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| | Information analysis of human splice site mutations |
 | | Functional analyses of splicing were not reported for mutations #31, 32, 54 and 55 in Table 1, #14, 15, 23, 34-38, and 44, 45, 46 in Table 2, and #1, 7 and 8 (the natural site at 2621) in Table 3. |
 | | Splicing patterns for several nucleotide substitutions #1, 2, 3, and 7 (Table 3) were not reported, however, based on information analysis, these changes would not be predicted to alter mRNA splicing. |
 | | Splicing varies among 3 common alleles that differ in length in the polymorphic polythymidine tract of the IVS 8 acceptor of the gene encoding the cystic fibrosis transmembrane regulator [CFTR; M55114] (Table 1, #6). |
| www.lecb.ncifcrf.gov /~toms/paper/rfs/latex/paper.html (5647 words) |
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