34435475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56585179-A-G

34435487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56585167-G-T

34435633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56585018-G-A

34435633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56585018-G-T

34435647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56585010-G-C

34435660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56584993-G-T

34435672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56584981-A-G

34435698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56584953-T-C

34435702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56584949-T-C

34435720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56584941-A-G

34436263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56583150-C-G

34443977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56578811-A-G

34443993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56578794-A-G

http://identifiers.org/hco/13/GRCh38#34444125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56578653-A-C

http://identifiers.org/hco/13/GRCh38#34445510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56577788-C-A

34445637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577668-A-T

34445831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577494-T-G

34445902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577438-G-A

34445905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577435-G-A

34446138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577201-T-C

34446210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577122-A-T

34446228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577104-T-C

http://identifiers.org/hco/13/GRCh38#34449386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56573609-C-A

34449631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56572400-C-T

34449791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56572253-C-T

http://identifiers.org/hco/13/GRCh38#34450556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56571537-A-C

http://identifiers.org/hco/13/GRCh38#34450564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56571529-A-C

34450584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56571509-C-T

34450838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56571251-C-T

34450907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56571182-C-T

34451038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56571048-T-C

34451161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570930-C-T

34451358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570782-G-T

34451438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570699-T-C

http://identifiers.org/hco/13/GRCh38#34452560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56569633-A-C

34452636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56569575-T-C

34453413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56568834-G-A

34454253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56568232-A-G

34454328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56568154-C-T

34454518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567969-G-A

34454518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567969-G-C

34454912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567627-T-C

34455486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567395-T-G

34455660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567234-G-A

34455829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567190-G-A

34456316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56566766-G-T

34457055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56566085-T-C

34457202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56565945-C-G

34459543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56562860-C-G

34459771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56562662-G-T

34459882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56562547-T-C

http://identifiers.org/hco/13/GRCh38#34461684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56560974-C-A

34461685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560973-C-T

34461776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560871-G-A

34461916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560773-T-G

34462035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560653-C-G

34462035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560653-C-T

http://identifiers.org/hco/13/GRCh38#34462113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56560412-A-C

http://identifiers.org/hco/13/GRCh38#34462118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56560407-C-A

34462284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560094-T-C

34462437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559968-C-T

34462548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559876-G-C

http://identifiers.org/hco/13/GRCh38#34462935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56559531-C-A

34462935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559531-C-G

34462935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559531-C-T

34462936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559530-G-A

34463045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559420-G-A

34464607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56557900-C-T

34464640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56557862-A-G

34464889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56557663-G-T

34465173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56557377-T-G

http://identifiers.org/hco/13/GRCh38#34465284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56557275-A-C

34466748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56555106-G-T

34467046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554925-G-A

34467137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554832-T-C

34467578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554418-G-A

34467617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554375-G-T

34467683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554326-T-A

34467731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554297-C-G

34467731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554297-C-T

34467771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554257-G-A

34467771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554257-G-C

34467849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554192-G-T

34468372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553963-C-T

34468548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553863-A-G

34468556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553855-C-T

34468620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553796-A-G

34468664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553752-A-T

34469391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553233-C-T

34470538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56551388-T-G

34470610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56551324-C-T

34470910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56551070-T-C

34471444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550624-C-T

34471535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550526-A-T

34471544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550517-A-T

34471627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550437-A-G

34473513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549668-C-T

34473896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549087-A-G

34474265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548719-C-G

34474404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548577-C-T

34474658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548334-T-A

34475012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56547980-A-G

34475152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56547859-C-T

34475193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56547818-G-A

34476913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56546570-C-T

34476980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56546506-T-C

34477521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545269-G-T

34477714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545046-T-C

34477843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544753-C-T

34478172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544059-C-T

34478275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543949-T-A

34478373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543841-C-T

34478399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543814-A-G

34478410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543803-G-A

34480150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542297-G-A

34480150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542297-G-T

34480160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542287-T-A

34486396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542110-G-A

34486454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542052-T-C

34486490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542020-A-G

34486597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56541156-C-T

34486828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540960-C-G

34486848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540940-T-A

34486848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540940-T-C

34486911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540861-A-G

34487101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540665-T-C

34487101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540665-T-G

http://identifiers.org/hco/13/GRCh38#34490935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56538704-C-A

34491239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538414-T-C

34491796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537734-A-T

34491965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537507-C-T

34492126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537346-T-A

34492240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537228-A-G

http://identifiers.org/hco/13/GRCh38#34492252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56537216-C-A

34492252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537216-C-T

34492257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537211-T-G

34492559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536889-T-C

34492650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536806-T-A

34492780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536697-A-G

34493764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536438-T-C

34493808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536401-G-T

34493828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536381-G-A

http://identifiers.org/hco/13/GRCh38#34494075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56536140-A-C

34500804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535899-C-T

34500855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535837-A-G

34500855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535837-A-T

34501190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56534787-T-C

34501216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56534761-G-A

34501234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56534743-A-G

34501487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56534517-T-C

34502573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56530404-A-G

34502580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56530411-G-A

34502612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56530441-G-T

34502651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56530481-T-C

34502724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56530554-G-A

34502852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56530686-G-A

34503078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531082-A-G

34503341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531267-G-A

34505116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56505144-G-T

34505321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56504942-A-G

34505548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56504753-C-G

34506455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56504373-C-G

34506545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56504282-A-G

34506918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56503943-G-T

34511090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93896692-T-C

34511090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93896692-T-G

34511117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

34511610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56502023-T-C

34511630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56502003-T-A

34512134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56501525-T-C

34512627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56500294-G-A

34512665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56500265-C-T

34512745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56500195-C-G

34512754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56500185-C-T

http://identifiers.org/hco/13/GRCh38#34512773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56500166-A-C

34512773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56500166-A-G

34512948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499994-C-T

34513084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499856-T-C

http://identifiers.org/hco/13/GRCh38#34513188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56499732-C-A

34513188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499732-C-T

34513326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499548-G-A

34513342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499531-A-G

34513586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499303-C-G

34513680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499219-T-C

http://identifiers.org/hco/13/GRCh38#34513691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56499208-A-C

34513692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499207-G-A

34513787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499124-T-C

34513833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499074-G-T

34513880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499035-T-G

34514232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56498686-T-C

34514263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56498655-T-G

34514332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56498600-C-G

34514333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56498599-C-T

34514401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56498549-G-A

34515156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56497808-T-C

34515322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56497651-G-A

34515387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56497587-C-G

34515526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56497447-C-G

34515548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56497425-C-G

34515548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56497425-C-T

34515597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56497381-T-C

34515733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56497284-A-G

34519473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495577-A-G

34519522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495532-C-G

34519583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495473-A-G

http://identifiers.org/hco/13/GRCh38#34519633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56495437-C-A

34520320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494754-A-G

34520428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494646-G-T

http://identifiers.org/hco/13/GRCh38#34520573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56494515-C-A

34520763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494347-C-G

http://identifiers.org/hco/13/GRCh38#34520833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56494283-C-A

34520833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494283-C-T

34520883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494235-G-C

34520890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494228-G-A

34521061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493872-G-A

34521139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493791-G-A

34521180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493766-G-A

http://identifiers.org/hco/13/GRCh38#34521346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56493629-A-C

34521419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493567-G-A

34521419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493567-G-T

http://identifiers.org/hco/13/GRCh38#34521428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56493558-A-C

34533277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56488080-T-C

34533454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56487887-C-T

34533588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56487768-G-A

34533778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56486571-A-G

34534029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56486369-G-T

34534072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56486324-A-G

http://identifiers.org/hco/13/GRCh38#34534118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56486256-C-A

34534122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56486252-G-T

34534185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56486202-G-A

34534531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485881-C-T

34534680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485733-G-T

34534740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485677-G-A

34534787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485630-G-A

34535137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485533-T-C

http://identifiers.org/hco/13/GRCh38#34535138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56485532-C-A

34535138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485532-C-G

34535153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485517-C-T

34535401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485306-C-T

34535596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485137-G-A

34535596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485137-G-T

34535802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56484732-G-A

34538859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56481643-T-C

34538956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56481565-A-T

34539041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56481487-T-A

34539127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56481404-G-T

34539208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56481323-C-T

34539313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56481215-T-C

34539315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56481211-T-G

34539531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56481001-G-A

http://identifiers.org/hco/13/GRCh38#34539705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56480801-C-A

34539764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56480697-T-C

http://identifiers.org/hco/13/GRCh38#34539810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56480645-C-A

34539810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56480645-C-G

http://identifiers.org/hco/13/GRCh38#34541804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56480265-A-C

34541807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56480262-A-G

http://identifiers.org/hco/13/GRCh38#34541812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56480257-A-C

34541812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56480257-A-G

34541898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56480171-A-T

34542086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56479984-A-G

34542086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56479984-A-T

34542157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56479911-A-G

34542319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56479744-C-T

34544848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469364-T-C

34545037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469169-G-A

http://identifiers.org/hco/13/GRCh38#34545047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56469159-C-A

34545075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469135-T-G

http://identifiers.org/hco/13/GRCh38#34545807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56468241-C-A

http://identifiers.org/hco/13/GRCh38#34545869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56468188-C-A

34545869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468188-C-T

http://identifiers.org/hco/13/GRCh38#34545953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56468123-A-C

34545957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56468119-T-C

34545961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56468115-C-G

34546001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56468074-T-C

34546063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468013-G-T

34546147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56467928-C-T

34546556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56467279-T-A

34546675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56467167-G-A

34546731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56467114-T-C

http://identifiers.org/hco/13/GRCh38#34546847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56466978-C-A

34547023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56466130-G-C

34547162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56466008-T-C

34547346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465898-A-G

34547360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465881-C-T

34547401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465845-G-A

34547409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465836-A-G

34547426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465818-G-A

34547456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465779-C-T

34547461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465774-G-A

34547563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465701-C-T

34547577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465688-A-G

34547964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465180-G-T

http://identifiers.org/hco/13/GRCh38#34548342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56463335-A-C

34549887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462896-T-A

34550215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462638-T-C

34550262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462602-C-G

34550271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462593-A-T

http://identifiers.org/hco/13/GRCh38#34550625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56462360-A-C

34550625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462360-A-G

34550709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462284-C-T

34550738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462253-C-T

34550833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462200-T-G

34551013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462021-C-T

34551117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56461962-A-G

34552485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453838-G-A

34553027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453826-A-T

34553029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453824-A-T

34553082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453766-C-T

34553120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453727-C-T

34553143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453704-G-A

http://identifiers.org/hco/13/GRCh38#34553148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56453699-C-A

34553280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453578-G-A

34553332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453524-G-A

34553332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453524-G-C

34553749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453316-G-A

34553749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453316-G-T

34553889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453198-C-G

34553889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453198-C-T

http://identifiers.org/hco/13/GRCh38#34553937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56453148-C-A

34558021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443510-G-A

34558185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443358-A-G

34558491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443069-T-C

34558853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56439545-C-G

34558931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56439485-C-T

34558941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56439475-A-G

34559240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56438722-C-T

34559249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56438713-C-T

34559631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56438349-T-C

34559714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56438272-A-G

34559754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56438229-C-G

34559976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56438029-C-T

34560016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56437992-T-G

34560794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56436172-T-A

34560856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56436120-G-A

34560964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56436016-C-T

34561042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56435944-A-G

34561126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56435861-A-G

http://identifiers.org/hco/13/GRCh38#34561375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56435630-C-A

34561913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56434881-A-G

34562211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56434656-G-A

34562223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56434644-C-G

34562366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56434504-C-G

34566261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56434150-C-T

34571860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56430334-T-C

34571933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56430258-T-C

34571943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56430248-T-C

34571971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56430220-C-T

http://identifiers.org/hco/13/GRCh38#34571979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56430213-A-C

34571979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56430213-A-G

34572029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56430165-G-A

34572029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56430165-G-C

34572351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56429886-T-C

34572857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56429315-T-C

34572996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56429110-C-T

34573012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56429095-G-C

34573033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56429080-T-C

http://identifiers.org/hco/13/GRCh38#34575194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56420890-C-A

34575546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56420563-A-G

34576231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56419730-C-T

34576237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56419724-C-T

34576239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56419722-G-C

34576371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56419579-G-T

34576522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56419453-T-C

34576719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56419275-T-G

34578830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56418445-T-C

34579047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56418242-G-C

34579081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56418209-G-T

34579197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56417869-A-G

34579197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56417869-A-T

34579243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56417823-T-C

34579739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56417406-A-T

34579820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56417334-C-T

34579899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56417257-C-T

34580326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56416876-T-C

34580372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56416835-T-C

34580983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56416208-A-G

34581075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56415730-C-T

http://identifiers.org/hco/13/GRCh38#34581450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56415412-C-A

34581482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56415378-A-G

34581497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56415362-G-C

34581980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56414875-T-C

34581986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56414869-G-C

34582031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56414824-C-T

http://identifiers.org/hco/13/GRCh38#34582173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56414708-C-A

34582226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56414649-A-G

34582236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56414639-C-T

34582311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56414575-T-G

34582505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56414393-C-T

http://identifiers.org/hco/13/GRCh38#34583110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56412773-C-A

34583234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56412662-C-G

34583270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56412623-G-T

34583625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56412252-A-T

34583636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56412241-C-T

34583676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56412201-T-G

34583703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56412180-G-T

34583837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56412004-T-C

34583861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56411979-A-G

34584262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56411591-G-T

34584837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56410056-G-A

34584837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56410056-G-C

34585127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56409720-C-T

34585330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56409544-A-G

http://identifiers.org/hco/13/GRCh38#34585356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56409518-A-C

34587394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407199-C-T

34587552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407036-G-A

34587729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406859-T-C

http://identifiers.org/hco/13/GRCh38#34588357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56406473-C-A

34588357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406473-C-G

34588406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406440-C-T

34588410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406436-G-C

http://identifiers.org/hco/13/GRCh38#34588456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56406392-C-A

34588507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406340-C-T

34588557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406251-G-A

34588557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406251-G-T

34588579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406229-G-A

34588643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406165-A-G

34589465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404384-G-A

34589984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403739-C-T

34590110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403617-G-A

34590149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403581-T-G

34590292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403465-C-T

34590745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402810-G-C

http://identifiers.org/hco/13/GRCh38#34590965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56402635-C-A

34591014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402586-T-C

34591503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402319-G-A

http://identifiers.org/hco/13/GRCh38#34591882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56402146-A-C

http://identifiers.org/hco/13/GRCh38#34591886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56402142-A-C

34592005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402021-C-T

34592555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401421-A-T

34592780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401215-G-A

34592829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401166-C-T

34593193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400828-G-A

34593227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400793-T-G

34593471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400580-G-A

34593741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400332-C-T

34593971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400108-A-G

34594245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56399588-G-A

34594247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56399586-G-A

34594251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56399582-T-G

34594410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56399432-G-T

34594688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56399154-C-T

34594730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56399112-A-G

34594954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56398900-G-A

34595004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56398866-C-T

34595825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56398527-T-C

http://identifiers.org/hco/13/GRCh38#34596418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56397588-A-C

34596462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397541-G-A

34596586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397427-G-C

34596603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397416-G-C

34596606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397413-G-C

34596614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397405-T-A

http://identifiers.org/hco/13/GRCh38#34596696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56397345-C-A

34596696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397345-C-G

34596871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397239-T-C

34596886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397222-G-C

34599526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56393768-T-C

34599672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56393660-T-C

34599990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56393358-C-T

34600797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56392927-T-G

34600938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56392789-G-T

34601572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56392608-T-C

34601636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56392571-G-T

34601771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56392426-G-T

34601842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56392336-A-G

34601842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56392336-A-T

34602334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56391885-C-T

34602346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56391873-A-G

34602363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56391865-T-C

34603190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390984-C-T

34603381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390796-G-A

34603748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56387413-A-G

34604047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56387133-T-C

34604574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56386330-T-C

34604583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56386321-T-C

34608190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384553-A-G

34608276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384501-A-G

34608350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384437-G-A

34608350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384437-G-T

34608362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384425-A-G

http://identifiers.org/hco/13/GRCh38#34608365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56384423-A-C

34608365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384423-A-G

34608365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384423-A-T

34608392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384403-G-T

34608482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56384346-G-T

34617473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56383660-C-T

34617660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56383556-G-A

34617858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56383360-C-T

34618110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56383152-G-A

34618235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56383027-A-G

http://identifiers.org/hco/13/GRCh38#34618248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56383014-C-A

http://identifiers.org/hco/13/GRCh38#34618309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56382961-A-C

34618692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56381966-G-A

http://identifiers.org/hco/13/GRCh38#34618789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56381874-A-C

34618790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56381873-G-T

34619334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56380395-G-C

34619468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56380262-T-G

34619469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56380261-G-A

34619551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56380182-A-G

34619622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56380113-A-T

34619637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56380097-A-G

http://identifiers.org/hco/13/GRCh38#34619649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56380079-A-C

34619730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379979-A-G

34620072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379651-T-C

34620089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379634-C-T

34620212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379517-T-A

34620212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379517-T-C

34620341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379392-T-C

34620505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379238-T-C

34620543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379200-A-G

34620543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379200-A-T

34620545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379198-A-G

34620798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378966-A-G

34621183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378555-G-T

34621339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378414-G-C

34621366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378382-G-T

34621474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378289-G-C

34621732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377584-G-A

34621816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377510-G-T

34621859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377467-T-A

34621875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377462-T-C

34621875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377462-T-G

http://identifiers.org/hco/13/GRCh38#34622180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56377150-A-C

34622236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377107-T-G

34622284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377061-T-G

34622311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377031-T-C

34622330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377012-T-C

34623414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56376814-A-G

34623610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56376651-C-T

34624403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56376005-G-A

34624405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56376003-A-G

34624827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56375586-G-A

34624953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56375459-G-C

34624953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56375459-G-T

34624990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56375422-T-C

34625036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56375377-A-G

34625072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56375341-A-G

34625186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56375245-T-A

http://identifiers.org/hco/13/GRCh38#34625442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56375022-C-A

34627187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374498-G-A

34627280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374379-A-G

http://identifiers.org/hco/13/GRCh38#34627290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56374369-C-A

34627290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374369-C-T

34627303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374355-G-A

34627321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374338-T-G

34627426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374260-A-G

34627516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374177-C-T

34628014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56373676-G-A

34628147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56373521-C-T

34628170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56373498-A-G

34629196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56371503-A-G

34629233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56371465-C-T

34629289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56371426-C-T

http://identifiers.org/hco/13/GRCh38#34629329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56371386-C-A

34629737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56370426-G-C

34630521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56370190-G-A

34630831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56369918-T-G

34631114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56369604-G-A

34637296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56369039-G-A

34637633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56368704-T-C

34637651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56368686-A-G

34637805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56368532-C-G

34637823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56368515-A-G

34637994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56368357-A-G

34638565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56367613-T-C

http://identifiers.org/hco/13/GRCh38#34638579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#56367600-C-A

34638866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56367295-C-T

34638868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56367293-G-A

34638994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56367168-T-A

34640049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56366092-G-T

34640316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56365839-G-A

34640555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56365619-G-T

34640565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56365609-A-G

34640755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56365429-G-A

34640755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42805
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56365429-G-C