Usher syndrome 2A (autosomal recessive, mild) (USH2A) - 1319 nt intron 68 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.787899
gttagtttctgactcctgtttctcagtgtggaaggcgctctgttccccagctttacggga  c.14968+60

         .         .         .         .         .         .  g.787959
tgctaaatctgaaagctgaccagcagatgctcaccattaaaatgtcttggtttaagtgcc  c.14968+120

         .         .         .         .         .         .  g.788019
cccttcttgtgaaaaagttactgctcaggataaataaggttttctttccttcccatttgc  c.14968+180

         .         .         .         .         .         .  g.788079
agcttgacagcactgcagttataatgcagttcaaggggacagcgctgcctccacaggact  c.14968+240

         .         .         .         .         .         .  g.788139
ggagggtccccaggaagggataagacccaagggccagttgggttcacaaaagaaatagca  c.14968+300

         .         .         .         .         .         .  g.788199
cccatacatagtcaatgactaccctaaaataatacacttctagcaacttcatagattttc  c.14968+360

         .         .         .         .         .         .  g.788259
ttgctgtatctccagtctccaaacagagccctatcaggaaataactatctccaactcatg  c.14968+420

         .         .         .         .         .         .  g.788319
aggacctgaataaggggtttccttaaccttccttgatatcagcccctgaaagaacaatct  c.14968+480

         .         .         .         .         .         .  g.788379
tgaccctctaaaatggagttccttcttcctgtttacttacatgtcccttttctccttgcc  c.14968+540

         .         .         .         .         .         .  g.788439
ttgtttttaaattgaaatgagaaaatgctttacaaggtgctaagtattttatagtgatca  c.14968+600

         .         .         .         .         .         .  g.788499
gcatgctcacaggaccaatgttcactatataatgaattgattaatgagtattttattttg  c.14968+660

--------------------- middle of intron ---------------------
          .         .         .         .         .           g.788558
 gctgtaaggtagaggtaaacagtgagctccagcattgcatgtatagtaatagaaactta  c.14969-601

.         .         .         .         .         .           g.788618
ataacatttttacaaagattcagctacacatgttcattgttacagttcatggtcacctgg  c.14969-541

.         .         .         .         .         .           g.788678
gcagctctttgggaaaggaaggtggcctgatggttgggagacacaggttctacctggcca  c.14969-481

.         .         .         .         .         .           g.788738
ggcctataaccatctgtgtgaccttgcaagggtcacttccctcaggttcctggccattgg  c.14969-421

.         .         .         .         .         .           g.788798
aagagcaatttagaccatgtgatttctaggatcccttttgagctctcctgttcagtaaga  c.14969-361

.         .         .         .         .         .           g.788858
aactctaggtcatttagtggaaagtacacctgtaaattttaaaggaaggatttaaaccgt  c.14969-301

.         .         .         .         .         .           g.788918
gtgcagaacaagatgcgctttgtgtattaccctttactcgtctgatgttcttttcctttg  c.14969-241

.         .         .         .         .         .           g.788978
ctgtataagctctaattttccttagctctattacttatggataggctattattacactaa  c.14969-181

.         .         .         .         .         .           g.789038
tgatagctttttttcttaaacattttaaaattagaagtaattttgaatattatataaaac  c.14969-121

.         .         .         .         .         .           g.789098
gtcataacttgctttggaatcctatttttcatgctatgatgcattgctcttttaaaagca  c.14969-61

.         .         .         .         .         .           g.789158
tgtgccctatttgtaggtgttgaatgaacaagtcatttaccagttcttccttttgtctag  c.14969-1