R40R (p.Arg40Arg) variant of MYD88 (Q99836)
R40R (p.Arg40Arg) in MYD88 (Q99836) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
R40R (p.Arg40Arg) variant details
- p.Arg40Arg
- rs1365188058
- gnomAD 3-38138820-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.149
- CADD 9.62
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available