Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.5774_14768del | CA2580610836 | |||
MT | m.5794_14876del | CA250414 | ClinVar | ||
MT | m.6470_15588del | CA645373332 | ClinVar | ||
MT | m.8839_14895del | CA645373339 | ClinVar | ||
MT | m.9062_16052del | CA2580618296 | |||
MT | m.10106_15067del | CA645373340 | ClinVar | ||
MT | m.10775_14941del | CA2740090229 | |||
MT | m.10950_15540del | CA2580102079 | ClinVar | ||
MT | m.11263_15374del | CA645373341 | ClinVar | ||
MT | m.14495A= | CA2499568513 | MT-ND6 | c.179T= (p.Leu60=) | |
MT | m.14495A>C | CA414822742 | MT-ND6 | c.179T>G (p.Leu60Ter) | |
MT | m.14495A>G | CA340933 | MT-ND6 | c.179T>C (p.Leu60Ser) | ClinVar dbSNP |
MT | m.14495A>T | CA414822745 | MT-ND6 | c.179T>A (p.Leu60Ter) | |
MT | m.14496A= | CA2499568514 | MT-ND6 | c.178T= (p.Leu60=) | |
MT | m.14496A>C | CA414822747 | MT-ND6 | c.178T>G (p.Leu60Val) | |
MT | m.14496A>G | CA913171666 | MT-ND6 | c.178T>C (p.Leu60=) | dbSNP |
MT | m.14496A>T | CA414822749 | MT-ND6 | c.178T>A (p.Leu60Ile) | |
MT | m.14497A= | CA2499568515 | MT-ND6 | c.177T= (p.Tyr59=) | |
MT | m.14497A>C | CA414822751 | MT-ND6 | c.177T>G (p.Tyr59Ter) | |
MT | m.14497A>G | CA913171667 | MT-ND6 | c.177T>C (p.Tyr59=) | dbSNP |
MT | m.14497A>T | CA414822752 | MT-ND6 | c.177T>A (p.Tyr59Ter) | |
MT | m.14498T>A | CA414822755 | MT-ND6 | c.176A>T (p.Tyr59Phe) | |
MT | m.14498T>C | CA356574 | MT-ND6 | c.176A>G (p.Tyr59Cys) | ClinVar dbSNP |
MT | m.14498T>G | CA414822757 | MT-ND6 | c.176A>C (p.Tyr59Ser) | |
MT | m.14498T= | CA2499568516 | MT-ND6 | c.176A= (p.Tyr59=) | |
MT | m.14499A= | CA2573327256 | MT-ND6 | c.175T= (p.Tyr59=) | |
MT | m.14499A>C | CA414822761 | MT-ND6 | c.175T>G (p.Tyr59Asp) | |
MT | m.14499A>G | CA414822762 | MT-ND6 | c.175T>C (p.Tyr59His) | |
MT | m.14499A>T | CA414822763 | MT-ND6 | c.175T>A (p.Tyr59Asn) | |
MT | m.14500A= | CA2499568517 | MT-ND6 | c.174T= (p.Ile58=) | |
MT | m.14500A>C | CA414822766 | MT-ND6 | c.174T>G (p.Ile58Met) | |
MT | m.14500A>G | CA913171669 | MT-ND6 | c.174T>C (p.Ile58=) | dbSNP |
MT | m.14500A>T | CA913171668 | MT-ND6 | c.174T>A (p.Ile58=) | |
MT | m.14501A= | CA2573327258 | MT-ND6 | c.173T= (p.Ile58=) | |
MT | m.14501A>C | CA414822768 | MT-ND6 | c.173T>G (p.Ile58Ser) | |
MT | m.14501A>G | CA414822771 | MT-ND6 | c.173T>C (p.Ile58Thr) | |
MT | m.14501A>T | CA414822772 | MT-ND6 | c.173T>A (p.Ile58Asn) | |
MT | m.14502T>A | CA414822777 | MT-ND6 | c.172A>T (p.Ile58Phe) | |
MT | m.14502T>C | CA337100074 | MT-ND6 | c.172A>G (p.Ile58Val) | ClinVar dbSNP |
MT | m.14502T>G | CA414822775 | MT-ND6 | c.172A>C (p.Ile58Leu) | |
MT | m.14502T= | CA2499568518 | MT-ND6 | c.172A= (p.Ile58=) | |
MT | m.14502_14503del | CA2573105304 | MT-ND6 | c.171_172del (p.Leu57PhefsTer19) | |
MT | m.14503T>A | CA414822779 | MT-ND6 | c.171A>T (p.Leu57Phe) | |
MT | m.14503T>C | CA337100076 | MT-ND6 | c.171A>G (p.Leu57=) | dbSNP |
MT | m.14503T>G | CA414822782 | MT-ND6 | c.171A>C (p.Leu57Phe) | |
MT | m.14503T= | CA2499568519 | MT-ND6 | c.171A= (p.Leu57=) | |
MT | m.14503_14504delinsTA | CA2499568520 | MT-ND6 | c.170_171delinsTA (p.Leu57=) | |
MT | m.14504A= | CA2573327262 | MT-ND6 | c.170T= (p.Leu57=) | |
MT | m.14504A>C | CA414822784 | MT-ND6 | c.170T>G (p.Leu57Ter) | |
MT | m.14504A>G | CA414822786 | MT-ND6 | c.170T>C (p.Leu57Ser) |