S16C (p.Ser16Cys) variant of MYD88 (Q99836)
S16C (p.Ser16Cys) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
S16C (p.Ser16Cys) variant details
- p.Ser16Cys
- gnomAD rs1300553231
- Missense
- Variant Prioritization Score for Impact Estimate 0.253
- CADD 13.70
- PolyPhen-2 0.00
- SIFT 0.06
- Most common in the Finnish in Finland (FIN) population (allele frequency 3.8e-05)
- Structural context available