RGD:405247238 Rat Genome Database

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Variant: RGD:405247238 -  Homo sapiens

RGD ID: 405247238
ClinVar ID: CV2966707
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTNNA1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 5 138,266,179
GRCh38 5 138,930,490
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.1659T>C
NM_001290309.3:c.1719T>C
NM_001323986.2:c.1935T>C
NM_001290307.3:c.2028T>C
More... 		11/23/2022 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003685625 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CTNNA1 CLINVAR
OMIM 116805 CLINVAR