Usher syndrome 1G (autosomal recessive) (USH1G) - 1377 nt intron 02 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.8863
gtgagtgtccagcctggcgggggggatggaggagcaggagttggaaggcccctggggagg  c.1382+60

         .         .         .         .         .         .  g.8923
gggtacagatctgcctattcaggagtagggggtgggggatactgtatttcataaaatcga  c.1382+120

         .         .         .         .         .         .  g.8983
aatgaggccatcgatgataaaaggcacccttattttatttaccaccagctcagaaaaaga  c.1382+180

         .         .         .         .         .         .  g.9043
agtggccaatttaatgatgacccgaggcattcttatcacagtgaaagtgcacctcgattc  c.1382+240

         .         .         .         .         .         .  g.9103
tggggacatcgacaagtggggaaatgggcctcttaatgtcaatgaatttcaacagtcaca  c.1382+300

         .         .         .         .         .         .  g.9163
ggaatcacagctggggtgtttttgagccctcccacctcctaggtgctgggttgtgccctt  c.1382+360

         .         .         .         .         .         .  g.9223
gaacaagtcctcttgcttaatccctctaaaagcctgtgtgcgctggactatattggtgga  c.1382+420

         .         .         .         .         .         .  g.9283
ttatatcgttcccattttacagccaatgagcaagtggaggctcagacagttagaatagct  c.1382+480

         .         .         .         .         .         .  g.9343
cacctcaaggtcctgctgctgctcagcatggagctaggcttgatccctggtctgcatggc  c.1382+540

         .         .         .         .         .         .  g.9403
tttagagcctggggtcaaggtggctgccatgggatgcagggcgtgcagtcagcagggcct  c.1382+600

         .         .         .         .         .         .  g.9463
ctcaattgcccaagacctcaggcagatttttttttttttttttttgagacagtttccctc  c.1382+660

         .         .           g.9492
ttgtcatccaggctggagtgcagtggcac  c.1382+689

--------------------- middle of intron ---------------------
                    g.9493              .         .           g.9520
                    c.1383-688  aatcactgtaacctccacctcccgggtt  c.1383-661

.         .         .         .         .         .           g.9580
caagcgattctcctgcctcagcctcctgagtagctgggattacaggagtgcaccaccatg  c.1383-601

.         .         .         .         .         .           g.9640
cccagctaatttctgtatttttagtagagatggggttttgccatgttggccaggctggtc  c.1383-541

.         .         .         .         .         .           g.9700
tcgaactcctgacctcaagtgatctgcccactctggcctcccaaagtgctgggattacag  c.1383-481

.         .         .         .         .         .           g.9760
gcgtgagccaccgcgcctggccttagggagatgttttacctactgttcctgaactttgca  c.1383-421

.         .         .         .         .         .           g.9820
atcaggaacgtgggcaaatgctcccaagagggtcagcagcagccctggaggcagagttca  c.1383-361

.         .         .         .         .         .           g.9880
tgttccaaaggccgtcatagttgcccaaggctgccaccacaatggtcatgctgtggccag  c.1383-301

.         .         .         .         .         .           g.9940
cccctgccctggcccctccccaatggcatcccacaggcccaacaaactttgtcctcattt  c.1383-241

.         .         .         .         .         .           g.10000
cctcttaggtatctatggccgttatcctgaatggctggggcagggatgggtgtggggagg  c.1383-181

.         .         .         .         .         .           g.10060
caggctggttcagagttttggggatggggaggtcacccataggctggcgtcccccatccc  c.1383-121

.         .         .         .         .         .           g.10120
tgacaattggcctgccgagagatggggaggctaagttgtccagatggctgccctgggtga  c.1383-61

.         .         .         .         .         .           g.10180
aaatgatgcctctggagggcctcatgtgagatctgtttctttctgtctcttcctccacag  c.1383-1