S27G (p.Ser27Gly) variant of ETV4 (ETS translocation variant 4)
S27G (p.Ser27Gly) in ETV4 (ETS translocation variant 4) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data.
S27G (p.Ser27Gly) variant details
- p.Ser27Gly
- TOPMed rs1300666313
- gnomAD rs1300666313
- Missense
- Variant Prioritization Score for Impact Estimate 0.304
- REVEL 0.16
- CADD 23.00
- PolyPhen-2 0.01
- SIFT 0.50
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)