S19T (p.Ser19Thr) variant of MYD88 (Q99836)
S19T (p.Ser19Thr) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data, published literature, and structural context.
S19T (p.Ser19Thr) variant details
- p.Ser19Thr
- gnomAD 3-38138755-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.288
- CADD 14.50
- PolyPhen-2 0.03
- SIFT 0.23
- Most common in the Non-Finnish European population (allele frequency 3.4e-06)
- Structural context available
- Literature evidence available