V15M (p.Val15Met) variant of RAD51C (O43502)
V15M (p.Val15Met) in RAD51C (O43502) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as benign in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
V15M (p.Val15Met) variant details
- p.Val15Met
- NCI-TCGA Cosmic COSV9954
- cosmic curated COSV99542
- Ensembl rs2143674492
- Benign
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Benign (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available