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.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) | |
MT | m.12755T>G | CA414814704 | MT-ND5 | c.419T>G (p.Leu140Arg) | |
MT | m.12755T= | CA2573321402 | MT-ND5 | c.419T= (p.Leu140=) | |
MT | m.12756G>A | CA645611414 | MT-ND5 | c.420G>A (p.Leu140=) | dbSNP COSMIC |
MT | m.12756G>C | CA913170503 | MT-ND5 | c.420G>C (p.Leu140=) | dbSNP |
MT | m.12756G= | CA2499567716 | MT-ND5 | c.420G= (p.Leu140=) | |
MT | m.12756G>T | CA913170504 | MT-ND5 | c.420G>T (p.Leu140=) | |
MT | m.12757T>A | CA414814710 | MT-ND5 | c.421T>A (p.Phe141Ile) | |
MT | m.12757T>C | CA414814709 | MT-ND5 | c.421T>C (p.Phe141Leu) | ClinVar dbSNP |
MT | m.12757T>G | CA414814707 | MT-ND5 | c.421T>G (p.Phe141Val) | |
MT | m.12757T= | CA2499567717 | MT-ND5 | c.421T= (p.Phe141=) | |
MT | m.12758T>A | CA414814712 | MT-ND5 | c.422T>A (p.Phe141Tyr) | |
MT | m.12758T>C | CA414814714 | MT-ND5 | c.422T>C (p.Phe141Ser) | dbSNP |
MT | m.12758T>G | CA414814716 | MT-ND5 | c.422T>G (p.Phe141Cys) | |
MT | m.12758T= | CA2499567718 | MT-ND5 | c.422T= (p.Phe141=) | |
MT | m.12759C>A | CA414814718 | MT-ND5 | c.423C>A (p.Phe141Leu) | |
MT | m.12759C= | CA2499567719 | MT-ND5 | c.423C= (p.Phe141=) | |
MT | m.12759C>G | CA414814720 | MT-ND5 | c.423C>G (p.Phe141Leu) | |
MT | m.12759C>T | CA913170505 | MT-ND5 | c.423C>T (p.Phe141=) | dbSNP |
MT | m.12760A= | CA2573321417 | MT-ND5 | c.424A= (p.Ile142=) | |
MT | m.12760A>C | CA414814723 | MT-ND5 | c.424A>C (p.Ile142Leu) | |
MT | m.12760A>G | CA414814724 | MT-ND5 | c.424A>G (p.Ile142Val) | |
MT | m.12760A>T | CA414814726 | MT-ND5 | c.424A>T (p.Ile142Phe) | |
MT | m.12761T>A | CA414814728 | MT-ND5 | c.425T>A (p.Ile142Asn) | |
MT | m.12761T>C | CA414814730 | MT-ND5 | c.425T>C (p.Ile142Thr) |