F36F (p.Phe36Phe) variant of MYD88 (Q99836)
F36F (p.Phe36Phe) in MYD88 (Q99836) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data, published literature, and structural context.
F36F (p.Phe36Phe) variant details
- p.Phe36Phe
- rs2125775512
- gnomAD 3-38138808-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.344
- CADD 14.30
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available
- Literature evidence available