S16G (p.Ser16Gly) variant of ETV1 (ETS translocation variant 1)
S16G (p.Ser16Gly) in ETV1 (ETS translocation variant 1) 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 and structural context.
S16G (p.Ser16Gly) variant details
- p.Ser16Gly
- gnomAD rs1453046202
- Missense
- Variant Prioritization Score for Impact Estimate 0.314
- REVEL 0.10
- CADD 24.40
- PolyPhen-2 0.05
- SIFT 0.09
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available