Werner syndrome, RecQ helicase-like (WRN) - 301 nt intron 14 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.62331
gtaagttgtacttaagcaaaacctaatcctttaaaaaaataaaacataaagagtttgaaa  c.1720+60

         .         .         .         .         .         .  g.62391
tgcttaatctttcattaaactctcaaaatacaaatgcaactacaaatgatgtaaactata  c.1720+120

         .         .         .   g.62422
gaagagagtgaacaaagaacagatgctcaga  c.1720+151

--------------------- middle of intron ---------------------
                  g.62423     .         .         .           g.62452
                  c.1721-150  tttatgtatcaattagcttttaggaagata  c.1721-121

.         .         .         .         .         .           g.62512
gcatactagtattgaccattcatctgtataagtacattgtaaaaagaaatgaaagcatca  c.1721-61

.         .         .         .         .         .           g.62572
aaggtttatttttatttctatatttttttcattttatttttatatttttttcatttcaag  c.1721-1