G7V (p.Gly7Val) variant of MYD88 (Q99836)
G7V (p.Gly7Val) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
G7V (p.Gly7Val) variant details
- p.Gly7Val
- Ensembl rs2125775205
- Missense
- Variant Prioritization Score for Impact Estimate 0.0568
- CADD 0.12
- PolyPhen-2 0.00
- SIFT 0.28
- Most common in the Non-Finnish European population (allele frequency 5.8e-05)
- Structural context available