E27D (p.Glu27Asp) variant of VHL (P40337)
E27D (p.Glu27Asp) in VHL (P40337) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; Chuvash polycythemia; Von Hippel-Lindau. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes published literature and structural context.
E27D (p.Glu27Asp) variant details
- p.Glu27Asp
- rs2125124618
- Ensembl rs2125124618
- ClinGen CA351747482
- ClinVar RCV002427900
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Chuvash polycythemia; Von Hippel-Lindau
- Missense
- Variant Prioritization Score for Impact Estimate 0.405
- AlphaMissense 0.10
- MetaLR 0.35
- MetaSVM -0.67
- PolyPhen-2 0.07
- SIFT 0.03
- MutPred 0.19
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Chuvash polycythemia; V)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: Clinical utility gene card for: familial erythrocytosis. (PMID 22274579)
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)