| 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.12083T>A | CA414812423 | MT-ND4 | c.1324T>A (p.Ser442Thr) | |
| MT | m.12083T>C | CA414812420 | MT-ND4 | c.1324T>C (p.Ser442Pro) | |
| MT | m.12083T>G | CA414812422 | MT-ND4 | c.1324T>G (p.Ser442Ala) | ClinVar dbSNP |
| MT | m.12083T= | CA2499567402 | MT-ND4 | c.1324T= (p.Ser442=) | |
| MT | m.12084C>A | CA414812426 | MT-ND4 | c.1325C>A (p.Ser442Tyr) | |
| MT | m.12084C= | CA2499567403 | MT-ND4 | c.1325C= (p.Ser442=) | |
| MT | m.12084C>G | CA414812427 | MT-ND4 | c.1325C>G (p.Ser442Cys) | dbSNP |
| MT | m.12084C>T | CA414812429 | MT-ND4 | c.1325C>T (p.Ser442Phe) | ClinVar dbSNP |
| MT | m.12085C>A | CA913169395 | MT-ND4 | c.1326C>A (p.Ser442=) | |
| MT | m.12085C= | CA2499567404 | MT-ND4 | c.1326C= (p.Ser442=) | |
| MT | m.12085C>G | CA913169393 | MT-ND4 | c.1326C>G (p.Ser442=) | |
| MT | m.12085C>T | CA913169394 | MT-ND4 | c.1326C>T (p.Ser442=) | dbSNP |
| MT | m.12086C>A | CA414812432 | MT-ND4 | c.1327C>A (p.Pro443Thr) | |
| MT | m.12086C= | CA2499567405 | MT-ND4 | c.1327C= (p.Pro443=) | |
| MT | m.12086C>G | CA414812433 | MT-ND4 | c.1327C>G (p.Pro443Ala) | |
| MT | m.12086C>T | CA414812435 | MT-ND4 | c.1327C>T (p.Pro443Ser) | dbSNP |
| MT | m.12087C>A | CA414812437 | MT-ND4 | c.1328C>A (p.Pro443His) | |
| MT | m.12087C= | CA2573328864 | MT-ND4 | c.1328C= (p.Pro443=) | |
| MT | m.12087C>G | CA414812439 | MT-ND4 | c.1328C>G (p.Pro443Arg) | |
| MT | m.12087C>T | CA414812441 | MT-ND4 | c.1328C>T (p.Pro443Leu) | |
| MT | m.12088C>A | CA913169398 | MT-ND4 | c.1329C>A (p.Pro443=) | |
| MT | m.12088C= | CA2499567406 | MT-ND4 | c.1329C= (p.Pro443=) | |
| MT | m.12088C>G | CA913169397 | MT-ND4 | c.1329C>G (p.Pro443=) | |
| MT | m.12088C>T | CA337099382 | MT-ND4 | c.1329C>T (p.Pro443=) | dbSNP |
| MT | m.12089A= | CA2573328868 | MT-ND4 | c.1330A= (p.Ile444=) | |
| MT | m.12089A>C | CA414812448 | MT-ND4 | c.1330A>C (p.Ile444Leu) | |
| MT | m.12089A>G | CA414812445 | MT-ND4 | c.1330A>G (p.Ile444Val) | |
| MT | m.12089A>T | CA414812446 | MT-ND4 | c.1330A>T (p.Ile444Phe) | |
| MT | m.12090T>A | CA414812451 | MT-ND4 | c.1331T>A (p.Ile444Asn) | |
| MT | m.12090T>C | CA414812452 | MT-ND4 | c.1331T>C (p.Ile444Thr) | |
| MT | m.12090T>G | CA414812454 | MT-ND4 | c.1331T>G (p.Ile444Ser) |