P18A (p.Pro18Ala) variant of RAD51C (O43502)
P18A (p.Pro18Ala) in RAD51C (O43502) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely benign in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
P18A (p.Pro18Ala) variant details
- p.Pro18Ala
- 1000Genomes rs547142453
- ExAC rs547142453
- gnomAD rs547142453
- Likely benign
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Likely benign (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available