Annotation Detail
Information
- Associated Genes
- NRAS
- Associated Variants
-
NRAS p.Gly12Arg (p.G12R)
(
ENST00000369535.5 )
NRAS p.Gly12Arg (p.G12R) ( ENST00000369535.5 ) - Associated Disease
- multiple myeloma
- Source Database
- ClinVar
- Description
- NM_002524.5(NRAS):c.34G>C (p.Gly12Arg) AND Multiple myeloma
- ClinVar Allele ID
- 48939
- ClinVar RefSeq Alternation Syntax
- NM_002524.5:c.34G>C
- 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/RCV000420396
- ClinVar Disease
- Multiple myeloma
- Observed Origin Sample
- somatic
Drugs