RGD:8637876 Rat Genome Database

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Variant: RGD:8637876 -  Homo sapiens

RGD ID: 8637876
ClinVar ID: CV93102
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SSX6P  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 47,976,462
GRCh38 X 48,117,080
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000023.11:g.48117080G>A
NC_000023.10:g.47976462G>A
NR_028366.1:c.471G>A
NR_028366.1:n.471G>A
More... 		non-coding transcript variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:SSX6P
Accession:NR_028366
Location:EXON;NON-CODING

Variant Samples