Annotation Detail
Information
- Associated Genes
- NRAS
- Associated Variants
-
NRAS p.Gly13Val (p.G13V)
(
ENST00000369535.5 )
NRAS p.Gly13Val (p.G13V) ( ENST00000369535.5 ) - Source Database
- ClinVar
- Description
- NM_002524.5(NRAS):c.38G>T (p.Gly13Val) AND Transitional cell carcinoma of the bladder
- ClinVar Allele ID
- 362755
- ClinVar RefSeq Alternation Syntax
- NM_002524.5:c.38G>T
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2016-05-31
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000436237
- Observed Origin Sample
- somatic
Drugs