40045047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80595738-G-A

40045188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80595897-G-C

40045408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, undefined
orthologous variants: 80596114-G-T

40045412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, undefined
orthologous variants: 80596118-G-A

40045412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, undefined
orthologous variants: 80596118-G-T

http://identifiers.org/hco/22/GRCh38#40045442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80596145-C-A

40045599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80596251-T-C

40045603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80596255-C-T

40045649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80596311-T-A

40045649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80596311-T-C

40045879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80596563-C-T

40046255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80596781-T-C

40046663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80597306-G-A

40046663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80597306-G-T

40046715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80597362-G-A

40046715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80597362-G-T

40046735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80597382-C-T

40046757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80597389-G-A

40046793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80597424-C-T

40046801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80597432-C-T

40051544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80598825-T-A

40051637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80598913-A-G

40051677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80598953-G-C

40051942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80599238-A-G

40051977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80599273-G-C

http://identifiers.org/hco/22/GRCh38#40052145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80599443-A-C

http://identifiers.org/hco/22/GRCh38#40052361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80599952-A-C

40052361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80599952-A-G

40052453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80600045-T-C

40052647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80600185-C-G

40052688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80600250-A-G

40052693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80600255-C-G

40057742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80606331-G-A

40058092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80606651-G-A

40058092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80606651-G-T

40058225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80606798-A-G

http://identifiers.org/hco/22/GRCh38#40058231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80606804-A-C

40058314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80606937-G-A

40058334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80606957-T-A

40058994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80607670-C-T

40071453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80613928-C-T

http://identifiers.org/hco/22/GRCh38#40082089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80616733-C-A

40082117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80616759-A-G

40082331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80616943-T-C

40082689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80617573-T-C

40082705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80617681-A-G

40082706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80617682-T-C

40082720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80617696-G-A

40083010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80618135-C-T

40083050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80618172-A-G

40083212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80618338-C-T

40083391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80618515-A-G

40083450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80618574-G-C

40094982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80619893-C-T

40095052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80619958-G-C

40095193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80620109-T-C

http://identifiers.org/hco/22/GRCh38#40107354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80623150-A-C

40107354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80623150-A-G

40107662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80623503-T-C

40108223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, undefined
orthologous variants: 80624047-C-G

40108223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, undefined
orthologous variants: 80624047-C-T

40109720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80625836-T-A

40110921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80626932-C-T

40110923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80626934-A-G

40110955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80626966-C-T

40114134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80628713-T-C

40114134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80628713-T-G

40115400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80629714-C-T

40115401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80629715-G-A

40116232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80630475-G-A

40116307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80630518-G-A

40116307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80630518-G-C

40116440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80630549-A-G

http://identifiers.org/hco/22/GRCh38#40116835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80631428-A-C

40116835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80631428-A-G

40116968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80631512-G-T

40116989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80631532-T-C

http://identifiers.org/hco/22/GRCh38#40117030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80631583-C-A

40117834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80633529-G-A

40117834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80633529-G-T

40117849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80633543-A-G

40118169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80637972-A-G

40120937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80637187-T-C

40120998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80637250-C-T

40121009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80637261-G-A

40121009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80637261-G-C

40121053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80637293-C-G

40121970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80638126-T-C

40122014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80638155-T-C

40122810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80638973-T-C

http://identifiers.org/hco/22/GRCh38#40123000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80639154-C-A

40123000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80639154-C-T

http://identifiers.org/hco/22/GRCh38#40123375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80639510-A-C

40124012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80640637-A-G

http://identifiers.org/hco/22/GRCh38#40125149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80642643-C-A

40125185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80642677-C-T

40125630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80643610-G-A

40125630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80643610-G-C

40125630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80643610-G-T

http://identifiers.org/hco/22/GRCh38#40125906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80643878-A-C

40125906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80643878-A-G

40128395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80644743-G-A

40128395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80644743-G-T

40128885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80645061-G-T

40128959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80645129-A-G

40128966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80645136-G-T

40129018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80645192-G-A

40129394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80645528-C-T

40129675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80646206-T-C

40129817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80646360-A-G

http://identifiers.org/hco/22/GRCh38#40129903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80646446-A-C

40131503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80647491-G-A

40132015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80648349-T-C

40133034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80648444-C-T

40133125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80648512-A-G

40133191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80648573-C-T

40133252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80648632-A-T

40133259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80648639-C-T

40133409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80648788-G-A

40134429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80649297-A-G

40134506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80649370-C-T

40134822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80649535-A-G

40134823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80649536-A-T

40146045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80652465-A-T

40155709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80668551-T-C

http://identifiers.org/hco/22/GRCh38#40156006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80668838-C-A

40156006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80668838-C-T

http://identifiers.org/hco/22/GRCh38#40156011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80668843-C-A

40156085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, undefined
orthologous variants: 80668911-G-A

40156085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, undefined
orthologous variants: 80668911-G-T

http://identifiers.org/hco/22/GRCh38#40156241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#80669063-C-A

40156281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, undefined
orthologous variants: 80669103-G-A

http://identifiers.org/hco/22/GRCh38#40156486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80669297-A-C

http://identifiers.org/hco/22/GRCh38#40158488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80670905-C-A

40158766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80671247-A-G

40168599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80674008-A-T

40168741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80674129-C-T

40175663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80680617-T-C

40175810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80680759-C-G

40177386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, undefined
orthologous variants: 80682266-T-A

40177452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80682324-C-T

http://identifiers.org/hco/22/GRCh38#40177817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#80682685-C-A

40177817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, undefined
orthologous variants: 80682685-C-T

http://identifiers.org/hco/22/GRCh38#40177833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80682701-A-C

40177833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80682701-A-G

40178015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 80682881-T-G

40178312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80683176-A-G

40178458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80683320-A-T

http://identifiers.org/hco/22/GRCh38#40179323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80684184-C-A

40179323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80684184-C-T

40179327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80684188-T-A

40179327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80684188-T-G

40179619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80684473-G-C

40179619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80684473-G-T

40180523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80685375-G-C

40180872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80685709-A-G

40180929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80685752-A-G

40180929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80685752-A-T

40181291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80686150-C-T

40182754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80686898-G-C

40182798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80687222-G-A

40183105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80687520-G-T

40183509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80688316-C-G

40183509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80688316-C-T

40183519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80688326-G-C

40183525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80688332-T-G

40184151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80688634-C-G

40184351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80690375-A-G

40184677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80690690-G-C

40184946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80690887-G-A

40184995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80690933-A-T

40186024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80691925-T-G

40186219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80692087-C-T

40186324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80692197-G-A

40187292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80692768-T-A

40187292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80692768-T-C

40187369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80692841-T-C

http://identifiers.org/hco/22/GRCh38#40187456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80692928-C-A

40187636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80693112-C-T

40187640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80693116-G-A

40187640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80693116-G-C

40187642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80693118-C-T

40187699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80693310-C-T

40188494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80694313-G-A

40188497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80694316-G-C

40189431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80695274-A-G

http://identifiers.org/hco/22/GRCh38#40189440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80695283-C-A

40189440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80695283-C-T

http://identifiers.org/hco/22/GRCh38#40189496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80695334-C-A

40190476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80697834-T-G

40190499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80697857-G-A

40192806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80699035-G-A

40192806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80699035-G-C

40193332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80699386-A-G

40193510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80699536-A-G

40193838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80700450-G-C

40193851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80700457-C-G

40194461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80700972-G-A

40195139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80701927-T-A

40196101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80702552-C-T

40197141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80703252-C-T

40198628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80704143-C-G

40198628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80704143-C-T

40204314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706277-A-G

40205434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80708113-G-T

40205436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80708115-T-G

40206281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80709238-A-G

40206713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80709804-G-A

40206869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80709969-T-C

40206989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80710088-G-A

40207384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80710368-G-A

http://identifiers.org/hco/22/GRCh38#40207544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80710432-A-C

40207620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80710515-C-G

40208406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80711078-C-T

40208697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80711310-A-G

40208925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80711529-T-C

40208950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80711555-A-G

40208950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80711555-A-T

http://identifiers.org/hco/22/GRCh38#40211692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80715185-A-C

40211692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80715185-A-T

40212049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80715513-C-G

40212277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80715711-G-A

40212669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80716214-A-G

40214882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80717778-G-A

40215523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80718617-C-T

40215603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80718711-C-G

40215701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80718778-C-G

40215818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80718898-G-A

40218890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80720504-G-A

40219280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80720875-T-G

40219379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80720933-C-T

40220398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80723156-C-T

40220403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80723169-C-T

40220672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80723399-T-G

40220854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80723585-T-G

40220875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80723606-G-T

40222224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80724823-A-G

40224401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80726032-C-G

40224462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80726085-T-C

40224586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80726205-C-T

40224865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80726403-C-T

40225041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80726513-C-T

40225338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80727010-T-A

40225370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80727040-G-A

40225451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80727131-G-A

40225931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80727668-C-T

40226003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80727728-T-C

40226226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80727958-A-G

40226630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80728406-T-C

40226683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80728469-A-G

http://identifiers.org/hco/22/GRCh38#40226787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80728577-C-A

40227113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80728746-T-G

40227204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80728838-C-T

40227764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80729223-G-A

40227919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80729359-A-G

40227950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80729389-A-G

40228117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80729549-G-A

40229105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80729988-A-G

40229176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80730037-A-G

40229382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80730218-G-C

40229456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80730287-T-C

40229824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80730614-G-A

40229897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80730682-T-A

40234630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80731015-A-G

http://identifiers.org/hco/22/GRCh38#40234828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80731211-A-C

40235562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80731924-G-A

40236056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80733093-C-T

40236076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80733113-T-C

40236293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80733289-C-T

40237623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80734125-T-G

http://identifiers.org/hco/22/GRCh38#40237761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80734290-C-A

40237790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80734316-G-A

40238014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80734555-T-A

40238091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80734634-A-G

40239357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80735623-G-A

40239402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80735673-T-C

40240292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80737517-G-A

40241237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80738765-C-T

40241681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80739242-T-C

40241753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80739304-G-A

40241789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80739340-T-C

40243238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80740035-A-G

40243934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80740401-T-A

40244017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80740475-T-C

40244515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80741419-C-G

40244616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80741520-C-T

40245011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80741875-A-T

40245351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80742319-A-G

40245550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80742496-C-T

40245611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80742545-T-C

40245983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80742848-T-C

40246405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: -G-A

40246687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80743222-A-T

40247072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80743736-C-T

40247117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80743782-T-C

40247411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80744081-A-G

40247523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80744196-A-G

40247663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80744330-G-A

40248454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80744895-T-C

40248454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80744895-T-G

40248456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80744897-G-A

40248460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80744901-G-C

40248460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80744901-G-T

40248563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80745383-T-A

40248612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80745437-G-A

40248622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80745446-G-A

40249124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80745945-C-G

40249277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80746098-A-G

40249564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80746460-C-T

40249655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80746555-C-T

40249875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80746774-G-A

40249909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80746808-G-T

40250126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80747596-A-G

40250207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80747676-T-G

40250212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80747681-G-A

40250246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80747715-T-C

40250360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80747834-T-C

40250370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80747844-A-G

40250791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748210-G-A

http://identifiers.org/hco/22/GRCh38#40250813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80748229-C-A

40250922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748340-T-C

40250975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748392-G-T

40251047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748449-T-C

40251073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748475-G-A

40251073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748475-G-T

40251114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748518-A-G

40251114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748518-A-T

40251160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748564-T-C

http://identifiers.org/hco/22/GRCh38#40251164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80748568-C-A

40251164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748568-C-G

40251261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748645-T-C

http://identifiers.org/hco/22/GRCh38#40251276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80748660-C-A

40251276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748660-C-T

http://identifiers.org/hco/22/GRCh38#40251294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80748675-A-C

40251294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748675-A-G

40251301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748682-G-A

40251301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748682-G-T

40251313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80748694-A-G

40252298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80749315-A-T

40252873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80749839-G-A

40253207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80749969-G-A

40253279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80750047-A-G

http://identifiers.org/hco/22/GRCh38#40253599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80750413-A-C

40253599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80750413-A-G

40253638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80750451-G-C

40253840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80750620-G-A

40253853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80750633-G-C

40254102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80751261-G-A

http://identifiers.org/hco/22/GRCh38#40254252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80751401-C-A

40254252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80751401-C-T

40254919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80751597-T-C

40255106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80751762-G-C

40255208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80751848-A-G

40257180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80757161-T-C

40258117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80757485-T-C

40258837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80758696-C-T

40258900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80758745-A-G

40259662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80759106-A-G

40260085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80759531-C-T

40260230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80759634-A-T

40260293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80759695-T-C

40260349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80759752-A-T

40260387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80759785-A-G

40260394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80759792-A-T

40262167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80760856-G-A

40262167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80760856-G-T

40262246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80760909-A-G

40262292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80760939-A-G

40262553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80761104-A-G

40264024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80762347-G-A

40264247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80762536-A-T

40264355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80762637-C-T

40264546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80762855-T-G

40264601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80762984-G-T

40264613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80762999-G-A

40264613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80762999-G-C

40264615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80763006-A-G

40264618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80763009-G-A

40264618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80763009-G-C

40264760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80763140-A-G

http://identifiers.org/hco/22/GRCh38#40264761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80763141-C-A

40264761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80763141-C-T

40265100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80763480-G-C

40265193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80763573-G-A

40265701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80764081-T-C

40266645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80765025-A-G

40267137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80765505-A-G

http://identifiers.org/hco/22/GRCh38#40267188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80765554-A-C

40267336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80765737-T-C

40267409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80765806-A-G

40269997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80767034-G-C

http://identifiers.org/hco/22/GRCh38#40270062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80767087-C-A

40270062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80767087-C-G

40270062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80767087-C-T

40270073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80767102-G-A

40272862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80767674-G-A

40273294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80768284-A-G

40274973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80769480-A-G

http://identifiers.org/hco/22/GRCh38#40275023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80769524-A-C

40276220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80770481-G-T

40276343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80770593-A-G

40276561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80770702-A-G

40276792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80770943-A-T

http://identifiers.org/hco/22/GRCh38#40276822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80770973-C-A

40276822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80770973-C-T

40277011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80771100-A-G

40277062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80771146-G-T

40277064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80771148-T-C

http://identifiers.org/hco/22/GRCh38#40277185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80771269-C-A

40277274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80771339-G-T

40277889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80771911-A-T

40277906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80771928-G-A

40278070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80772100-T-C

http://identifiers.org/hco/22/GRCh38#40278189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80772221-C-A

40279438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80772722-A-G

40279664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80772950-A-T

http://identifiers.org/hco/22/GRCh38#40279869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80773109-C-A

40279869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80773109-C-T

40279967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80773199-T-C

40280186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80773399-G-A

40280186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80773399-G-T

http://identifiers.org/hco/22/GRCh38#40280280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80773492-C-A

40280280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80773492-C-T

40280327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80773539-C-T

40280529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80773745-G-A

40280687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80773882-G-A

40281361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80774549-A-G

40281361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80774549-A-T

40281384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80774570-T-C

40281384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80774570-T-G

40281414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80774600-T-A

40281423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80774610-G-A

40281423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80774610-G-C

40281423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80774610-G-T

40281665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80775031-T-G

40281771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80775312-C-T

40281805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80775338-A-G

http://identifiers.org/hco/22/GRCh38#40281903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80775416-C-A

40281903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80775416-C-G

40282275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80775720-C-G

40282430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80775867-G-A

40282911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80776459-C-T

40283641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80776672-G-T

40283815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80776753-G-T

40284340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80777110-T-A

40284517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80777252-G-T

40284651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80777386-G-A

40284904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80777680-C-T

40285430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80778309-G-A

40285552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80778444-G-T

40285647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 80778532-C-T

40285780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80778665-T-C

40285869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80778744-A-G

40286083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80778864-T-C

http://identifiers.org/hco/22/GRCh38#40286114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80778895-C-A

40292345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80781940-T-C

40292345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80781940-T-G

40292697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80782249-C-T

40292712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80782264-C-T

40298291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80784742-T-C

40298364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80784813-C-T

40298498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80784931-T-A

40298498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80784931-T-C

40300104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80785767-G-T

http://identifiers.org/hco/22/GRCh38#40300347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80785993-C-A

http://identifiers.org/hco/22/GRCh38#40300382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80786027-C-A

40300382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80786027-C-T

http://identifiers.org/hco/22/GRCh38#40300383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80786028-A-C

40300395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80786040-T-G

http://identifiers.org/hco/22/GRCh38#40300407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80786052-A-C

40300407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80786052-A-G

40300598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80786228-A-T

40300603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80786233-C-T

40300621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80786251-G-A

40300621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80786251-G-T

http://identifiers.org/hco/22/GRCh38#40300729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80786337-C-A

40300799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80786400-T-C

40300804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80786405-A-G

http://identifiers.org/hco/22/GRCh38#40300863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80786451-C-A

40300863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80786451-C-G

40300863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80786451-C-T

40300906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 80786485-G-A

http://identifiers.org/hco/22/GRCh38#40301031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80786613-A-C

40301031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80786613-A-G

40301085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80786657-G-A

40301179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80786759-G-A

40301314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80786894-A-G

40302225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80788131-G-A

http://identifiers.org/hco/22/GRCh38#40302502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80788395-A-C

40302755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80788651-G-A

40302843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80788708-A-G

40305147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80795171-A-G

40305172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80795196-G-A

40306541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80795991-A-G

http://identifiers.org/hco/22/GRCh38#40307065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80796326-A-C

40307066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80796327-T-A

40307066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80796327-T-C

40307073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80796333-G-T

40307474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80796706-T-C

40307474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80796706-T-G

40307527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80796751-C-T

40307831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80797000-C-T

http://identifiers.org/hco/22/GRCh38#40308306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80797328-C-A

40308306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80797328-C-T

40308445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80797439-G-A

http://identifiers.org/hco/22/GRCh38#40309319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80799373-A-C

40309780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80799799-C-G

40309808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80799827-C-G

40310209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80800185-G-A

40310248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80800218-G-C

40310298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80800268-A-G

40310560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80800520-A-T

40310790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80800860-A-G

40312374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80801991-T-A

40312378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80801995-G-T

http://identifiers.org/hco/22/GRCh38#40312467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80802117-C-A

40312467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80802117-C-T

40312692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80802337-A-G

40312692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80802337-A-T

40312777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80802426-A-G

http://identifiers.org/hco/22/GRCh38#40312856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80802664-C-A

40312856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80802664-C-G

40312856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80802664-C-T

40312858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80802666-G-A

40312858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80802666-G-C

40313036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80802841-T-G

40313089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80802888-T-C

40313115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80802914-G-A

40313115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80802914-G-T

40313124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80802923-A-T

40313215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80803025-G-T

http://identifiers.org/hco/22/GRCh38#40313406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80803204-C-A

40313406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80803204-C-T

40314499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80806613-A-G

40314499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80806613-A-T

40314866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80807187-A-G

40314989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80807321-T-C

http://identifiers.org/hco/22/GRCh38#40315187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80807576-C-A

http://identifiers.org/hco/22/GRCh38#40315229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80807610-C-A

40315554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80807914-G-A

40315554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80807914-G-C

40315556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80807916-T-A

40315631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80807977-T-G

40315804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80808146-A-G

40315923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80808269-T-A

40315923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80808269-T-C

http://identifiers.org/hco/22/GRCh38#40316104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80808446-A-C

http://identifiers.org/hco/22/GRCh38#40316151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80808485-A-C

40316151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80808485-A-G

40316215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80808561-A-G

40320523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80811097-C-T

40320818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80811324-C-T

40320929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80811632-C-T

40321058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80811768-G-C

40321078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80811789-A-G

40321263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80811970-C-T

40321264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80811971-A-G

40321286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80811991-G-A

40321286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80811991-G-T

40321386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80812076-G-A

40321901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80812376-G-T

40321947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80812423-C-G

40322143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80812609-A-G

40322319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80812795-C-T

40322391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80812872-G-A

40322459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80812984-A-G

40322828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron variant
orthologous variants: 80813270-A-G

http://identifiers.org/hco/22/GRCh38#40322850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80813286-C-A

40322850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 80813286-C-G

http://identifiers.org/hco/22/GRCh38#40323712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80814146-C-A

http://identifiers.org/hco/22/GRCh38#40323730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80814164-A-C

40323730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80814164-A-G

40323730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80814164-A-T

http://identifiers.org/hco/22/GRCh38#40323872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80814305-C-A

40323872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80814305-C-T

40323974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80814426-T-A

40323974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80814426-T-C

40324006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80814459-T-C

40324007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80814460-G-A

40324312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80814754-A-G

40324312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80814754-A-T

40324556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80814987-G-T

40324615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80815057-G-T

40324628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80815070-G-A

40324672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80815114-G-A

40324672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80815114-G-C

40324672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80815114-G-T

http://identifiers.org/hco/22/GRCh38#40324717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80815159-C-A

http://identifiers.org/hco/22/GRCh38#40324752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80815190-C-A

http://identifiers.org/hco/22/GRCh38#40325057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80815523-C-A

40325057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80815523-C-T

40325462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80815939-T-C

40325803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80816256-G-A

40325803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80816256-G-C

40325803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80816256-G-T

http://identifiers.org/hco/22/GRCh38#40325884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80816345-C-A

40325884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80816345-C-G

40325884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80816345-C-T

40326049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80816514-G-A

http://identifiers.org/hco/22/GRCh38#40326219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80816779-C-A

40326513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80817072-A-G

40326534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80817091-A-G

40326822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80817388-G-T

http://identifiers.org/hco/22/GRCh38#40326918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80817490-C-A

40327214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80817770-A-G

40327245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80817799-G-A

40327245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80817799-G-T

40327535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80818088-G-A

40327821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80818315-T-A

40327881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80818373-G-C

40327881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80818373-G-T

40327937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80818427-A-G

40327937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80818427-A-T

40327983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80818468-G-A

40327983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80818468-G-T

40328218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80818727-G-A

40328330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80818819-G-T

40328497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80819012-G-A

http://identifiers.org/hco/22/GRCh38#40329132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80819578-C-A

40329252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80819657-C-T

40329457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80819815-A-T

40329505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80819863-C-T

40329618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80820102-G-T

40329637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80820122-G-A

40329694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80820150-G-A

40329694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80820150-G-C

40329694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80820150-G-T

40330218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80820567-C-T

40330471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80820722-A-G

40330668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80820888-G-A

40330668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80820888-G-T

40330746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80820967-G-A

40330890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80821053-G-T

40330937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80821106-C-T

http://identifiers.org/hco/22/GRCh38#40331024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80821179-C-A

40331028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80821183-G-A

40331028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80821183-G-T

40331136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80821303-C-T

40331371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80821552-T-G

40331670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80821803-T-A

40331670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80821803-T-C

40331670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80821803-T-G

http://identifiers.org/hco/22/GRCh38#40331671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80821804-C-A

40331671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80821804-C-G

40331671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80821804-C-T

http://identifiers.org/hco/22/GRCh38#40331672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80821805-A-C

40331672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80821805-A-G

40331672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80821805-A-T

40331883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80822003-G-T

40331885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80822009-G-T

http://identifiers.org/hco/22/GRCh38#40331903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80822027-C-A

40332350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80822377-C-T

40332364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80822391-G-C

40332452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80822472-T-A

40332514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80822532-C-T

http://identifiers.org/hco/22/GRCh38#40332572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80822586-C-A

40332572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80822586-C-T

http://identifiers.org/hco/22/GRCh38#40332583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80822597-C-A

http://identifiers.org/hco/22/GRCh38#40332972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80822953-C-A

40332972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80822953-C-G

http://identifiers.org/hco/22/GRCh38#40333019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80822982-C-A

40333019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80822982-C-T

40333077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80823000-C-G

40333080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80823003-A-G

40333095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80823015-G-A

40333163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80823036-G-A

40333163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80823036-G-C

40333551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80823226-G-A

40333559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80823234-G-C

http://identifiers.org/hco/22/GRCh38#40334029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80823582-C-A

40334029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80823582-C-T

40334056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80823606-T-A

40334056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80823606-T-C

http://identifiers.org/hco/22/GRCh38#40334187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80823739-C-A

40334187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80823739-C-G

40334187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80823739-C-T

40334191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29190
most severe consequence: 3 prime UTR variant
orthologous variants: 80823743-G-A