A9P (p.Ala9Pro) variant of PTPN4 (P29074)
A9P (p.Ala9Pro) in PTPN4 (P29074) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data, published literature, and structural context.
A9P (p.Ala9Pro) variant details
- p.Ala9Pro
- gnomAD 2-119809878-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.509
- REVEL 0.49
- ESM-1b 0.00
- AlphaMissense 0.21
- MetaLR 0.57
- MetaSVM 0.01
- CADD 32.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available