A12V (p.Ala12Val) variant of MYD88 (Q99836)
A12V (p.Ala12Val) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
A12V (p.Ala12Val) variant details
- p.Ala12Val
- cosmic curated COSV57180
- gnomAD rs1157980099
- Missense
- Variant Prioritization Score for Impact Estimate 0.328
- CADD 11.70
- PolyPhen-2 0.00
- SIFT 0.30
- Most common in the Non-Finnish European population (allele frequency 3.4e-06)
- Structural context available