G

70085474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24430241-T-C

70085786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24429937-A-G

70085786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24429937-A-T

70085787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24429936-C-G

70085928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24429791-G-C

70087085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24428632-T-C

70088952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24427652-T-C

70089150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24426978-A-G

70089305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24426837-A-T

http://identifiers.org/hco/6/GRCh38#70089507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24426669-A-C

70089635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24426542-G-A

70089858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24426318-T-A

70089955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24426256-T-C

70089955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24426256-T-G

http://identifiers.org/hco/6/GRCh38#70089960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24426250-A-C

70090662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24426122-G-T

70090953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24425870-G-C

70091076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24425754-C-G

70091184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24425648-G-A

70091226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24425606-G-A

70091492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24425376-C-T

70091511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24425359-G-A

70091511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24425359-G-C

70091635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24425237-A-G

70091919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24424996-A-G

70091988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24424922-A-G

70092153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24424760-A-G

70092176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24424751-G-A

70092838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24424540-A-G

70092990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24424369-A-G

70093219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24424146-G-A

70093223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24424142-T-C

70093279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24424094-C-T

70093299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24424073-T-A

http://identifiers.org/hco/6/GRCh38#70093486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24423911-C-A

70093542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24423843-G-C

70093665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24423425-A-G

70093900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24423030-G-A

70094014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24422838-C-G

70094078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24422775-G-A

70094314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24422526-T-G

70094335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24422505-T-A

70094494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24422352-A-G

70094812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24422021-C-T

70095008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24421817-C-G

70095229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24421390-T-C

70095243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24421342-G-A

70095243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24421342-G-T

70095249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24421336-A-G

70095390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24421053-G-A

70095479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24420960-A-G

70095488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24420951-G-A

70095490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24420949-A-G

70095544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24420932-A-G

70095762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24420752-C-T

70095809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24420705-T-C

70095813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24420701-T-C

70095909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24420604-A-G

70096702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24419043-G-T

70097046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24422284-A-G

70097180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24422145-C-T

70099824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24417476-G-A

70099864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24417426-A-G

70099964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24417334-G-A

70100131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24417186-A-G

70100387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24416943-G-A

http://identifiers.org/hco/6/GRCh38#70100513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24416819-A-C

70100923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24415885-A-G

70101066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24415804-T-C

http://identifiers.org/hco/6/GRCh38#70102038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24413842-C-A

http://identifiers.org/hco/6/GRCh38#70102039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24413841-A-C

70102039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24413841-A-G

70102039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24413841-A-T

70102072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24413817-T-C

70104632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24413476-T-C

70104650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24413463-T-G

70104727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24413400-G-A

70104749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24413385-T-C

70105103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24413058-G-A

70105483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24411593-A-G

http://identifiers.org/hco/6/GRCh38#70105720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24411380-A-C

70105743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24411351-A-G

70105835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24411244-T-G

70106160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24410944-T-C

http://identifiers.org/hco/6/GRCh38#70106229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24410862-C-A

70106231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24410860-G-A

70106275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24410818-C-T

70106326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24410759-G-A

70106976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24408211-A-G

70106986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24408202-G-A

70107011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24408179-A-G

70107069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24408122-A-G

70107092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24408099-T-C

70107354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24407869-C-G

70107354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24407869-C-T

70107400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24407835-C-T

70107497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24407740-T-G

70107753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24407501-C-G

70107833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24407422-T-C

70107884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24407372-T-A

70107912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24407344-C-T

http://identifiers.org/hco/6/GRCh38#70107915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24407341-A-C

70107922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24407334-T-C

70108026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24407231-T-C

http://identifiers.org/hco/6/GRCh38#70108231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24407035-C-A

70108231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24407035-C-T

70108319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24406949-T-C

70108654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24406613-G-T

70109428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24405254-G-A

70109479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24405212-T-C

70109533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24405148-G-A

70110010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24404631-C-T

70110220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24404445-T-A

70110233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24404432-A-G

70110233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24404432-A-T

70110242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24404423-C-T

70110335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24404354-T-G

70110349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24404341-A-G

70110408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24404277-C-T

70110448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24404238-T-A

70110514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24404142-T-G

70110515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24404141-C-T

70110803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24403865-A-G

70110886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24403801-G-C

70110902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24403785-C-T

70110930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24403758-A-T

70110934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24403754-G-A

70111061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24403628-C-T

70111062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24403627-G-A

70111062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24403627-G-C

70111062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24403627-G-T

http://identifiers.org/hco/6/GRCh38#70111178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24403499-A-C

70111352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24403339-A-G

http://identifiers.org/hco/6/GRCh38#70111442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24403253-C-A

70111468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24403230-A-G

70111619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24402804-T-C

70112118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24402295-C-T

70112334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24402087-T-A

70112492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24401900-G-T

70112561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24401829-G-A

70112596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24401792-A-G

70112662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24401726-C-T

70112729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24401659-T-A

70112839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24401549-C-T

70112841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24401547-A-G

70112965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24401423-A-G

70113126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24401259-G-A

70113348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24400580-T-C

70113374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24400551-T-A

70113374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24400551-T-C

70113378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24400547-A-G

70113579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24400355-T-C

70113590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24400344-C-T

70113630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24400306-A-G

70115516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24398703-T-C

70115916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24398289-A-G

70115920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24398285-C-T

70115956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24398247-A-G

70116513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24397435-T-C

70116647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24397310-T-A

70116647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24397310-T-G

70116679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24397286-A-G

70116731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24397235-T-C

http://identifiers.org/hco/6/GRCh38#70116763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24397199-A-C

70116766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24397196-C-T

http://identifiers.org/hco/6/GRCh38#70116873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24397097-A-C

70116917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24397054-A-G

70116993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24396966-G-A

70116997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24396962-C-T

70117007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24396952-C-G

70117118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24396853-G-C

70117384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24396597-G-A

70117446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24396506-T-C

http://identifiers.org/hco/6/GRCh38#70117454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24396498-C-A

70117940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24395993-T-C

70118076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24395878-G-A

http://identifiers.org/hco/6/GRCh38#70118341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24395604-C-A

70118341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24395604-C-T

70118408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24395166-G-A

70118411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24395163-G-A

70118751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24394836-T-C

70118836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24394763-T-C

http://identifiers.org/hco/6/GRCh38#70118897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24394702-A-C

70118917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24394688-C-T

70118924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24394681-G-A

70119024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24394586-A-G

70119024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24394586-A-T

70119429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24394175-T-G

70120410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24392814-T-C

70120477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24392748-G-A

70120606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24392634-T-C

70120684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24392559-G-C

70120762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24392481-A-T

70120766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24392477-G-C

70120829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24392415-T-C

70120907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24392350-G-C

70120948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24392308-C-T

70121065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24392123-C-T

70121404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24391840-A-G

70121507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24391750-A-G

70121658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24391595-A-G

70121823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24391461-A-G

70121823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24391461-A-T

70121899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24391395-G-A

70121899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24391395-G-C

70121948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24391355-G-A

70121948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24391355-G-T

http://identifiers.org/hco/6/GRCh38#70121949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24391354-C-A

70121949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 24391354-C-T

70121964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24391339-A-G

70122018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24391284-A-G

http://identifiers.org/hco/6/GRCh38#70122022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24391280-C-A

http://identifiers.org/hco/6/GRCh38#70122027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24391275-C-A

70122033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24391269-A-T

70122074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24391227-T-C

70122467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24390647-A-T

70122547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24390565-T-A

70122663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24390427-G-A

70124243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24390074-C-G

70124594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24389739-A-G

70124970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24389371-T-C

http://identifiers.org/hco/6/GRCh38#70125043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24389309-C-A

70125085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24389272-G-C

70125209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24389154-C-T

70125527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24388840-C-G

70125573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24388800-G-T

70125589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24388784-A-T

70125647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24388738-G-A

70125691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24388709-G-A

70125708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24388692-T-C

70125741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24388655-C-G

70125924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24388469-A-G

70125999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24388420-G-A

70126099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24388333-T-C

70126174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24388269-C-G

70128202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24378107-T-A

70128260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24378068-T-G

70128383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24377963-C-G

70129744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24377404-A-T

70129873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24377304-G-A

70129950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24377234-A-G

70130090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24377096-A-T

70130181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 24377019-G-A

70130194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, missense_variant
orthologous variants: 24377006-C-T

70130203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, missense_variant
orthologous variants: 24376997-G-A

http://identifiers.org/hco/6/GRCh38#70130229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24376971-C-A

70130251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24376949-A-G

70130251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24376949-A-T

http://identifiers.org/hco/6/GRCh38#70130254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24376946-C-A

70130254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24376946-C-G

70130254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24376946-C-T

http://identifiers.org/hco/6/GRCh38#70130732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24376407-A-C

70130872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24376206-G-A

70130959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24376116-T-A

70130959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24376116-T-G

70130975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24376100-A-T

70131045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 24376029-A-T

70131135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24375934-T-C

70131161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24375912-T-C

70131161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24375912-T-G

http://identifiers.org/hco/6/GRCh38#70131164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24375909-C-A

70131172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24375901-G-A

70131172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24375901-G-T

http://identifiers.org/hco/6/GRCh38#70131200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24375855-C-A

70131200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24375855-C-T

70131238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24375814-G-T

http://identifiers.org/hco/6/GRCh38#70131292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24375759-C-A

70131655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24375407-A-G

70131832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24375239-A-G

70131832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24375239-A-T

70131905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, undefined
orthologous variants: 24375166-A-G

http://identifiers.org/hco/6/GRCh38#70131957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24375107-A-C

70131958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24375106-G-T

70132092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24374966-A-G

http://identifiers.org/hco/6/GRCh38#70132498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24374875-A-C

70132498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24374875-A-T

70132714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24374712-T-C

70132851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24374586-C-T

70133158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24374298-G-T

70134035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24374231-C-T

70134122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24374144-T-C

70134269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24374034-T-C

70137236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24371963-C-T

70137356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24371845-T-A

70137356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24371845-T-C

http://identifiers.org/hco/6/GRCh38#70137573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24371624-A-C

70137650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24371598-A-G

70137651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24371597-T-A

70137651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24371597-T-C

70137651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24371597-T-G

70138031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24371299-A-G

70138090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24371264-G-A

70138557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24370028-C-T

70138765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24369814-G-A

70138977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24369659-T-G

70139048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24369601-A-G

70139048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24369601-A-T

70139065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24369587-A-G

70139127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24369556-G-A

70139164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24369522-C-T

70139273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24369440-T-G

70139377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24369333-T-C

70140059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24368589-G-A

70140059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24368589-G-T

http://identifiers.org/hco/6/GRCh38#70140892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24367212-C-A

70140892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24367212-C-T

70141053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24367055-T-C

http://identifiers.org/hco/6/GRCh38#70141701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24365435-A-C

70141701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24365435-A-G

70141709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24365421-A-G

70141769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24365364-T-C

70141822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24365314-T-C

http://identifiers.org/hco/6/GRCh38#70141850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24365287-C-A

70141857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24365280-T-C

70141857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24365280-T-G

70141859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24365278-A-G

70141967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24365168-A-G

70142006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24365129-T-C

70142008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24365127-C-T

70142011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24365123-C-T

70142078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: splice donor variant
orthologous variants: 24365056-T-C

70142153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24364969-G-A

70142195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24364928-A-T

70142208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24364915-G-A

70142208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24364915-G-T

70142211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24364912-G-T

http://identifiers.org/hco/6/GRCh38#70142226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24364896-C-A

70142430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24364692-T-G

70142600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24364527-C-T

http://identifiers.org/hco/6/GRCh38#70142624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24364503-C-A

70142624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24364503-C-G

70142624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24364503-C-T

70142676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24364461-G-C

70142676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24364461-G-T

70142838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24364311-G-A

http://identifiers.org/hco/6/GRCh38#70142926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24364255-A-C

70143166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24364073-A-G

70143992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24363005-T-A

70144194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362830-A-G

70144247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24362777-G-C

70144258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24362766-G-C

70144258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: stop gained
orthologous variants: 24362766-G-T

70144267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362757-T-A

70144267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362757-T-C

70144267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362757-T-G

70144292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362731-T-G

70144329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362701-G-A

70144329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362701-G-T

70144392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362628-T-A

70144392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362628-T-C

70144395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362625-A-G

http://identifiers.org/hco/6/GRCh38#70144399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24362621-C-A

70144399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362621-C-T

70144402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362618-C-G

70144402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362618-C-T

70144533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362505-G-A

70144563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362475-A-T

70144590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362454-G-A

http://identifiers.org/hco/6/GRCh38#70144735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24362279-A-C

70144769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362245-G-C

70144769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362245-G-T

70144778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362232-G-A

70144778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362232-G-T

70144806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362217-A-G

http://identifiers.org/hco/6/GRCh38#70144822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24362201-C-A

70144822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362201-C-T

70144863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362163-A-T

70144898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362127-T-A

70144898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362127-T-C

http://identifiers.org/hco/6/GRCh38#70144924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24362101-C-A

70144924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24362101-C-T

http://identifiers.org/hco/6/GRCh38#70144960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24362065-C-A

70144960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24362065-C-T

70144975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24362050-G-A

70144975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24362050-G-C

70145022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362004-T-A

70145022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362004-T-C

70145022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362004-T-G

70145023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362003-T-C

70145023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24362003-T-G

http://identifiers.org/hco/6/GRCh38#70145042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24361984-C-A

70145045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24361981-G-T

70146278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24361706-T-C

70146531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24361471-T-C

70146572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24361436-A-T

70146603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24361399-A-G

70146764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24361238-A-G

http://identifiers.org/hco/6/GRCh38#70146845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24361156-C-A

70146857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24361144-G-A

70146857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24361144-G-T

70146873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24361128-G-T

70146893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24361108-A-G

70149435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24357052-C-T

70149543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356956-G-A

70149572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356928-T-A

70149589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356912-T-C

70149591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356910-G-A

http://identifiers.org/hco/6/GRCh38#70149595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24356906-A-C

70149595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356906-A-T

70149611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356890-A-T

http://identifiers.org/hco/6/GRCh38#70149678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24356834-A-C

70149678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356834-A-G

70149806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356702-A-G

70149896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24356620-G-A

70150001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24356515-G-C

http://identifiers.org/hco/6/GRCh38#70150088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24356428-C-A

70150088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356428-C-T

70150089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356427-C-T

70150189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356327-G-A

70150189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356327-G-T

70150220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356296-C-T

70150239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24356239-T-G

70150526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24355950-T-C

70150568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24355908-C-T

70150708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24355781-C-T

70150901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24355621-C-T

70150984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24355428-T-C

70151025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24355305-C-T

70151062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24355266-C-T

70151153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24355173-A-G

70151424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24354491-G-A

70151424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24354491-G-C

70151433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24354482-C-T

70151474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24354441-T-A

http://identifiers.org/hco/6/GRCh38#70151485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24354430-A-C

70151588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24354335-G-A

70151588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24354335-G-C

70151847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24353891-G-C

70151870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24353876-G-T

70151895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24353855-C-T

70152080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24353715-T-A

70152105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24353697-T-C

70152106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24353696-G-A

70152219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24353594-G-A

70155835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351921-T-C

70155898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351841-A-G

70155899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351840-A-G

70155989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351752-T-C

70155991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351750-A-T

70156078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351679-T-C

70156120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 24351638-T-C

70156253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351506-T-C

http://identifiers.org/hco/6/GRCh38#70156255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24351504-A-C

70156264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351495-G-T

70156274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351485-T-C

70156274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351485-T-G

70156310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 24351450-T-C

http://identifiers.org/hco/6/GRCh38#70156382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24351378-C-A

70156382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351378-C-G

70156382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351378-C-T

70156392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351368-T-A

70156392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351368-T-G

http://identifiers.org/hco/6/GRCh38#70156547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24351314-A-C

70156547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351314-A-G

70156547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351314-A-T

70156597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351259-G-A

70156655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351194-G-A

70156663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 24351186-T-C

70156773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351096-G-A

70156773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351096-G-C

http://identifiers.org/hco/6/GRCh38#70156777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24351092-C-A

70156777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24351092-C-T

70157147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24350233-C-T

70157223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24350154-A-T

70157237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24350145-A-G

70157237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24350145-A-T

70157297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24350085-G-A

http://identifiers.org/hco/6/GRCh38#70157686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24349690-A-C

70157862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24349494-G-C

70157957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24349401-G-A

http://identifiers.org/hco/6/GRCh38#70157966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24349393-A-C

70158010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24349349-C-T

70158121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24349251-C-T

70158122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24349250-G-A

http://identifiers.org/hco/6/GRCh38#70158201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24349210-C-A

70158266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24349146-T-A

70158342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24349070-T-C

70158429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24348988-G-A

70158566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24348865-C-T

70158888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24348624-T-C

70158929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24348583-A-G

70158930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24348582-T-C

70159414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24348126-A-G

70159578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24347975-A-G

70159616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24347454-C-T

70159680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24347403-C-T

70159740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24347344-G-A

70161918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24346760-G-A

70161918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24346760-G-T

70161976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24346702-G-A

http://identifiers.org/hco/6/GRCh38#70161993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24346685-C-A

70161993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24346685-C-T

70162030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24346650-T-C

70162038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24346642-G-T

70162062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24346622-G-A

70162062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24346622-G-T

70162092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24346592-T-A

70162138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24346547-G-A

70162194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24346498-T-C

70162288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24346411-C-G

70162517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24346210-G-C

70163148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345588-T-C

70163225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345510-G-A

70163225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345510-G-T

http://identifiers.org/hco/6/GRCh38#70163226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24345509-C-A

70163226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345509-C-T

70163238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345497-G-C

70163238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345497-G-T

70163270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345465-A-G

http://identifiers.org/hco/6/GRCh38#70163318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24345417-A-C

70163318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345417-A-G

70163430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345325-T-C

70163440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345315-A-G

70163472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345283-A-G

70163486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345269-G-A

70163494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345261-T-C

70163515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345236-A-G

70163526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345225-T-C

70163528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345223-T-C

70163539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24345212-T-A

70164041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24344723-C-T

70164260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24344159-A-G

70164319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24344097-A-G

70164342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24344074-A-G

70164368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24344048-G-A

70164469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24343954-A-G

70164507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24343923-T-A

70164825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24343619-G-C

http://identifiers.org/hco/6/GRCh38#70165088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24343395-C-A

70165149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24343334-G-A

70165306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24343169-G-A

70165654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342856-G-A

70165679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342832-T-G

70165716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342800-A-G

70165764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342753-T-C

70165808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342706-G-T

70165853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342661-G-T

70165897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342625-G-A

70165913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342609-C-T

70165919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342601-T-C

http://identifiers.org/hco/6/GRCh38#70165933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24342587-C-A

70165933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 24342587-C-T

70166074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342469-A-G

70166144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342319-T-G

70166148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342315-T-C

70166148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342315-T-G

70166192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342267-T-A

70166192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342267-T-C

70166297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342179-C-T

70166449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24342033-G-C

70166936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24341583-T-C

70166936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24341583-T-G

70167181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24341381-T-C

70167206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24341356-A-T

70167538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340998-T-G

70167718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340822-C-T

70167945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340590-T-C

70167959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340576-G-T

70168009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340545-T-C

http://identifiers.org/hco/6/GRCh38#70168013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24340541-C-A

70168101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340453-A-G

70168124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340429-T-C

http://identifiers.org/hco/6/GRCh38#70168187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24340382-C-A

70168187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24340382-C-T

http://identifiers.org/hco/6/GRCh38#70168201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24340368-C-A

70168207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24340362-G-A

70168207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24340362-G-C

70168207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24340362-G-T

http://identifiers.org/hco/6/GRCh38#70168260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24340309-C-A

70168260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340309-C-T

http://identifiers.org/hco/6/GRCh38#70168276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24340297-C-A

70168294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340279-T-C

70168299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340274-T-A

70168299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340274-T-C

http://identifiers.org/hco/6/GRCh38#70168324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24340249-C-A

70168324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340249-C-T

http://identifiers.org/hco/6/GRCh38#70168334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24340239-C-A

70168334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340239-C-T

70168351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340223-T-A

70168418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340161-G-A

70168460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24340119-A-G

http://identifiers.org/hco/6/GRCh38#70168547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24339804-C-A

70168616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24339734-T-C

70168642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24339711-G-A

70168700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24339654-T-C

70168719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24339648-T-C

http://identifiers.org/hco/6/GRCh38#70168750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24339620-C-A

70168750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24339620-C-T

http://identifiers.org/hco/6/GRCh38#70168850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24339522-A-C

70169269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24339094-A-G

70169352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24339002-T-G

70169365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24338989-A-G

70169404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24338950-C-G

70169426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24338928-A-G

http://identifiers.org/hco/6/GRCh38#70169635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24338737-C-A

70169793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24338567-C-T

http://identifiers.org/hco/6/GRCh38#70169915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24338446-A-C

70169966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24338394-T-C

70169972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24338388-C-G

70170062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24338294-T-C

http://identifiers.org/hco/6/GRCh38#70170144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24338214-C-A

http://identifiers.org/hco/6/GRCh38#70170260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24338094-C-A

70170376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24337972-C-T

70170710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24337278-A-G

70170710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24337278-A-T

70170903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24337084-A-G

70170904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24337083-C-T

70170934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24336859-A-G

70171354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24336454-G-A

70171359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24336449-G-A

70171565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24336253-C-G

70171625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24336193-A-G

http://identifiers.org/hco/6/GRCh38#70171753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24336065-C-A

70171830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24336000-A-G

70171831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24335999-T-C

70171926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24335912-A-G

70171934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24335904-T-C

70172025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 24335831-C-T

70172027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24335829-G-A

70172042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24335814-T-A

70172043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24335813-T-G

70172066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24335795-G-A

70172070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24335791-A-G

70172176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24335680-A-G

70175935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24333069-A-G

http://identifiers.org/hco/6/GRCh38#70175997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24333009-A-C

70176045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24332961-T-C

70176048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24332958-T-A

70176296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24332700-A-T

70176400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24332484-T-C

70176406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24332427-T-A

http://identifiers.org/hco/6/GRCh38#70176468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24332250-C-A

70176496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24332221-A-G

http://identifiers.org/hco/6/GRCh38#70176644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24332074-C-A

70176644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24332074-C-T

70176672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24332048-T-A

70176672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24332048-T-C

70176770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24331980-T-C

http://identifiers.org/hco/6/GRCh38#70177148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24331616-C-A

70177306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24331457-C-T

70177416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24331370-C-T

70177518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24331267-G-A

http://identifiers.org/hco/6/GRCh38#70177530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24331256-A-C

70177530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24331256-A-T

70177596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24331149-A-G

70177625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24331121-T-G

70177687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24331063-C-T

70177863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24330927-A-G

70177914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24330876-C-T

70177942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24330849-C-T

70177968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24330823-G-A

70178069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24330729-A-G

70178438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24330667-T-G

70178493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24330612-C-T

70178794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24330367-A-G

70178822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24330340-G-A

70178824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24330338-G-A

http://identifiers.org/hco/6/GRCh38#70179754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24329100-C-A

70179764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24329090-T-A

70180217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24329024-A-G

70180250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24329007-G-T

70180255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24329002-A-G

70180259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24328998-G-T

70180379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24328890-G-T

70180393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24328876-T-C

70180398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24328871-T-C

70180424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24328846-G-A

70180424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24328846-G-C

70180424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24328846-G-T

70180512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24328757-T-A

70180557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24328711-T-C

70180559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24328710-G-A

70180570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24328699-T-C

70180571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24327827-A-G

70180619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24327781-G-T

70180652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24327757-G-A

70180652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24327757-G-T

70180681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24327714-T-C

70183713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24325675-A-G

70183744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24325644-G-C

70183784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24325604-C-T

70183808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24325582-T-C

70183918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24325473-G-A

70183959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24325438-A-G

70184268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24325120-T-C

70184309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324837-A-G

70184444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324647-T-G

70184449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324642-C-G

70184461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324619-G-A

70184461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324619-G-T

70184479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324602-T-G

70184547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324509-T-C

70184562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324494-T-G

http://identifiers.org/hco/6/GRCh38#70184595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24324461-C-A

70184595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324461-C-T

70184608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324448-T-C

http://identifiers.org/hco/6/GRCh38#70184670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24324398-A-C

http://identifiers.org/hco/6/GRCh38#70184727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24324344-C-A

70184727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24324344-C-T

70184819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324243-T-A

70184819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324243-T-G

70184835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324231-C-T

70184851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324196-T-C

70184913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 24324134-C-G

70184913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 24324134-C-T

70184940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324107-T-C

http://identifiers.org/hco/6/GRCh38#70184945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24324102-C-A

70184945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324102-C-T

http://identifiers.org/hco/6/GRCh38#70184968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24324079-C-A

70184968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324079-C-G

70184968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24324079-C-T

70185157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24323909-G-A

70185182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24323887-T-C

70185223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24323846-T-A

70185273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24323794-A-G

70185659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24323339-T-C

70185715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24323274-G-A

70185748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24323251-C-T

70185766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24323233-G-T

70185785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24323216-T-C

70185928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24323070-A-G

70185970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24323030-C-T

70186372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24322522-G-A

70186412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24322506-T-A

70186412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24322506-T-C

70186423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24322497-G-A

70186424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24322496-T-C

70186512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24322410-C-T

http://identifiers.org/hco/6/GRCh38#70187593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24322123-C-A

70187872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321870-C-T

http://identifiers.org/hco/6/GRCh38#70187892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24321854-C-A

70187892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321854-C-G

70187892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321854-C-T

70187920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321820-C-T

70187929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321811-G-T

70187937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321803-G-A

70187937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321803-G-T

70187942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321798-G-T

70187971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321771-A-T

70187994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321748-A-G

70187994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321748-A-T

70188031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321706-A-G

70188186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24321555-T-C

70188189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24321552-A-G

http://identifiers.org/hco/6/GRCh38#70188221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24321520-C-A

70188221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: synonymous variant
orthologous variants: 24321520-C-T

70188281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321476-T-C

http://identifiers.org/hco/6/GRCh38#70188289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24321468-C-A

70188289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321468-C-T

70188320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321437-T-C

http://identifiers.org/hco/6/GRCh38#70188359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24321404-C-A

70188359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321404-C-G

70188396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321382-T-A

70188396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321382-T-G

http://identifiers.org/hco/6/GRCh38#70188445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24321341-C-A

70188504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24321286-G-A

70188877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24320826-A-G

70189130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24320154-T-G

70189194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24320093-G-A

70189244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24320058-A-G

70189273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24320029-A-G

70189629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24319684-A-G

70189795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24319558-A-T

70189868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24319500-T-C

70190045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24319328-C-T

70190145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24319230-T-C

70190186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24319192-G-A

70190186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24319192-G-T

http://identifiers.org/hco/6/GRCh38#70190212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24319166-C-A

70190212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24319166-C-T

70190250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24319141-T-C

http://identifiers.org/hco/6/GRCh38#70190251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24319140-A-C

70190318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24319074-G-A

70190360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24319032-G-A

http://identifiers.org/hco/6/GRCh38#70190449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24318952-C-A

http://identifiers.org/hco/6/GRCh38#70190504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24318905-C-A

70190504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24318905-C-G

70190584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24318836-A-G

70190588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24318832-T-G

70190666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24318759-C-T

http://identifiers.org/hco/6/GRCh38#70193180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24315880-C-A

70193213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24315847-A-T

70193227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24315829-C-T

http://identifiers.org/hco/6/GRCh38#70193387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24315701-C-A

70193387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24315701-C-G

70193406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24315681-C-T

70194042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24315069-T-G

70194057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24315055-T-C

70194160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314974-G-A

http://identifiers.org/hco/6/GRCh38#70194252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24314884-A-C

70194423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314733-C-T

70194551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314606-G-A

70194564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314593-T-C

70194655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314499-T-G

70194663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314491-C-T

http://identifiers.org/hco/6/GRCh38#70194709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24314445-C-A

70194734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314420-T-C

70194768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314395-G-A

70194789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314373-T-C

70195022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314205-T-G

70195084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314154-G-A

70195086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314152-A-G

70195101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314136-A-G

70195131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24314106-T-A

70195371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24313910-A-T

70195923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24313538-G-A

70196184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24313320-A-G

70196186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24313318-T-A

70196473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24313048-G-A

70196473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24313048-G-T

70196496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24312991-G-A

70196603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24312905-T-G

70196623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24312885-T-C

70196634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24312877-C-T

70196689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24312825-T-C

70196735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24312813-T-C

70196794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24312755-C-G

70197081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24312461-T-C

70197113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24312434-A-G

70198390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24312219-A-G

70198888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24310248-A-T

70198944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24310214-G-A

70198996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24310174-C-T

70199026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24310141-T-A

70199026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24310141-T-C

70199033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24310134-T-C

70199033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24310134-T-G

70199089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24310093-G-T

70199163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24310021-A-T

70199186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309998-A-G

70199332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309872-G-T

70199387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309826-C-G

70199504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309676-T-C

70199537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309644-T-C

70199537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309644-T-G

70199562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309618-A-G

70199595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309586-T-C

http://identifiers.org/hco/6/GRCh38#70199596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24309585-C-A

70199596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309585-C-T

70199756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309425-A-G

70199852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309346-A-G

70199856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309342-A-T

70199912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309286-T-C

70199966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309239-T-A

70199966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309239-T-C

70199975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309230-A-G

70200007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309201-A-G

70200008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309200-T-A

70200008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309200-T-C

http://identifiers.org/hco/6/GRCh38#70200074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24309141-C-A

70200074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309141-C-G

70200074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24309141-C-T

http://identifiers.org/hco/6/GRCh38#70200289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24308525-A-C

http://identifiers.org/hco/6/GRCh38#70201063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24307464-A-C

70201071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24307456-T-A

70201302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24307233-A-G

70201453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24307066-G-A

70201488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24307039-T-C

70201707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24306788-A-G

70201974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24306459-T-A

70201974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24306459-T-G

70202068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24306399-T-C

70202577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24306106-A-G

http://identifiers.org/hco/6/GRCh38#70202660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24306022-C-A

70202660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24306022-C-T

70202667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24306015-A-G

70202733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24305961-T-C

70202783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24305911-G-T

http://identifiers.org/hco/6/GRCh38#70202785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24305909-A-C

70202884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24305809-C-T

70202906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24305789-C-T

70202908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24305787-T-G

70206226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24304708-C-G

70206660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24304351-G-T

http://identifiers.org/hco/6/GRCh38#70206698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24304307-A-C

70206698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24304307-A-T

http://identifiers.org/hco/6/GRCh38#70206724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24304282-A-C

http://identifiers.org/hco/6/GRCh38#70206763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24304259-A-C

70206763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24304259-A-T

70206803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24304219-T-A

70206832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24304191-G-A

70206832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24304191-G-T

70206894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 24304128-C-T

70207003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24304022-C-G

http://identifiers.org/hco/6/GRCh38#70207105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24303939-C-A

70207129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: intron variant
orthologous variants: 24303915-T-G

70207164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: missense variant
orthologous variants: 24303879-T-C

70207322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303721-G-A

70207322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303721-G-T

70207338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303696-G-A

70207338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303696-G-C

70207338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303696-G-T

70207355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303679-T-A

70207355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303679-T-C

70207355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303679-T-G

http://identifiers.org/hco/6/GRCh38#70207439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24303594-A-C

http://identifiers.org/hco/6/GRCh38#70207495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24303538-C-A

70207495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303538-C-T

http://identifiers.org/hco/6/GRCh38#70207550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24303488-C-A

70207550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303488-C-T

70207575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303467-T-C

70207600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303445-T-A

70207604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303441-G-T

70207606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303439-T-C

70207638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303409-G-T

70207668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303379-G-T

70207704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303337-T-C

70207753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303280-A-G

70207789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24303249-T-A

http://identifiers.org/hco/6/GRCh38#70207804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24303233-C-A

70208129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302952-C-G

http://identifiers.org/hco/6/GRCh38#70208187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24302894-C-A

70208187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302894-C-G

70208239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302850-G-T

http://identifiers.org/hco/6/GRCh38#70208281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24302800-C-A

70208292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302789-G-T

http://identifiers.org/hco/6/GRCh38#70208341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24302740-A-C

http://identifiers.org/hco/6/GRCh38#70208358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24302723-A-C

70208358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302723-A-T

70208381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302702-G-A

70208381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302702-G-T

70208430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302649-T-C

http://identifiers.org/hco/6/GRCh38#70208456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24302564-C-A

http://identifiers.org/hco/6/GRCh38#70208468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24302536-C-A

70208468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302536-C-T

70208469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302535-A-T

70208522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302488-T-C

70208536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302474-C-T

70208565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302445-G-A

70208691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302328-A-G

70208696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302323-G-T

70208716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302317-G-A

70208716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24302317-G-T

70209292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24301736-T-C

70209436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24301557-G-T

70209463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24301528-T-C

70209569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24301422-G-C

70209569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24301422-G-T

70209741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24301292-G-A

70210189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24300943-T-C

70210361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24300786-T-G

http://identifiers.org/hco/6/GRCh38#70210411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#24300741-A-C

70210432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24300720-T-C

70210432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24300720-T-G

70210552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24300587-T-G

70210719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24300421-A-G

70211032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24300113-T-C

70211036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24300109-C-T

70211498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24299667-T-C

70211790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24299386-A-G

70211803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24299373-T-C

70211868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24299308-G-A

70211917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24299281-A-G

70212141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24299088-T-C

70212186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24299052-T-C

70212190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24299048-T-C

70212413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24298830-A-G

70212413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2196
most severe consequence: 3 prime UTR variant
orthologous variants: 24298830-A-T