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.7731_11256del | CA645373334 | ClinVar | ||
MT | m.8282_8290del | CA2573104974 | |||
MT | m.8287_8292delinsCTAGAG | CA2499565566 | |||
MT | m.8289_8298dup | CA920609096 | dbSNP | ||
MT | m.8288_8291del | CA2573104983 | |||
MT | m.8288_8292del | CA920609100 | dbSNP | ||
MT | m.8290G>A | CA2499565574 | dbSNP | ||
MT | m.8290G>C | CA2573329212 | |||
MT | m.8290G= | CA2499565573 | |||
MT | m.8290G>T | CA2573104985 | |||
MT | m.8290_13040del | CA645373335 | ClinVar | ||
MT | m.8291A= | CA2499565575 | |||
MT | m.8291A>C | CA2573329213 | |||
MT | m.8291A>G | CA337097832 | dbSNP | ||
MT | m.8291A>T | CA2573329214 | |||
MT | m.8292G>A | CA2499565577 | dbSNP | ||
MT | m.8292G>C | CA2499565578 | dbSNP | ||
MT | m.8292G= | CA2499565576 | |||
MT | m.8292G>T | CA2573329215 | |||
MT | m.8293_8299dup | CA2740101891 | |||
MT | m.8293C>A | CA2573329220 | |||
MT | m.8293C= | CA2573329219 | |||
MT | m.8293C>G | CA2573329218 | |||
MT | m.8293C>T | CA2573104986 | |||
MT | m.8294C>A | CA2573329221 | |||
MT | m.8294C= | CA2573329223 | |||
MT | m.8294C>G | CA2573329224 | |||
MT | m.8294C>T | CA2573104987 | |||
MT | m.8295C>A | CA913178859 | |||
MT | m.8295C= | CA2573329226 | |||
MT | m.8295C>G | CA913178857 | |||
MT | m.8295C>T | CA913178856 | |||
MT | m.8296A= | CA2499565579 | |||
MT | m.8296A>C | CA913178861 | dbSNP | ||
MT | m.8296A>G | CA120557 | ClinVar dbSNP | ||
MT | m.8296A>T | CA913178860 | |||
MT | m.8297C>A | CA913178865 | |||
MT | m.8297C= | CA2573329229 | |||
MT | m.8297C>G | CA913178864 | |||
MT | m.8297C>T | CA913178863 | |||
MT | m.8298T>A | CA913178869 | |||
MT | m.8298T>C | CA913178868 | ClinVar dbSNP |