Search for variants found at specified frequencies in your choice of haplogroups or lineages - originally developed as a "Marker Finder" but has many uses!
Retrieve haplogroup-specific GenBank sequences and their variants
Get info for specified variants - find lineage & haplogroup-specific frequencies for both variant and rCRS alleles
Haplotype your sequences and get variant information - including frequencies, conservation, references, and more. Input can be sequences in FASTA format, GenBank numbers, or SNVs. The SNV query is especially useful for novel variants.
Search for variants by position - a quick way to pull up info on general population variants and patient variants. For variants not currently listed in Mitomap, use the SNV query function in MITOMASTER, above.
Retrieve sequence IDs from our current database, from GenBank, and elsewhere. Download a real-time listing of all variants found in Mitomap's set of GenBank sequences.
Download raw data from the Mitomap database.