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.6005_11222del | CA645373331 | ClinVar | ||
MT | m.6470_15588del | CA645373332 | ClinVar | ||
MT | m.7129_13991del | CA645373333 | ClinVar | ||
MT | m.7731_11256del | CA645373334 | 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.11199C>A | CA414809679 | MT-ND4 | c.440C>A (p.Thr147Lys) | |
MT | m.11199C= | CA2573327444 | MT-ND4 | c.440C= (p.Thr147=) | |
MT | m.11199C>G | CA414809680 | MT-ND4 | c.440C>G (p.Thr147Arg) | |
MT | m.11199C>T | CA414809681 | MT-ND4 | c.440C>T (p.Thr147Ile) | |
MT | m.11200A= | CA2573327445 | MT-ND4 | c.441A= (p.Thr147=) | |
MT | m.11200A>C | CA913166231 | MT-ND4 | c.441A>C (p.Thr147=) | |
MT | m.11200A>G | CA913166233 | MT-ND4 | c.441A>G (p.Thr147=) | |
MT | m.11200A>T | CA913166232 | MT-ND4 | c.441A>T (p.Thr147=) | |
MT | m.11201T>A | CA414809682 | MT-ND4 | c.442T>A (p.Tyr148Asn) | |
MT | m.11201T>C | CA414809683 | MT-ND4 | c.442T>C (p.Tyr148His) | |
MT | m.11201T>G | CA414809684 | MT-ND4 | c.442T>G (p.Tyr148Asp) | |
MT | m.11201T= | CA2573327446 | MT-ND4 | c.442T= (p.Tyr148=) | |
MT | m.11202A= | CA2573327451 | MT-ND4 | c.443A= (p.Tyr148=) | |
MT | m.11202A>C | CA414809687 | MT-ND4 | c.443A>C (p.Tyr148Ser) | |
MT | m.11202A>G | CA414809685 | MT-ND4 | c.443A>G (p.Tyr148Cys) | |
MT | m.11202A>T | CA414809686 | MT-ND4 | c.443A>T (p.Tyr148Phe) | |
MT | m.11203C>A | CA414809688 | MT-ND4 | c.444C>A (p.Tyr148Ter) | |
MT | m.11203C= | CA2499567186 | MT-ND4 | c.444C= (p.Tyr148=) | |
MT | m.11203C>G | CA414809689 | MT-ND4 | c.444C>G (p.Tyr148Ter) | |
MT | m.11203C>T | CA913166244 | MT-ND4 | c.444C>T (p.Tyr148=) | dbSNP |
MT | m.11204T>A | CA414809690 | MT-ND4 | c.445T>A (p.Phe149Ile) | |
MT | m.11204T>C | CA337099117 | MT-ND4 | c.445T>C (p.Phe149Leu) | ClinVar dbSNP |
MT | m.11204T>G | CA414809691 | MT-ND4 | c.445T>G (p.Phe149Val) | |
MT | m.11204T= | CA2499567187 | MT-ND4 | c.445T= (p.Phe149=) | |
MT | m.11205T>A | CA414809692 | MT-ND4 | c.446T>A (p.Phe149Tyr) | |
MT | m.11205T>C | CA414809693 | MT-ND4 | c.446T>C (p.Phe149Ser) | |
MT | m.11205T>G | CA414809694 | MT-ND4 | c.446T>G (p.Phe149Cys) | |
MT | m.11205T= | CA2573327455 | MT-ND4 | c.446T= (p.Phe149=) | |
MT | m.11206C>A | CA337099119 | MT-ND4 | c.447C>A (p.Phe149Leu) | dbSNP |
MT | m.11206C= | CA2499567188 | MT-ND4 | c.447C= (p.Phe149=) |