R37G (p.Arg37Gly) variant of ETV1 (ETS translocation variant 1)
R37G (p.Arg37Gly) in ETV1 (ETS translocation variant 1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
R37G (p.Arg37Gly) variant details
- p.Arg37Gly
- TOPMed rs1782714207
- Missense
- Variant Prioritization Score for Impact Estimate 0.332
- REVEL 0.13
- CADD 23.60
- PolyPhen-2 0.14
- SIFT 0.11
- Most common in the African/African-American population (allele frequency 0.00031)
- Structural context available