F141V (p.Phe141Val) variant of PTPN2 (P17706)
F141V (p.Phe141Val) in PTPN2 (P17706) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.65 / 1. The record also includes population frequency data, published literature, and structural context.
F141V (p.Phe141Val) variant details
- p.Phe141Val
- rs1055535966
- gnomAD 18-12788092-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.647
- CADD 13.00
- Most common in the 1KG:MXL population (allele frequency 0.0081)
- Structural context available
- Literature evidence available