RGD:405156123 Rat Genome Database

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Variant: RGD:405156123 -  Homo sapiens

RGD ID: 405156123
ClinVar ID: CV3049093
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TP63  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 189,586,482
GRCh38 3 189,868,693
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_428t1:c.1106A>G
NM_001329964.2:c.1100A>G
NM_001114978.2:c.1106A>G
NM_001114979.2:c.1106A>G
More... 		03/10/2023 missense variant uncertain significance

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003756762 CLINVAR
MedGen CN239305 CLINVAR
NCBI Gene TP63 CLINVAR
OMIM 603273 CLINVAR