W47R (p.Trp47Arg) variant of MYD88 (Q99836)
W47R (p.Trp47Arg) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.68 / 1. The record also includes population frequency data, published literature, and structural context.
W47R (p.Trp47Arg) variant details
- p.Trp47Arg
- gnomAD 3-38138839-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.681
- CADD 32.00
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the South Asian population (allele frequency 0.00044)
- Structural context available
- Literature evidence available