RGD:405182237 Rat Genome Database

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Variant: RGD:405182237 -  Homo sapiens

RGD ID: 405182237
ClinVar ID: CV3024448
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTNNA1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 138,163,373
GRCh38 5 138,827,684
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001290307.3:c.1028C>T
NM_001323982.2:c.1028C>T
NM_001323983.1:c.1028C>T
NM_001323984.2:c.1028C>T
More... 		08/11/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003705651 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CTNNA1 CLINVAR
OMIM 116805 CLINVAR