E53G (p.Glu53Gly) variant of MYD88 (Q99836)
E53G (p.Glu53Gly) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
E53G (p.Glu53Gly) variant details
- p.Glu53Gly
- gnomAD rs1337358823
- Missense
- Variant Prioritization Score for Impact Estimate 0.42
- CADD 24.40
- PolyPhen-2 0.34
- SIFT 0.28
- Most common in the Non-Finnish European population (allele frequency 3.4e-06)
- Structural context available