RGD:8626918 Rat Genome Database

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Variant: RGD:8626918 -  Homo sapiens

RGD ID: 8626918
ClinVar ID: CV82062
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: USP47  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 11,964,675
GRCh38 11 11,943,128
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000011.8:g.11921251G>A
NM_017944.3:c.2887+16G>A
NC_000011.10:g.11943128G>A
NC_000011.9:g.11964675G>A
 intron|intron variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:USP47
Accession:NM_001372096
Location:INTRON

Gene Symbol:USP47
Accession:NM_017944
Location:INTRON

Gene Symbol:USP47
Accession:NM_001372101
Location:INTRON

Gene Symbol:USP47
Accession:NM_001372095
Location:INTRON

Gene Symbol:USP47
Accession:NM_001282659
Location:INTRON

Gene Symbol:USP47
Accession:NM_001330208
Location:INTRON

Gene Symbol:USP47
Accession:NM_001372092
Location:INTRON

Gene Symbol:USP47
Accession:XM_011520196
Location:INTRON

Gene Symbol:USP47
Accession:NM_001372093
Location:INTRON

Gene Symbol:USP47
Accession:NM_001372103
Location:INTRON

Gene Symbol:USP47
Accession:NM_001372099
Location:INTRON

Gene Symbol:USP47
Accession:NM_001372102
Location:INTRON

Gene Symbol:USP47
Accession:NM_001372097
Location:INTRON

Gene Symbol:USP47
Accession:XM_017017954
Location:INTRON

Gene Symbol:USP47
Accession:NM_001372094
Location:INTRON

Gene Symbol:USP47
Accession:NM_001372100
Location:INTRON

Gene Symbol:USP47
Accession:NM_001372098
Location:INTRON

Gene Symbol:USP47
Accession:NM_001372091
Location:INTRON

Variant Samples