RGD:405182711 Rat Genome Database

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Variant: RGD:405182711 -  Homo sapiens

RGD ID: 405182711
ClinVar ID: CV3159654
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTNNA1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 138,264,985
GRCh38 5 138,929,296
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001290310.3:c.1581C>T
NM_001290309.3:c.1641C>T
NM_001323986.2:c.1857C>T
NM_001290307.3:c.1950C>T
More... 		09/17/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003858905 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CTNNA1 CLINVAR
OMIM 116805 CLINVAR