Annotation Detail
Information
- Associated Genes
- PTPN11
- Associated Variants
-
PTPN11 p.Thr472Met (p.T472M)
(
ENST00000351677.7,
ENST00000635625.1,
ENST00000639857.2,
ENST00000687906.1,
ENST00000688597.1,
ENST00000690210.1 )
PTPN11 p.Thr472Met (p.T472M) ( ENST00000351677.7, ENST00000635625.1, ENST00000639857.2, ENST00000687906.1, ENST00000688597.1, ENST00000690210.1 ) - Associated Disease
- PTPN11-related disorder
- Source Database
- ClinVar
- Description
- NM_002834.5(PTPN11):c.1403C>T (p.Thr468Met) AND PTPN11-related disorder
- ClinVar Allele ID
- 28370
- ClinVar RefSeq Alternation Syntax
- NM_001374625.1:c.1400C>T
- ClinVar RefSeq Alternation Syntax
- NM_002834.5:c.1403C>T
- ClinVar RefSeq Alternation Syntax
- NM_001330437.2:c.1415C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2018-07-05
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000723326
- ClinVar Disease
- PTPN11-related disorder
- Observed Origin Sample
- germline
Drugs