chr3:178927980:T>C Detail (hg19) (PIK3CA)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr3:178,927,980-178,927,980 |
hg38 | chr3:179,210,192-179,210,192 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_006218.3:c.1258T>C | NP_006209.2:p.Cys420Arg |
Ensemble | ENST00000263967.4:c.1258T>C | ENST00000263967.4:p.Cys420Arg |
ENST00000643187.1:c.1258T>C | ENST00000643187.1:p.Cys420Arg |
Summary
MGeND
Clinical significance |
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Variant entry | 24 |
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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pyloric antrum |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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descending colon |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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colon, unspecified |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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malignant neoplasm of rectosigmoid junction |
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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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Serous surface papillary carcinoma (morphologic abnormality)__Primary malignant neoplasm of uterus (disorder) |
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MGS000021
(TMGS000080) |
Manabu Muto | Kyoto University | ||||
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breast |
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MGS000038
(TMGS000091) |
Manabu Muto Ichiro Kinoshita |
Kyoto University Department of Medical Oncology Faculty of Medicine and Graduate School of Medicine Hokkaido University |
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Endometrial cancer |
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MGS000018
(TMGS000110) |
Hitoshi Nakagama | National Cancer Center Japan |
30742731
|
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pyloric antrum |
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MGS000042
(TMGS000093) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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caecum |
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MGS000042
(TMGS000093) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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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 | ||||
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sigmoid colon |
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MGS000042
(TMGS000093) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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colon, unspecified |
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MGS000042
(TMGS000093) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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bronchus or lung, unspecified |
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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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criteria provided, single submitter | CLOVES syndrome |
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Detail | |
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2010-10-08 | criteria provided, single submitter | Neoplasm of ovary |
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Detail |
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2014-04-23 | no assertion criteria provided | PIK3CA related overgrowth syndrome |
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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 | adenoid cystic carcinoma |
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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 | gastric 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 | Malignant neoplasm of body of uterus |
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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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2021-10-01 | criteria provided, single submitter | CLAPO syndrome |
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Detail |
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no assertion criteria provided |
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Detail | ||
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criteria provided, single submitter | Capillary malformation |
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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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2024-01-01 | criteria provided, multiple submitters, no conflicts | not provided |
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Detail |
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2023-12-12 | criteria provided, single submitter | Cowden syndrome |
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Detail |
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2024-03-19 | no assertion criteria provided | Rare combined vascular malformation |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.129 | ovarian neoplasm | NA | CLINVAR | Detail | |
0.361 | Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi | NA | CLINVAR | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND CLOVES syndrome | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND Neoplasm of ovary | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND PIK3CA related overgrowth syndrome | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND Prostate adenocarcinoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND Adenoid cystic carcinoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND Breast neoplasm | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND Gastric adenocarcinoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND Neoplasm of the large intestine | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND Malignant neoplasm of body of uterus | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND Squamous cell lung carcinoma | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND CLAPO syndrome | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND Abnormal cardiovascular system morphology | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND Capillary malformation | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND Segmental undergrowth associated with lymphatic malf... | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND not provided | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND Cowden syndrome | ClinVar | Detail |
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg) AND Rare combined vascular malformation | ClinVar | 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
- rs121913272 dbSNP
- Genome
- hg19
- Position
- chr3:178,927,980-178,927,980
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- C
- Variant (CIViC) (CIViC Variant)
- C420R
- Transcript 1 (CIViC Variant)
- ENST00000263967.3
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/931
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