chr3:179218306:C>G Detail (hg38) (PIK3CA)

Information

Genome

Assembly Position
hg19 chr3:178,936,094-178,936,094 View the variant detail on this assembly version.
hg38 chr3:179,218,306-179,218,306

HGVS

Type Transcript Protein
RefSeq NM_006218.3:c.1636C>G NP_006209.2:p.Gln546Glu
Ensemble ENST00000263967.4:c.1636C>G ENST00000263967.4:p.Gln546Glu
ENST00000643187.1:c.1636C>G ENST00000643187.1:p.Gln546Glu
Summary

MGeND

Clinical significance
Variant entry
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 COSM6147 COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2004-11-01 no assertion criteria provided breast adenocarcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Malignant melanoma of skin 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 glioblastoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided uterine carcinosarcoma somatic Detail
Pathogenic 2016-05-31 no assertion criteria provided Breast neoplasm 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 medulloblastoma somatic Detail
Pathogenic 2016-05-31 no assertion criteria provided Neoplasm of the large intestine 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 Squamous cell carcinoma of the head and neck somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided gastric adenocarcinoma somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided prostate adenocarcinoma somatic Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.120 breast adenocarcinoma NA CLINVAR Detail
0.131 colon carcinoma NA CLINVAR Detail
0.128 Epithelial ovarian cancer NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Breast adenocarcinoma ClinVar Detail
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Malignant melanoma of skin ClinVar Detail
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Neoplasm of uterine cervix ClinVar Detail
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Glioblastoma ClinVar Detail
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Transitional cell carcinoma of the bladder ClinVar Detail
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Uterine carcinosarcoma ClinVar Detail
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Breast neoplasm ClinVar Detail
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Neoplasm of brain ClinVar Detail
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Medulloblastoma ClinVar Detail
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Neoplasm of the large intestine ClinVar Detail
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Malignant neoplasm of body of uterus ClinVar Detail
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Squamous cell carcinoma of the head and neck ClinVar Detail
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Gastric adenocarcinoma ClinVar Detail
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu) AND Prostate adenocarcinoma ClinVar Detail
NA DisGeNET Detail
NA DisGeNET 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
rs121913286 dbSNP
Genome
hg38
Position
chr3:179,218,306-179,218,306
Variant Type
snv
Reference Allele
C
Alternative Allele
G
Variant (CIViC) (CIViC Variant)
Q546E
Transcript 1 (CIViC Variant)
ENST00000263967.3
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/886
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