MITOMAP
A human mitochondrial genome database
A compendium of polymorphisms and mutations in human mitochondrial DNA
MITOMAP reports published data on human mitochondrial DNA variation. If you would like to add a paper and its data into MITOMAP, please email a pdf to mitomap@chop.edu. We appreciate your help. |  |  |
2026 Update #1:
On
January 15, 2026 we added
2,745 new full-length (FL)
(but we als removed 15 bad sequences)
and
510 new control region (CR) GenBank sequences to our database.
This brings our total number of FL sequences to
65,286 and
the number of CR sequences to
82,288. Our SNVs now total
19,973.
We update our GenBank sequences every 4-6 months. Hand curation
of variants and references continues weekly.
See the
GenBank Frequency Info
page for details about our current sequence sets.
We have starred our user Favorites for seeking information on specific variants and for understanding the contents of our database.
MITOMAP Quick Reference & Tools
Allele Search - get point mutation data based on position
MITOMASTER - analyze any human mito SNV or nucleotide sequence
Tool Launchpad
The rCRS is GenBank number
NC_012920.1.
Click here for details.
 | Map of the Human Mitochondrial DNA |
~☆~ Celebrating years! ~☆~
Mitomap has been continuously updated since 1996.
PhyloTree Markers
tRNAdb