RGD:11051010 Rat Genome Database

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Variant: RGD:11051010 -  Homo sapiens

RGD ID: 11051010
RS ID: rs869312567
ClinVar ID: CV225457
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTNNA1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 138,217,297
GRCh38 5 138,881,608
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001290307.3:c.1063-4604G>T
NM_001323994.1:c.-48-4604G>T
NM_001324001.1:c.-48-4604G>T
NM_001323999.1:c.-49+471G>T
More... 		12/01/2015 intron variant likely benign Cancer predisposition; Hereditary Cancer Syndrome; Hereditary neoplastic syndrome; Neoplastic Syndromes, Hereditary; Tumor predisposition
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CTNNA1
Accession:NM_001324002
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001323987
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001324000
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001324012
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001324001
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001324009
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001290312
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001323993
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001324006
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001324010
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001323999
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001324003
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001323995
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001323996
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001323997
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001323998
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001323991
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001324008
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001324013
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001323988
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001323992
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001323994
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001324011
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001324004
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001324005
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001324007
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001323990
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001323989
Location:5UTRS;INTRON

Gene Symbol:CTNNA1
Accession:NM_001290310
Location:INTRON

Gene Symbol:CTNNA1
Accession:NM_001290307
Location:INTRON

Gene Symbol:CTNNA1
Accession:NM_001323982
Location:INTRON

Gene Symbol:CTNNA1
Accession:NM_001323983
Location:INTRON

Gene Symbol:CTNNA1
Accession:NM_001290309
Location:INTRON

Gene Symbol:CTNNA1
Accession:NM_001903
Location:INTRON

Gene Symbol:CTNNA1
Accession:NM_001323984
Location:INTRON

Gene Symbol:CTNNA1
Accession:NM_001323985
Location:INTRON

Gene Symbol:CTNNA1
Accession:NM_001323986
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000209024 CLINVAR
dbSNP (RS) rs869312567 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene CTNNA1 CLINVAR
OMIM 116805 CLINVAR
SNOMED CT 699346009 CLINVAR