Usher syndrome 1C (autosomal recessive, severe) (USH1C) - 284 nt intron 11 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.26266
gtaagtccagaatgagctggtgggagccccttgaccttcatccccagcccctctgacctt  c.876+60

         .         .         .         .         .         .  g.26326
tgatctctgccacacactcccagggtggctggtctccttccctgaagctctgacagagca  c.876+120

         .         .    g.26348
gagcgagaggacttctgcccag  c.876+142

--------------------- middle of intron ---------------------
                           g.26349      .         .           g.26370
                           c.877-142  caagaagtttgggtcagggatt  c.877-121

.         .         .         .         .         .           g.26430
gcgggagccgcagtgcctgatggtgctgagaagaccacctgcatctcggcccccaggggt  c.877-61

.         .         .         .         .         .           g.26490
gtgtcaggggatccccaggttccccgggggctgagcaaggggcctcttttctcccatgag  c.877-1