RGD:405144948 Rat Genome Database

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Variant: RGD:405144948 -  Homo sapiens

RGD ID: 405144948
ClinVar ID: CV3027390
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTNNA1  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 5 138,240,032
GRCh38 5 138,904,343
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001324006.1:c.-211-6T>G
NM_001324007.1:c.-211-6T>G
NM_001324008.1:c.-211-6T>G
NM_001324009.1:c.-211-6T>G
More... 		05/24/2023 intron variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003702838 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CTNNA1 CLINVAR
OMIM 116805 CLINVAR