General mutations and polymorphisms
Find information about allele frequencies from different polymorphic areas in the human genome.
Search for information Cre transgenic mouse lines.
Search for sequence elements conserved between human and mouse that are involved in the pathogenesis of genetic disorders.
Search for well-annotated polymorphic sequences in the Drosophila genus.
An established software for haplotype association analysis of nuclear families.
Identify and prioritize high-risk SNPs according to their phenotypic risks and putative functional effects.
A high-density SNP database of Drosophila melanogaster.
Find information about potential associations of genes to a trait of interest.
Analyze mutant-based experiments and synthesize genetic networks.
A Variational Bayes within-sample SNP genotyping algorithm that does not require a reference population.
Search approved symbols for human genes.
multiplex tag SNP design SNPs tagging tag SNPs selection tool tag SNPs evaluation tool genome-wide association studies genotyping tool allele frequency estimation Association mapping disease association studies SNPs genotyping haplotype frequencies estimation
Study comprehensive linkage between the human disease genes compiled in Online Mendelian Inheritance in Man (OMIM) and the complete Drosophila genomic sequence.
Map recessive traits in consanguineous families.
A web resource for individual human genomics.
Find information about genetic disease common in Indian (India) populations.
Detect substitution and indel SNPs in sequencing traces.
Find murine models of immune processes and immunological diseases.
Conduct single nucleotide polymorphisms diversity measurements among homologous sequences from the Mammalia class.
Explore a comprehensive map of regulatory elements in the human genome.
Integration of publicly available databases of human genetic variation with molecular features and clinical phenotype data.
A system that uses genome-wide genotype data to estimate disease susceptibility.
Find whole genome epigenetic datasets.
Search for nuclear receptor mutation information.
Search an evolving collection of human and mouse Open Reading Frame (ORF) clones (UltimateTM ORF Clones).
Search for up-to-date information on inherited disorders and other familial traits in non-laboratory animals.
Display and analyze polymorphisms in genes.
Find information about SNPs and genetic association analysis.
Search for polymorphic sequences in large databases and estimate their genetic diversity.
Find information about the polymorphisms associated with notable pain phenotypes.
A database of potential intron polymorphism markers in plants.
Search for comprehensive information on documented protein mutants.
Search for single nucleotide polymorphisms (SNPs) with potential phenotypic effect.
Find information about genes related to pain phenotypes in mice.
Search for images of the abnormal histology associated with spontaneous and induced mutations of both embryonic and adult mice including those produced by transgenesis, targeted mutagenesis and chemical mutagenesis.
Compare fluorescence-based sequences across traces obtained from different individuals to identify heterozygous sites for single nucleotide substitutions.
Search for naturally occurring DNA variations in putative microRNA target sites.
Search for information on within-species sequence polymorphism in the nuclear, mitochondrial and chloroplastic genomes of Eukaryota species.
Estimate frequencies of single-nucleotide polymorphism (SNP) haplotypes from DNA pools.
Select single nucleotide polymorphisms (SNPs) with potential phenotypic effect.
Select single nucleotide polymorphisms (SNPs) with potential phenotypic effect.
Predict what amino acid substitutions will affect protein function.
Find suitable restriction enzymes for assays on a batch of SNPs and genes from the human, rat, and mouse genomes.
Visualize SNPs and mutations in genes.
Find information about SNPs.
Perform essential statistical analyses of SNPs in a common computational environment.
Search for information on compound microsatellite-SNP markers in human, dog, mouse, rat and chicken.
Perform automated identification of SNPs and mutations in fluorescence-based resequencing reads.
Carry out automatic masking of SNPs and repeats across eukaryotic genomes.
Conduct genome-wide identification of SNPs in microorganisms.
Find information about populations carrying polymorphisms within protein binding pockets that make them susceptible to serious adverse drug reaction (SADR).
A web server for mapping and modeling nsSNPs on protein structures with linkage to metabolic pathways.
Software for analysis of population variation in community genomic datasets.
Search for information on transgenic animals and targeted mutations generated and analyzed worldwide.
Search for various information and analyze repeats in genomic DNA.
Select and evaluate taged SNPs from genotype data.
Search for insertions in genes (Gene trap mutagenesis) expressed in mouse embryonic stem cells, under specific in vitro conditions, or based upon sequence identity via an online searchable database.
Search for comprehensive information on polymorphisms in various organisms.
A database on genetic polymorphism.
Perform oligo sequence silent mutation analysis, restriction analysis, and scanning for amplification-created restriction sites for the detection of single nucleotide polymorphisms.
Browse and download data from the first Asian diploid genome.
A database server mapping nsSNPs on protein structures.
Find information about chromosome rearrangements and associated diseases in humans.
Find information about SNPs that might be duplicated-gene nucleotide variants.
Search for data from wide association (GWA) studies.
Find the presence of Single Nucleotide Polymorphism in a nucleotide sequence.
A tool for exploring multi-locus associations in candidate genes and regions.
Investigate the influence of mutations in regulatory gene regions onto DNA interaction with nuclear proteins.