I13M (p.Ile13Met) variant of SLC37A4 (O43826)
I13M (p.Ile13Met) in SLC37A4 (O43826) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data and structural context.
I13M (p.Ile13Met) variant details
- p.Ile13Met
- TOPMed rs1943677629
- gnomAD rs1943677629
- Missense
- Variant Prioritization Score for Impact Estimate 0.534
- CADD 24.50
- Most common in the Ashkenazi Jewish population (allele frequency 0.00029)
- Structural context available