V14V (p.Val14Val) variant of MYD88 (Q99836)
V14V (p.Val14Val) in MYD88 (Q99836) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
V14V (p.Val14Val) variant details
- p.Val14Val
- rs763301680
- gnomAD 3-38138742-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0919
- CADD 1.59
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available