Fraser syndrome 1 (FRAS1) - 1312 nt intron 55 reference sequence

(intronic numbering for coding DNA Reference Sequence)


         .         .         .         .         .         .  g.425552
gtctgttggttccacaggtgacaaagagctataataattgctaacatttattgagttcct  c.8098+60

         .         .         .         .         .         .  g.425612
attatgtgctaagcactcatctcatgcattatcttaactcacatgtgtactttccactta  c.8098+120

         .         .         .         .         .         .  g.425672
ttaactcatttggttcccacaacaaccctgatgatgattctatccatagtgactaccatc  c.8098+180

         .         .         .         .         .         .  g.425732
agaaagcctcttttcttagttcaagttgttagagctcccatttactcttaaattggacta  c.8098+240

         .         .         .         .         .         .  g.425792
gaagactggttatatttagccttctaaattattcatgaatcagtattcttaatcaatcac  c.8098+300

         .         .         .         .         .         .  g.425852
ccaatccataaaatatttagtaaccttggtcaaggagggaagttacagttcataaggact  c.8098+360

         .         .         .         .         .         .  g.425912
ggctttccatcttattcttggaagacagaaatatgctgaaaatttccctatgtgacagtc  c.8098+420

         .         .         .         .         .         .  g.425972
atatgtagagctcagatgagaaataaactatgtgtaagaaataaagggcaattctttttt  c.8098+480

         .         .         .         .         .         .  g.426032
tgttttatttttgactgatacatagtaattgtgcatgttgataaaagggcaattcttgag  c.8098+540

         .         .         .         .         .         .  g.426092
gagttggaaataaaaataaacatcatatggaattttgattgtgcaagattgagactttaa  c.8098+600

         .         .         .         .         .        g.426148
aacacatggaaattgaacccccattcaaaggcacaacaagactgtaaatgatgatt  c.8098+656

--------------------- middle of intron ---------------------
          .         .         .         .         .           g.426204
    ttgggtttctttcttgaatctgctgactgggtattagtgtaacaaatactgtagat  c.8099-601

.         .         .         .         .         .           g.426264
agcaaaaacccttggtaatgccacttggaaaacaagcaagcctcattgattgctctgggc  c.8099-541

.         .         .         .         .         .           g.426324
caccaagccaggcccagaacaggctgtcaccaagggaagtggcagccctaataagtaaag  c.8099-481

.         .         .         .         .         .           g.426384
tcatttgtatacagtggcagattttattttgttttgtctttctctttttaaataagcctg  c.8099-421

.         .         .         .         .         .           g.426444
tttctttctgggaattaaagtatagaagtttattcagaaaggcagtgaactgtgcttata  c.8099-361

.         .         .         .         .         .           g.426504
gcactaccttcaggacacaattactttcctacttaaagtaccaaatatgtgtcatatctt  c.8099-301

.         .         .         .         .         .           g.426564
tccacctgctgtggtcttagatggtgggcaatgagtcttgcaaattaacagagcacaaaa  c.8099-241

.         .         .         .         .         .           g.426624
ttcacagaataggaaatccattttgagttgtttgatgaagtatctggggtatattaaatc  c.8099-181

.         .         .         .         .         .           g.426684
ctcaagtggtttataccacaggctcaaagaaactgcaattcaggaaggttttatgtcaga  c.8099-121

.         .         .         .         .         .           g.426744
gtttgaacagaaatagtgatggactgtttgggagggaccaagctcattaacttaccagag  c.8099-61

.         .         .         .         .         .           g.426804
gttttaaaatctgagaagcactcattcaaatgctttggttttttgccatttgtatttcag  c.8099-1


Powered by LOVD v.3.0 Build 18
©2004-2017 Leiden University Medical Center