rs961575949 Rat Genome Database

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Variant: rs961575949 -  Homo sapiens

RGD ID: 127267943
RS ID: rs961575949
ClinVar ID: CV1107031
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127893228  SAMHD1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 20 35,575,211
GRCh38 20 36,946,808
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001363729.2:c.209-4A>G
NM_001363733.2:c.209-4A>G
NM_015474.4:c.209-4A>G
LRG_281:g.10036A>G
More... 		12/15/2023 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SAMHD1
Accession:NM_001363729
Location:INTRON

Gene Symbol:SAMHD1
Accession:NM_001363733
Location:INTRON

Gene Symbol:SAMHD1
Accession:NM_015474
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001440654 CLINVAR
  RCV002555574 CLINVAR
dbSNP (RS) rs961575949 CLINVAR
MedGen C0950123 CLINVAR
  C2749659 CLINVAR
NCBI Gene SAMHD1 CLINVAR
OMIM 606754 CLINVAR
  612952 CLINVAR