G5V (p.Gly5Val) variant of MYD88 (Q99836)
G5V (p.Gly5Val) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
G5V (p.Gly5Val) variant details
- p.Gly5Val
- ESP rs371896760
- ExAC rs371896760
- TOPMed rs371896760
- gnomAD rs371896760
- Missense
- Variant Prioritization Score for Impact Estimate 0.0641
- CADD 0.14
- PolyPhen-2 0.00
- SIFT 0.51
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Structural context available