RGD:597674336 Rat Genome Database

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Variant: RGD:597674336 -  Homo sapiens

RGD ID: 597674336
ClinVar ID: CV3620818
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TNFRSF8  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 12,202,413
GRCh38 1 12,142,356
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NP_001268359.2:p.Arg426Gln
NP_001234.3:p.Arg538Gln
NM_001281430.3:c.1277G>A
NM_001243.5:c.1613G>A
More... 		12/03/2024 missense variant likely benign AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004882857 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene TNFRSF8 CLINVAR
OMIM 153243 CLINVAR