F7F (p.Phe7Phe) variant of SDHAF2 (Q9NX18)
F7F (p.Phe7Phe) in SDHAF2 (Q9NX18) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
F7F (p.Phe7Phe) variant details
- p.Phe7Phe
- rs892955355
- gnomAD 11-61430167-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.39
- CADD 6.19
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available