MitoTIP Sub-Scoring for Variant 9997C

MitoTIP Scoring Details


rCRS Position rCRS NT Query NT Numerical Scores Percentile Status
Variant Hx and Conservation Variant Location 2° Structure Prediction
9997 T C 9.829 1.857 5.267 16.952 80.30% 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% ( 1 / 33273 )
    H 0.01% ( 1 / 9486 )