Annotation Detail
Information
- Associated Genes
- PTEN
- Associated Variants
-
PTEN p.Arg335Ter (p.R335*)
(
ENST00000371953.8,
ENST00000472832.3,
ENST00000688308.1,
ENST00000700021.1,
ENST00000700029.2,
ENST00000713839.1 )
PTEN p.Arg335Ter (p.R335*) ( ENST00000371953.8, ENST00000472832.3, ENST00000688308.1, ENST00000700021.1, ENST00000700029.2, ENST00000713839.1 ) - Source Database
- ClinVar
- Description
- NM_000314.8(PTEN):c.1003C>T (p.Arg335Ter) AND Abnormality of the nervous system
- ClinVar Allele ID
- 22872
- ClinVar RefSeq Alternation Syntax
- NM_000314.8:c.1003C>T
- ClinVar RefSeq Alternation Syntax
- NM_001304717.5:c.1522C>T
- ClinVar RefSeq Alternation Syntax
- NM_001304718.2:c.412C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-07-10
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001813965
- Observed Origin Sample
- de novo
Drugs