chr3:178952074:G>A Detail (hg19) (PIK3CA)

Information

Genome

Assembly Position
hg19 chr3:178,952,074-178,952,074
hg38 chr3:179,234,286-179,234,286 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_006218.3:c.3129G>A NP_006209.2:p.Met1043Ile
Ensemble ENST00000263967.4:c.3129G>A ENST00000263967.4:p.Met1043Ile
ENST00000643187.1:c.*209G>A
Summary

MGeND

Clinical significance not provided
Variant entry 7
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic Likely 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 COSM29313 COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
not provided fundus of stomach not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
not provided ill-defined sites within the digestive system not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
not provided pyloric antrum not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
not provided malignant neoplasm of rectum not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
not provided body of pancreas not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
not provided Tumors of unknown primary site somatic MGS000018
(TMGS000110)
Hitoshi Nakagama National Cancer Center Japan 30742731
not provided bronchus or lung, unspecified not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Likely pathogenic 2013-07-19 criteria provided, single submitter Non-small cell lung carcinoma somatic Detail
Pathogenic 2015-01-20 no assertion criteria provided PIK3CA related overgrowth syndrome somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Malignant neoplasm of body of uterus somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Breast neoplasm 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 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 Neoplasm of the large intestine somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided gastric adenocarcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided glioblastoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided adenoid cystic carcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Thyroid tumor somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided somatic Detail
Pathogenic 2022-07-05 criteria provided, single submitter Cowden syndrome germline Detail
Pathogenic criteria provided, single submitter Megalencephaly-capillary malformation-polymicrogyria syndrome somatic Detail
Pathogenic 2022-10-20 criteria provided, single submitter not provided germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.137 Non-small cell lung carcinoma NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Non-small cell lung carcinoma ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND PIK3CA related overgrowth syndrome ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Malignant neoplasm of body of uterus ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Breast neoplasm ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Squamous cell carcinoma of the head and neck ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Pancreatic adenocarcinoma ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Neoplasm of brain ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Neoplasm of the large intestine ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Gastric adenocarcinoma ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Glioblastoma ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Adenoid cystic carcinoma ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Thyroid tumor ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Transitional cell carcinoma of the bladder ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Cowden syndrome ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND Megalencephaly-capillary malformation-polymicrogyri... ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) AND not provided 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
rs121913283 dbSNP
Genome
hg19
Position
chr3:178,952,074-178,952,074
Variant Type
snv
Reference Allele
G
Alternative Allele
A
Genome browser