S10F (p.Ser10Phe) variant of MYD88 (Q99836)
S10F (p.Ser10Phe) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data and structural context.
S10F (p.Ser10Phe) variant details
- p.Ser10Phe
- gnomAD rs1337361092
- Missense
- Variant Prioritization Score for Impact Estimate 0.522
- CADD 19.50
- PolyPhen-2 0.41
- SIFT 0.00
- Most common in the Ashkenazi Jewish population (allele frequency 5.1e-05)
- Structural context available