N32D (p.Asn32Asp) variant of PTPN4 (P29074)
N32D (p.Asn32Asp) in PTPN4 (P29074) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
N32D (p.Asn32Asp) variant details
- p.Asn32Asp
- ExAC rs766410710
- TOPMed rs766410710
- gnomAD rs766410710
- Missense
- Variant Prioritization Score for Impact Estimate 0.442
- REVEL 0.34
- ESM-1b 1.00
- AlphaMissense 0.16
- MetaLR 0.47
- MetaSVM -0.28
- CADD 24.60
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available