D141G (p.Asp141Gly) variant of VWF (von Willebrand factor)
D141G (p.Asp141Gly) in VWF (von Willebrand factor) is a missense change. The available record places it in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.78 / 1. The record also includes structural context.
D141G (p.Asp141Gly) variant details
- p.Asp141Gly
- rs61753993
- ClinGen CA228563
- ClinVar RCV000086746
- Ensembl rs61753993
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.777
- MutPred 0.78
- ClinVar: not provided (not provided)
- UniProt: Not provided
- Structural context available