D19A (p.Asp19Ala) variant of FLNC (Filamin-C)
D19A (p.Asp19Ala) in FLNC (Filamin-C) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
D19A (p.Asp19Ala) variant details
- p.Asp19Ala
- TOPMed rs1807849997
- Missense
- Variant Prioritization Score for Impact Estimate 0.306
- REVEL 0.10
- CADD 22.70
- PolyPhen-2 0.00
- SIFT 0.47
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Structural context available