F26V (p.Phe26Val) variant of SLC25A20 (O43772)
F26V (p.Phe26Val) in SLC25A20 (O43772) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
F26V (p.Phe26Val) variant details
- p.Phe26Val
- gnomAD rs1439890633
- Missense
- Variant Prioritization Score for Impact Estimate 0.442
- REVEL 0.38
- MetaLR 0.18
- MetaSVM -0.76
- CADD 23.40
- SIFT 0.85
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available