G7G (p.Gly7Gly) variant of MYD88 (Q99836)
G7G (p.Gly7Gly) in MYD88 (Q99836) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
G7G (p.Gly7Gly) variant details
- p.Gly7Gly
- gnomAD 3-38138721-C-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.122
- CADD 5.86
- Most common in the Non-Finnish European population (allele frequency 5e-05)
- Structural context available
- Literature evidence available