L38W (p.Leu38Trp) variant of SLC37A4 (O43826)
L38W (p.Leu38Trp) 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.
L38W (p.Leu38Trp) variant details
- p.Leu38Trp
- Ensembl rs1268979184
- Missense
- Variant Prioritization Score for Impact Estimate 0.661
- CADD 28.60
- PolyPhen-2 0.96
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available