Annotation Detail
Information
- Associated Genes
- PTEN
- Associated Variants
-
PTEN p.Asn356Tyr (p.N356Y)
(
ENST00000371953.8,
ENST00000700029.2,
ENST00000688308.1,
ENST00000700021.1,
ENST00000713839.1 )
PTEN p.Asn356Tyr (p.N356Y) ( ENST00000371953.8, ENST00000688308.1, ENST00000700021.1, ENST00000700029.2, ENST00000713839.1 ) - Associated Disease
- PTEN hamartoma tumor syndrome
- Source Database
- ClinVar
- Description
- NM_000314.8(PTEN):c.1066A>T (p.Asn356Tyr) AND PTEN hamartoma tumor syndrome
- ClinVar Allele ID
- 187389
- ClinVar RefSeq Alternation Syntax
- NM_000314.8:c.1066A>T
- ClinVar RefSeq Alternation Syntax
- NM_001304718.2:c.475A>T
- ClinVar RefSeq Alternation Syntax
- NM_001304717.5:c.1585A>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-06-25
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000456755
- ClinVar Disease
- PTEN hamartoma tumor syndrome
- Observed Origin Sample
- germline
Drugs