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.11696G>A | CA120635 | MT-ND4 | c.937G>A (p.Val313Ile) | ClinVar dbSNP |
MT | m.11696G>C | CA414810758 | MT-ND4 | c.937G>C (p.Val313Leu) | |
MT | m.11696G= | CA2499567247 | MT-ND4 | c.937G= (p.Val313=) | |
MT | m.11696G>T | CA414810759 | MT-ND4 | c.937G>T (p.Val313Phe) | |
MT | m.11697T>A | CA414810760 | MT-ND4 | c.938T>A (p.Val313Asp) | |
MT | m.11697T>C | CA414810761 | MT-ND4 | c.938T>C (p.Val313Ala) | |
MT | m.11697T>G | CA414810762 | MT-ND4 | c.938T>G (p.Val313Gly) | |
MT | m.11697T= | CA2573328232 | MT-ND4 | c.938T= (p.Val313=) | |
MT | m.11698C>A | CA913168257 | MT-ND4 | c.939C>A (p.Val313=) | |
MT | m.11698C= | CA2499567248 | MT-ND4 | c.939C= (p.Val313=) | |
MT | m.11698C>G | CA913168255 | MT-ND4 | c.939C>G (p.Val313=) | dbSNP |
MT | m.11698C>T | CA913168253 | MT-ND4 | c.939C>T (p.Val313=) | |
MT | m.11699A= | CA2573328234 | MT-ND4 | c.940A= (p.Ile314=) | |
MT | m.11699A>C | CA414810763 | MT-ND4 | c.940A>C (p.Ile314Leu) | |
MT | m.11699A>G | CA414810764 | MT-ND4 | c.940A>G (p.Ile314Val) | |
MT | m.11699A>T | CA414810765 | MT-ND4 | c.940A>T (p.Ile314Phe) | |
MT | m.11700T>A | CA414810766 | MT-ND4 | c.941T>A (p.Ile314Asn) | |
MT | m.11700T>C | CA414810768 | MT-ND4 | c.941T>C (p.Ile314Thr) | |
MT | m.11700T>G | CA414810767 | MT-ND4 | c.941T>G (p.Ile314Ser) | |
MT | m.11700T= | CA2573328237 | MT-ND4 | c.941T= (p.Ile314=) | |
MT | m.11701T>A | CA913168277 | MT-ND4 | c.942T>A (p.Ile314=) | |
MT | m.11701T>C | CA913168278 | MT-ND4 | c.942T>C (p.Ile314=) | dbSNP |
MT | m.11701T>G | CA414810769 | MT-ND4 | c.942T>G (p.Ile314Met) | |
MT | m.11701T= | CA2499567249 | MT-ND4 | c.942T= (p.Ile314=) | |
MT | m.11702C>A | CA414810770 | MT-ND4 | c.943C>A (p.Leu315Ile) | |
MT | m.11702C= | CA2573328240 | MT-ND4 | c.943C= (p.Leu315=) | |
MT | m.11702C>G | CA414810771 | MT-ND4 | c.943C>G (p.Leu315Val) | |
MT | m.11702C>T | CA414810772 | MT-ND4 | c.943C>T (p.Leu315Phe) | |
MT | m.11703T>A | CA414810773 | MT-ND4 | c.944T>A (p.Leu315His) | |
MT | m.11703T>C | CA414810774 | MT-ND4 | c.944T>C (p.Leu315Pro) | |
MT | m.11703T>G | CA414810775 | MT-ND4 | c.944T>G (p.Leu315Arg) |