E27Q (p.Glu27Gln) variant of NTHL1 (Endonuclease III-like protein 1)
E27Q (p.Glu27Gln) in NTHL1 (Endonuclease III-like protein 1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; not provided. The record also includes variant effect predictions, published literature, and structural context.
E27Q (p.Glu27Gln) variant details
- p.Glu27Gln
- rs2084517936
- ClinGen CA394298345
- ClinVar RCV001297281
- ClinVar RCV003365303
- Uncertain significance
- Hereditary cancer-predisposing syndrome; not provided
- Missense
- MutPred 0.20
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; not provided)
- 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)