chr10:89692953:T>A Detail (hg19) (PTEN)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr10:89,692,953-89,692,953
hg38	chr10:87,933,196-87,933,196 View the variant detail on this assembly version.

HGVS

PTEN

Type	Transcript	Protein
RefSeq	NM_000314.6:c.437T>A	NP_000305.3:p.Leu146Ter
	NM_001304717.2:c.437T>A	NP_001291646.2:p.Leu146Ter
	NM_001304718.1:c.437T>A	NP_001291647.1:p.Leu146Ter
Ensemble	ENST00000371953.8:c.437T>A	ENST00000371953.8:p.Leu146Ter
	ENST00000472832.3:c.437T>A	ENST00000472832.3:p.Leu146Ter
	ENST00000688308.1:c.437T>A	ENST00000688308.1:p.Leu146Ter
	ENST00000700021.1:c.392T>A	ENST00000700021.1:p.Leu131Ter
	ENST00000700029.2:c.437T>A	ENST00000700029.2:p.Leu146Ter
	ENST00000713839.1:c.530T>A	ENST00000713839.1:p.Leu177Ter

Summary

MGeND

Clinical significance	not provided
Variant entry	1
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic
Review star
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Links

PTEN

Type	Database	ID	Link
Gene	MIM	601728	OMIM
	HGNC	9588	HGNC
	Ensembl	ENSG00000171862	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC	COSM921098	COSMIC
	MONDO

Disease area statistics

MGeND

Clinical significance	Last evaluated	Condition	Origin	Submission ID	Submitter	Institute	Citation	Comment	Image
not provided		descending colon	not provided	MGS000041 (TMGS000094)	Hitoshi Nakagama	National Cancer Center Japan

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2014-04-21	criteria provided, single submitter	not provided	germline	Detail
Pathogenic	2016-09-07	criteria provided, single submitter	Hereditary cancer-predisposing syndrome	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.126	PTEN hamartoma tumor syndrome	NA	CLINVAR		Detail
0.122	Neoplastic Syndromes, Hereditary	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000314.8(PTEN):c.437T>A (p.Leu146Ter) AND not provided	ClinVar	Detail
NM_000314.8(PTEN):c.437T>A (p.Leu146Ter) AND Hereditary cancer-predisposing syndrome	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: rs786204933 dbSNP
Genome: hg19
Position: chr10:89,692,953-89,692,953
Variant Type: snv
Reference Allele: T
Alternative Allele: A

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