RGD:28896448 Rat Genome Database

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Variant: RGD:28896448 -  Homo sapiens

RGD ID: 28896448
RS ID: rs533069935
ClinVar ID: CV879975
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNASEH2A  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 12,924,403
GRCh38 19 12,813,589
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000019.10:g.12813589G>A
LRG_278t1:c.*123G>A
NM_006397.3:c.*123G>A
LRG_278:g.11976G>A
More... 		01/13/2018 3 prime utr variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:RNASEH2A
Accession:NM_006397
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001122849 CLINVAR
dbSNP (RS) rs533069935 CLINVAR
MedGen C1835912 CLINVAR
NCBI Gene RNASEH2A CLINVAR
OMIM 606034 CLINVAR
  610333 CLINVAR