RGD:405227827 Rat Genome Database

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Variant: RGD:405227827 -  Homo sapiens

RGD ID: 405227827
ClinVar ID: CV2889017
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTNNA1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 138,253,548
GRCh38 5 138,917,859
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.1138G>A
NM_001290309.3:c.1198G>A
NM_001323986.2:c.1414G>A
NM_001290307.3:c.1507G>A
More... 		01/14/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003554859 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CTNNA1 CLINVAR
OMIM 116805 CLINVAR