R40P (p.Arg40Pro) variant of MYD88 (Q99836)
R40P (p.Arg40Pro) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
R40P (p.Arg40Pro) variant details
- p.Arg40Pro
- gnomAD 3-38138819-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.305
- CADD 16.90
- PolyPhen-2 0.01
- SIFT 0.39
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available
- Literature evidence available