| 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.8290_13040del | CA645373335 | ClinVar | ||
| MT | m.8350_13450del | CA915952048 | ClinVar | ||
| MT | m.8483_13459del | CA645373336 | ClinVar | ||
| MT | m.8480_13440del | CA915952050 | ClinVar | ||
| MT | m.8587_12967del | CA645373337 | 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.11947A= | CA2499567343 | MT-ND4 | c.1188A= (p.Thr396=) | |
| MT | m.11947A>C | CA913169190 | MT-ND4 | c.1188A>C (p.Thr396=) | |
| MT | m.11947A>G | CA337099354 | MT-ND4 | c.1188A>G (p.Thr396=) | dbSNP |
| MT | m.11947A>T | CA913169191 | MT-ND4 | c.1188A>T (p.Thr396=) | |
| MT | m.11948G>A | CA414811804 | MT-ND4 | c.1189G>A (p.Gly397Arg) | COSMIC |
| MT | m.11948G>C | CA414811806 | MT-ND4 | c.1189G>C (p.Gly397Arg) | |
| MT | m.11948G= | CA2573328597 | MT-ND4 | c.1189G= (p.Gly397=) | |
| MT | m.11948G>T | CA414811808 | MT-ND4 | c.1189G>T (p.Gly397Ter) | |
| MT | m.11949G>A | CA414811810 | MT-ND4 | c.1190G>A (p.Gly397Glu) | |
| MT | m.11949G>C | CA414811812 | MT-ND4 | c.1190G>C (p.Gly397Ala) | |
| MT | m.11949G= | CA2573328598 | MT-ND4 | c.1190G= (p.Gly397=) | |
| MT | m.11949G>T | CA414811814 | MT-ND4 | c.1190G>T (p.Gly397Val) | |
| MT | m.11950A= | CA2499567344 | MT-ND4 | c.1191A= (p.Gly397=) | |
| MT | m.11950A>C | CA913169192 | MT-ND4 | c.1191A>C (p.Gly397=) | |
| MT | m.11950A>G | CA913169193 | MT-ND4 | c.1191A>G (p.Gly397=) | dbSNP |
| MT | m.11950A>T | CA913169194 | MT-ND4 | c.1191A>T (p.Gly397=) | |
| MT | m.11951C>A | CA414811820 | MT-ND4 | c.1192C>A (p.Leu398Ile) | |
| MT | m.11951C= | CA2573328602 | MT-ND4 | c.1192C= (p.Leu398=) | |
| MT | m.11951C>G | CA414811818 | MT-ND4 | c.1192C>G (p.Leu398Val) | |
| MT | m.11951C>T | CA414811816 | MT-ND4 | c.1192C>T (p.Leu398Phe) | |
| MT | m.11952T>A | CA414811822 | MT-ND4 | c.1193T>A (p.Leu398His) | |
| MT | m.11952T>C | CA414811824 | MT-ND4 | c.1193T>C (p.Leu398Pro) | |
| MT | m.11952T>G | CA414811826 | MT-ND4 | c.1193T>G (p.Leu398Arg) | |
| MT | m.11952T= | CA2573328605 | MT-ND4 | c.1193T= (p.Leu398=) | |
| MT | m.11953C>A | CA913169200 | MT-ND4 | c.1194C>A (p.Leu398=) | |
| MT | m.11953C= | CA2573328608 | MT-ND4 | c.1194C= (p.Leu398=) | |
| MT | m.11953C>G | CA913169198 | MT-ND4 | c.1194C>G (p.Leu398=) | |
| MT | m.11953C>T | CA913169199 | MT-ND4 | c.1194C>T (p.Leu398=) | dbSNP |
| MT | m.11954A= | CA2573328611 | MT-ND4 | c.1195A= (p.Asn399=) | |
| MT | m.11954A>C | CA414811829 | MT-ND4 | c.1195A>C (p.Asn399His) | |
| MT | m.11954A>G | CA414811830 | MT-ND4 | c.1195A>G (p.Asn399Asp) |