Usher syndrome 2A (autosomal recessive, mild) (USH2A) - 537 nt intron 39 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.527702
gtgagcattctactttgtccattctatcagctgggttatacaatatagacataacatttt  c.7451+60

         .         .         .         .         .         .  g.527762
tgaagagtaggtcagttctcatttgcaaaaaatataggttaccttttaaaagtacaaaaa  c.7451+120

         .         .         .         .         .         .  g.527822
aaccccaaacaattagaggataatcatttgctttgcaaaaatatctatttttcatttatg  c.7451+180

         .         .         .         .         .         .  g.527882
tagcatttaaagtaggatttcttcccactgaaacttttcatgagcacatgcattacataa  c.7451+240

         .         .           g.527911
agcaatgaaactaacaaaatgatgtctga  c.7451+269

--------------------- middle of intron ---------------------
                    g.527912            .         .           g.527939
                    c.7452-268  actgtcgctaacaaattataatacctat  c.7452-241

.         .         .         .         .         .           g.527999
tctacaaatccacatggcagtcagtctcaatactactaggatttacatctcgtataaaca  c.7452-181

.         .         .         .         .         .           g.528059
caagattacagactcagccaatggctacttattttaaaagagatctcatttgatggcaga  c.7452-121

.         .         .         .         .         .           g.528119
aaattacaatacttaaatgtatgttgacatcctctaaaatttttttgtagtaagaaattt  c.7452-61

.         .         .         .         .         .           g.528179
acttgcttttatttctttgaatgtcgaaaacttcctaattgacatttatttcccatacag  c.7452-1