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.12092C>A | CA414812460 | MT-ND4 | c.1333C>A (p.Leu445Ile) | ClinVar dbSNP |
MT | m.12092C= | CA2499567408 | MT-ND4 | c.1333C= (p.Leu445=) | |
MT | m.12092C>G | CA414812462 | MT-ND4 | c.1333C>G (p.Leu445Val) | |
MT | m.12092C>T | CA414812463 | MT-ND4 | c.1333C>T (p.Leu445Phe) | ClinVar dbSNP |
MT | m.12093T>A | CA414812466 | MT-ND4 | c.1334T>A (p.Leu445His) | |
MT | m.12093T>C | CA414812468 | MT-ND4 | c.1334T>C (p.Leu445Pro) | |
MT | m.12093T>G | CA414812469 | MT-ND4 | c.1334T>G (p.Leu445Arg) | |
MT | m.12093T= | CA2573328875 | MT-ND4 | c.1334T= (p.Leu445=) | |
MT | m.12094C>A | CA913169407 | MT-ND4 | c.1335C>A (p.Leu445=) | |
MT | m.12094C= | CA2573328878 | MT-ND4 | c.1335C= (p.Leu445=) | |
MT | m.12094C>G | CA913169406 | MT-ND4 | c.1335C>G (p.Leu445=) | |
MT | m.12094C>T | CA913169405 | MT-ND4 | c.1335C>T (p.Leu445=) | |
MT | m.12095C>A | CA414812472 | MT-ND4 | c.1336C>A (p.Leu446Ile) | |
MT | m.12095C= | CA2573328879 | MT-ND4 | c.1336C= (p.Leu446=) | |
MT | m.12095C>G | CA414812475 | MT-ND4 | c.1336C>G (p.Leu446Val) | |
MT | m.12095C>T | CA414812474 | MT-ND4 | c.1336C>T (p.Leu446Phe) | |
MT | m.12096T>A | CA414812478 | MT-ND4 | c.1337T>A (p.Leu446His) | |
MT | m.12096T>C | CA414812482 | MT-ND4 | c.1337T>C (p.Leu446Pro) | |
MT | m.12096T>G | CA414812480 | MT-ND4 | c.1337T>G (p.Leu446Arg) | |
MT | m.12096T= | CA2573328881 | MT-ND4 | c.1337T= (p.Leu446=) | |
MT | m.12097C>A | CA913169409 | MT-ND4 | c.1338C>A (p.Leu446=) | |
MT | m.12097C= | CA2499567409 | MT-ND4 | c.1338C= (p.Leu446=) | |
MT | m.12097C>G | CA913169408 | MT-ND4 | c.1338C>G (p.Leu446=) | |
MT | m.12097C>T | CA337099386 | MT-ND4 | c.1338C>T (p.Leu446=) | dbSNP |
MT | m.12098C>A | CA414812486 | MT-ND4 | c.1339C>A (p.Leu447Ile) | |
MT | m.12098C= | CA2573328884 | MT-ND4 | c.1339C= (p.Leu447=) | |
MT | m.12098C>G | CA414812487 | MT-ND4 | c.1339C>G (p.Leu447Val) | |
MT | m.12098C>T | CA913169410 | MT-ND4 | c.1339C>T (p.Leu447=) | |
MT | m.12099T>A | CA414812489 | MT-ND4 | c.1340T>A (p.Leu447Gln) | |
MT | m.12099T>C | CA414812491 | MT-ND4 | c.1340T>C (p.Leu447Pro) | |
MT | m.12099T>G | CA414812493 | MT-ND4 | c.1340T>G (p.Leu447Arg) |