nephrosis 1, congenital, Finnish type (nephrin) (NPHS1) - 710 nt intron 05 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.23984
gtgtggaaactgaaacaaccccccaaccttgacccctaattttccccatgggaaccccag  c.608+60

         .         .         .         .         .         .  g.24044
accccagggatgcaagcatgaagcttgggctaggtatgaacatctgggacccaattcttc  c.608+120

         .         .         .         .         .         .  g.24104
atcctgactctcaaagcttcttcatggggaacagaggtggtggctcatgcctgtaatccc  c.608+180

         .         .         .         .         .         .  g.24164
agcactttgggaggctgaggtgggcggatcacctgaggtcaggagttcaagatcagctgg  c.608+240

         .         .         .         .         .         .  g.24224
gtcaacatggtgaaaccctgttttcactaaaaatacaaaaattagccgggtgtggtggcg  c.608+300

         .         .         .         .         .       g.24279
catgcctgtactcccagctcctcagggggctgaggcaggagaatcacttgaaccc  c.608+355

--------------------- middle of intron ---------------------
          .         .         .         .         .           g.24334
     aagaagtggaggttgcagtgagctgagattgtaccactgcactccagcctgggtg  c.609-301

.         .         .         .         .         .           g.24394
atagagccagattctgtctcaaaagacaaacaaacaaataaacaaacaaaaaaacttcat  c.609-241

.         .         .         .         .         .           g.24454
gggaacctcagttctagagtcccaagcactaaagttttggtcagatgtggggctctctag  c.609-181

.         .         .         .         .         .           g.24514
gctccaattctcactgttcacccccaaaatctctcccatggaaccctggatcccagagga  c.609-121

.         .         .         .         .         .           g.24574
gatcagcatggggacttagaccaggtgtggggaccagaggtgacatccccacctcttctc  c.609-61

.         .         .         .         .         .           g.24634
cctgactccccaaatttcagatgatgactctgactctataaccctgacttctcatcccag  c.609-1