S15C (p.Ser15Cys) variant of MYD88 (Q99836)
S15C (p.Ser15Cys) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
S15C (p.Ser15Cys) variant details
- p.Ser15Cys
- ExAC rs771227546
- gnomAD rs771227546
- Missense
- Variant Prioritization Score for Impact Estimate 0.129
- CADD 9.72
- PolyPhen-2 0.00
- SIFT 0.21
- Most common in the HGDP:BIAKA population (allele frequency 0.93)
- Structural context available