P17Q (p.Pro17Gln) variant of ERBB2 (P04626)
P17Q (p.Pro17Gln) in ERBB2 (P04626) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
P17Q (p.Pro17Gln) variant details
- p.Pro17Gln
- gnomAD 17-39699582-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.247
- CADD 8.58
- Population evidence available
- Structural context available
- Literature evidence available