G9G (p.Gly9Gly) variant of MYD88 (Q99836)
G9G (p.Gly9Gly) in MYD88 (Q99836) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data, published literature, and structural context.
G9G (p.Gly9Gly) variant details
- p.Gly9Gly
- rs2125775230
- gnomAD 3-38138727-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.199
- CADD 5.84
- Most common in the African/African-American population (allele frequency 2.8e-05)
- Structural context available
- Literature evidence available