R31L (p.Arg31Leu) variant of MYD88 (Q99836)
R31L (p.Arg31Leu) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data, published literature, and structural context.
R31L (p.Arg31Leu) variant details
- p.Arg31Leu
- gnomAD 3-38138792-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.513
- CADD 23.30
- PolyPhen-2 0.39
- SIFT 0.17
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available