P17P (p.Pro17Pro) variant of ERBB2 (P04626)
P17P (p.Pro17Pro) in ERBB2 (P04626) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
P17P (p.Pro17Pro) variant details
- p.Pro17Pro
- gnomAD 17-39699565-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.128
- CADD 6.67
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available
- Literature evidence available