deafness, autosomal recessive 31 (DFNB31) - 556 nt intron 10 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.106621
gtgagccaggaggaggaggatgcagagggctgagaggaacacgggccccaggcacagaat  c.2418+60

         .         .         .         .         .         .  g.106681
gggaggtcccgggaccagggctcagcttggcaagtgaccacaaagggaggtagtgagctc  c.2418+120

         .         .         .         .         .         .  g.106741
cctataactggagggatttggacgtcctggaggagcactggattaggaatctggaggccc  c.2418+180

         .         .         .         .         .         .  g.106801
agtttcagctctgcctttgcactgacactaggggctgaggctgagattggtcttgggaat  c.2418+240

         .         .         .          g.106839
ctttaagctcctctcagttttgacatggccaggtggct  c.2418+278

--------------------- middle of intron ---------------------
          g.106840            .         .         .           g.106877
          c.2419-278  gagacagtcttcggagtcaggcttcgattcaagtcctg  c.2419-241

.         .         .         .         .         .           g.106937
atgccaccaccagacagccttaggcaagctccttaacctcctgagcctcggggattttgg  c.2419-181

.         .         .         .         .         .           g.106997
tgaggattaaagagccaagaacacaagtgcttggcttagtgcgttgcacacctgaggctc  c.2419-121

.         .         .         .         .         .           g.107057
ccgacacagggctggagcctgagctctgctgacccagggtggtgtcacggcccggcccag  c.2419-61

.         .         .         .         .         .           g.107117
ccccctggccaggcctgccaactgcgaaggcctcagtggtgtccttcctaatacccacag  c.2419-1