R31H (p.Arg31His) variant of MYD88 (Q99836)
R31H (p.Arg31His) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data and structural context.
R31H (p.Arg31His) variant details
- p.Arg31His
- ExAC rs751153924
- gnomAD rs751153924
- Missense
- Variant Prioritization Score for Impact Estimate 0.494
- CADD 23.20
- PolyPhen-2 0.01
- SIFT 0.13
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Structural context available