Usher syndrome 1C (autosomal recessive, severe) (USH1C) - 151 nt intron 10 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.26058
gtgagatgtgggggtcttcacctgttggcccttgtcatctccacaccccacttctcatcc  c.819+60

         .        g.26074
ccaccaccctggagcc  c.819+76

--------------------- middle of intron ---------------------
                                   g.26075        .           g.26089
                                   c.820-75  tggggccttctgtgc  c.820-61

.         .         .         .         .         .           g.26149
tctctgcctggactgctgtggtctgtcaggcctcggcccactgtccttctgtccccacag  c.820-1