Annotation Detail
Information
- Associated Genes
- PTPN11
- Associated Variants
-
PTPN11 p.Phe71Leu (p.F71L)
(
ENST00000687906.1,
ENST00000351677.7,
ENST00000392597.5,
ENST00000688597.1,
ENST00000639857.2,
ENST00000635625.1,
ENST00000690210.1 )
PTPN11 p.Phe71Leu (p.F71L) ( ENST00000351677.7, ENST00000392597.5, ENST00000635625.1, ENST00000639857.2, ENST00000687906.1, ENST00000688597.1, ENST00000690210.1 ) - Associated Disease
- Noonan syndrome 3
- Source Database
- ClinVar
- Description
- NM_002834.5(PTPN11):c.211T>C (p.Phe71Leu) AND Noonan syndrome 3
- ClinVar Allele ID
- 48969
- ClinVar RefSeq Alternation Syntax
- NM_001330437.2:c.211T>C
- ClinVar RefSeq Alternation Syntax
- NM_080601.3:c.211T>C
- ClinVar RefSeq Alternation Syntax
- NM_001374625.1:c.208T>C
- ClinVar RefSeq Alternation Syntax
- NM_002834.5:c.211T>C
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2017-03-27
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000586528
- ClinVar Disease
- Noonan syndrome 3
- Observed Origin Sample
- germline
Drugs