| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| MT | m.5774_14768del | CA2580610836 | |||
| MT | m.5780_14107del | CA2580610932 | |||
| MT | m.5782_13922del | CA250413 | ClinVar | ||
| MT | m.5788_13923del | CA2580618295 | |||
| MT | m.5794_14876del | CA250414 | ClinVar | ||
| MT | m.6470_15588del | CA645373332 | ClinVar | ||
| MT | m.7129_13991del | CA645373333 | ClinVar | ||
| MT | m.8815_13722del | CA645373338 | ClinVar | ||
| MT | m.8839_14895del | CA645373339 | ClinVar | ||
| MT | m.9062_16052del | CA2580618296 | |||
| MT | m.10106_15067del | CA645373340 | ClinVar | ||
| MT | m.10775_14941del | CA2740090229 | |||
| MT | m.10950_15540del | CA2580102079 | ClinVar | ||
| MT | m.11263_15374del | CA645373341 | ClinVar | ||
| MT | m.12114_14420del | CA645373342 | ClinVar | ||
| MT | m.13608T>A | CA913171075 | MT-ND5 | c.1272T>A (p.Thr424=) | |
| MT | m.13608T>C | CA913171076 | MT-ND5 | c.1272T>C (p.Thr424=) | |
| MT | m.13608T>G | CA913171077 | MT-ND5 | c.1272T>G (p.Thr424=) | |
| MT | m.13608T= | CA2573324868 | MT-ND5 | c.1272T= (p.Thr424=) | |
| MT | m.13609C>A | CA913171078 | MT-ND5 | c.1273C>A (p.Arg425=) | |
| MT | m.13609C= | CA2499568075 | MT-ND5 | c.1273C= (p.Arg425=) | |
| MT | m.13609C>G | CA337099752 | MT-ND5 | c.1273C>G (p.Arg425Gly) | dbSNP |
| MT | m.13609C>T | CA414818744 | MT-ND5 | c.1273C>T (p.Arg425Ter) | |
| MT | m.13610G>A | CA414818746 | MT-ND5 | c.1274G>A (p.Arg425Gln) | |
| MT | m.13610G>C | CA414818747 | MT-ND5 | c.1274G>C (p.Arg425Pro) | |
| MT | m.13610G= | CA2573324874 | MT-ND5 | c.1274G= (p.Arg425=) | |
| MT | m.13610G>T | CA414818750 | MT-ND5 | c.1274G>T (p.Arg425Leu) | |
| MT | m.13611A= | CA2499568076 | MT-ND5 | c.1275A= (p.Arg425=) | |
| MT | m.13611A>C | CA913171079 | MT-ND5 | c.1275A>C (p.Arg425=) | |
| MT | m.13611A>G | CA913171080 | MT-ND5 | c.1275A>G (p.Arg425=) | dbSNP |
| MT | m.13611A>T | CA913171081 | MT-ND5 | c.1275A>T (p.Arg425=) | |
| MT | m.13612A= | CA2499568077 | MT-ND5 | c.1276A= (p.Ile426=) | |
| MT | m.13612A>C | CA414818752 | MT-ND5 | c.1276A>C (p.Ile426Leu) | |
| MT | m.13612A>G | CA414818753 | MT-ND5 | c.1276A>G (p.Ile426Val) | |
| MT | m.13612A>T | CA414818755 | MT-ND5 | c.1276A>T (p.Ile426Leu) | ClinVar dbSNP |
| MT | m.13613T>A | CA414818758 | MT-ND5 | c.1277T>A (p.Ile426Lys) | |
| MT | m.13613T>C | CA414818760 | MT-ND5 | c.1277T>C (p.Ile426Thr) | |
| MT | m.13613T>G | CA414818759 | MT-ND5 | c.1277T>G (p.Ile426Arg) | |
| MT | m.13613T= | CA2573324885 | MT-ND5 | c.1277T= (p.Ile426=) | |
| MT | m.13614A= | CA2499568078 | MT-ND5 | c.1278A= (p.Ile426=) | |
| MT | m.13614A>C | CA913171082 | MT-ND5 | c.1278A>C (p.Ile426=) | |
| MT | m.13614A>G | CA414818763 | MT-ND5 | c.1278A>G (p.Ile426Met) | dbSNP |
| MT | m.13614A>T | CA913171083 | MT-ND5 | c.1278A>T (p.Ile426=) | |
| MT | m.13615A= | CA2499568079 | MT-ND5 | c.1279A= (p.Ile427=) | |
| MT | m.13615A>C | CA414818765 | MT-ND5 | c.1279A>C (p.Ile427Leu) | |
| MT | m.13615A>G | CA414818768 | MT-ND5 | c.1279A>G (p.Ile427Val) | ClinVar dbSNP |
| MT | m.13615A>T | CA414818770 | MT-ND5 | c.1279A>T (p.Ile427Phe) | |
| MT | m.13616T>A | CA414818772 | MT-ND5 | c.1280T>A (p.Ile427Asn) | |
| MT | m.13616T>C | CA414818776 | MT-ND5 | c.1280T>C (p.Ile427Thr) | ClinVar dbSNP |
| MT | m.13616T>G | CA414818774 | MT-ND5 | c.1280T>G (p.Ile427Ser) |