chr3:178916936:G>A Detail (hg19) (PIK3CA)

Information

Genome

Assembly Position
hg19 chr3:178,916,936-178,916,936
hg38 chr3:179,199,148-179,199,148 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_006218.3:c.323G>A NP_006209.2:p.Arg108His
Ensemble ENST00000263967.4:c.323G>A ENST00000263967.4:p.Arg108His
ENST00000643187.1:c.323G>A ENST00000643187.1:p.Arg108His
Summary

MGeND

Clinical significance not provided
Variant entry 11
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Conflicting classifications of pathogenicity
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 COSM27497 COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
not provided body of stomach not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
not provided malignant neoplasm of rectosigmoid junction 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 fundus of stomach not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
not provided caecum not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
not provided ascending colon not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
not provided sigmoid colon not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
not provided colon, unspecified not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
not provided malignant neoplasm of rectosigmoid junction not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
not provided head of pancreas not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2023-05-14 criteria provided, single submitter not provided germline Detail
Uncertain significance 2019-09-20 criteria provided, single submitter not specified germline Detail
Pathogenic Likely pathogenic 2023-01-13 criteria provided, multiple submitters, no conflicts Megalencephaly-capillary malformation-polymicrogyria syndrome germline unknown Detail
Likely pathogenic 2022-07-29 criteria provided, single submitter Cowden syndrome germline Detail
Likely pathogenic 2021-12-08 criteria provided, single submitter unknown Detail
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
NM_006218.4(PIK3CA):c.323G>A (p.Arg108His) AND not provided ClinVar Detail
NM_006218.4(PIK3CA):c.323G>A (p.Arg108His) AND not specified ClinVar Detail
NM_006218.4(PIK3CA):c.323G>A (p.Arg108His) AND Megalencephaly-capillary malformation-polymicrogyria ... ClinVar Detail
NM_006218.4(PIK3CA):c.323G>A (p.Arg108His) AND Cowden syndrome ClinVar Detail
NM_006218.4(PIK3CA):c.323G>A (p.Arg108His) AND See cases ClinVar 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
rs886042002 dbSNP
Genome
hg19
Position
chr3:178,916,936-178,916,936
Variant Type
snv
Reference Allele
G
Alternative Allele
A
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