MitoTIP Sub-Scoring for Variant 5789C

MitoTIP Scoring Details


rCRS Position rCRS NT Query NT Numerical Scores Percentile Status
Variant Hx and Conservation Variant Location 2° Structure Prediction
5789 T C 9.463 1.737 5.267 16.466 77.30% likely pathogenic

GenBank Frequency Information

L lineages
African
M lineages
Asian
N lineages
Eurasian
Highest hg lineage(s)
0.00% ( 0 / 6672 ) 0.00% ( 0 / 12461 ) 0.00% ( 0 / 41991 ) NA