exons nonsense splicing indel missense start ATG readthrough synonymous introns UTRs intergenic miRNA piRNA scRNA snRNA, snoRNA tRNA, rRNA other ncRNA
SNVs indels
Enter a comma separated list of gene and/or sequence names (e.g. unc-6, F15B9.7). Wildcards (e.g. unc-*) are supported.
Show only mutations affecting the following domain(s) (enter one or more domain abbreviations, see column 'domain affected' in the output table). You can use wildcards (*). suggest domains
Chromosome (e.g. I, X, mtDNA) from to
Enter one or more strain names (e.g. VC20167, VC20124)
Enter a comma separated list of Ensembl IDs of human genes (e.g. ENSG00000335203).
web page text only Sort by sequence name gene name strain allele position
collapse identical mutations in different strains show restriction enzymes recognizing the polymorphisms show Grantham and conservation scores show Ensembl IDs of human homologs