Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.4195A= | CA2573329414 | MT-ND1 | c.889A= (p.Thr297=) | |
MT | m.4195A>C | CA414774395 | MT-ND1 | c.889A>C (p.Thr297Pro) | |
MT | m.4195A>G | CA414774396 | MT-ND1 | c.889A>G (p.Thr297Ala) | |
MT | m.4195A>T | CA414774397 | MT-ND1 | c.889A>T (p.Thr297Ser) | |
MT | m.4196C>A | CA414774398 | MT-ND1 | c.890C>A (p.Thr297Asn) | |
MT | m.4196C= | CA2573329418 | MT-ND1 | c.890C= (p.Thr297=) | |
MT | m.4196C>G | CA414774400 | MT-ND1 | c.890C>G (p.Thr297Ser) | |
MT | m.4196C>T | CA414774399 | MT-ND1 | c.890C>T (p.Thr297Ile) | |
MT | m.4197C>A | CA913177218 | MT-ND1 | c.891C>A (p.Thr297=) | |
MT | m.4197C= | CA2499563776 | MT-ND1 | c.891C= (p.Thr297=) | |
MT | m.4197C>G | CA913177219 | MT-ND1 | c.891C>G (p.Thr297=) | |
MT | m.4197C>T | CA913177220 | MT-ND1 | c.891C>T (p.Thr297=) | dbSNP |
MT | m.4198C>A | CA414774401 | MT-ND1 | c.892C>A (p.Leu298Ile) | |
MT | m.4198C= | CA2499563777 | MT-ND1 | c.892C= (p.Leu298=) | |
MT | m.4198C>G | CA414774402 | MT-ND1 | c.892C>G (p.Leu298Val) | |
MT | m.4198C>T | CA337096819 | MT-ND1 | c.892C>T (p.Leu298=) | dbSNP |
MT | m.4199T>A | CA414774403 | MT-ND1 | c.893T>A (p.Leu298Gln) | |
MT | m.4199T>C | CA414774404 | MT-ND1 | c.893T>C (p.Leu298Pro) | |
MT | m.4199T>G | CA414774405 | MT-ND1 | c.893T>G (p.Leu298Arg) | |
MT | m.4199T= | CA2513226723 | MT-ND1 | c.893T= (p.Leu298=) | |
MT | m.4200A= | CA2499563778 | MT-ND1 | c.894A= (p.Leu298=) | |
MT | m.4200A>C | CA913177232 | MT-ND1 | c.894A>C (p.Leu298=) | |
MT | m.4200A>G | CA913177233 | MT-ND1 | c.894A>G (p.Leu298=) | dbSNP |
MT | m.4200A>T | CA913177235 | MT-ND1 | c.894A>T (p.Leu298=) | dbSNP |
MT | m.4201G>A | CA414774406 | MT-ND1 | c.895G>A (p.Ala299Thr) | |
MT | m.4201G>C | CA414774407 | MT-ND1 | c.895G>C (p.Ala299Pro) | |
MT | m.4201G= | CA2573329422 | MT-ND1 | c.895G= (p.Ala299=) | |
MT | m.4201G>T | CA414774408 | MT-ND1 | c.895G>T (p.Ala299Ser) | |
MT | m.4202C>A | CA414774409 | MT-ND1 | c.896C>A (p.Ala299Glu) | |
MT | m.4202C= | CA2573329424 | MT-ND1 | c.896C= (p.Ala299=) | |
MT | m.4202C>G | CA414774410 | MT-ND1 | c.896C>G (p.Ala299Gly) | |
MT | m.4202C>T | CA414774411 | MT-ND1 | c.896C>T (p.Ala299Val) | |
MT | m.4203A= | CA2499563779 | MT-ND1 | c.897A= (p.Ala299=) | |
MT | m.4203A>C | CA913177255 | MT-ND1 | c.897A>C (p.Ala299=) | dbSNP |
MT | m.4203A>G | CA913177252 | MT-ND1 | c.897A>G (p.Ala299=) | dbSNP |
MT | m.4203A>T | CA913177250 | MT-ND1 | c.897A>T (p.Ala299=) | |
MT | m.4204T>A | CA414774412 | MT-ND1 | c.898T>A (p.Leu300Ile) | |
MT | m.4204T>C | CA913177257 | MT-ND1 | c.898T>C (p.Leu300=) | dbSNP |
MT | m.4204T>G | CA414774413 | MT-ND1 | c.898T>G (p.Leu300Val) | |
MT | m.4204T= | CA2499563780 | MT-ND1 | c.898T= (p.Leu300=) | |
MT | m.4205T>A | CA414774414 | MT-ND1 | c.899T>A (p.Leu300Ter) | |
MT | m.4205T>C | CA414774416 | MT-ND1 | c.899T>C (p.Leu300Ser) | ClinVar dbSNP |
MT | m.4205T>G | CA414774415 | MT-ND1 | c.899T>G (p.Leu300Ter) | |
MT | m.4205T= | CA2499563781 | MT-ND1 | c.899T= (p.Leu300=) | |
MT | m.4206A= | CA2573329430 | MT-ND1 | c.900A= (p.Leu300=) | |
MT | m.4206A>C | CA414774417 | MT-ND1 | c.900A>C (p.Leu300Phe) | |
MT | m.4206A>G | CA913177262 | MT-ND1 | c.900A>G (p.Leu300=) | |
MT | m.4206A>T | CA414774418 | MT-ND1 | c.900A>T (p.Leu300Phe) | |
MT | m.4207C>A | CA414774419 | MT-ND1 | c.901C>A (p.Leu301Ile) | |
MT | m.4207C= | CA2573329431 | MT-ND1 | c.901C= (p.Leu301=) |