F42F (p.Phe42Phe) variant of FLNC (Filamin-C)
F42F (p.Phe42Phe) in FLNC (Filamin-C) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data, published literature, and structural context.
F42F (p.Phe42Phe) variant details
- p.Phe42Phe
- rs746857110
- gnomAD 7-128830763-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.431
- CADD 16.10
- Most common in the Non-Finnish European population (allele frequency 5e-05)
- Structural context available
- Literature evidence available