RGD:405170151 Rat Genome Database

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Variant: RGD:405170151 -  Homo sapiens

RGD ID: 405170151
ClinVar ID: CV3047615
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TP63  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 189,612,148
GRCh38 3 189,894,359
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_428t1:c.1900C>T
NM_001329144.2:c.*128C>T
NM_001329145.2:c.*128C>T
NM_001329149.2:c.*128C>T
More... 		11/15/2023 3 prime utr variant uncertain significance

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003758121 CLINVAR
MedGen CN239305 CLINVAR
NCBI Gene TP63 CLINVAR
OMIM 603273 CLINVAR