spastic paraplegia 11 (autosomal recessive) (SPG11) - 189 nt intron 05 reference sequence

(intronic numbering for coding DNA Reference Sequence)


         .         .         .         .         .         .  g.16610
gtacagaaacttccttttcatgtagtttattgttcttattttttatcatgctgacgctgt  c.1007+60

         .         .         .       g.16645
accctttcattaaaggtctttatttgatagatact  c.1007+95

--------------------- middle of intron ---------------------
               g.16646        .         .         .           g.16679
               c.1008-94  ttttttttttaagaacatctttgccctggtttag  c.1008-61

.         .         .         .         .         .           g.16739
tgttttacatagtgccttttactgtgacaggtgttaagttatattttaccttgtttccag  c.1008-1


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