chr3:179199690:G>A Detail (hg38) (PIK3CA)

Information

Genome

Assembly Position
hg19 chr3:178,917,478-178,917,478 View the variant detail on this assembly version.
hg38 chr3:179,199,690-179,199,690

HGVS

Type Transcript Protein
RefSeq NM_006218.3:c.353G>A NP_006209.2:p.Gly118Asp
Ensemble ENST00000263967.4:c.353G>A ENST00000263967.4:p.Gly118Asp
ENST00000643187.1:c.353G>A ENST00000643187.1:p.Gly118Asp
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 171834 OMIM
HGNC 8975 HGNC
Ensembl ENSG00000121879 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC COSM751 COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2013-01-10 no assertion criteria provided Cowden syndrome 5 germline Detail
Likely pathogenic 2016-05-31 no assertion criteria provided glioblastoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Squamous cell carcinoma of the head and neck somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Breast neoplasm somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided gastric adenocarcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Squamous cell lung carcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided pancreatic adenocarcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Neoplasm of brain somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Thyroid tumor somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided prostate adenocarcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Neoplasm of uterine cervix somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Malignant neoplasm of body of uterus somatic Detail
Pathogenic 2021-08-01 criteria provided, single submitter not provided germline Detail
Pathogenic 2016-06-07 no assertion criteria provided somatic Detail
Pathogenic 2021-02-22 criteria provided, single submitter Angioosteohypertrophic syndrome somatic unknown Detail
Pathogenic 2022-06-07 criteria provided, single submitter Cowden syndrome germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.240 Cowden syndrome 5 NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Cowden syndrome 5 ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Glioblastoma ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Squamous cell carcinoma of the head and neck ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Breast neoplasm ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Gastric adenocarcinoma ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Squamous cell lung carcinoma ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Pancreatic adenocarcinoma ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Neoplasm of brain ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Thyroid tumor ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Prostate adenocarcinoma ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Neoplasm of uterine cervix ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Malignant neoplasm of body of uterus ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND not provided ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Keratoacanthoma ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Angioosteohypertrophic syndrome ClinVar Detail
NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Cowden syndrome ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs587777790 dbSNP
Genome
hg38
Position
chr3:179,199,690-179,199,690
Variant Type
snv
Reference Allele
G
Alternative Allele
A
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