| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| MT | m.5491C>A | CA414780557 | MT-ND2 | c.1022C>A (p.Pro341His) | |
| MT | m.5491C= | CA2513084297 | MT-ND2 | c.1022C= (p.Pro341=) | |
| MT | m.5491C>G | CA414780561 | MT-ND2 | c.1022C>G (p.Pro341Arg) | |
| MT | m.5491C>T | CA414780558 | MT-ND2 | c.1022C>T (p.Pro341Leu) | |
| MT | m.5492T>A | CA913179679 | MT-ND2 | c.1023T>A (p.Pro341=) | |
| MT | m.5492T>C | CA337097154 | MT-ND2 | c.1023T>C (p.Pro341=) | dbSNP |
| MT | m.5492T>G | CA913179680 | MT-ND2 | c.1023T>G (p.Pro341=) | |
| MT | m.5492T= | CA2499564337 | MT-ND2 | c.1023T= (p.Pro341=) | |
| MT | m.5493T>A | CA414780566 | MT-ND2 | c.1024T>A (p.Phe342Ile) | |
| MT | m.5493T>C | CA414780564 | MT-ND2 | c.1024T>C (p.Phe342Leu) | ClinVar dbSNP |
| MT | m.5493T>G | CA414780568 | MT-ND2 | c.1024T>G (p.Phe342Val) | |
| MT | m.5493T= | CA2499564338 | MT-ND2 | c.1024T= (p.Phe342=) | |
| MT | m.5494T>A | CA414780570 | MT-ND2 | c.1025T>A (p.Phe342Tyr) | |
| MT | m.5494T>C | CA414780573 | MT-ND2 | c.1025T>C (p.Phe342Ser) | dbSNP |
| MT | m.5494T>G | CA414780571 | MT-ND2 | c.1025T>G (p.Phe342Cys) | ClinVar dbSNP |
| MT | m.5494T= | CA2499564339 | MT-ND2 | c.1025T= (p.Phe342=) | |
| MT | m.5495T>A | CA414780575 | MT-ND2 | c.1026T>A (p.Phe342Leu) | |
| MT | m.5495T>C | CA337097156 | MT-ND2 | c.1026T>C (p.Phe342=) | dbSNP |
| MT | m.5495T>G | CA414780578 | MT-ND2 | c.1026T>G (p.Phe342Leu) | |
| MT | m.5495T= | CA2499564340 | MT-ND2 | c.1026T= (p.Phe342=) | |
| MT | m.5496A= | CA2499564341 | MT-ND2 | c.1027A= (p.Ile343=) | |
| MT | m.5496A>C | CA414780580 | MT-ND2 | c.1027A>C (p.Ile343Leu) | |
| MT | m.5496A>G | CA337097158 | MT-ND2 | c.1027A>G (p.Ile343Val) | ClinVar dbSNP |
| MT | m.5496A>T | CA414780583 | MT-ND2 | c.1027A>T (p.Ile343Leu) | |
| MT | m.5497T>A | CA414780585 | MT-ND2 | c.1028T>A (p.Ile343Lys) | |
| MT | m.5497T>C | CA414780587 | MT-ND2 | c.1028T>C (p.Ile343Thr) | |
| MT | m.5497T>G | CA414780589 | MT-ND2 | c.1028T>G (p.Ile343Arg) | |
| MT | m.5497T= | CA2573331247 | MT-ND2 | c.1028T= (p.Ile343=) | |
| MT | m.5498A= | CA2499564342 | MT-ND2 | c.1029A= (p.Ile343=) | |
| MT | m.5498A>C | CA913179682 | MT-ND2 | c.1029A>C (p.Ile343=) | |
| MT | m.5498A>G | CA337097160 | MT-ND2 | c.1029A>G (p.Ile343Met) | dbSNP |
| MT | m.5498A>T | CA913179683 | MT-ND2 | c.1029A>T (p.Ile343=) | |
| MT | m.5499C>A | CA414780594 | MT-ND2 | c.1030C>A (p.Leu344Ile) | |
| MT | m.5499C= | CA2573331248 | MT-ND2 | c.1030C= (p.Leu344=) | |
| MT | m.5499C>G | CA414780592 | MT-ND2 | c.1030C>G (p.Leu344Val) | |
| MT | m.5499C>T | CA913179684 | MT-ND2 | c.1030C>T (p.Leu344=) | |
| MT | m.5500T>A | CA414780595 | MT-ND2 | c.1031T>A (p.Leu344Gln) | |
| MT | m.5500T>C | CA414780598 | MT-ND2 | c.1031T>C (p.Leu344Pro) | |
| MT | m.5500T>G | CA414780600 | MT-ND2 | c.1031T>G (p.Leu344Arg) | |
| MT | m.5500T= | CA2573331249 | MT-ND2 | c.1031T= (p.Leu344=) | |
| MT | m.5501A= | CA2499564343 | MT-ND2 | c.1032A= (p.Leu344=) | |
| MT | m.5501A>C | CA913179689 | MT-ND2 | c.1032A>C (p.Leu344=) | |
| MT | m.5501A>G | CA913179686 | MT-ND2 | c.1032A>G (p.Leu344=) | dbSNP |
| MT | m.5501A>T | CA913179685 | MT-ND2 | c.1032A>T (p.Leu344=) | |
| MT | m.5502A= | CA2499564344 | MT-ND2 | c.1033A= (p.Ile345=) | |
| MT | m.5502A>C | CA414780601 | MT-ND2 | c.1033A>C (p.Ile345Leu) | |
| MT | m.5502A>G | CA414780603 | MT-ND2 | c.1033A>G (p.Ile345Val) | dbSNP |
| MT | m.5502A>T | CA414780605 | MT-ND2 | c.1033A>T (p.Ile345Leu) | |
| MT | m.5503T>A | CA414780607 | MT-ND2 | c.1034T>A (p.Ile345Lys) | |
| MT | m.5503T>C | CA414780609 | MT-ND2 | c.1034T>C (p.Ile345Thr) | dbSNP |