Fig. 3From: Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITFChromosomal localization of the MITF missense mutation. The NM_198159.2:c.1013C > T variant on chromosome 3 is visualized Using the IGV software. Both parents (I.1 and I.2) carry the heterozygous form (blue and red), whereas both affected daughters carry the homozygous form (red). The amino acids are shown in the lower panel below their corresponding codons, whereas a straight blue line was shown under the nucleotides that correspond to the intronic regionBack to article page