Skip to main content
Fig. 3 | BMC Medical Genomics

Fig. 3

From: Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A

Fig. 3

The types of MYO15A reported splice-site variants. Green boxes are exons and white boxes are introns. A yellow asterisk indicates the site of variant. A Canonical donor splice-site variant leads to intro retention; B Canonical acceptor splice-site variant leads to exon skipping; C Non-canonical splice-site variant. Deep intronic variants creating new splice sites

Back to article page