V13M (p.Val13Met) variant of GNA13 (Q14344)
V13M (p.Val13Met) in GNA13 (Q14344) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data.
V13M (p.Val13Met) variant details
- p.Val13Met
- TOPMed rs1210500843
- gnomAD rs1210500843
- Missense
- Variant Prioritization Score for Impact Estimate 0.435
- REVEL 0.33
- MetaLR 0.44
- MetaSVM -0.44
- CADD 22.20
- PolyPhen-2 0.18
- SIFT 0.30
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)