nephrosis 1, congenital, Finnish type (nephrin) (NPHS1) - 209 nt intron 12 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.28340
gtgagggctcgcactgctgaggcccgggggcggggcgggagggacagagccaggtggggc  c.1627+60

         .         .         .         .       g.28385
agggacccagcgaaccctggacccggggaaagcgggcggaggcgg  c.1627+105

--------------------- middle of intron ---------------------
    g.28386         .         .         .         .           g.28429
    c.1628-104  ggtgggggacccgagactgggcggagcctggggtgcaggcgggg  c.1628-61

.         .         .         .         .         .           g.28489
tggacgcagaccaggccgcccctaacctctgagtctcgctcctccaaccccgtctcccag  c.1628-1