T17T (p.Thr17Thr) variant of MYD88 (Q99836)
T17T (p.Thr17Thr) in MYD88 (Q99836) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
T17T (p.Thr17Thr) variant details
- p.Thr17Thr
- gnomAD 3-38138751-A-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.391
- CADD 6.42
- Most common in the Ashkenazi Jewish population (allele frequency 5.1e-05)
- Structural context available
- Literature evidence available