G68A (p.Gly68Ala) variant of SLC37A4 (O43826)
G68A (p.Gly68Ala) in SLC37A4 (O43826) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.78 / 1. The record also includes population frequency data and structural context.
G68A (p.Gly68Ala) variant details
- p.Gly68Ala
- gnomAD rs1325803224
- Missense
- Variant Prioritization Score for Impact Estimate 0.776
- CADD 24.80
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 2.3e-05)
- Structural context available