optic atrophy 1 (autosomal dominant) (OPA1) - 486 nt intron 22 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.70912
gtaagtggagacacggcttattgagttctgagttcacagtggtgaaggagtcatccaact  c.2275+60

         .         .         .         .         .         .  g.70972
ttagtgaacatttgtagaaatagattgaacatttcaaagtctttgtcattaatactatag  c.2275+120

         .         .         .         .         .         .  g.71032
tcgaatattatttgtggaatttttttagtcaactgctttgtaactactaaaaccaatgaa  c.2275+180

         .         .         .         .         .         .  g.71092
taaaatggacacatgatgcttatatgcatttatattctataaagctataatgcagaatat  c.2275+240

     g.71095
ttt  c.2275+243

--------------------- middle of intron ---------------------
                                             g.71096          g.71098
                                             c.2276-243  agt  c.2276-241

.         .         .         .         .         .           g.71158
gtgttcgctactgtacttataggaattttataagcaattatacttttaggtatcttaaac  c.2276-181

.         .         .         .         .         .           g.71218
acatatataattaaactcttacacatgtgccatatcagtcatgtgggttttttcctttat  c.2276-121

.         .         .         .         .         .           g.71278
ttcaactgccttcatattgatatagcactttgaaatagttaagaaagcaagaccattatt  c.2276-61

.         .         .         .         .         .           g.71338
agttataatttgtgtgtgtgtaagtgataaaattcttgattaattaatttttttttctag  c.2276-1