Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.4160T>A | CA414774315 | MT-ND1 | c.854T>A (p.Leu285His) | |
MT | m.4160T>C | CA340942 | MT-ND1 | c.854T>C (p.Leu285Pro) | ClinVar dbSNP |
MT | m.4160T>G | CA414774316 | MT-ND1 | c.854T>G (p.Leu285Arg) | |
MT | m.4160T= | CA2499563759 | MT-ND1 | c.854T= (p.Leu285=) | |
MT | m.4160_4161insG | CA2573104456 | MT-ND1 | c.854_855insG (p.Ile286HisfsTer?) | |
MT | m.4161C>A | CA913177047 | MT-ND1 | c.855C>A (p.Leu285=) | |
MT | m.4161C= | CA2499563760 | MT-ND1 | c.855C= (p.Leu285=) | |
MT | m.4161C>G | CA913177045 | MT-ND1 | c.855C>G (p.Leu285=) | |
MT | m.4161C>T | CA913177049 | MT-ND1 | c.855C>T (p.Leu285=) | dbSNP |
MT | m.4162A= | CA2573329362 | MT-ND1 | c.856A= (p.Ile286=) | |
MT | m.4162A>C | CA414774317 | MT-ND1 | c.856A>C (p.Ile286Leu) | |
MT | m.4162A>G | CA414774318 | MT-ND1 | c.856A>G (p.Ile286Val) | |
MT | m.4162A>T | CA414774319 | MT-ND1 | c.856A>T (p.Ile286Leu) | |
MT | m.4162_4163insGTGGTGAGGGTGTTTATTATAATAATGTTTATG | CA2573104457 | MT-ND1 | c.856_857insGTGGTGAGGGTGTTTATTATAATAATGTTTATG (p.Ile286delinsSerGlyGluGlyValTyrTyrAsnAsnValTyrVal) | |
MT | m.4163T>A | CA414774320 | MT-ND1 | c.857T>A (p.Ile286Lys) | |
MT | m.4163T>C | CA414774321 | MT-ND1 | c.857T>C (p.Ile286Thr) | dbSNP |
MT | m.4163T>G | CA414774322 | MT-ND1 | c.857T>G (p.Ile286Arg) | |
MT | m.4163T= | CA2499563761 | MT-ND1 | c.857T= (p.Ile286=) | |
MT | m.4164A= | CA2499563762 | MT-ND1 | c.858A= (p.Ile286=) | |
MT | m.4164A>C | CA337096814 | MT-ND1 | c.858A>C (p.Ile286=) | |
MT | m.4164A>G | CA414774323 | MT-ND1 | c.858A>G (p.Ile286Met) | dbSNP |
MT | m.4164A>T | CA337096812 | MT-ND1 | c.858A>T (p.Ile286=) | |
MT | m.4165C>A | CA414774326 | MT-ND1 | c.859C>A (p.His287Asn) | |
MT | m.4165C= | CA2499563763 | MT-ND1 | c.859C= (p.His287=) | |
MT | m.4165C>G | CA414774324 | MT-ND1 | c.859C>G (p.His287Asp) | ClinVar dbSNP |
MT | m.4165C>T | CA414774325 | MT-ND1 | c.859C>T (p.His287Tyr) | |
MT | m.4166_4168del | CA2573104458 | MT-ND1 | c.860_862del (p.His287del) | |
MT | m.4166A= | CA2573329364 | MT-ND1 | c.860A= (p.His287=) | |
MT | m.4166A>C | CA414774327 | MT-ND1 | c.860A>C (p.His287Pro) | |
MT | m.4166A>G | CA414774328 | MT-ND1 | c.860A>G (p.His287Arg) | |
MT | m.4166A>T | CA414774329 | MT-ND1 | c.860A>T (p.His287Leu) | |
MT | m.4167C>A | CA414774330 | MT-ND1 | c.861C>A (p.His287Gln) | |
MT | m.4167C= | CA2499563764 | MT-ND1 | c.861C= (p.His287=) | |
MT | m.4167C>G | CA414774331 | MT-ND1 | c.861C>G (p.His287Gln) | |
MT | m.4167C>T | CA913177052 | MT-ND1 | c.861C>T (p.His287=) | ClinVar dbSNP |
MT | m.4168C>A | CA414774332 | MT-ND1 | c.862C>A (p.Leu288Ile) | |
MT | m.4168C= | CA2573329367 | MT-ND1 | c.862C= (p.Leu288=) | |
MT | m.4168C>G | CA414774333 | MT-ND1 | c.862C>G (p.Leu288Val) | |
MT | m.4168C>T | CA414774334 | MT-ND1 | c.862C>T (p.Leu288Phe) | |
MT | m.4169T>A | CA414774335 | MT-ND1 | c.863T>A (p.Leu288His) | |
MT | m.4169T>C | CA414774336 | MT-ND1 | c.863T>C (p.Leu288Pro) | |
MT | m.4169T>G | CA414774337 | MT-ND1 | c.863T>G (p.Leu288Arg) | |
MT | m.4169T= | CA2513112278 | MT-ND1 | c.863T= (p.Leu288=) | |
MT | m.4170C>A | CA913177056 | MT-ND1 | c.864C>A (p.Leu288=) | |
MT | m.4170C= | CA2499563765 | MT-ND1 | c.864C= (p.Leu288=) | |
MT | m.4170C>G | CA913177058 | MT-ND1 | c.864C>G (p.Leu288=) | |
MT | m.4170C>T | CA913177059 | MT-ND1 | c.864C>T (p.Leu288=) | dbSNP |
MT | m.4171C>A | CA340948 | MT-ND1 | c.865C>A (p.Leu289Ile) | ClinVar dbSNP |
MT | m.4171C= | CA2499563766 | MT-ND1 | c.865C= (p.Leu289=) | |
MT | m.4171C>G | CA414774338 | MT-ND1 | c.865C>G (p.Leu289Val) |