| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| MT | m.8815_13722del | CA645373338 | ClinVar | ||
| MT | m.13708G>A | CA340935 | MT-ND5 | c.1372G>A (p.Ala458Thr) | ClinVar dbSNP |
| MT | m.13708G>C | CA414819169 | MT-ND5 | c.1372G>C (p.Ala458Pro) | |
| MT | m.13708G= | CA2499568120 | MT-ND5 | c.1372G= (p.Ala458=) | |
| MT | m.13708G>T | CA414819167 | MT-ND5 | c.1372G>T (p.Ala458Ser) | |
| MT | m.13708_13755del | CA2740098359 | MT-ND5 | c.1372_1419del (p.Ala458_Ser473del) | |
| MT | m.13709C>A | CA414819171 | MT-ND5 | c.1373C>A (p.Ala458Glu) | |
| MT | m.13709C= | CA2573325219 | MT-ND5 | c.1373C= (p.Ala458=) | |
| MT | m.13709C>G | CA414819173 | MT-ND5 | c.1373C>G (p.Ala458Gly) | |
| MT | m.13709C>T | CA414819175 | MT-ND5 | c.1373C>T (p.Ala458Val) | |
| MT | m.13709_13713del | CA2740098360 | MT-ND5 | c.1373_1377del (p.Ala458GlyfsTer11) | |
| MT | m.13710A= | CA2499568121 | MT-ND5 | c.1374A= (p.Ala458=) | |
| MT | m.13710A>C | CA337099776 | MT-ND5 | c.1374A>C (p.Ala458=) | dbSNP |
| MT | m.13710A>G | CA645611422 | MT-ND5 | c.1374A>G (p.Ala458=) | dbSNP COSMIC |
| MT | m.13710A>T | CA913171151 | MT-ND5 | c.1374A>T (p.Ala458=) | |
| MT | m.13711G>A | CA337099778 | MT-ND5 | c.1375G>A (p.Ala459Thr) | ClinVar dbSNP COSMIC |
| MT | m.13711G>C | CA414819179 | MT-ND5 | c.1375G>C (p.Ala459Pro) | |
| MT | m.13711G= | CA2499568122 | MT-ND5 | c.1375G= (p.Ala459=) | |
| MT | m.13711G>T | CA414819181 | MT-ND5 | c.1375G>T (p.Ala459Ser) | |
| MT | m.13712C>A | CA414819183 | MT-ND5 | c.1376C>A (p.Ala459Asp) | |
| MT | m.13712C= | CA2499568123 | MT-ND5 | c.1376C= (p.Ala459=) | |
| MT | m.13712C>G | CA414819185 | MT-ND5 | c.1376C>G (p.Ala459Gly) | |
| MT | m.13712C>T | CA414819187 | MT-ND5 | c.1376C>T (p.Ala459Val) | ClinVar dbSNP |
| MT | m.13713C>A | CA16040635 | MT-ND5 | c.1377C>A (p.Ala459=) | ClinVar dbSNP |
| MT | m.13713C= | CA2499568124 | MT-ND5 | c.1377C= (p.Ala459=) | |
| MT | m.13713C>G | CA913171152 | MT-ND5 | c.1377C>G (p.Ala459=) | |
| MT | m.13713C>T | CA913171153 | MT-ND5 | c.1377C>T (p.Ala459=) | dbSNP |
| MT | m.13714G>A | CA414819192 | MT-ND5 | c.1378G>A (p.Gly460Arg) | |
| MT | m.13714G>C | CA414819194 | MT-ND5 | c.1378G>C (p.Gly460Arg) | |
| MT | m.13714G= | CA2573325243 | MT-ND5 | c.1378G= (p.Gly460=) | |
| MT | m.13714G>T | CA414819190 | MT-ND5 | c.1378G>T (p.Gly460Ter) | |
| MT | m.13715G>A | CA414819200 | MT-ND5 | c.1379G>A (p.Gly460Glu) | |
| MT | m.13715G>C | CA414819196 | MT-ND5 | c.1379G>C (p.Gly460Ala) | |
| MT | m.13715G= | CA2573325246 | MT-ND5 | c.1379G= (p.Gly460=) | |
| MT | m.13715G>T | CA414819198 | MT-ND5 | c.1379G>T (p.Gly460Val) | |
| MT | m.13716A= | CA2499568125 | MT-ND5 | c.1380A= (p.Gly460=) | |
| MT | m.13716A>C | CA913171154 | MT-ND5 | c.1380A>C (p.Gly460=) | |
| MT | m.13716A>G | CA913171155 | MT-ND5 | c.1380A>G (p.Gly460=) | dbSNP |
| MT | m.13716A>T | CA913171156 | MT-ND5 | c.1380A>T (p.Gly460=) | |
| MT | m.13716_13720del | CA2740098361 | MT-ND5 | c.1380_1384del (p.Ser461IlefsTer8) | |
| MT | m.13717A= | CA2499568126 | MT-ND5 | c.1381A= (p.Ser461=) | |
| MT | m.13717A>C | CA414819202 | MT-ND5 | c.1381A>C (p.Ser461Arg) | |
| MT | m.13717A>G | CA414819204 | MT-ND5 | c.1381A>G (p.Ser461Gly) | dbSNP |
| MT | m.13717A>T | CA414819206 | MT-ND5 | c.1381A>T (p.Ser461Cys) | |
| MT | m.13718G>A | CA414819208 | MT-ND5 | c.1382G>A (p.Ser461Asn) | |
| MT | m.13718G>C | CA414819210 | MT-ND5 | c.1382G>C (p.Ser461Thr) | dbSNP |
| MT | m.13718G= | CA2499568127 | MT-ND5 | c.1382G= (p.Ser461=) | |
| MT | m.13718G>T | CA414819212 | MT-ND5 | c.1382G>T (p.Ser461Ile) | |
| MT | m.13719C>A | CA414819214 | MT-ND5 | c.1383C>A (p.Ser461Arg) | |
| MT | m.13719C= | CA2499568128 | MT-ND5 | c.1383C= (p.Ser461=) |