P56S (p.Pro56Ser) variant of RAD51 (Q06609)
P56S (p.Pro56Ser) in RAD51 (Q06609) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as benign in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data and structural context.
P56S (p.Pro56Ser) variant details
- p.Pro56Ser
- rs45623838
- ClinGen CA7483931
- cosmic curated COSV10586
- ClinVar RCV002643767
- Benign
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.452
- REVEL 0.26
- CADD 21.80
- PolyPhen-2 0.02
- SIFT 0.11
- ClinVar: Benign (not provided)
- EBI: Benign
- UniProt: Benign
- Population evidence available
- Structural context available