I89M (p.Ile89Met) variant of IFT172 (Q9UG01)
I89M (p.Ile89Met) in IFT172 (Q9UG01) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
I89M (p.Ile89Met) variant details
- p.Ile89Met
- TOPMed rs1668656318
- Missense
- Variant Prioritization Score for Impact Estimate 0.395
- REVEL 0.25
- CADD 23.20
- PolyPhen-2 0.74
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available