Q67H (p.Gln67His) variant of GNA13 (Q14344)
Q67H (p.Gln67His) in GNA13 (Q14344) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.78 / 1. The record also includes population frequency data and structural context.
Q67H (p.Gln67His) variant details
- p.Gln67His
- gnomAD rs1908061421
- Missense
- Variant Prioritization Score for Impact Estimate 0.779
- REVEL 0.83
- MetaLR 0.91
- MetaSVM 1.07
- CADD 25.70
- SIFT 0.09
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.5e-05)
- Structural context available