spastic paraplegia 11 (autosomal recessive) (SPG11) - 207 nt intron 37 reference sequence

(intronic numbering for coding DNA Reference Sequence)


         .         .         .         .         .         .  g.102522
gtaacccaaaggcttttttcagactggccttgggacttgctgtctgcagtaaaattattt  c.6843+60

         .         .         .         .      g.102566
tcttttgtccttgggctctttccaggtgaagcgggagggcatca  c.6843+104

--------------------- middle of intron ---------------------
     g.102567       .         .         .         .           g.102609
     c.6844-103  taggccaaccaggaacagaaggggtgaataccgttgtgagggt  c.6844-61

.         .         .         .         .         .           g.102669
tcacacaggaggtgacaactaggtctttctctactgtgcctctccacccttgttcctcag  c.6844-1


Powered by LOVD v.3.0 Build 13
©2004-2015 Leiden University Medical Center