G9E (p.Gly9Glu) variant of MYD88 (Q99836)
G9E (p.Gly9Glu) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
G9E (p.Gly9Glu) variant details
- p.Gly9Glu
- Ensembl rs905392063
- Missense
- Variant Prioritization Score for Impact Estimate 0.0786
- CADD 2.40
- PolyPhen-2 0.00
- SIFT 0.41
- Most common in the Non-Finnish European population (allele frequency 2.3e-05)
- Structural context available