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.6005_11222del | CA645373331 | ClinVar | ||
MT | m.6470_15588del | CA645373332 | ClinVar | ||
MT | m.7129_13991del | CA645373333 | ClinVar | ||
MT | m.7731_11256del | CA645373334 | 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.10879A= | CA2573326916 | MT-ND4 | c.120A= (p.Leu40=) | |
MT | m.10879A>C | CA913165051 | MT-ND4 | c.120A>C (p.Leu40=) | |
MT | m.10879A>G | CA913165054 | MT-ND4 | c.120A>G (p.Leu40=) | |
MT | m.10879A>T | CA913165059 | MT-ND4 | c.120A>T (p.Leu40=) | |
MT | m.10880T>A | CA414807323 | MT-ND4 | c.121T>A (p.Phe41Ile) | |
MT | m.10880T>C | CA414807325 | MT-ND4 | c.121T>C (p.Phe41Leu) | |
MT | m.10880T>G | CA414807326 | MT-ND4 | c.121T>G (p.Phe41Val) | |
MT | m.10880T= | CA2573326919 | MT-ND4 | c.121T= (p.Phe41=) | |
MT | m.10885del | CA2573105076 | MT-ND4 | c.126del (p.Phe42LeufsTer20) | |
MT | m.10881T>A | CA414807329 | MT-ND4 | c.122T>A (p.Phe41Tyr) | |
MT | m.10881T>C | CA414807331 | MT-ND4 | c.122T>C (p.Phe41Ser) | dbSNP |
MT | m.10881T>G | CA414807332 | MT-ND4 | c.122T>G (p.Phe41Cys) | |
MT | m.10881T= | CA2499567011 | MT-ND4 | c.122T= (p.Phe41=) | |
MT | m.10882T>A | CA414807338 | MT-ND4 | c.123T>A (p.Phe41Leu) | |
MT | m.10882T>C | CA337099039 | MT-ND4 | c.123T>C (p.Phe41=) | dbSNP |
MT | m.10882T>G | CA414807336 | MT-ND4 | c.123T>G (p.Phe41Leu) | |
MT | m.10882T= | CA2499567013 | MT-ND4 | c.123T= (p.Phe41=) | |
MT | m.10883T>A | CA414807341 | MT-ND4 | c.124T>A (p.Phe42Ile) | |
MT | m.10883T>C | CA414807342 | MT-ND4 | c.124T>C (p.Phe42Leu) | dbSNP |
MT | m.10883T>G | CA414807345 | MT-ND4 | c.124T>G (p.Phe42Val) | |
MT | m.10883T= | CA2499567014 | MT-ND4 | c.124T= (p.Phe42=) | |
MT | m.10884T>A | CA414807346 | MT-ND4 | c.125T>A (p.Phe42Tyr) | |
MT | m.10884T>C | CA414807348 | MT-ND4 | c.125T>C (p.Phe42Ser) | |
MT | m.10884T>G | CA414807350 | MT-ND4 | c.125T>G (p.Phe42Cys) | |
MT | m.10884T= | CA2573326923 | MT-ND4 | c.125T= (p.Phe42=) | |
MT | m.10885T>A | CA414807352 | MT-ND4 | c.126T>A (p.Phe42Leu) | |
MT | m.10885T>C | CA913165088 | MT-ND4 | c.126T>C (p.Phe42=) | dbSNP |
MT | m.10885T>G | CA414807354 | MT-ND4 | c.126T>G (p.Phe42Leu) | |
MT | m.10885T= | CA2499567016 | MT-ND4 | c.126T= (p.Phe42=) | |
MT | m.10886A= | CA2573326926 | MT-ND4 | c.127A= (p.Asn43=) | |
MT | m.10886A>C | CA414807356 | MT-ND4 | c.127A>C (p.Asn43His) |