Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.3697G>A | CA120647 | MT-ND1 | c.391G>A (p.Gly131Ser) | ClinVar dbSNP COSMIC COSMIC |
MT | m.3697G>C | CA414773328 | MT-ND1 | c.391G>C (p.Gly131Arg) | |
MT | m.3697G= | CA2499563557 | MT-ND1 | c.391G= (p.Gly131=) | |
MT | m.3697G>T | CA414773329 | MT-ND1 | c.391G>T (p.Gly131Cys) | |
MT | m.3698G>A | CA414773330 | MT-ND1 | c.392G>A (p.Gly131Asp) | |
MT | m.3698G>C | CA414773331 | MT-ND1 | c.392G>C (p.Gly131Ala) | |
MT | m.3698G= | CA2573328325 | MT-ND1 | c.392G= (p.Gly131=) | |
MT | m.3698G>T | CA414773332 | MT-ND1 | c.392G>T (p.Gly131Val) | |
MT | m.3699C>A | CA913170166 | MT-ND1 | c.393C>A (p.Gly131=) | |
MT | m.3699C= | CA2499563558 | MT-ND1 | c.393C= (p.Gly131=) | |
MT | m.3699C>G | CA913170167 | MT-ND1 | c.393C>G (p.Gly131=) | dbSNP |
MT | m.3699C>T | CA913170165 | MT-ND1 | c.393C>T (p.Gly131=) | |
MT | m.3700G>A | CA344828 | MT-ND1 | c.394G>A (p.Ala132Thr) | ClinVar dbSNP |
MT | m.3700G>C | CA414773333 | MT-ND1 | c.394G>C (p.Ala132Pro) | |
MT | m.3700G= | CA2499563559 | MT-ND1 | c.394G= (p.Ala132=) | |
MT | m.3700G>T | CA414773334 | MT-ND1 | c.394G>T (p.Ala132Ser) | |
MT | m.3701C>A | CA414773336 | MT-ND1 | c.395C>A (p.Ala132Glu) | |
MT | m.3701C= | CA2499563560 | MT-ND1 | c.395C= (p.Ala132=) | |
MT | m.3701C>G | CA414773337 | MT-ND1 | c.395C>G (p.Ala132Gly) | |
MT | m.3701C>T | CA414773335 | MT-ND1 | c.395C>T (p.Ala132Val) | ClinVar dbSNP |
MT | m.3702A= | CA2499563561 | MT-ND1 | c.396A= (p.Ala132=) | |
MT | m.3702A>C | CA913170172 | MT-ND1 | c.396A>C (p.Ala132=) | |
MT | m.3702A>G | CA913170171 | MT-ND1 | c.396A>G (p.Ala132=) | dbSNP |
MT | m.3702A>T | CA913170170 | MT-ND1 | c.396A>T (p.Ala132=) | |
MT | m.3703C>A | CA414773338 | MT-ND1 | c.397C>A (p.Leu133Met) | |
MT | m.3703C= | CA2573328345 | MT-ND1 | c.397C= (p.Leu133=) | |
MT | m.3703C>G | CA414773339 | MT-ND1 | c.397C>G (p.Leu133Val) | |
MT | m.3703C>T | CA913170174 | MT-ND1 | c.397C>T (p.Leu133=) | |
MT | m.3704T>A | CA414773340 | MT-ND1 | c.398T>A (p.Leu133Gln) | |
MT | m.3704T>C | CA414773341 | MT-ND1 | c.398T>C (p.Leu133Pro) | |
MT | m.3704T>G | CA414773342 | MT-ND1 | c.398T>G (p.Leu133Arg) | |
MT | m.3704T= | CA2573328347 | MT-ND1 | c.398T= (p.Leu133=) | |
MT | m.3705G>A | CA337096647 | MT-ND1 | c.399G>A (p.Leu133=) | dbSNP |
MT | m.3705G>C | CA337096643 | MT-ND1 | c.399G>C (p.Leu133=) | |
MT | m.3705G= | CA2499563562 | MT-ND1 | c.399G= (p.Leu133=) | |
MT | m.3705G>T | CA337096645 | MT-ND1 | c.399G>T (p.Leu133=) | |
MT | m.3706C>A | CA913170177 | MT-ND1 | c.400C>A (p.Arg134=) | |
MT | m.3706C= | CA2573328357 | MT-ND1 | c.400C= (p.Arg134=) | |
MT | m.3706C>G | CA414773343 | MT-ND1 | c.400C>G (p.Arg134Gly) | |
MT | m.3706C>T | CA414773344 | MT-ND1 | c.400C>T (p.Arg134Ter) | |
MT | m.3707G>A | CA414773345 | MT-ND1 | c.401G>A (p.Arg134Gln) | COSMIC COSMIC |
MT | m.3707G>C | CA414773346 | MT-ND1 | c.401G>C (p.Arg134Pro) | |
MT | m.3707G= | CA2573328360 | MT-ND1 | c.401G= (p.Arg134=) | |
MT | m.3707G>T | CA414773347 | MT-ND1 | c.401G>T (p.Arg134Leu) | |
MT | m.3708A= | CA2573328363 | MT-ND1 | c.402A= (p.Arg134=) | |
MT | m.3708A>C | CA913170178 | MT-ND1 | c.402A>C (p.Arg134=) | |
MT | m.3708A>G | CA913170179 | MT-ND1 | c.402A>G (p.Arg134=) | |
MT | m.3708A>T | CA913170180 | MT-ND1 | c.402A>T (p.Arg134=) | |
MT | m.3709G>A | CA414773348 | MT-ND1 | c.403G>A (p.Ala135Thr) | ClinVar dbSNP |
MT | m.3709G>C | CA414773350 | MT-ND1 | c.403G>C (p.Ala135Pro) |