| 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.12748T>A | CA414814664 | MT-ND5 | c.412T>A (p.Phe138Ile) | |
| MT | m.12748T>C | CA414814665 | MT-ND5 | c.412T>C (p.Phe138Leu) | |
| MT | m.12748T>G | CA414814667 | MT-ND5 | c.412T>G (p.Phe138Val) | |
| MT | m.12748T= | CA2573321365 | MT-ND5 | c.412T= (p.Phe138=) | |
| MT | m.12749T>A | CA414814670 | MT-ND5 | c.413T>A (p.Phe138Tyr) | |
| MT | m.12749T>C | CA414814673 | MT-ND5 | c.413T>C (p.Phe138Ser) | |
| MT | m.12749T>G | CA414814671 | MT-ND5 | c.413T>G (p.Phe138Cys) | |
| MT | m.12749T= | CA2573321370 | MT-ND5 | c.413T= (p.Phe138=) | |
| MT | m.12750C>A | CA414814676 | MT-ND5 | c.414C>A (p.Phe138Leu) | |
| MT | m.12750C= | CA2499567714 | MT-ND5 | c.414C= (p.Phe138=) | |
| MT | m.12750C>G | CA414814677 | MT-ND5 | c.414C>G (p.Phe138Leu) | |
| MT | m.12750C>T | CA913170500 | MT-ND5 | c.414C>T (p.Phe138=) | dbSNP |
| MT | m.12751C>A | CA414814680 | MT-ND5 | c.415C>A (p.Gln139Lys) | |
| MT | m.12751C= | CA2573321382 | MT-ND5 | c.415C= (p.Gln139=) | |
| MT | m.12751C>G | CA414814683 | MT-ND5 | c.415C>G (p.Gln139Glu) | |
| MT | m.12751C>T | CA414814682 | MT-ND5 | c.415C>T (p.Gln139Ter) | |
| MT | m.12752A= | CA2573321385 | MT-ND5 | c.416A= (p.Gln139=) | |
| MT | m.12752A>C | CA414814686 | MT-ND5 | c.416A>C (p.Gln139Pro) | |
| MT | m.12752A>G | CA414814688 | MT-ND5 | c.416A>G (p.Gln139Arg) | |
| MT | m.12752A>T | CA414814689 | MT-ND5 | c.416A>T (p.Gln139Leu) | |
| MT | m.12753A= | CA2499567715 | MT-ND5 | c.417A= (p.Gln139=) | |
| MT | m.12753A>C | CA414814692 | MT-ND5 | c.417A>C (p.Gln139His) | |
| MT | m.12753A>G | CA913170501 | MT-ND5 | c.417A>G (p.Gln139=) | dbSNP |
| MT | m.12753A>T | CA414814694 | MT-ND5 | c.417A>T (p.Gln139His) | |
| MT | m.12754C>A | CA414814697 | MT-ND5 | c.418C>A (p.Leu140Met) | |
| MT | m.12754C= | CA2573321395 | MT-ND5 | c.418C= (p.Leu140=) | |
| MT | m.12754C>G | CA414814698 | MT-ND5 | c.418C>G (p.Leu140Val) | |
| MT | m.12754C>T | CA913170502 | MT-ND5 | c.418C>T (p.Leu140=) | |
| MT | m.12755T>A | CA414814700 | MT-ND5 | c.419T>A (p.Leu140Gln) | |
| MT | m.12755T>C | CA414814703 | MT-ND5 | c.419T>C (p.Leu140Pro) |