N40D (p.Asn40Asp) variant of FLNC (Filamin-C)
N40D (p.Asn40Asp) in FLNC (Filamin-C) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and structural context.
N40D (p.Asn40Asp) variant details
- p.Asn40Asp
- gnomAD rs1807852608
- Missense
- Variant Prioritization Score for Impact Estimate 0.507
- REVEL 0.40
- CADD 28.90
- Most common in the Non-Finnish European population (allele frequency 5e-05)
- Structural context available