D67G (p.Asp67Gly) variant of VCL (Vinculin)
D67G (p.Asp67Gly) in VCL (Vinculin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data and structural context.
D67G (p.Asp67Gly) variant details
- p.Asp67Gly
- gnomAD rs1215296365
- Missense
- Variant Prioritization Score for Impact Estimate 0.634
- REVEL 0.59
- CADD 32.00
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available