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.11807A= | CA2499567285 | MT-ND4 | c.1048A= (p.Thr350=) | |
MT | m.11807A>C | CA414811167 | MT-ND4 | c.1048A>C (p.Thr350Pro) | |
MT | m.11807A>G | CA414811168 | MT-ND4 | c.1048A>G (p.Thr350Ala) | ClinVar dbSNP |
MT | m.11807A>T | CA414811170 | MT-ND4 | c.1048A>T (p.Thr350Ser) | |
MT | m.11808C>A | CA414811173 | MT-ND4 | c.1049C>A (p.Thr350Asn) | |
MT | m.11808C= | CA2513268984 | MT-ND4 | c.1049C= (p.Thr350=) | |
MT | m.11808C>G | CA414811174 | MT-ND4 | c.1049C>G (p.Thr350Ser) | |
MT | m.11808C>T | CA414811176 | MT-ND4 | c.1049C>T (p.Thr350Ile) | |
MT | m.11809T>A | CA913168729 | MT-ND4 | c.1050T>A (p.Thr350=) | |
MT | m.11809T>C | CA913168726 | MT-ND4 | c.1050T>C (p.Thr350=) | dbSNP |
MT | m.11809T>G | CA913168725 | MT-ND4 | c.1050T>G (p.Thr350=) | |
MT | m.11809T= | CA2499567286 | MT-ND4 | c.1050T= (p.Thr350=) | |
MT | m.11810C>A | CA414811178 | MT-ND4 | c.1051C>A (p.Leu351Ile) | |
MT | m.11810C= | CA2573328409 | MT-ND4 | c.1051C= (p.Leu351=) | |
MT | m.11810C>G | CA414811180 | MT-ND4 | c.1051C>G (p.Leu351Val) | |
MT | m.11810C>T | CA913168735 | MT-ND4 | c.1051C>T (p.Leu351=) | |
MT | m.11811T>A | CA414811183 | MT-ND4 | c.1052T>A (p.Leu351Gln) | |
MT | m.11811T>C | CA414811184 | MT-ND4 | c.1052T>C (p.Leu351Pro) | |
MT | m.11811T>G | CA414811186 | MT-ND4 | c.1052T>G (p.Leu351Arg) | |
MT | m.11811T= | CA2573328412 | MT-ND4 | c.1052T= (p.Leu351=) | |
MT | m.11812A= | CA2499567287 | MT-ND4 | c.1053A= (p.Leu351=) | |
MT | m.11812A>C | CA337099298 | MT-ND4 | c.1053A>C (p.Leu351=) | dbSNP |
MT | m.11812A>G | CA337099300 | MT-ND4 | c.1053A>G (p.Leu351=) | dbSNP |
MT | m.11812A>T | CA337099302 | MT-ND4 | c.1053A>T (p.Leu351=) | |
MT | m.11813C>A | CA414811192 | MT-ND4 | c.1054C>A (p.Leu352Ile) | |
MT | m.11813C= | CA2499567288 | MT-ND4 | c.1054C= (p.Leu352=) | |
MT | m.11813C>G | CA414811194 | MT-ND4 | c.1054C>G (p.Leu352Val) | |
MT | m.11813C>T | CA414811196 | MT-ND4 | c.1054C>T (p.Leu352Phe) | dbSNP |
MT | m.11814T>A | CA414811198 | MT-ND4 | c.1055T>A (p.Leu352His) | |
MT | m.11814T>C | CA414811200 | MT-ND4 | c.1055T>C (p.Leu352Pro) | dbSNP COSMIC |
MT | m.11814T>G | CA414811202 | MT-ND4 | c.1055T>G (p.Leu352Arg) |