W77R (p.Trp77Arg) variant of MBP (Myelin basic protein)
W77R (p.Trp77Arg) in MBP (Myelin basic protein) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
W77R (p.Trp77Arg) variant details
- p.Trp77Arg
- rs1209144688
- gnomAD 18-76980010-A-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0812
- CADD 0.08
- Most common in the African/African-American population (allele frequency 0.00041)
- Structural context available
- Literature evidence available