Fig. 3From: Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing lossResults of in silico predictions. A-C rows represent the analysis results of three in silico prediction tools, respectively. A Human Splicing Finder3.1. B NetGene 2 service. C NNSPLICE 0.9. According to each tool, the result of c.6177 + 1G > T mutation is in the left side and the result of c.9690 + 1G > A mutation is in the right sideBack to article page