Annotation Detail
Information
- Associated Genes
- NRAS
- Associated Variants
-
NRAS p.Gly12Cys (p.G12C)
(
ENST00000369535.5 )
NRAS p.Gly12Cys (p.G12C) ( ENST00000369535.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_002524.5(NRAS):c.34G>T (p.Gly12Cys) AND not provided
- ClinVar Allele ID
- 48938
- ClinVar RefSeq Alternation Syntax
- NM_002524.5:c.34G>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2012-06-02
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000158979
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs