| 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.8290_13040del | CA645373335 | ClinVar | ||
| MT | m.8350_13450del | CA915952048 | ClinVar | ||
| MT | m.8483_13459del | CA645373336 | ClinVar | ||
| MT | m.8480_13440del | CA915952050 | ClinVar | ||
| MT | m.8587_12967del | CA645373337 | 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 | ClinVar | ||
| MT | m.10950_15540del | CA2580102079 | ClinVar | ||
| MT | m.11263_15374del | CA645373341 | ClinVar | ||
| MT | m.12114_14420del | CA645373342 | ClinVar | ||
| MT | m.12706T>A | CA414814475 | MT-ND5 | c.370T>A (p.Phe124Ile) | |
| MT | m.12706T>C | CA120628 | MT-ND5 | c.370T>C (p.Phe124Leu) | ClinVar dbSNP |
| MT | m.12706T>G | CA414814472 | MT-ND5 | c.370T>G (p.Phe124Val) | |
| MT | m.12706T= | CA2499567696 | MT-ND5 | c.370T= (p.Phe124=) | |
| MT | m.12707T>A | CA414814479 | MT-ND5 | c.371T>A (p.Phe124Tyr) | |
| MT | m.12707T>C | CA414814480 | MT-ND5 | c.371T>C (p.Phe124Ser) | dbSNP |
| MT | m.12707T>G | CA414814482 | MT-ND5 | c.371T>G (p.Phe124Cys) | |
| MT | m.12707T= | CA2499567697 | MT-ND5 | c.371T= (p.Phe124=) | |
| MT | m.12708C>A | CA414814485 | MT-ND5 | c.372C>A (p.Phe124Leu) | |
| MT | m.12708C= | CA2499567698 | MT-ND5 | c.372C= (p.Phe124=) | |
| MT | m.12708C>G | CA414814486 | MT-ND5 | c.372C>G (p.Phe124Leu) | |
| MT | m.12708C>T | CA913170471 | MT-ND5 | c.372C>T (p.Phe124=) | dbSNP |
| MT | m.12709C>A | CA414814489 | MT-ND5 | c.373C>A (p.Leu125Ile) | |
| MT | m.12709C= | CA2573321077 | MT-ND5 | c.373C= (p.Leu125=) | |
| MT | m.12709C>G | CA414814490 | MT-ND5 | c.373C>G (p.Leu125Val) | |
| MT | m.12709C>T | CA913170472 | MT-ND5 | c.373C>T (p.Leu125=) | |
| MT | m.12710T>A | CA414814493 | MT-ND5 | c.374T>A (p.Leu125Gln) | |
| MT | m.12710T>C | CA414814494 | MT-ND5 | c.374T>C (p.Leu125Pro) | |
| MT | m.12710T>G | CA414814496 | MT-ND5 | c.374T>G (p.Leu125Arg) | |
| MT | m.12710T= | CA2573321079 | MT-ND5 | c.374T= (p.Leu125=) | |
| MT | m.12711A= | CA2573321081 | MT-ND5 | c.375A= (p.Leu125=) | |
| MT | m.12711A>C | CA913170475 | MT-ND5 | c.375A>C (p.Leu125=) | |
| MT | m.12711A>G | CA913170473 | MT-ND5 | c.375A>G (p.Leu125=) | |
| MT | m.12711A>T | CA913170474 | MT-ND5 | c.375A>T (p.Leu125=) | |
| MT | m.12712A= | CA2573321086 | MT-ND5 | c.376A= (p.Ile126=) | |
| MT | m.12712A>C | CA414814500 | MT-ND5 | c.376A>C (p.Ile126Leu) | |
| MT | m.12712A>G | CA414814502 | MT-ND5 | c.376A>G (p.Ile126Val) | |
| MT | m.12712A>T | CA414814498 | MT-ND5 | c.376A>T (p.Ile126Phe) | |
| MT | m.12713T>A | CA414814504 | MT-ND5 | c.377T>A (p.Ile126Asn) | |
| MT | m.12713T>C | CA414814506 | MT-ND5 | c.377T>C (p.Ile126Thr) | ClinVar dbSNP COSMIC |