S22N (p.Ser22Asn) variant of GNA13 (Q14344)
S22N (p.Ser22Asn) in GNA13 (Q14344) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data.
S22N (p.Ser22Asn) variant details
- p.Ser22Asn
- TOPMed rs1313821721
- gnomAD rs1313821721
- Missense
- Variant Prioritization Score for Impact Estimate 0.315
- REVEL 0.18
- MetaLR 0.50
- MetaSVM -0.45
- CADD 15.20
- PolyPhen-2 0.01
- SIFT 0.27
- Most common in the Non-Finnish European population (allele frequency 9e-07)