P18T (p.Pro18Thr) variant of ERBB2 (P04626)
P18T (p.Pro18Thr) in ERBB2 (P04626) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data, published literature, and structural context.
P18T (p.Pro18Thr) variant details
- p.Pro18Thr
- gnomAD 17-39700290-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.213
- REVEL 0.16
- CADD 17.40
- PolyPhen-2 0.03
- SIFT 0.40
- Population evidence available
- Structural context available
- Literature evidence available