L8M (p.Leu8Met) variant of RAD51D (O75771)
L8M (p.Leu8Met) in RAD51D (O75771) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
L8M (p.Leu8Met) variant details
- p.Leu8Met
- NCI-TCGA Cosmic COSV9933
- cosmic curated COSV99338
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available