G13G (p.Gly13Gly) variant of FLNC (Filamin-C)
G13G (p.Gly13Gly) in FLNC (Filamin-C) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data, published literature, and structural context.
G13G (p.Gly13Gly) variant details
- p.Gly13Gly
- gnomAD 7-128830676-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.422
- CADD 14.30
- Most common in the Middle Eastern population (allele frequency 0.0011)
- Structural context available
- Literature evidence available