I136M (p.Ile136Met) variant of ETV4 (ETS translocation variant 4)
I136M (p.Ile136Met) in ETV4 (ETS translocation variant 4) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data.
I136M (p.Ile136Met) variant details
- p.Ile136Met
- ExAC rs747958996
- TOPMed rs747958996
- gnomAD rs747958996
- Missense
- Variant Prioritization Score for Impact Estimate 0.193
- REVEL 0.08
- CADD 18.60
- Most common in the HGDP:FRENCH population (allele frequency 0.019)