C69R (p.Cys69Arg) variant of VCP (P55072)
C69R (p.Cys69Arg) in VCP (P55072) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, published literature, and structural context.
C69R (p.Cys69Arg) variant details
- p.Cys69Arg
- rs1442790356
- gnomAD 9-35057156-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.328
- CADD 8.52
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available