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 |
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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 |
Disease area statistics
MGeND
Clinical significance | Last evaluated | Condition | Origin | Submission ID | Submitter | Institute | Citation | Comment | Image |
---|---|---|---|---|---|---|---|---|---|
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body of stomach |
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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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ill-defined sites within the digestive system |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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fundus of stomach |
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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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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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malignant neoplasm of rectosigmoid junction |
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MGS000042
(TMGS000093) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
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head of pancreas |
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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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2023-05-14 | criteria provided, single submitter | not provided |
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Detail |
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2019-09-20 | criteria provided, single submitter | not specified |
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Detail |
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2023-01-13 | criteria provided, multiple submitters, no conflicts | Megalencephaly-capillary malformation-polymicrogyria syndrome |
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Detail |
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2022-07-29 | criteria provided, single submitter | Cowden syndrome |
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Detail |
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2021-12-08 | criteria provided, single submitter |
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Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
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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