| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| MT | m.5774_14768del | CA2580610836 | |||
| MT | m.5780_14107del | CA2580610932 | |||
| MT | m.5782_13922del | CA250413 | ClinVar | ||
| MT | m.5788_13923del | CA2580618295 | |||
| MT | m.5794_14876del | CA250414 | ClinVar | ||
| MT | m.6470_15588del | CA645373332 | ClinVar | ||
| MT | m.7129_13991del | CA645373333 | ClinVar | ||
| MT | m.8815_13722del | CA645373338 | ClinVar | ||
| MT | m.8839_14895del | CA645373339 | ClinVar | ||
| MT | m.9062_16052del | CA2580618296 | |||
| MT | m.10106_15067del | CA645373340 | ClinVar | ||
| MT | m.10775_14941del | CA2740090229 | ClinVar | ||
| MT | m.10950_15540del | CA2580102079 | ClinVar | ||
| MT | m.11263_15374del | CA645373341 | ClinVar | ||
| MT | m.12114_14420del | CA645373342 | ClinVar | ||
| MT | m.13620_13622del | CA2573105290 | MT-ND5 | c.1284_1286del (p.Leu429del) | |
| MT | m.13620T>A | CA913171087 | MT-ND5 | c.1284T>A (p.Leu428=) | |
| MT | m.13620T>C | CA913171085 | MT-ND5 | c.1284T>C (p.Leu428=) | dbSNP |
| MT | m.13620T>G | CA913171086 | MT-ND5 | c.1284T>G (p.Leu428=) | |
| MT | m.13620T= | CA2499568082 | MT-ND5 | c.1284T= (p.Leu428=) | |
| MT | m.13621C>A | CA414818792 | MT-ND5 | c.1285C>A (p.Leu429Ile) | |
| MT | m.13621C= | CA2573324903 | MT-ND5 | c.1285C= (p.Leu429=) | |
| MT | m.13621C>G | CA414818794 | MT-ND5 | c.1285C>G (p.Leu429Val) | |
| MT | m.13621C>T | CA414818796 | MT-ND5 | c.1285C>T (p.Leu429Phe) | |
| MT | m.13622T>A | CA414818798 | MT-ND5 | c.1286T>A (p.Leu429His) | |
| MT | m.13622T>C | CA414818803 | MT-ND5 | c.1286T>C (p.Leu429Pro) | |
| MT | m.13622T>G | CA414818800 | MT-ND5 | c.1286T>G (p.Leu429Arg) | |
| MT | m.13622T= | CA2573324908 | MT-ND5 | c.1286T= (p.Leu429=) | |
| MT | m.13623C>A | CA913171090 | MT-ND5 | c.1287C>A (p.Leu429=) | |
| MT | m.13623C= | CA2499568083 | MT-ND5 | c.1287C= (p.Leu429=) | |
| MT | m.13623C>G | CA913171089 | MT-ND5 | c.1287C>G (p.Leu429=) | dbSNP |
| MT | m.13623C>T | CA913171088 | MT-ND5 | c.1287C>T (p.Leu429=) | dbSNP |
| MT | m.13624A= | CA2573324914 | MT-ND5 | c.1288A= (p.Thr430=) | |
| MT | m.13624A>C | CA414818805 | MT-ND5 | c.1288A>C (p.Thr430Pro) | |
| MT | m.13624A>G | CA414818806 | MT-ND5 | c.1288A>G (p.Thr430Ala) | |
| MT | m.13624A>T | CA414818808 | MT-ND5 | c.1288A>T (p.Thr430Ser) | |
| MT | m.13625C>A | CA414818810 | MT-ND5 | c.1289C>A (p.Thr430Asn) | |
| MT | m.13625C= | CA2573324918 | MT-ND5 | c.1289C= (p.Thr430=) | |
| MT | m.13625C>G | CA414818811 | MT-ND5 | c.1289C>G (p.Thr430Ser) | |
| MT | m.13625C>T | CA414818812 | MT-ND5 | c.1289C>T (p.Thr430Ile) | |
| MT | m.13626C>A | CA913171092 | MT-ND5 | c.1290C>A (p.Thr430=) | |
| MT | m.13626C= | CA2499568084 | MT-ND5 | c.1290C= (p.Thr430=) | |
| MT | m.13626C>G | CA913171091 | MT-ND5 | c.1290C>G (p.Thr430=) | |
| MT | m.13626C>T | CA337099756 | MT-ND5 | c.1290C>T (p.Thr430=) | dbSNP |
| MT | m.13627C>A | CA414818815 | MT-ND5 | c.1291C>A (p.Leu431Ile) | |
| MT | m.13627C= | CA2499568085 | MT-ND5 | c.1291C= (p.Leu431=) | |
| MT | m.13627C>G | CA414818816 | MT-ND5 | c.1291C>G (p.Leu431Val) | |
| MT | m.13627C>T | CA337099759 | MT-ND5 | c.1291C>T (p.Leu431=) | dbSNP |
| MT | m.13628T>A | CA414818820 | MT-ND5 | c.1292T>A (p.Leu431Gln) | |
| MT | m.13628T>C | CA414818821 | MT-ND5 | c.1292T>C (p.Leu431Pro) |