Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.13608T>A | CA913171075 | MT-ND5 | c.1272T>A (p.Thr424=) | |
MT | m.13608T>C | CA913171076 | MT-ND5 | c.1272T>C (p.Thr424=) | |
MT | m.13608T>G | CA913171077 | MT-ND5 | c.1272T>G (p.Thr424=) | |
MT | m.13608T= | CA2573324868 | MT-ND5 | c.1272T= (p.Thr424=) | |
MT | m.13609C>A | CA913171078 | MT-ND5 | c.1273C>A (p.Arg425=) | |
MT | m.13609C= | CA2499568075 | MT-ND5 | c.1273C= (p.Arg425=) | |
MT | m.13609C>G | CA337099752 | MT-ND5 | c.1273C>G (p.Arg425Gly) | dbSNP |
MT | m.13609C>T | CA414818744 | MT-ND5 | c.1273C>T (p.Arg425Ter) | |
MT | m.13610G>A | CA414818746 | MT-ND5 | c.1274G>A (p.Arg425Gln) | |
MT | m.13610G>C | CA414818747 | MT-ND5 | c.1274G>C (p.Arg425Pro) | |
MT | m.13610G= | CA2573324874 | MT-ND5 | c.1274G= (p.Arg425=) | |
MT | m.13610G>T | CA414818750 | MT-ND5 | c.1274G>T (p.Arg425Leu) | |
MT | m.13611A= | CA2499568076 | MT-ND5 | c.1275A= (p.Arg425=) | |
MT | m.13611A>C | CA913171079 | MT-ND5 | c.1275A>C (p.Arg425=) | |
MT | m.13611A>G | CA913171080 | MT-ND5 | c.1275A>G (p.Arg425=) | dbSNP |
MT | m.13611A>T | CA913171081 | MT-ND5 | c.1275A>T (p.Arg425=) | |
MT | m.13612A= | CA2499568077 | MT-ND5 | c.1276A= (p.Ile426=) | |
MT | m.13612A>C | CA414818752 | MT-ND5 | c.1276A>C (p.Ile426Leu) | |
MT | m.13612A>G | CA414818753 | MT-ND5 | c.1276A>G (p.Ile426Val) | |
MT | m.13612A>T | CA414818755 | MT-ND5 | c.1276A>T (p.Ile426Leu) | ClinVar dbSNP |
MT | m.13613T>A | CA414818758 | MT-ND5 | c.1277T>A (p.Ile426Lys) | |
MT | m.13613T>C | CA414818760 | MT-ND5 | c.1277T>C (p.Ile426Thr) | |
MT | m.13613T>G | CA414818759 | MT-ND5 | c.1277T>G (p.Ile426Arg) | |
MT | m.13613T= | CA2573324885 | MT-ND5 | c.1277T= (p.Ile426=) | |
MT | m.13614A= | CA2499568078 | MT-ND5 | c.1278A= (p.Ile426=) | |
MT | m.13614A>C | CA913171082 | MT-ND5 | c.1278A>C (p.Ile426=) | |
MT | m.13614A>G | CA414818763 | MT-ND5 | c.1278A>G (p.Ile426Met) | dbSNP |
MT | m.13614A>T | CA913171083 | MT-ND5 | c.1278A>T (p.Ile426=) | |
MT | m.13615A= | CA2499568079 | MT-ND5 | c.1279A= (p.Ile427=) | |
MT | m.13615A>C | CA414818765 | MT-ND5 | c.1279A>C (p.Ile427Leu) | |
MT | m.13615A>G | CA414818768 | MT-ND5 | c.1279A>G (p.Ile427Val) | ClinVar dbSNP |
MT | m.13615A>T | CA414818770 | MT-ND5 | c.1279A>T (p.Ile427Phe) | |
MT | m.13616T>A | CA414818772 | MT-ND5 | c.1280T>A (p.Ile427Asn) | |
MT | m.13616T>C | CA414818776 | MT-ND5 | c.1280T>C (p.Ile427Thr) | ClinVar dbSNP |
MT | m.13616T>G | CA414818774 | MT-ND5 | c.1280T>G (p.Ile427Ser) | |
MT | m.13616T= | CA2499568080 | MT-ND5 | c.1280T= (p.Ile427=) | |
MT | m.13620_13622del | CA2573105290 | MT-ND5 | c.1284_1286del (p.Leu429del) | |
MT | m.13617T>A | CA913171084 | MT-ND5 | c.1281T>A (p.Ile427=) | |
MT | m.13617T>C | CA337099754 | MT-ND5 | c.1281T>C (p.Ile427=) | ClinVar dbSNP |
MT | m.13617T>G | CA414818779 | MT-ND5 | c.1281T>G (p.Ile427Met) | |
MT | m.13617T= | CA2499568081 | MT-ND5 | c.1281T= (p.Ile427=) | |
MT | m.13618C>A | CA414818781 | MT-ND5 | c.1282C>A (p.Leu428Ile) | |
MT | m.13618C= | CA2573324895 | MT-ND5 | c.1282C= (p.Leu428=) | |
MT | m.13618C>G | CA414818782 | MT-ND5 | c.1282C>G (p.Leu428Val) | |
MT | m.13618C>T | CA414818784 | MT-ND5 | c.1282C>T (p.Leu428Phe) | |
MT | m.13619T>A | CA414818786 | MT-ND5 | c.1283T>A (p.Leu428His) | |
MT | m.13619T>C | CA414818788 | MT-ND5 | c.1283T>C (p.Leu428Pro) | |
MT | m.13619T>G | CA414818790 | MT-ND5 | c.1283T>G (p.Leu428Arg) | |
MT | m.13619T= | CA2573324900 | MT-ND5 | c.1283T= (p.Leu428=) | |
MT | m.13620T>A | CA913171087 | MT-ND5 | c.1284T>A (p.Leu428=) |