Usher syndrome 2A (autosomal recessive, mild) (USH2A) - 472 nt intron 07 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.104289
gtatgaatatttttaaacaattaatttaatagactgattggttattaataatgtacaagt  c.1328+60

         .         .         .         .         .         .  g.104349
atgctagctctctaggctggtggagacttcccttcaccaccaacttccttgaggcagatt  c.1328+120

         .         .         .         .         .         .  g.104409
ctcctaagtcttatccctaaattgggcttaaaactatgtttaaagttcttgtaaaagaca  c.1328+180

         .         .         .         .         .        g.104465
ttagagtgactcttatttcaatctcactgatgtttcacaatctgattttcagattg  c.1328+236

--------------------- middle of intron ---------------------
          .         .         .         .         .           g.104521
    tttggcaagttatctatgtaaatagaattttcattatgttttcaaggaactgtttt  c.1329-181

.         .         .         .         .         .           g.104581
agtgtggctttctatgataatcctgtattgtttatatatgaaatatatggaatatgcttt  c.1329-121

.         .         .         .         .         .           g.104641
tcctagaatgaataatttaagcttttattgatactgtgtagtaatttctcaacattttga  c.1329-61

.         .         .         .         .         .           g.104701
tttctgttttgccaaaaatgtgaatagattttcatgacatcgaatttctttcattaacag  c.1329-1