Annotation Detail
Information
- Associated Genes
- NRAS
- Associated Variants
-
NRAS p.Gly12Ser (p.G12S)
(
ENST00000369535.5 )
NRAS p.Gly12Ser (p.G12S) ( ENST00000369535.5 ) - Associated Disease
- RASopathy
- Source Database
- ClinVar
- Description
- NM_002524.5(NRAS):c.34G>A (p.Gly12Ser) AND RASopathy
- ClinVar Allele ID
- 172332
- ClinVar RefSeq Alternation Syntax
- NM_002524.5:c.34G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-07-24
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001066799
- ClinVar Disease
- RASopathy
- Observed Origin Sample
- germline
Drugs