T41T (p.Thr41Thr) variant of MYD88 (Q99836)
T41T (p.Thr41Thr) in MYD88 (Q99836) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
T41T (p.Thr41Thr) variant details
- p.Thr41Thr
- gnomAD 3-38138823-A-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.15
- CADD 9.73
- Most common in the HGDP:MBUTI population (allele frequency 0.083)
- Structural context available
- Literature evidence available