N47N (p.Asn47Asn) variant of FLNC (Filamin-C)
N47N (p.Asn47Asn) in FLNC (Filamin-C) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
N47N (p.Asn47Asn) variant details
- p.Asn47Asn
- rs1331955110
- gnomAD 7-128830778-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.255
- CADD 11.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available