V39M (p.Val39Met) variant of SLC37A4 (O43826)
V39M (p.Val39Met) in SLC37A4 (O43826) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data and structural context.
V39M (p.Val39Met) variant details
- p.Val39Met
- TOPMed rs1334488398
- gnomAD rs1334488398
- Missense
- Variant Prioritization Score for Impact Estimate 0.557
- CADD 18.50
- PolyPhen-2 0.53
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available