V9G (p.Val9Gly) variant of VWF (von Willebrand factor)
V9G (p.Val9Gly) in VWF (von Willebrand factor) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
V9G (p.Val9Gly) variant details
- p.Val9Gly
- gnomAD rs1945449461
- Missense
- Variant Prioritization Score for Impact Estimate 0.235
- REVEL 0.14
- MetaLR 0.10
- MetaSVM -0.98
- CADD 21.40
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available