L20I (p.Leu20Ile) variant of MYD88 (Q99836)
L20I (p.Leu20Ile) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data, published literature, and structural context.
L20I (p.Leu20Ile) variant details
- p.Leu20Ile
- gnomAD 3-38138758-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.263
- CADD 1.50
- PolyPhen-2 0.01
- SIFT 1.00
- Most common in the Ashkenazi Jewish population (allele frequency 7.7e-05)
- Structural context available
- Literature evidence available