A2T (p.Ala2Thr) variant of MYD88 (Q99836)
A2T (p.Ala2Thr) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
A2T (p.Ala2Thr) variant details
- p.Ala2Thr
- gnomAD rs1167556183
- Missense
- Variant Prioritization Score for Impact Estimate 0.356
- CADD 18.20
- PolyPhen-2 0.07
- SIFT 0.02
- Most common in the South Asian population (allele frequency 0.00044)
- Structural context available