M10V (p.Met10Val) variant of IL7R (P16871)
M10V (p.Met10Val) in IL7R (P16871) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
M10V (p.Met10Val) variant details
- p.Met10Val
- ESP rs145097494
- ExAC rs145097494
- TOPMed rs145097494
- gnomAD rs145097494
- Missense
- Variant Prioritization Score for Impact Estimate 0.107
- REVEL 0.14
- CADD 0.70
- PolyPhen-2 0.00
- SIFT 0.19
- Most common in the Finnish in Finland (FIN) population (allele frequency 3.8e-05)
- Structural context available