P17A (p.Pro17Ala) variant of ERBB2 (P04626)
P17A (p.Pro17Ala) in ERBB2 (P04626) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
P17A (p.Pro17Ala) variant details
- p.Pro17Ala
- TOPMed rs1307888184
- gnomAD rs1307888184
- Missense
- Variant Prioritization Score for Impact Estimate 0.168
- REVEL 0.11
- CADD 14.30
- PolyPhen-2 0.00
- SIFT 0.51
- Most common in the Non-Finnish European population (allele frequency 9.8e-07)
- Structural context available