R77W (p.Arg77Trp) variant of VSIR (Q9H7M9)
R77W (p.Arg77Trp) in VSIR (Q9H7M9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
R77W (p.Arg77Trp) variant details
- p.Arg77Trp
- gnomAD rs1304665446
- Missense
- Variant Prioritization Score for Impact Estimate 0.16
- REVEL 0.08
- CADD 17.20
- PolyPhen-2 0.02
- SIFT 0.06
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available