T67A (p.Thr67Ala) variant of NBN (Nibrin)
T67A (p.Thr67Ala) 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 0.35 / 1. The record also includes published literature and structural context.
T67A (p.Thr67Ala) variant details
- p.Thr67Ala
- rs876660922
- ClinGen CA10578807
- ClinVar RCV000220748
- ClinVar RCV000636750
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Microcephaly, normal intelligence and i
- Missense
- Variant Prioritization Score for Impact Estimate 0.35
- AlphaMissense 0.13
- MetaLR 0.16
- MetaSVM -0.87
- PolyPhen-2 1.00
- SIFT 0.02
- MutPred 0.59
- 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)