MitoTIP Sub-Scoring for Variant 7567T
MitoTIP Scoring Details
| rCRS Position | rCRS NT | Query NT | Numerical Scores | Percentile | Status | |||
|---|---|---|---|---|---|---|---|---|
| Variant Hx and Conservation | Variant Location | 2° Structure | Prediction | |||||
| 7567 | C | T | 2.829 | 1.468 | 0.000 | 4.296 | 11.80% | likely benign |
GenBank Frequency Information
| L lineages African |
M lineages Asian |
N lineages Eurasian |
Highest hg lineage(s) |
|---|---|---|---|
| 0.00% ( 0 / 6668 ) | 0.00% ( 0 / 12798 ) | 0.01% ( 6 / 42378 ) |
|