Annotation Detail
Information
- Associated Genes
- PTEN
- Associated Variants
-
PTEN p.Gln17Ter (p.Q17*)
(
ENST00000371953.8,
ENST00000472832.3,
ENST00000688308.1,
ENST00000700021.1,
ENST00000700029.2,
ENST00000713839.1 )
PTEN p.Gln17Ter (p.Q17*) ( 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.49C>T (p.Gln17Ter) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 187323
- ClinVar RefSeq Alternation Syntax
- NM_001304717.5:c.568C>T
- ClinVar RefSeq Alternation Syntax
- NM_001304718.2:c.-657C>T
- ClinVar RefSeq Alternation Syntax
- NM_000314.8:c.49C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-02-28
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000169851
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs