RGD:405191947 Rat Genome Database

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Variant: RGD:405191947 -  Homo sapiens

RGD ID: 405191947
ClinVar ID: CV2984905
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTNNA1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 138,223,294
GRCh38 5 138,887,605
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NP_001277239.1:p.Ala297Asp
NP_001277238.1:p.Ala317Asp
NP_001277236.1:p.Ala420Asp
NP_001310911.1:p.Ala420Asp
More... 		12/10/2022 5 prime utr variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003706545 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CTNNA1 CLINVAR
OMIM 116805 CLINVAR