N38D (p.Asn38Asp) variant of PTPN4 (P29074)
N38D (p.Asn38Asp) in PTPN4 (P29074) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
N38D (p.Asn38Asp) variant details
- p.Asn38Asp
- Ensembl rs1691549703
- Missense
- Variant Prioritization Score for Impact Estimate 0.303
- REVEL 0.21
- ESM-1b 0.00
- AlphaMissense 0.13
- MetaLR 0.15
- MetaSVM -0.97
- CADD 21.30
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available