Variant Search, aka "Marker Finder" Search for variants found at specified frequencies in your choice of haplogroups or lineages - originally developed as a "Marker Finder" but has many uses.
Variants Satisfying BA1 or BS1 Frequency Cutoffs Real-time report of all variants in our GenBank Full Length Sequence Set that meet current ClinGen frequency levels for standalone* or supporting "Benign" assessment [*barring any disqualifying factors].
MITOMASTER 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. This tools is available through your browser or our web API.
Allele Search 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.
Sequence and Variant Downloads 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.
Data Downloads Download raw data in various formats from the Mitomap database.