P18H (p.Pro18His) variant of ERBB2 (P04626)
P18H (p.Pro18His) in ERBB2 (P04626) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
P18H (p.Pro18His) variant details
- p.Pro18His
- gnomAD 17-39700291-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.392
- REVEL 0.30
- CADD 21.00
- PolyPhen-2 0.25
- SIFT 0.56
- Population evidence available
- Structural context available
- Literature evidence available