W9G (p.Trp9Gly) variant of ERBB2 (P04626)
W9G (p.Trp9Gly) in ERBB2 (P04626) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data, published literature, and structural context.
W9G (p.Trp9Gly) variant details
- p.Trp9Gly
- gnomAD 17-39700263-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.501
- REVEL 0.44
- CADD 25.80
- PolyPhen-2 0.35
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 9.7e-07)
- Structural context available
- Literature evidence available