RGD:150497599 Rat Genome Database

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Variant: RGD:150497599 -  Homo sapiens

RGD ID: 150497599
RS ID: rs7910253
ClinVar ID: CV1219432
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: POLR3A  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 79,767,216
GRCh38 10 78,007,458
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.2074+244C>T
NG_029648.1:g.27083C>T
NC_000010.11:g.78007458G>A
NC_000010.10:g.79767216G>A
 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 RCV001620101 CLINVAR
dbSNP (RS) rs7910253 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene POLR3A CLINVAR
OMIM 614258 CLINVAR