RGD:407454002 Rat Genome Database

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Variant: RGD:407454002 -  Homo sapiens

RGD ID: 407454002
ClinVar ID: CV3490596
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRIM50  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 72,738,773
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001281450.1:c.13G>A
NM_001281451.1:c.13G>A
NM_178125.3:c.13G>A
NG_023242.2:g.1620C>T
More... 		06/16/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004684740 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene TRIM50 CLINVAR
OMIM 612548 CLINVAR