Werner syndrome, RecQ helicase-like (WRN) - 235 nt intron 29 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.118927
gtaaggcttttgtaaaaaggtaattagtttatgataggatagttatgattctatgtatgc  c.3459+60

         .         .         .         .         .          g.118985
ttaaaattctgtattttgccagcattttaaaaattgttcttaagctaagagtctgagt  c.3459+118

--------------------- middle of intron ---------------------
          .         .         .         .         .           g.119042
   ttatatttcagtttatattcattctaaggaaaaatgtggtatctgaagctctaaaaa  c.3460-61

.         .         .         .         .         .           g.119102
taaaggactagatcttttaagtacactttaaaaagtgttgtttctttgttttttgttcag  c.3460-1