Wolf-Hirschhorn syndrome candidate 1 (WHSC1) - 352 nt intron 13 reference sequence

(intronic numbering for coding DNA Reference Sequence)


         .         .         .         .         .         .  g.89005
gtgaggggcctgggggtgtctgcggcacacgcctctcacactcccaggagccacatatca  c.2518+60

         .         .         .         .         .         .  g.89065
aggcaggctcattccttgtctgcgctgtgttcattgatgttgacagtgttctgtgcgtct  c.2518+120

         .         .         .         .         .        g.89121
tcacgttaatagtatatcacagtagctctaaattaattgtaatcatttcgcaaaca  c.2518+176

--------------------- middle of intron ---------------------
          .         .         .         .         .           g.89177
    tacaggaaattatttgtggtgaaaatgacatttgctctcgtgctgatgtacagatc  c.2519-121

.         .         .         .         .         .           g.89237
gctgttttaaaactgatgtttataagttaaggctgtaataagtgtagactgtgaagcact  c.2519-61

.         .         .         .         .         .           g.89297
gaatctgggctgagccatagcagacaggctaagcctggccgcctcgccctcctcttgcag  c.2519-1


Powered by LOVD v.3.0 Build 28
©2004-2022 Leiden University Medical Center