RGD:150489728 Rat Genome Database

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Variant: RGD:150489728 -  Homo sapiens

RGD ID: 150489728
RS ID: rs60051748
ClinVar ID: CV1250909
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: POLR3A  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 79,764,421
GRCh38 10 78,004,663
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_007055.4:c.2247+53G>A
NG_029648.1:g.29878G>A
NC_000010.11:g.78004663C>T
NC_000010.10:g.79764421C>T
04/21/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:POLR3A
Accession:NM_007055
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001674576 CLINVAR
dbSNP (RS) rs60051748 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene POLR3A CLINVAR
OMIM 614258 CLINVAR