V39M (p.Val39Met) variant of IL15RA (Q13261)
V39M (p.Val39Met) in IL15RA (Q13261) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
V39M (p.Val39Met) variant details
- p.Val39Met
- ExAC rs780326185
- TOPMed rs780326185
- gnomAD rs780326185
- Missense
- Variant Prioritization Score for Impact Estimate 0.179
- REVEL 0.08
- CADD 20.70
- PolyPhen-2 0.97
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available