RGD:405215722 Rat Genome Database

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Variant: RGD:405215722 -  Homo sapiens

RGD ID: 405215722
ClinVar ID: CV2981726
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTNNA1  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 138,266,620
GRCh38 5 138,930,931
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NP_001310920.1:p.Asp395Val
NP_001310921.1:p.Asp395Val
NP_001310922.1:p.Asp395Val
NP_001310923.1:p.Asp395Val
More... 		12/14/2022 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003709290 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CTNNA1 CLINVAR
OMIM 116805 CLINVAR