RGD:150495821 Rat Genome Database

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Variant: RGD:150495821 -  Homo sapiens

RGD ID: 150495821
RS ID: rs77263147
ClinVar ID: CV1272727
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: POLR3A  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 79,782,281
GRCh38 10 78,022,523
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.646-139A>G
NG_029648.1:g.12018A>G
NC_000010.11:g.78022523T>C
NC_000010.10:g.79782281T>C
04/16/2021 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 RCV001688650 CLINVAR
dbSNP (RS) rs77263147 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene POLR3A CLINVAR
OMIM 614258 CLINVAR