G37S (p.Gly37Ser) variant of HOGA1 (Q86XE5)
G37S (p.Gly37Ser) in HOGA1 (Q86XE5) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.71 / 1. The record also includes population frequency data, published literature, and structural context.
G37S (p.Gly37Ser) variant details
- p.Gly37Ser
- gnomAD 10-97584812-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.709
- REVEL 0.80
- ESM-1b 1.00
- AlphaMissense 0.67
- MetaLR 0.99
- MetaSVM 0.98
- CADD 24.20
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available
- Literature evidence available