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.5788T>A | CA913180460 | |||
MT | m.5788T>C | CA913180459 | ClinVar dbSNP | ||
MT | m.5788T>G | CA913180458 | |||
MT | m.5788T= | CA2499564568 | |||
MT | m.5789T>A | CA913180463 | |||
MT | m.5789T>C | CA913180462 | |||
MT | m.5789T>G | CA913180461 | |||
MT | m.5789T= | CA2573322220 | |||
MT | m.5790C>A | CA913180466 | dbSNP | ||
MT | m.5790C= | CA2499564569 | |||
MT | m.5790C>G | CA913180467 | |||
MT | m.5790C>T | CA913180465 | |||
MT | m.5791G>A | CA658475697 | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC | ||
MT | m.5791G>C | CA913180469 | |||
MT | m.5791G= | CA2499564570 | |||
MT | m.5791G>T | CA913180471 | |||
MT | m.5791_5792del | CA2573104504 | |||
MT | m.5792A= | CA2573322231 | |||
MT | m.5792A>C | CA913180472 | |||
MT | m.5792A>G | CA913180473 | |||
MT | m.5792A>T | CA913180474 | |||
MT | m.5793A= | CA2499564571 | |||
MT | m.5793A>C | CA913180477 | |||
MT | m.5793A>G | CA913180475 | ClinVar dbSNP | ||
MT | m.5793A>T | CA913180476 | |||
MT | m.5794T>A | CA913180478 | |||
MT | m.5794T>C | CA913180479 | ClinVar dbSNP | ||
MT | m.5794T>G | CA913180482 | |||
MT | m.5794T= | CA2499564572 | |||
MT | m.5794_14876del | CA250414 | ClinVar | ||
MT | m.5795T>A | CA913180484 | |||
MT | m.5795T>C | CA913180485 | |||
MT | m.5795T>G | CA913180483 | |||
MT | m.5795T= | CA2573322243 | |||
MT | m.5796T>A | CA913180486 | |||
MT | m.5796T>C | CA337097238 | dbSNP | ||
MT | m.5796T>G | CA913180487 | |||
MT | m.5796T= | CA2499564573 | |||
MT | m.5797G>A | CA913180490 | |||
MT | m.5797G>C | CA913180489 | |||
MT | m.5797G= | CA2573322246 | |||
MT | m.5797G>T | CA913180488 | |||
MT | m.5798C>A | CA913180493 | |||
MT | m.5798C= | CA2573322252 | |||
MT | m.5798C>G | CA913180492 | |||
MT | m.5798C>T | CA913180491 |