K50Q (p.Lys50Gln) variant of RAD50 (DNA repair protein RAD50)
K50Q (p.Lys50Gln) 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 0.56 / 1. The record also includes population frequency data, published literature, and structural context.
K50Q (p.Lys50Gln) variant details
- p.Lys50Gln
- rs876658371
- ClinGen CA10578474
- ClinVar RCV000228619
- TOPMed rs876658371
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.562
- AlphaMissense 0.56
- MetaLR 0.10
- MetaSVM -1.02
- CADD 28.40
- PolyPhen-2 1.00
- SIFT 0.00
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 7.2e-06)
- 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)