RGD:11051225 Rat Genome Database

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Variant: RGD:11051225 -  Homo sapiens

RGD ID: 11051225
RS ID: rs869312614
ClinVar ID: CV225637
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIK3CA  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 178,926,428
GRCh38 3 179,208,640
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_310:g.65118A>G
NG_012113.2:g.65118A>G
NC_000003.12:g.179208640A>G
NC_000003.11:g.178926428A>G
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:PIK3CA
Accession:NM_006218
Location:INTRON

Gene Symbol:PIK3CA
Accession:XM_006713658
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000209612 CLINVAR
dbSNP (RS) rs869312614 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene PIK3CA CLINVAR
OMIM 171834 CLINVAR
SNOMED CT 699346009 CLINVAR