G4V (p.Gly4Val) variant of MYD88 (Q99836)
G4V (p.Gly4Val) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
G4V (p.Gly4Val) variant details
- p.Gly4Val
- TOPMed rs1162844242
- gnomAD rs1162844242
- Missense
- Variant Prioritization Score for Impact Estimate 0.176
- AlphaMissense 0.99
- MetaLR 0.08
- MetaSVM -1.08
- CADD 8.30
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available