A51G (p.Ala51Gly) variant of MYD88 (Q99836)
A51G (p.Ala51Gly) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.69 / 1. The record also includes population frequency data, published literature, and structural context.
A51G (p.Ala51Gly) variant details
- p.Ala51Gly
- gnomAD 3-38138852-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.693
- CADD 28.50
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the 1KG:GIH population (allele frequency 0.0053)
- Structural context available
- Literature evidence available