S58C (p.Ser58Cys) variant of NBN (Nibrin)
S58C (p.Ser58Cys) in NBN (Nibrin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; Microcephaly, normal intelligence and i. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes published literature and structural context.
S58C (p.Ser58Cys) variant details
- p.Ser58Cys
- rs1554568431
- ClinGen CA371662646
- ClinVar RCV000568176
- ClinVar RCV003617823
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Microcephaly, normal intelligence and i
- Missense
- Variant Prioritization Score for Impact Estimate 0.509
- AlphaMissense 0.09
- MetaLR 0.57
- MetaSVM 0.19
- PolyPhen-2 1.00
- SIFT 0.00
- MutPred 0.66
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Microcephaly, normal in)
- 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)
- Cited in: Nijmegen Breakage Syndrome. (PMID 20301355)