RGD:13504401 Rat Genome Database

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Variant: RGD:13504401 -  Homo sapiens

RGD ID: 13504401
RS ID: rs757666508
ClinVar ID: CV446034
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNASEH2A  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 19 12,924,019
GRCh38 19 12,813,205
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_278t1:c.760T>C
LRG_278:g.11592T>C
LRG_278p1:p.Trp254Arg
NM_006397.3:c.760T>C
More... 		09/05/2019 missense variant uncertain significance none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:RNASEH2A
Accession:NM_006397
Location:EXON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000519024 CLINVAR
  RCV001208798 CLINVAR
dbSNP (RS) rs757666508 CLINVAR
MedGen C1835912 CLINVAR
  CN517202 CLINVAR
NCBI Gene RNASEH2A CLINVAR
OMIM 606034 CLINVAR
  610333 CLINVAR