Annotation Detail
Information
- Associated Genes
- NRAS
- Associated Variants
-
NRAS p.Gly13Cys (p.G13C)
(
ENST00000369535.5 )
NRAS p.Gly13Cys (p.G13C) ( ENST00000369535.5 ) - Associated Disease
- melanoma
- Source Database
- ClinVar
- Description
- NM_002524.5(NRAS):c.37G>T (p.Gly13Cys) AND Melanoma
- ClinVar Allele ID
- 48941
- ClinVar RefSeq Alternation Syntax
- NM_002524.5:c.37G>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2015-07-14
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000445167
- ClinVar Disease
- Melanoma
- Observed Origin Sample
- somatic
Drugs