G36S (p.Gly36Ser) variant of GNAT1 (P11488)
G36S (p.Gly36Ser) in GNAT1 (P11488) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.93 / 1. The record also includes population frequency data and structural context.
G36S (p.Gly36Ser) variant details
- p.Gly36Ser
- TOPMed rs1487464362
- gnomAD rs1487464362
- Missense
- Variant Prioritization Score for Impact Estimate 0.932
- REVEL 0.99
- CADD 35.00
- PolyPhen-2 0.98
- SIFT 0.01
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available