I22M (p.Ile22Met) variant of SLC18A2 (Q05940)
I22M (p.Ile22Met) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
I22M (p.Ile22Met) variant details
- p.Ile22Met
- ExAC rs773686320
- TOPMed rs773686320
- gnomAD rs773686320
- Missense
- Variant Prioritization Score for Impact Estimate 0.474
- CADD 25.20
- PolyPhen-2 0.94
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available