Overview

Variant ID 112
Entrez Gene ID 5290
Gene PIK3CA (GeneCards)
Location hg19 3:178927980-178927980
hg38 3:179210192-179210192
Disease Congenital lipomatous overgrowth vascular malformations and epidermal nevi (view all the variants in this disease)
Method Massively Parallel RNA Sequencing
Mutation(HGVS format) NC_000003.11:g.178927980 A>G (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein 420
Amino acid changes in protein C > R
Position in cDNA 1258
Changes in cDNA T > C
mRNA accession NM_006218.2
mRNA length 3207
Reference length 198022430

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.5248
CADD Raw score (version 1.3) 3.689411 (Deleterious)
FATHMM raw prediction score 0.98626 (Tolerated)
SIFT score 0.051 (Tolerated)
LRT score 0 (Deleterious)
MutationTaster score 1 (Deleterious)
MutatioinAssessor score 2.34 (Deleterious)
PROVEAN score -4.02 (Deleterious)
MetaSVM score -0.556 (Tolerated)
MetaLR score 0.314 (Tolerated)
MCAP score 0.084 (Deleterious)
FitCons score 0.732 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 5.51
PhyloP score based on multiple alignment of 100 vertebrates 7.674
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 15.621
Deleterious probability by DeFine 0.9664 (Deleterious)
Entrez Gene ID 5290 (NCBI Gene)
Official Gene Symbol PIK3CA (GeneCards)
Number of variants in PIK3CA in this database 109 (view all the variants)
Full name phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
Band 3q26.32
Other IDs Vega: OTTHUMG00000157311
OMIM: 171834
HGNC: HGNC:8975
Ensembl: ENSG00000121879
Other names MCM, CWS5, MCAP, PI3K, CLOVE, MCMTC, PI3K-alpha, p110-alpha
Summary Phosphatidylinositol 3-kinase is composed of an 85 kDa regulatory subunit and a 110 kDa catalytic subunit. The protein encoded by this gene represents the catalytic subunit, which uses ATP to phosphorylate PtdIns, PtdIns4P and PtdIns(4,5)P2. This gene has been found to be oncogenic and has been implicated in cervical cancers. A pseudogene of this gene has been defined on chromosome 22. [provided by RefSeq, Apr 2016]

Individual #1

Individual ID 22658544.05 (view all the variants in this individual)
Pubmed ID 22658544
Whose mosaic mutation Male Patient  
Phenotype 3  
Disease Congenital lipomatous overgrowth vascular malformations and epidermal nevi (view all the variants in this disease)
OMIM ID 612918

Publication #1: 22658544

Pubmed ID 22658544
Title Somatic Mosaic Activating Mutations in PIK3CA Cause CLOVES Syndrome
Journal American Journal of Human Genetics
Publication date 2012.06
Disease Congenital lipomatous overgrowth vascular malformations and epidermal nevi
Number of cases Male cases: 3; Female cases: 3;