T48S (p.Thr48Ser) variant of MYD88 (Q99836)
T48S (p.Thr48Ser) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
T48S (p.Thr48Ser) variant details
- p.Thr48Ser
- Ensembl rs2125775610
- Missense
- Variant Prioritization Score for Impact Estimate 0.326
- CADD 14.00
- PolyPhen-2 0.02
- SIFT 0.50
- Most common in the South Asian population (allele frequency 0.00044)
- Structural context available