chr3:179234286:G>A Detail (hg38) (PIK3CA)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr3:178,952,074-178,952,074 View the variant detail on this assembly version. |
hg38 | chr3:179,234,286-179,234,286 |
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 | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
Clinical Significance |
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Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2013-07-19 | criteria provided, single submitter | Non-small cell lung carcinoma |
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Detail |
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2015-01-20 | no assertion criteria provided | PIK3CA related overgrowth syndrome |
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Detail |
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2016-05-31 | no assertion criteria provided | Malignant neoplasm of body of uterus |
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Detail |
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2016-05-31 | no assertion criteria provided | Breast neoplasm |
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Detail |
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2016-05-31 | no assertion criteria provided | Squamous cell carcinoma of the head and neck |
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Detail |
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2016-05-31 | no assertion criteria provided | pancreatic adenocarcinoma |
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Detail |
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2016-05-31 | no assertion criteria provided | Neoplasm of brain |
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Detail |
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2016-05-31 | no assertion criteria provided | Neoplasm of the large intestine |
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Detail |
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2016-05-31 | no assertion criteria provided | gastric adenocarcinoma |
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Detail |
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2016-05-31 | no assertion criteria provided | glioblastoma |
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Detail |
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2016-05-31 | no assertion criteria provided | adenoid cystic carcinoma |
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Detail |
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2016-05-31 | no assertion criteria provided | Thyroid tumor |
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Detail |
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2016-05-31 | no assertion criteria provided |
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Detail | |
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2022-07-05 | criteria provided, single submitter | Cowden syndrome |
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Detail |
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criteria provided, single submitter | Megalencephaly-capillary malformation-polymicrogyria syndrome |
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Detail | |
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2022-10-20 | criteria provided, single submitter | not provided |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.137 | Non-small cell lung carcinoma | NA | CLINVAR | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
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 |
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Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs121913283 dbSNP
- Genome
- hg38
- Position
- chr3:179,234,286-179,234,286
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
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