S33F (p.Ser33Phe) variant of RAD51D (O75771)
S33F (p.Ser33Phe) 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.
S33F (p.Ser33Phe) variant details
- p.Ser33Phe
- NCI-TCGA Cosmic COSV5010
- cosmic curated COSV50100
- Ensembl rs2142477736
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available