<p>Coding variants include missense, nonsense, frameshift, in-frame deletions and insertions and readthrough variants.</p><p>Essential splice variants include all variants found in the first two base pairs or the last two base pairs of introns.</p>a<p>Both homozygous and heterozygous variations are included.</p
<p>ASM-1 constitutes the reference sequence to which all other ASM variants are compared. The novel ...
*<p>Whole exome sequencing of genomic DNA from two <i>P43</i> mutants was performed. All mutations (...
<p>* Exome Aggregation Consortium (<a href="http://exac.broadinstitude.org/" target="_blank">http://...
<p>Coding variants include missense, nonsense, frameshift, in-frame deletions and insertions and rea...
<p>Exome sequence variants shared by all affected individuals in homozygous or compound heterozygous...
The advent of next-generation sequencing technologies has revolutionized the study of genetic variat...
Alternative splicing of genes is an efficient means of generating variation in protein function. Sev...
Alternative splicing of genes is an efficient means of generating variation in protein function. Sev...
<p>The number of functional variants (non-synonymous/splice acceptor and donor site/insertions or de...
Mutations that lead to splicing defects can have severe consequences on gene function and cause dise...
<p>Exon constitutes coding variants only. Splice junction constitutes +/−5 bp around an exon. A full...
<div><p>DNA variants that affect alternative splicing and the relative quantities of different gene ...
Variants found to satisfy the criteria of the women being homozygous with a minor allele and the men...
Alternative splicing diversifies mRNA transcripts in human cells. This sequence-driven process can b...
a<p>Number of variants not found in dbSNP or 1000 Genomes or HapMap and <0.001% in our database;</p>...
<p>ASM-1 constitutes the reference sequence to which all other ASM variants are compared. The novel ...
*<p>Whole exome sequencing of genomic DNA from two <i>P43</i> mutants was performed. All mutations (...
<p>* Exome Aggregation Consortium (<a href="http://exac.broadinstitude.org/" target="_blank">http://...
<p>Coding variants include missense, nonsense, frameshift, in-frame deletions and insertions and rea...
<p>Exome sequence variants shared by all affected individuals in homozygous or compound heterozygous...
The advent of next-generation sequencing technologies has revolutionized the study of genetic variat...
Alternative splicing of genes is an efficient means of generating variation in protein function. Sev...
Alternative splicing of genes is an efficient means of generating variation in protein function. Sev...
<p>The number of functional variants (non-synonymous/splice acceptor and donor site/insertions or de...
Mutations that lead to splicing defects can have severe consequences on gene function and cause dise...
<p>Exon constitutes coding variants only. Splice junction constitutes +/−5 bp around an exon. A full...
<div><p>DNA variants that affect alternative splicing and the relative quantities of different gene ...
Variants found to satisfy the criteria of the women being homozygous with a minor allele and the men...
Alternative splicing diversifies mRNA transcripts in human cells. This sequence-driven process can b...
a<p>Number of variants not found in dbSNP or 1000 Genomes or HapMap and <0.001% in our database;</p>...
<p>ASM-1 constitutes the reference sequence to which all other ASM variants are compared. The novel ...
*<p>Whole exome sequencing of genomic DNA from two <i>P43</i> mutants was performed. All mutations (...
<p>* Exome Aggregation Consortium (<a href="http://exac.broadinstitude.org/" target="_blank">http://...