Annotation Detail
Information
- Associated Genes
- PTPN11
- Associated Variants
-
PTPN11 p.Ser506Thr (p.S506T)
(
ENST00000351677.7,
ENST00000635625.1,
ENST00000639857.2,
ENST00000687906.1,
ENST00000688597.1,
ENST00000690210.1 )
PTPN11 p.Ser506Thr (p.S506T) ( ENST00000351677.7, ENST00000635625.1, ENST00000688597.1, ENST00000690210.1, ENST00000639857.2, ENST00000687906.1 ) - Associated Disease
- Noonan syndrome juvenile myelomonocytic leukemia
- Source Database
- ClinVar
- Description
- NM_002834.5(PTPN11):c.1504T>A (p.Ser502Thr) AND Noonan Syndrome with Juvenile Myelomonocytic Leukemia
- ClinVar Allele ID
- 28371
- ClinVar RefSeq Alternation Syntax
- NM_001330437.2:c.1516T>A
- ClinVar RefSeq Alternation Syntax
- NM_001374625.1:c.1501T>A
- ClinVar RefSeq Alternation Syntax
- NM_002834.5:c.1504T>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2015-09-29
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000033543
- ClinVar Disease
- Noonan syndrome
- ClinVar Disease
- Juvenile myelomonocytic leukemia
- Observed Origin Sample
- germline
Drugs