Fig. 2
From: A de novo FBN1 variant likely causes congenital bilateral ectopia lentis in a crossbred horse
Sanger sequencing traces of the identified de novo coding variant in FBN1 (NC_009144.3:g.142398596 C > T) in the affected foal and his sire and dam. The affected foal was found to be heterozygous for the identified cytosine to thymine substitution in FBN1 (denoted by the red box) while his sire and dam are homozygous for the reference allele, cytosine.
