Usher syndrome 2A (autosomal recessive, mild) (USH2A) - 673 nt intron 01 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.5243
gtaactcagcttatttatcaatacaattacttgcacagtattagggatccatgtgtaacc  c.-205+60

         .         .         .         .         .         .  g.5303
tacaaattcatagtcatatgaggaaacacagaaacattttgctaaatattaaagcatagg  c.-205+120

         .         .         .         .         .         .  g.5363
acagacagatggtgttgggtttctaatcagctttactctgagcttaaagttgctgcacat  c.-205+180

         .         .         .         .         .         .  g.5423
gctgggataaggggaaaggcccaaagtcctttgccagctttattttgggcatctgtaagt  c.-205+240

         .         .         .         .         .         .  g.5483
tagctctgggttacaatgtacagtgcatgtgtaaagaaaatctacaagattcttttccct  c.-205+300

         .         .         .         g.5520
gttaagtagagctggtaatgccattgctaattccctg  c.-205+337

--------------------- middle of intron ---------------------
            g.5521            .         .         .           g.5556
            c.-204-336  gggtgaagtaacaacacaaaattattgtatgtgtaa  c.-204-301

.         .         .         .         .         .           g.5616
tatattattaataattatatatatataaaacacacacatatattatataaatatttatgt  c.-204-241

.         .         .         .         .         .           g.5676
ataactggttataaatattactggttgtcctgtggacttataaagtgcttgatttgccca  c.-204-181

.         .         .         .         .         .           g.5736
atgcaatcaagagatttaccaaaaggatgagtattttactctgagcactgtgcttcaaaa  c.-204-121

.         .         .         .         .         .           g.5796
tgttttttgagaagttcagtagtgttgcttctaggagctcaaagtcctcaggcctgggat  c.-204-61

.         .         .         .         .         .           g.5856
gagcttcagttttaaaggtgcagcagctttcccttgacgccctacgtttttgattcccag  c.-204-1