MitoTIP Sub-Scoring for Variant 8344G

MitoTIP Scoring Details


rCRS Position rCRS NT Query NT Numerical Scores Percentile Status
Variant Hx and Conservation Variant Location 2° Structure Prediction
8344 A G 10.088 1.166 0.000 11.254 38.10% confirmed pathogenic *
* Additional lines of evidence led to confirmation of pathogenicity for this tRNA variant. Examples of factors supporting confirmation of pathogencity: determination of heteroplasmy levels; correlation of heteroplasmy with phenotype; presence of variant in multiple unrelated affected families; functional cybrid studies; tRNA steady state levels; single fiber studies.

GenBank Frequency Information

L lineages
African
M lineages
Asian
N lineages
Eurasian
Highest hg lineage(s)
0.00% ( 0 / 5991 ) 0.01% ( 1 / 10520 ) 0.01% ( 3 / 32371 )
    V 0.14% ( 1 / 693 )