RGD:15123437 Rat Genome Database

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Variant: RGD:15123437 -  Homo sapiens

RGD ID: 15123437
RS ID: rs202006168
ClinVar ID: CV760897
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: XRCC1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 44,058,790
GRCh38 19 43,554,638
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006297.3:c.414+8G>A
NG_033799.1:g.25941G>A
NC_000019.10:g.43554638C>T
NC_000019.9:g.44058790C>T
More... 		04/10/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:XRCC1
Accession:NM_006297
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000918821 CLINVAR
dbSNP (RS) rs202006168 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene XRCC1 CLINVAR
OMIM 194360 CLINVAR