MitoTIP Sub-Scoring for Variant 4467A

MitoTIP Scoring Details


rCRS Position rCRS NT Query NT Numerical Scores Percentile Status
Variant Hx and Conservation Variant Location 2° Structure Prediction
4467 C A 7.715 2.328 6.254 16.297 75.60% likely pathogenic

GenBank Frequency Information

L lineages
African
M lineages
Asian
N lineages
Eurasian
Highest hg lineage(s)
0.00% ( 0 / 6191 ) 0.00% ( 0 / 10711 ) 0.00% ( 0 / 33273 ) NA