Annotation Detail
Information
- Associated Genes
- PTEN
- Associated Variants
-
PTEN p.Ile253LysfsTer2 (p.I253Kfs*2)
(
ENST00000700021.1,
ENST00000472832.3,
ENST00000713839.1,
ENST00000371953.8,
ENST00000700029.2,
ENST00000688308.1 )
PTEN p.Ile253LysfsTer2 (p.I253Kfs*2) ( ENST00000371953.8, ENST00000472832.3, ENST00000688308.1, ENST00000700021.1, ENST00000700029.2, ENST00000713839.1 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_000314.8(PTEN):c.758_761del (p.Ile253fs) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 187374
- ClinVar RefSeq Alternation Syntax
- NM_001304717.5:c.1277_1280del
- ClinVar RefSeq Alternation Syntax
- NM_001304718.2:c.167_170del
- ClinVar RefSeq Alternation Syntax
- NM_000314.8:c.758_761del
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2014-03-25
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000169844
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs