RGD:405164928 Rat Genome Database

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Variant: RGD:405164928 -  Homo sapiens

RGD ID: 405164928
ClinVar ID: CV3002033
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TP63  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 189,587,184
GRCh38 3 189,869,395
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_428t1:c.1201T>C
NM_001329148.2:c.1189T>C
NM_001329964.2:c.1195T>C
NM_001114978.2:c.1201T>C
More... 		12/25/2022 synonymous variant likely benign

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003757618 CLINVAR
MedGen CN239305 CLINVAR
NCBI Gene TP63 CLINVAR
OMIM 603273 CLINVAR