G37R (p.Gly37Arg) variant of HOGA1 (Q86XE5)
G37R (p.Gly37Arg) in HOGA1 (Q86XE5) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.73 / 1. The record also includes population frequency data and structural context.
G37R (p.Gly37Arg) variant details
- p.Gly37Arg
- ExAC rs769193078
- TOPMed rs769193078
- gnomAD rs769193078
- Missense
- Variant Prioritization Score for Impact Estimate 0.734
- REVEL 0.82
- ESM-1b 1.00
- AlphaMissense 0.94
- MetaLR 0.99
- MetaSVM 1.02
- CADD 24.50
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available