H41Q (p.His41Gln) variant of ETV1 (ETS translocation variant 1)
H41Q (p.His41Gln) 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.
H41Q (p.His41Gln) variant details
- p.His41Gln
- TOPMed rs1334696169
- gnomAD rs1334696169
- Missense
- Variant Prioritization Score for Impact Estimate 0.312
- REVEL 0.11
- CADD 21.50
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available