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 | ClinVar | ||
MT | m.10950_15540del | CA2580102079 | ClinVar | ||
MT | m.11263_15374del | CA645373341 | ClinVar | ||
MT | m.12114_14420del | CA645373342 | ClinVar | ||
MT | m.14188A= | CA2499568365 | MT-ND6 | c.486T= (p.Val162=) | |
MT | m.14188A>C | CA913171485 | MT-ND6 | c.486T>G (p.Val162=) | |
MT | m.14188A>G | CA913171483 | MT-ND6 | c.486T>C (p.Val162=) | dbSNP |
MT | m.14188A>T | CA913171484 | MT-ND6 | c.486T>A (p.Val162=) | |
MT | m.14189A= | CA2499568366 | MT-ND6 | c.485T= (p.Val162=) | |
MT | m.14189A>C | CA414821303 | MT-ND6 | c.485T>G (p.Val162Gly) | |
MT | m.14189A>G | CA414821305 | MT-ND6 | c.485T>C (p.Val162Ala) | ClinVar dbSNP |
MT | m.14189A>T | CA414821307 | MT-ND6 | c.485T>A (p.Val162Asp) | |
MT | m.14190C>A | CA414821309 | MT-ND6 | c.484G>T (p.Val162Phe) | |
MT | m.14190C= | CA2573326624 | MT-ND6 | c.484G= (p.Val162=) | |
MT | m.14190C>G | CA414821310 | MT-ND6 | c.484G>C (p.Val162Leu) | |
MT | m.14190C>T | CA414821313 | MT-ND6 | c.484G>A (p.Val162Ile) | |
MT | m.14191A= | CA2573326627 | MT-ND6 | c.483T= (p.Phe161=) | |
MT | m.14191A>C | CA414821315 | MT-ND6 | c.483T>G (p.Phe161Leu) | |
MT | m.14191A>G | CA913171486 | MT-ND6 | c.483T>C (p.Phe161=) | |
MT | m.14191A>T | CA414821316 | MT-ND6 | c.483T>A (p.Phe161Leu) | |
MT | m.14192A= | CA2573326629 | MT-ND6 | c.482T= (p.Phe161=) | |
MT | m.14192A>C | CA414821320 | MT-ND6 | c.482T>G (p.Phe161Cys) | |
MT | m.14192A>G | CA414821322 | MT-ND6 | c.482T>C (p.Phe161Ser) | |
MT | m.14192A>T | CA414821319 | MT-ND6 | c.482T>A (p.Phe161Tyr) | |
MT | m.14193A= | CA2499568367 | MT-ND6 | c.481T= (p.Phe161=) | |
MT | m.14193A>C | CA414821325 | MT-ND6 | c.481T>G (p.Phe161Val) | |
MT | m.14193A>G | CA414821326 | MT-ND6 | c.481T>C (p.Phe161Leu) | ClinVar dbSNP |
MT | m.14193A>T | CA414821328 | MT-ND6 | c.481T>A (p.Phe161Ile) | |
MT | m.14194C>A | CA414821331 | MT-ND6 | c.480G>T (p.Leu160Phe) | |
MT | m.14194C= | CA2499568368 | MT-ND6 | c.480G= (p.Leu160=) | |
MT | m.14194C>G | CA414821333 | MT-ND6 | c.480G>C (p.Leu160Phe) | |
MT | m.14194C>T | CA913171487 | MT-ND6 | c.480G>A (p.Leu160=) | dbSNP |
MT | m.14195A= | CA2573326638 | MT-ND6 | c.479T= (p.Leu160=) | |
MT | m.14195A>C | CA414821336 | MT-ND6 | c.479T>G (p.Leu160Trp) | |
MT | m.14195A>G | CA414821337 | MT-ND6 | c.479T>C (p.Leu160Ser) | |
MT | m.14195A>T | CA414821339 | MT-ND6 | c.479T>A (p.Leu160Ter) | |
MT | m.14196A= | CA2573326641 | MT-ND6 | c.478T= (p.Leu160=) | |
MT | m.14196A>C | CA414821341 | MT-ND6 | c.478T>G (p.Leu160Val) | |
MT | m.14196A>G | CA913171488 | MT-ND6 | c.478T>C (p.Leu160=) | |
MT | m.14196A>T | CA414821342 | MT-ND6 | c.478T>A (p.Leu160Met) | |
MT | m.14197T>A | CA913171489 | MT-ND6 | c.477A>T (p.Thr159=) | |
MT | m.14197T>C | CA913171490 | MT-ND6 | c.477A>G (p.Thr159=) | dbSNP |
MT | m.14197T>G | CA913171491 | MT-ND6 | c.477A>C (p.Thr159=) | |
MT | m.14197T= | CA2499568369 | MT-ND6 | c.477A= (p.Thr159=) |