F88F (p.Phe88Phe) variant of SLC25A14 (O95258)
F88F (p.Phe88Phe) in SLC25A14 (O95258) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data, published literature, and structural context.
F88F (p.Phe88Phe) variant details
- p.Phe88Phe
- gnomAD X-130346638-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.657
- CADD 7.74
- Most common in the 1KG:FIN population (allele frequency 0.0051)
- Structural context available
- Literature evidence available