V13F (p.Val13Phe) variant of ETV1 (ETS translocation variant 1)
V13F (p.Val13Phe) in ETV1 (ETS translocation variant 1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
V13F (p.Val13Phe) variant details
- p.Val13Phe
- gnomAD rs1376879279
- Missense
- Variant Prioritization Score for Impact Estimate 0.363
- REVEL 0.14
- CADD 24.10
- PolyPhen-2 0.49
- SIFT 0.38
- Most common in the African/African-American population (allele frequency 0.00012)
- Structural context available