S19F (p.Ser19Phe) variant of MYD88 (Q99836)
S19F (p.Ser19Phe) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
S19F (p.Ser19Phe) variant details
- p.Ser19Phe
- ExAC rs759720432
- TOPMed rs759720432
- gnomAD rs759720432
- Missense
- Variant Prioritization Score for Impact Estimate 0.38
- CADD 18.70
- PolyPhen-2 0.06
- SIFT 0.00
- Most common in the East Asian population (allele frequency 2.8e-05)
- Structural context available