nephrosis 1, congenital, Finnish type (nephrin) (NPHS1) - 509 nt intron 16 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.30245
gtgagccccgcccaccatggaaaccacacccacccaaggaaccttgcccattgtggagtc  c.2212+60

         .         .         .         .         .         .  g.30305
tcctcattgtgggagctccgcccacccagggatagccacccatcctggaaccctcccgtt  c.2212+120

         .         .         .         .         .         .  g.30365
ctggaagtcccagccgcggtgtaaccacgcccactgcggaacccctcccactagagagac  c.2212+180

         .         .         .         .         .         .  g.30425
ccagtgtggaatctctgcccagagagggtgcccgcctagacacggaagctgctcccgtca  c.2212+240

         .       g.30440
ggaatgagagcccac  c.2212+255

--------------------- middle of intron ---------------------
                                  g.30441         .           g.30454
                                  c.2213-254  tgtataagccctgc  c.2213-241

.         .         .         .         .         .           g.30514
tacacacacaattctggaagcccactcaactcactctaattatcacagaggcatagtgga  c.2213-181

.         .         .         .         .         .           g.30574
gggtggagacaacctcaccaaccttgagaactctcctccaaccctttggtattaagggca  c.2213-121

.         .         .         .         .         .           g.30634
gattgtgtccacacccataaccttcctggaacccctaagacatccctcccacctggggcc  c.2213-61

.         .         .         .         .         .           g.30694
ctctcacacccagacctgtctgggcccaagtgtcttccccaagcctctgccttccaccag  c.2213-1