| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| MT | m.5438C>A | CA913179617 | MT-ND2 | c.969C>A (p.Thr323=) | |
| MT | m.5438C= | CA2499564311 | MT-ND2 | c.969C= (p.Thr323=) | |
| MT | m.5438C>G | CA913179616 | MT-ND2 | c.969C>G (p.Thr323=) | |
| MT | m.5438C>T | CA913179614 | MT-ND2 | c.969C>T (p.Thr323=) | dbSNP |
| MT | m.5439C>A | CA337097140 | MT-ND2 | c.970C>A (p.Pro324Thr) | dbSNP |
| MT | m.5439C= | CA2499564312 | MT-ND2 | c.970C= (p.Pro324=) | |
| MT | m.5439C>G | CA414780355 | MT-ND2 | c.970C>G (p.Pro324Ala) | |
| MT | m.5439C>T | CA414780356 | MT-ND2 | c.970C>T (p.Pro324Ser) | |
| MT | m.5440C>A | CA414780359 | MT-ND2 | c.971C>A (p.Pro324Gln) | |
| MT | m.5440C= | CA2573331221 | MT-ND2 | c.971C= (p.Pro324=) | |
| MT | m.5440C>G | CA414780362 | MT-ND2 | c.971C>G (p.Pro324Arg) | |
| MT | m.5440C>T | CA414780361 | MT-ND2 | c.971C>T (p.Pro324Leu) | |
| MT | m.5441A= | CA2499564313 | MT-ND2 | c.972A= (p.Pro324=) | |
| MT | m.5441A>C | CA913179620 | MT-ND2 | c.972A>C (p.Pro324=) | dbSNP |
| MT | m.5441A>G | CA913179619 | MT-ND2 | c.972A>G (p.Pro324=) | dbSNP |
| MT | m.5441A>T | CA913179618 | MT-ND2 | c.972A>T (p.Pro324=) | dbSNP |
| MT | m.5442T>A | CA414780365 | MT-ND2 | c.973T>A (p.Phe325Ile) | |
| MT | m.5442T>C | CA337097142 | MT-ND2 | c.973T>C (p.Phe325Leu) | ClinVar dbSNP |
| MT | m.5442T>G | CA414780367 | MT-ND2 | c.973T>G (p.Phe325Val) | |
| MT | m.5442T= | CA2499564314 | MT-ND2 | c.973T= (p.Phe325=) | |
| MT | m.5443T>A | CA414780370 | MT-ND2 | c.974T>A (p.Phe325Tyr) | |
| MT | m.5443T>C | CA337097144 | MT-ND2 | c.974T>C (p.Phe325Ser) | dbSNP |
| MT | m.5443T>G | CA414780372 | MT-ND2 | c.974T>G (p.Phe325Cys) | |
| MT | m.5443T= | CA2499564315 | MT-ND2 | c.974T= (p.Phe325=) | |
| MT | m.5444C>A | CA414780374 | MT-ND2 | c.975C>A (p.Phe325Leu) | ClinVar dbSNP |
| MT | m.5444C= | CA2499564316 | MT-ND2 | c.975C= (p.Phe325=) | |
| MT | m.5444C>G | CA414780376 | MT-ND2 | c.975C>G (p.Phe325Leu) | |
| MT | m.5444C>T | CA913179622 | MT-ND2 | c.975C>T (p.Phe325=) | dbSNP |
| MT | m.5445C>A | CA414780378 | MT-ND2 | c.976C>A (p.Leu326Ile) | |
| MT | m.5445C= | CA2573331222 | MT-ND2 | c.976C= (p.Leu326=) | |
| MT | m.5445C>G | CA414780380 | MT-ND2 | c.976C>G (p.Leu326Val) | |
| MT | m.5445C>T | CA414780382 | MT-ND2 | c.976C>T (p.Leu326Phe) | |
| MT | m.5446T>A | CA414780384 | MT-ND2 | c.977T>A (p.Leu326His) | |
| MT | m.5446T>C | CA414780387 | MT-ND2 | c.977T>C (p.Leu326Pro) | dbSNP |
| MT | m.5446T>G | CA414780386 | MT-ND2 | c.977T>G (p.Leu326Arg) | |
| MT | m.5446T= | CA2499564317 | MT-ND2 | c.977T= (p.Leu326=) | |
| MT | m.5447C>A | CA913179625 | MT-ND2 | c.978C>A (p.Leu326=) | dbSNP |
| MT | m.5447C= | CA2499564318 | MT-ND2 | c.978C= (p.Leu326=) | |
| MT | m.5447C>G | CA913179624 | MT-ND2 | c.978C>G (p.Leu326=) | |
| MT | m.5447C>T | CA913179626 | MT-ND2 | c.978C>T (p.Leu326=) | |
| MT | m.5448C>A | CA414780390 | MT-ND2 | c.979C>A (p.Pro327Thr) | |
| MT | m.5448C= | CA2573331223 | MT-ND2 | c.979C= (p.Pro327=) | |
| MT | m.5448C>G | CA414780391 | MT-ND2 | c.979C>G (p.Pro327Ala) | |
| MT | m.5448C>T | CA414780393 | MT-ND2 | c.979C>T (p.Pro327Ser) | |
| MT | m.5449C>A | CA414780395 | MT-ND2 | c.980C>A (p.Pro327His) | |
| MT | m.5449C= | CA2573331224 | MT-ND2 | c.980C= (p.Pro327=) | |
| MT | m.5449C>G | CA414780397 | MT-ND2 | c.980C>G (p.Pro327Arg) | |
| MT | m.5449C>T | CA414780399 | MT-ND2 | c.980C>T (p.Pro327Leu) | |
| MT | m.5450C>A | CA913179629 | MT-ND2 | c.981C>A (p.Pro327=) | |
| MT | m.5450C= | CA2499564319 | MT-ND2 | c.981C= (p.Pro327=) |