W9L (p.Trp9Leu) variant of ERBB2 (P04626)
W9L (p.Trp9Leu) in ERBB2 (P04626) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data, published literature, and structural context.
W9L (p.Trp9Leu) variant details
- p.Trp9Leu
- gnomAD 17-39700264-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.509
- REVEL 0.39
- CADD 23.30
- PolyPhen-2 0.26
- SIFT 0.11
- Most common in the Finnish in Finland (FIN) population (allele frequency 3e-05)
- Structural context available
- Literature evidence available