RGD:405159923 Rat Genome Database

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Variant: RGD:405159923 -  Homo sapiens

RGD ID: 405159923
ClinVar ID: CV3021396
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTNNA1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 5 138,266,619
GRCh38 5 138,930,930
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001324011.1:c.1090G>C
NM_001290312.1:c.1183G>C
NM_001323987.1:c.1183G>C
NM_001323988.1:c.1183G>C
More... 		04/19/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003703890 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CTNNA1 CLINVAR
OMIM 116805 CLINVAR