S18F (p.Ser18Phe) variant of MYD88 (Q99836)
S18F (p.Ser18Phe) 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 and structural context.
S18F (p.Ser18Phe) variant details
- p.Ser18Phe
- ESP rs377224266
- ExAC rs377224266
- gnomAD rs377224266
- Missense
- Variant Prioritization Score for Impact Estimate 0.146
- CADD 11.10
- PolyPhen-2 0.00
- SIFT 0.40
- Most common in the South Asian population (allele frequency 0.00044)
- Structural context available