Y9C (p.Tyr9Cys) variant of SLC37A4 (O43826)
Y9C (p.Tyr9Cys) in SLC37A4 (O43826) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data and structural context.
Y9C (p.Tyr9Cys) variant details
- p.Tyr9Cys
- ExAC rs781813179
- gnomAD rs781813179
- Missense
- Variant Prioritization Score for Impact Estimate 0.656
- CADD 27.90
- PolyPhen-2 0.86
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available