S15F (p.Ser15Phe) variant of MYD88 (Q99836)
S15F (p.Ser15Phe) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
S15F (p.Ser15Phe) variant details
- p.Ser15Phe
- ExAC rs771227546
- gnomAD rs771227546
- Missense
- Variant Prioritization Score for Impact Estimate 0.144
- CADD 8.88
- Most common in the Middle Eastern population (allele frequency 0.0011)
- Structural context available