F each mutation within its exon, calculated as percentage of exon length. The lone spike around the 80–90% position is an abundance of mutations from the experimental mutagenesis data on exon #10 of the CFTR gene.<p><b>Copyright information:</b></p><p>Taken from "The Alternative Splicing Mutation Database: a hub for investigations of alternative splicing using mutational evidence"</p><p>http://www.biomedcentral.com/1756-0500/1/3</p><p>BMC Research Notes 2008;1():3-3.</p><p>Published online 26 Feb 2008</p><p>PMCID:PMC2518265.</p><p></p
Cystic Fibrosis is the most common recessive autosomal rare disease found in Caucasians. It is cause...
<p><b>Copyright information:</b></p><p>Taken from "Computational analysis of splicing errors and mut...
<p><b>Copyright information:</b></p><p>Taken from "Computational analysis of splicing errors and mut...
T a count of the splicing effects, not the mutations in that category.<p><b>Copyright information:</...
T a count of the splicing effects, not the mutations in that category.<p><b>Copyright information:</...
Ensus value (CV) method. Donor and acceptor sites are considered separately. The vertical dashed lin...
links to further views of the data. The colored boxes next to the SE values code the accuracy of the...
links to further views of the data. The colored boxes next to the SE values code the accuracy of the...
ASMD ID in the search results). The mutation position is highlighted in red. The splice site strengt...
ASMD ID in the search results). The mutation position is highlighted in red. The splice site strengt...
International audienceBackground: the majority of variants of unknown clinical significance (VUCS) i...
Copyright © 2015 Raëd Farhat et al. This is an open access article distributed under the Creative C...
Background The CFTR gene encodes for a chlorine-transporting protein essential for the correct hyd...
<p>(A) Number of splicing events and genes detected for 5 classes of alternative splicing events: ca...
AbstractBackgroundCystic fibrosis is caused by mutations in the cystic fibrosis transmembrane conduc...
Cystic Fibrosis is the most common recessive autosomal rare disease found in Caucasians. It is cause...
<p><b>Copyright information:</b></p><p>Taken from "Computational analysis of splicing errors and mut...
<p><b>Copyright information:</b></p><p>Taken from "Computational analysis of splicing errors and mut...
T a count of the splicing effects, not the mutations in that category.<p><b>Copyright information:</...
T a count of the splicing effects, not the mutations in that category.<p><b>Copyright information:</...
Ensus value (CV) method. Donor and acceptor sites are considered separately. The vertical dashed lin...
links to further views of the data. The colored boxes next to the SE values code the accuracy of the...
links to further views of the data. The colored boxes next to the SE values code the accuracy of the...
ASMD ID in the search results). The mutation position is highlighted in red. The splice site strengt...
ASMD ID in the search results). The mutation position is highlighted in red. The splice site strengt...
International audienceBackground: the majority of variants of unknown clinical significance (VUCS) i...
Copyright © 2015 Raëd Farhat et al. This is an open access article distributed under the Creative C...
Background The CFTR gene encodes for a chlorine-transporting protein essential for the correct hyd...
<p>(A) Number of splicing events and genes detected for 5 classes of alternative splicing events: ca...
AbstractBackgroundCystic fibrosis is caused by mutations in the cystic fibrosis transmembrane conduc...
Cystic Fibrosis is the most common recessive autosomal rare disease found in Caucasians. It is cause...
<p><b>Copyright information:</b></p><p>Taken from "Computational analysis of splicing errors and mut...
<p><b>Copyright information:</b></p><p>Taken from "Computational analysis of splicing errors and mut...