nephrosis 1, congenital, Finnish type (nephrin) (NPHS1) - 149 nt intron 26 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.43052
gtaagtgggggtggccctggtgaccccacaatcagggcaccgacggcgactgaagccctg  c.3387+60

         .       g.43067
ccgttagcatcaggt  c.3387+75

--------------------- middle of intron ---------------------
                                   g.43068        .           g.43081
                                   c.3388-74  tgatcattgccctt  c.3388-61

.         .         .         .         .         .           g.43141
ccgggcacagtggggtcagaggatggaaagggctttgtttgttttgcgtgtggggaacag  c.3388-1