Annotation Detail
Information
- Associated Genes
- PTPN11
- Associated Variants
-
PTPN11 p.Pro495Thr (p.P495T)
(
ENST00000688597.1,
ENST00000690210.1,
ENST00000639857.2,
ENST00000635625.1,
ENST00000687906.1,
ENST00000351677.7 )
PTPN11 p.Pro495Thr (p.P495T) ( ENST00000351677.7, ENST00000635625.1, ENST00000639857.2, ENST00000687906.1, ENST00000688597.1, ENST00000690210.1 ) - Associated Disease
- Noonan syndrome 1
- Source Database
- ClinVar
- Description
- NM_002834.5(PTPN11):c.1471C>A (p.Pro491Thr) AND Noonan syndrome 1
- ClinVar Allele ID
- 49019
- ClinVar RefSeq Alternation Syntax
- NM_001330437.2:c.1483C>A
- ClinVar RefSeq Alternation Syntax
- NM_002834.5:c.1471C>A
- ClinVar RefSeq Alternation Syntax
- NM_001374625.1:c.1468C>A
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2019-06-06
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000660240
- ClinVar Disease
- Noonan syndrome 1
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs