G92R (p.Gly92Arg) variant of SLC25A20 (O43772)
G92R (p.Gly92Arg) in SLC25A20 (O43772) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.81 / 1. The record also includes population frequency data and structural context.
G92R (p.Gly92Arg) variant details
- p.Gly92Arg
- TOPMed rs1222742008
- gnomAD rs1222742008
- Missense
- Variant Prioritization Score for Impact Estimate 0.809
- REVEL 0.85
- MetaLR 0.71
- MetaSVM 0.57
- CADD 26.10
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available