W9R (p.Trp9Arg) variant of ERBB2 (P04626)
W9R (p.Trp9Arg) in ERBB2 (P04626) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
W9R (p.Trp9Arg) variant details
- p.Trp9Arg
- rs1211697061
- gnomAD 17-39699575-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.108
- CADD 3.86
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available
- Literature evidence available