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.11299T>A | CA913166589 | MT-ND4 | c.540T>A (p.Thr180=) | |
MT | m.11299T>C | CA337099154 | MT-ND4 | c.540T>C (p.Thr180=) | dbSNP |
MT | m.11299T>G | CA913166591 | MT-ND4 | c.540T>G (p.Thr180=) | |
MT | m.11299T= | CA2499566863 | MT-ND4 | c.540T= (p.Thr180=) | |
MT | m.11300C>A | CA414809882 | MT-ND4 | c.541C>A (p.Leu181Ile) | |
MT | m.11300C= | CA2573327616 | MT-ND4 | c.541C= (p.Leu181=) | |
MT | m.11300C>G | CA414809883 | MT-ND4 | c.541C>G (p.Leu181Val) | |
MT | m.11300C>T | CA414809884 | MT-ND4 | c.541C>T (p.Leu181Phe) | |
MT | m.11301T>A | CA414809885 | MT-ND4 | c.542T>A (p.Leu181His) | |
MT | m.11301T>C | CA414809886 | MT-ND4 | c.542T>C (p.Leu181Pro) | ClinVar dbSNP COSMIC |
MT | m.11301T>G | CA414809887 | MT-ND4 | c.542T>G (p.Leu181Arg) | |
MT | m.11301T= | CA2499566866 | MT-ND4 | c.542T= (p.Leu181=) | |
MT | m.11302C>A | CA913166614 | MT-ND4 | c.543C>A (p.Leu181=) | |
MT | m.11302C= | CA2499566869 | MT-ND4 | c.543C= (p.Leu181=) | |
MT | m.11302C>G | CA913166616 | MT-ND4 | c.543C>G (p.Leu181=) | dbSNP |
MT | m.11302C>T | CA913166619 | MT-ND4 | c.543C>T (p.Leu181=) | dbSNP |
MT | m.11303A= | CA2573327620 | MT-ND4 | c.544A= (p.Thr182=) | |
MT | m.11303A>C | CA414809888 | MT-ND4 | c.544A>C (p.Thr182Pro) | |
MT | m.11303A>G | CA414809890 | MT-ND4 | c.544A>G (p.Thr182Ala) | |
MT | m.11303A>T | CA414809889 | MT-ND4 | c.544A>T (p.Thr182Ser) | |
MT | m.11304C>A | CA414809891 | MT-ND4 | c.545C>A (p.Thr182Asn) | |
MT | m.11304C= | CA2573327622 | MT-ND4 | c.545C= (p.Thr182=) | |
MT | m.11304C>G | CA414809893 | MT-ND4 | c.545C>G (p.Thr182Ser) | |
MT | m.11304C>T | CA414809892 | MT-ND4 | c.545C>T (p.Thr182Ile) | |
MT | m.11305T>A | CA913166644 | MT-ND4 | c.546T>A (p.Thr182=) | |
MT | m.11305T>C | CA913166650 | MT-ND4 | c.546T>C (p.Thr182=) | dbSNP |
MT | m.11305T>G | CA913166653 | MT-ND4 | c.546T>G (p.Thr182=) | |
MT | m.11305T= | CA2499566871 | MT-ND4 | c.546T= (p.Thr182=) | |
MT | m.11306G>A | CA414809894 | MT-ND4 | c.547G>A (p.Ala183Thr) | |
MT | m.11306G>C | CA414809896 | MT-ND4 | c.547G>C (p.Ala183Pro) | |
MT | m.11306G= | CA2573327626 | MT-ND4 | c.547G= (p.Ala183=) |