chr3:178952074:G>T 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>T NP_006209.2:p.Met1043Ile
Ensemble ENST00000643187.1:c.*209G>T
ENST00000263967.4:c.3129G>T ENST00000263967.4:p.Met1043Ile
Summary

MGeND

Clinical significance not provided
Variant entry 4
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 COSM773 COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
not provided malignant neoplasm of rectum not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
not provided descending colon not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
not provided malignant neoplasm of rectum not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
not provided intrahepatic bile duct carcinoma not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic criteria provided, single submitter PIK3CA related overgrowth syndrome de novo somatic Detail
Likely pathogenic 2015-07-14 no assertion criteria provided Neoplasm of the large intestine somatic Detail
Pathogenic 2021-07-13 criteria provided, single submitter Cowden syndrome germline Detail
Pathogenic 2023-08-09 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>T (p.Met1043Ile) AND PIK3CA related overgrowth syndrome ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>T (p.Met1043Ile) AND Neoplasm of the large intestine ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>T (p.Met1043Ile) AND Cowden syndrome ClinVar Detail
NM_006218.4(PIK3CA):c.3129G>T (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
T
Variant (CIViC) (CIViC Variant)
M1043I
Transcript 1 (CIViC Variant)
ENST00000263967.3
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/937
Genome browser