S15P (p.Ser15Pro) variant of MYD88 (Q99836)
S15P (p.Ser15Pro) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
S15P (p.Ser15Pro) variant details
- p.Ser15Pro
- gnomAD 3-38138743-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.146
- AlphaMissense 0.62
- MetaLR 0.06
- MetaSVM -1.14
- CADD 0.97
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available