V12G (p.Val12Gly) variant of RAD50 (DNA repair protein RAD50)
V12G (p.Val12Gly) 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 0.49 / 1. The record also includes published literature and structural context.
V12G (p.Val12Gly) variant details
- p.Val12Gly
- rs1580974376
- ClinGen CA360950917
- ClinVar RCV000792723
- Ensembl rs1580974376
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.488
- AlphaMissense 0.95
- MetaLR 0.13
- MetaSVM -0.89
- PolyPhen-2 1.00
- SIFT 0.00
- EVE 0.95
- 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)