S22T (p.Ser22Thr) variant of GNA13 (Q14344)
S22T (p.Ser22Thr) in GNA13 (Q14344) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data.
S22T (p.Ser22Thr) variant details
- p.Ser22Thr
- TOPMed rs1313821721
- gnomAD rs1313821721
- Missense
- Variant Prioritization Score for Impact Estimate 0.318
- REVEL 0.19
- MetaLR 0.45
- MetaSVM -0.51
- CADD 15.20
- PolyPhen-2 0.19
- SIFT 0.22
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)