I17M (p.Ile17Met) variant of TRDN (Triadin)
I17M (p.Ile17Met) in TRDN (Triadin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
I17M (p.Ile17Met) variant details
- p.Ile17Met
- ESP rs375486432
- ExAC rs375486432
- TOPMed rs375486432
- gnomAD rs375486432
- Missense
- Variant Prioritization Score for Impact Estimate 0.28
- REVEL 0.25
- CADD 21.40
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available