Usher syndrome 2A (autosomal recessive, mild) (USH2A) - 541 nt intron 53 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.645719
gtattgagatacctttaaaatacaaataacaaaatcccataaattcataagaaaattgaa  c.10585+60

         .         .         .         .         .         .  g.645779
atgagtacaatctacatttaattgccctatgcatctaaccactagaaaagtatgttccga  c.10585+120

         .         .         .         .         .         .  g.645839
taaagggaactgtaattatgtgacaactaatcactcactttgtggtgtagtcctcgtaga  c.10585+180

         .         .         .         .         .         .  g.645899
tttttagcctaaataagtaaaaaaatagaaatgaaagttccttgaatcccagaatatatc  c.10585+240

         .         .         .   g.645930
tgagctgctttcaaaacaagcaaggcatatt  c.10585+271

--------------------- middle of intron ---------------------
                 g.645931     .         .         .           g.645960
                 c.10586-270  cagagaaggggaaagagttttaatattgaa  c.10586-241

.         .         .         .         .         .           g.646020
agtaaatttgtttcatagtgaaaggaaataaacataaatgactcttatcatttatgtcaa  c.10586-181

.         .         .         .         .         .           g.646080
gaatccatctcctccataatagtataattaggaactgcttgagacagcaatataatagga  c.10586-121

.         .         .         .         .         .           g.646140
aattaaaattaaataaagctatagtattgcatttcttccgaacactaagatttgtaagtt  c.10586-61

.         .         .         .         .         .           g.646200
gtttgcaaatagttaaaatgatatcacattcaaatgcagtcatttttctgcttcttttag  c.10586-1