RGD:597674354 Rat Genome Database

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Variant: RGD:597674354 -  Homo sapiens

RGD ID: 597674354
ClinVar ID: CV3620820
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TNFRSF8  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 12,186,245
GRCh38 1 12,126,188
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001243.5:c.1261C>T
NM_001281430.3:c.928C>T
NG_029573.2:g.67812C>T
NC_000001.11:g.12126188C>T
More... 		09/03/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004882859 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene TNFRSF8 CLINVAR
OMIM 153243 CLINVAR