V69G (p.Val69Gly) variant of IFT172 (Q9UG01)
V69G (p.Val69Gly) in IFT172 (Q9UG01) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.71 / 1. The record also includes population frequency data and structural context.
V69G (p.Val69Gly) variant details
- p.Val69Gly
- gnomAD rs1410849775
- Missense
- Variant Prioritization Score for Impact Estimate 0.707
- REVEL 0.74
- CADD 28.20
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Ashkenazi Jewish population (allele frequency 3.8e-05)
- Structural context available