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.12063C>A | CA414812325 | MT-ND4 | c.1304C>A (p.Thr435Asn) | |
MT | m.12063C= | CA2499567392 | MT-ND4 | c.1304C= (p.Thr435=) | |
MT | m.12063C>G | CA414812327 | MT-ND4 | c.1304C>G (p.Thr435Ser) | |
MT | m.12063C>T | CA414812329 | MT-ND4 | c.1304C>T (p.Thr435Ile) | ClinVar dbSNP |
MT | m.12064C>A | CA913169368 | MT-ND4 | c.1305C>A (p.Thr435=) | |
MT | m.12064C= | CA2499567393 | MT-ND4 | c.1305C= (p.Thr435=) | |
MT | m.12064C>G | CA913169369 | MT-ND4 | c.1305C>G (p.Thr435=) | |
MT | m.12064C>T | CA913169373 | MT-ND4 | c.1305C>T (p.Thr435=) | dbSNP |
MT | m.12065C>A | CA414812331 | MT-ND4 | c.1306C>A (p.Leu436Ile) | |
MT | m.12065C= | CA2573328825 | MT-ND4 | c.1306C= (p.Leu436=) | |
MT | m.12065C>G | CA414812333 | MT-ND4 | c.1306C>G (p.Leu436Val) | |
MT | m.12065C>T | CA414812335 | MT-ND4 | c.1306C>T (p.Leu436Phe) | |
MT | m.12066T>A | CA414812338 | MT-ND4 | c.1307T>A (p.Leu436His) | |
MT | m.12066T>C | CA414812339 | MT-ND4 | c.1307T>C (p.Leu436Pro) | |
MT | m.12066T>G | CA414812341 | MT-ND4 | c.1307T>G (p.Leu436Arg) | |
MT | m.12066T= | CA2573328828 | MT-ND4 | c.1307T= (p.Leu436=) | |
MT | m.12067C>A | CA913169376 | MT-ND4 | c.1308C>A (p.Leu436=) | |
MT | m.12067C= | CA2499567394 | MT-ND4 | c.1308C= (p.Leu436=) | |
MT | m.12067C>G | CA913169375 | MT-ND4 | c.1308C>G (p.Leu436=) | |
MT | m.12067C>T | CA913169374 | MT-ND4 | c.1308C>T (p.Leu436=) | dbSNP |
MT | m.12068A= | CA2499567395 | MT-ND4 | c.1309A= (p.Met437=) | |
MT | m.12068A>C | CA414812345 | MT-ND4 | c.1309A>C (p.Met437Leu) | |
MT | m.12068A>G | CA414812348 | MT-ND4 | c.1309A>G (p.Met437Val) | dbSNP |
MT | m.12068A>T | CA414812344 | MT-ND4 | c.1309A>T (p.Met437Leu) | |
MT | m.12069T>A | CA414812350 | MT-ND4 | c.1310T>A (p.Met437Lys) | |
MT | m.12069T>C | CA414812354 | MT-ND4 | c.1310T>C (p.Met437Thr) | |
MT | m.12069T>G | CA414812351 | MT-ND4 | c.1310T>G (p.Met437Arg) | |
MT | m.12069T= | CA2573328831 | MT-ND4 | c.1310T= (p.Met437=) | |
MT | m.12070G>A | CA414812356 | MT-ND4 | c.1311G>A (p.Met437Ile) | dbSNP |
MT | m.12070G>C | CA414812360 | MT-ND4 | c.1311G>C (p.Met437Ile) | |
MT | m.12070G= | CA2499567396 | MT-ND4 | c.1311G= (p.Met437=) |