nephrosis 1, congenital, Finnish type (nephrin) (NPHS1) - 128 nt intron 13 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.28679
gtgggagtgcgagggatccctcccctctctggtctggcctcgccccctccacgcatgtcc  c.1757+60

      g.28683
cgcc  c.1757+64

--------------------- middle of intron ---------------------
                                             g.28684          g.28687
                                             c.1758-64  cccg  c.1758-61

.         .         .         .         .         .           g.28747
cctagtgcctctccagcctctggctccgctcgcagccctggcttgaccccggttccacag  c.1758-1