S9T (p.Ser9Thr) variant of GNA13 (Q14344)
S9T (p.Ser9Thr) in GNA13 (Q14344) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data.
S9T (p.Ser9Thr) variant details
- p.Ser9Thr
- ExAC rs773338310
- gnomAD rs773338310
- Missense
- Variant Prioritization Score for Impact Estimate 0.33
- REVEL 0.21
- MetaLR 0.44
- MetaSVM -0.34
- CADD 22.50
- PolyPhen-2 0.01
- SIFT 0.11
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)