I52L (p.Ile52Leu) variant of RAD50 (DNA repair protein RAD50)
I52L (p.Ile52Leu) in RAD50 (DNA repair protein RAD50) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes published literature and structural context.
I52L (p.Ile52Leu) variant details
- p.Ile52Leu
- rs1060501969
- ClinGen CA360953345
- ClinVar RCV003027239
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.293
- AlphaMissense 0.06
- MetaLR 0.02
- MetaSVM -1.05
- PolyPhen-2 0.00
- SIFT 0.55
- EVE 0.25
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)