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.6005_11222del | CA645373331 | ClinVar | ||
MT | m.6470_15588del | CA645373332 | ClinVar | ||
MT | m.7129_13991del | CA645373333 | ClinVar | ||
MT | m.7486G>A | CA645509243 | ClinVar dbSNP | ||
MT | m.7486G>C | CA913177182 | |||
MT | m.7486G= | CA2499565192 | |||
MT | m.7486G>T | CA913177181 | |||
MT | m.7487C>A | CA913177183 | |||
MT | m.7487C= | CA2499565193 | |||
MT | m.7487C>G | CA913177186 | |||
MT | m.7487C>T | CA913177185 | ClinVar dbSNP | ||
MT | m.7488C>A | CA913177191 | |||
MT | m.7488C= | CA2573327466 | |||
MT | m.7488C>G | CA913177190 | |||
MT | m.7488C>T | CA913177189 | |||
MT | m.7489A= | CA2573327468 | |||
MT | m.7489A>C | CA913177194 | |||
MT | m.7489A>G | CA913177193 | |||
MT | m.7489A>T | CA913177192 | |||
MT | m.7490A= | CA2499565194 | |||
MT | m.7490A>C | CA913177197 | |||
MT | m.7490A>G | CA913177196 | ClinVar dbSNP | ||
MT | m.7490A>T | CA913177195 | |||
MT | m.7491C>A | CA913177199 | |||
MT | m.7491C= | CA2573327473 | |||
MT | m.7491C>G | CA913177198 | |||
MT | m.7491C>T | CA913177200 | |||
MT | m.7494del | CA2573104866 | |||
MT | m.7492C>A | CA913177203 | |||
MT | m.7492C= | CA2499565195 | |||
MT | m.7492C>G | CA913177202 | |||
MT | m.7492C>T | CA337097637 | dbSNP | ||
MT | m.7493C>A | CA913177207 | |||
MT | m.7493C= | CA2499565196 | |||
MT | m.7493C>G | CA913177206 | |||
MT | m.7493C>T | CA131014 | ClinVar dbSNP | ||
MT | m.7494C>A | CA913177208 | |||
MT | m.7494C= | CA2573327479 | |||
MT | m.7494C>G | CA913177210 | |||
MT | m.7494C>T | CA913177209 | |||
MT | m.7495A= | CA2573327481 | |||
MT | m.7495A>C | CA913177212 | |||
MT | m.7495A>G | CA913177211 | |||
MT | m.7495A>T | CA913177213 | |||
MT | m.7496T>A | CA913177214 |