G17R (p.Gly17Arg) variant of GNA13 (Q14344)
G17R (p.Gly17Arg) in GNA13 (Q14344) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data.
G17R (p.Gly17Arg) variant details
- p.Gly17Arg
- TOPMed rs1421154389
- gnomAD rs1421154389
- Missense
- Variant Prioritization Score for Impact Estimate 0.469
- REVEL 0.38
- MetaLR 0.52
- MetaSVM -0.18
- CADD 22.60
- PolyPhen-2 0.30
- SIFT 0.59
- Most common in the Non-Finnish European population (allele frequency 9e-07)