chr3:178952084:C>T Detail (hg19) (PIK3CA)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr3:178,952,084-178,952,084 |
hg38 | chr3:179,234,296-179,234,296 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_006218.3:c.3139C>T | NP_006209.2:p.His1047Tyr |
Ensemble | ENST00000263967.4:c.3139C>T | ENST00000263967.4:p.His1047Tyr |
ENST00000643187.1:c.*219C>T |
Summary
MGeND
Clinical significance |
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Variant entry | 9 |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
MGeND
Clinical significance | Last evaluated | Condition | Origin | Submission ID | Submitter | Institute | Citation | Comment | Image |
---|---|---|---|---|---|---|---|---|---|
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colon, unspecified |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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bronchus or lung, unspecified |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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descending colon |
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MGS000040
(TMGS000095) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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malignant neoplasm of rectosigmoid junction |
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MGS000040
(TMGS000095) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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2018/05/15 | stomach neoplasms |
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MGS000017
(TMGS000034) |
Kohei Miyazono | Tokyo University | |||
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Neoplasm of ovary (disorder) |
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MGS000021
(TMGS000080) |
Manabu Muto | Kyoto University | ||||
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other |
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MGS000073
(TMGS000155) |
Kenjiro Kosaki |
Keio University IRUD |
||||
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ascending colon |
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MGS000042
(TMGS000093) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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descending colon |
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MGS000042
(TMGS000093) |
Hitoshi Nakagama | National Cancer Center Japan |
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2022-03-08 | criteria provided, multiple submitters, no conflicts | Megalencephaly-capillary malformation-polymicrogyria syndrome |
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Detail |
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2011-03-01 | criteria provided, single submitter | Non-small cell lung carcinoma |
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Detail |
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2016-05-31 | no assertion criteria provided | medulloblastoma |
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Detail |
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2016-05-31 | no assertion criteria provided | hepatocellular carcinoma |
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Detail |
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2015-07-14 | no assertion criteria provided | Malignant tumor of floor of mouth |
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Detail |
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2016-05-31 | no assertion criteria provided | prostate adenocarcinoma |
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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 | Neoplasm of brain |
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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 | Squamous cell lung carcinoma |
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Detail |
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2016-05-31 | no assertion criteria provided | Malignant melanoma of skin |
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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 | Carcinoma of esophagus |
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Detail |
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2016-05-31 | no assertion criteria provided | lung adenocarcinoma |
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Detail |
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2016-05-31 | no assertion criteria provided | uterine carcinosarcoma |
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Detail |
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2016-05-31 | no assertion criteria provided | Neoplasm of uterine cervix |
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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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2016-05-31 | no assertion criteria provided |
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Detail | |
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2016-05-31 | no assertion criteria provided | ovarian serous cystadenocarcinoma |
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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 | Breast neoplasm |
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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 the large intestine |
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Detail |
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2016-05-31 | no assertion criteria provided | Papillary renal cell carcinoma type 1 |
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Detail |
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2016-05-31 | no assertion criteria provided | Adrenal cortex carcinoma |
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Detail |
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2023-10-13 | criteria provided, single submitter | Cowden syndrome |
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Detail |
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2018-10-31 | criteria provided, single submitter | epidermal nevus,CLOVES syndrome,Neoplasm of ovary,Neoplasm of stomach,hepatocellular carcinoma,Congenital macrodactylia,Familial cancer of breast,Carcinoma of colon,seborrheic keratosis,Megalencephaly-capillary malformation-polymicrogyria syndrome,Cowden syndrome 5,lung carcinoma,CLAPO syndrome |
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Detail |
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2018-10-31 | criteria provided, single submitter | epidermal nevus,CLOVES syndrome,Neoplasm of ovary,Neoplasm of stomach,hepatocellular carcinoma,Congenital macrodactylia,Familial cancer of breast,Carcinoma of colon,seborrheic keratosis,Megalencephaly-capillary malformation-polymicrogyria syndrome,Cowden syndrome 5,lung carcinoma,CLAPO syndrome |
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Detail |
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2018-10-31 | criteria provided, single submitter | epidermal nevus,CLOVES syndrome,Neoplasm of ovary,Neoplasm of stomach,hepatocellular carcinoma,Congenital macrodactylia,Familial cancer of breast,Carcinoma of colon,seborrheic keratosis,Megalencephaly-capillary malformation-polymicrogyria syndrome,Cowden syndrome 5,lung carcinoma,CLAPO syndrome |
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Detail |
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2018-10-31 | criteria provided, single submitter | epidermal nevus,CLOVES syndrome,Neoplasm of ovary,Neoplasm of stomach,hepatocellular carcinoma,Congenital macrodactylia,Familial cancer of breast,Carcinoma of colon,seborrheic keratosis,Megalencephaly-capillary malformation-polymicrogyria syndrome,Cowden syndrome 5,lung carcinoma,CLAPO syndrome |
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Detail |
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2018-10-31 | criteria provided, single submitter | epidermal nevus,CLOVES syndrome,Neoplasm of ovary,Neoplasm of stomach,hepatocellular carcinoma,Congenital macrodactylia,Familial cancer of breast,Carcinoma of colon,seborrheic keratosis,Megalencephaly-capillary malformation-polymicrogyria syndrome,Cowden syndrome 5,lung carcinoma,CLAPO syndrome |
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Detail |
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2018-10-31 | criteria provided, single submitter | epidermal nevus,CLOVES syndrome,Neoplasm of ovary,Neoplasm of stomach,hepatocellular carcinoma,Congenital macrodactylia,Familial cancer of breast,Carcinoma of colon,seborrheic keratosis,Megalencephaly-capillary malformation-polymicrogyria syndrome,Cowden syndrome 5,lung carcinoma,CLAPO syndrome |
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Detail |
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2018-10-31 | criteria provided, single submitter | epidermal nevus,CLOVES syndrome,Neoplasm of ovary,Neoplasm of stomach,hepatocellular carcinoma,Congenital macrodactylia,Familial cancer of breast,Carcinoma of colon,seborrheic keratosis,Megalencephaly-capillary malformation-polymicrogyria syndrome,Cowden syndrome 5,lung carcinoma,CLAPO syndrome |
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Detail |
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2018-10-31 | criteria provided, single submitter | epidermal nevus,CLOVES syndrome,Neoplasm of ovary,Neoplasm of stomach,hepatocellular carcinoma,Congenital macrodactylia,Familial cancer of breast,Carcinoma of colon,seborrheic keratosis,Megalencephaly-capillary malformation-polymicrogyria syndrome,Cowden syndrome 5,lung carcinoma,CLAPO syndrome |
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Detail |
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2018-10-31 | criteria provided, single submitter | epidermal nevus,CLOVES syndrome,Neoplasm of ovary,Neoplasm of stomach,hepatocellular carcinoma,Congenital macrodactylia,Familial cancer of breast,Carcinoma of colon,seborrheic keratosis,Megalencephaly-capillary malformation-polymicrogyria syndrome,Cowden syndrome 5,lung carcinoma,CLAPO syndrome |
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Detail |
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2018-10-31 | criteria provided, single submitter | epidermal nevus,CLOVES syndrome,Neoplasm of ovary,Neoplasm of stomach,hepatocellular carcinoma,Congenital macrodactylia,Familial cancer of breast,Carcinoma of colon,seborrheic keratosis,Megalencephaly-capillary malformation-polymicrogyria syndrome,Cowden syndrome 5,lung carcinoma,CLAPO syndrome |
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Detail |
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2018-10-31 | criteria provided, single submitter | epidermal nevus,CLOVES syndrome,Neoplasm of ovary,Neoplasm of stomach,hepatocellular carcinoma,Congenital macrodactylia,Familial cancer of breast,Carcinoma of colon,seborrheic keratosis,Megalencephaly-capillary malformation-polymicrogyria syndrome,Cowden syndrome 5,lung carcinoma,CLAPO syndrome |
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Detail |
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2018-10-31 | criteria provided, single submitter | epidermal nevus,CLOVES syndrome,Neoplasm of ovary,Neoplasm of stomach,hepatocellular carcinoma,Congenital macrodactylia,Familial cancer of breast,Carcinoma of colon,seborrheic keratosis,Megalencephaly-capillary malformation-polymicrogyria syndrome,Cowden syndrome 5,lung carcinoma,CLAPO syndrome |
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Detail |
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2018-10-31 | criteria provided, single submitter | epidermal nevus,CLOVES syndrome,Neoplasm of ovary,Neoplasm of stomach,hepatocellular carcinoma,Congenital macrodactylia,Familial cancer of breast,Carcinoma of colon,seborrheic keratosis,Megalencephaly-capillary malformation-polymicrogyria syndrome,Cowden syndrome 5,lung carcinoma,CLAPO syndrome |
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Detail |
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2020-11-30 | criteria provided, multiple submitters, no conflicts | not provided |
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Detail |
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2021-04-06 | criteria provided, single submitter |
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Detail | |
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2021-08-01 | criteria provided, single submitter | CLOVES syndrome |
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Detail |
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2023-10-11 | criteria provided, multiple submitters, no conflicts | PIK3CA related overgrowth syndrome |
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Detail |
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2012-06-24 | no assertion criteria provided | HEMIFACIAL MYOHYPERPLASIA, SOMATIC |
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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 | |
<0.001 | Oropharyngeal disorders | PIK3CA mutations were identified by Sanger sequencing in 23 of 75 (31%) HPV-posi... | BeFree | 24341335 | Detail |
0.360 | Megalencephaly cutis marmorata telangiectatica congenita | NA | CLINVAR | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Megalencephaly-capillary malformation-polymicrogyri... | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Non-small cell lung carcinoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Medulloblastoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Hepatocellular carcinoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Malignant tumor of floor of mouth | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Prostate adenocarcinoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Malignant neoplasm of body of uterus | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Neoplasm of brain | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Gastric adenocarcinoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Squamous cell lung carcinoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Malignant melanoma of skin | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Glioblastoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Carcinoma of esophagus | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Lung adenocarcinoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Uterine carcinosarcoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Neoplasm of uterine cervix | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Transitional cell carcinoma of the bladder | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Brainstem glioma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Ovarian serous cystadenocarcinoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Squamous cell carcinoma of the head and neck | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Breast neoplasm | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Pancreatic adenocarcinoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Neoplasm of the large intestine | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Papillary renal cell carcinoma type 1 | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Adrenal cortex carcinoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Cowden syndrome | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND multiple conditions | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND multiple conditions | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND multiple conditions | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND multiple conditions | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND multiple conditions | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND multiple conditions | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND multiple conditions | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND multiple conditions | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND multiple conditions | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND multiple conditions | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND multiple conditions | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND multiple conditions | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND multiple conditions | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND not provided | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND Segmental undergrowth associated with mainly venous... | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND CLOVES syndrome | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND PIK3CA related overgrowth syndrome | ClinVar | Detail |
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr) AND HEMIFACIAL MYOHYPERPLASIA, SOMATIC | ClinVar | Detail |
NA | DisGeNET | Detail |
PIK3CA mutations were identified by Sanger sequencing in 23 of 75 (31%) HPV-positive oropharyngeal c... | 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
- rs121913281 dbSNP
- Genome
- hg19
- Position
- chr3:178,952,084-178,952,084
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
- Variant (CIViC) (CIViC Variant)
- H1047Y
- Transcript 1 (CIViC Variant)
- ENST00000263967.3
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/938
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