S19C (p.Ser19Cys) variant of MYD88 (Q99836)
S19C (p.Ser19Cys) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
S19C (p.Ser19Cys) variant details
- p.Ser19Cys
- ExAC rs759720432
- TOPMed rs759720432
- gnomAD rs759720432
- Missense
- Variant Prioritization Score for Impact Estimate 0.419
- CADD 22.20
- PolyPhen-2 0.34
- SIFT 0.00
- Most common in the HGDP:MBUTI population (allele frequency 0.083)
- Structural context available