List of all SNPs. Column 4-43 indicate whether this SNP was noncoding (nc), non-synonymous (ns), synonymous (s), alternate stop codon (STOP), or homozygous reference allele (0). Column 44 indicates whether this mutation was analyzed by PROVEAN. Column 45 indicates PROVEAN score, if applicable. Column 46-50 indicate frequency of alternate allele in different classes of individuals
Table S4 BLAST results of SNP-associated sequences from masson pine accessions compared with the non...
<p><b>Non-synonymous substitutions.</b> Table of <i>Funci{SNP}</i>-identified single nucleotide miss...
Single nucleotide polymorphisms (SNPs) constitute the bulk of human genetic variation, occurring wit...
Table S1. Genetic diseases and sSNPs. The first column corresponds to the disease or genetic trait. ...
<p>PROVEAN scores are in parentheses. SNPs are predicted to have functional effect by PROVEAN if the...
<p>The four known mutations were analyzed by non-synonymous single nucleotide polymorphism (nsSNP) p...
<p>CHR: Chromosome; SNP: Single Nucleotide Polymorphism. The last four columns show the allele repor...
<p>Panel (a) describes key features of the SNP association approaches used. Panel (b) shows, for a s...
Single nucleotide polymorphisms (SNPs) are the most common form of human genetic variation, with mil...
Results of SIFT analyses identifying deleterious non-synonymous mutations. First column identifies t...
List of SNPs for H.paradoxus. Column 1 refers to the reference sequence. Column 2 to the position we...
<p>List of SNPs including Gene ID, accession number, mutant allele frequency and haplotype details w...
A major interest in human genetics is to determine whether a nonsynonymous single-base nucleotide po...
Table S2. SNP identification (Marker) and progressive number (N°), allelic variants (SNP), lines car...
OAK B188 Single nucleotide polymorphism (SNPs) are the most common form of sequence variation in the...
Table S4 BLAST results of SNP-associated sequences from masson pine accessions compared with the non...
<p><b>Non-synonymous substitutions.</b> Table of <i>Funci{SNP}</i>-identified single nucleotide miss...
Single nucleotide polymorphisms (SNPs) constitute the bulk of human genetic variation, occurring wit...
Table S1. Genetic diseases and sSNPs. The first column corresponds to the disease or genetic trait. ...
<p>PROVEAN scores are in parentheses. SNPs are predicted to have functional effect by PROVEAN if the...
<p>The four known mutations were analyzed by non-synonymous single nucleotide polymorphism (nsSNP) p...
<p>CHR: Chromosome; SNP: Single Nucleotide Polymorphism. The last four columns show the allele repor...
<p>Panel (a) describes key features of the SNP association approaches used. Panel (b) shows, for a s...
Single nucleotide polymorphisms (SNPs) are the most common form of human genetic variation, with mil...
Results of SIFT analyses identifying deleterious non-synonymous mutations. First column identifies t...
List of SNPs for H.paradoxus. Column 1 refers to the reference sequence. Column 2 to the position we...
<p>List of SNPs including Gene ID, accession number, mutant allele frequency and haplotype details w...
A major interest in human genetics is to determine whether a nonsynonymous single-base nucleotide po...
Table S2. SNP identification (Marker) and progressive number (N°), allelic variants (SNP), lines car...
OAK B188 Single nucleotide polymorphism (SNPs) are the most common form of sequence variation in the...
Table S4 BLAST results of SNP-associated sequences from masson pine accessions compared with the non...
<p><b>Non-synonymous substitutions.</b> Table of <i>Funci{SNP}</i>-identified single nucleotide miss...
Single nucleotide polymorphisms (SNPs) constitute the bulk of human genetic variation, occurring wit...
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