RGD:150463095 Rat Genome Database

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Variant: RGD:150463095 -  Homo sapiens

RGD ID: 150463095
RS ID: rs72642271
ClinVar ID: CV1276175
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: POLR3A  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 79,751,219
GRCh38 10 77,991,461
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.2788-294C>T
NG_029648.1:g.43080C>T
NC_000010.11:g.77991461G>A
NC_000010.10:g.79751219G>A
 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 RCV001710120 CLINVAR
dbSNP (RS) rs72642271 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene POLR3A CLINVAR
OMIM 614258 CLINVAR