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.10779C>A | CA414806819 | MT-ND4 | c.20C>A (p.Pro7Gln) | |
MT | m.10779C= | CA2573326747 | MT-ND4 | c.20C= (p.Pro7=) | |
MT | m.10779C>G | CA414806821 | MT-ND4 | c.20C>G (p.Pro7Arg) | |
MT | m.10779C>T | CA414806823 | MT-ND4 | c.20C>T (p.Pro7Leu) | |
MT | m.10780A= | CA2573326751 | MT-ND4 | c.21A= (p.Pro7=) | |
MT | m.10780A>C | CA913164654 | MT-ND4 | c.21A>C (p.Pro7=) | |
MT | m.10780A>G | CA913164658 | MT-ND4 | c.21A>G (p.Pro7=) | |
MT | m.10780A>T | CA913164656 | MT-ND4 | c.21A>T (p.Pro7=) | |
MT | m.10781A= | CA2573326754 | MT-ND4 | c.22A= (p.Thr8=) | |
MT | m.10781A>C | CA414806824 | MT-ND4 | c.22A>C (p.Thr8Pro) | |
MT | m.10781A>G | CA414806825 | MT-ND4 | c.22A>G (p.Thr8Ala) | |
MT | m.10781A>T | CA414806826 | MT-ND4 | c.22A>T (p.Thr8Ser) | |
MT | m.10782C>A | CA414806834 | MT-ND4 | c.23C>A (p.Thr8Lys) | |
MT | m.10782C= | CA2513690119 | MT-ND4 | c.23C= (p.Thr8=) | |
MT | m.10782C>G | CA414806830 | MT-ND4 | c.23C>G (p.Thr8Arg) | |
MT | m.10782C>T | CA414806832 | MT-ND4 | c.23C>T (p.Thr8Ile) | |
MT | m.10783A= | CA2499566957 | MT-ND4 | c.24A= (p.Thr8=) | |
MT | m.10783A>C | CA337099015 | MT-ND4 | c.24A>C (p.Thr8=) | dbSNP |
MT | m.10783A>G | CA913164666 | MT-ND4 | c.24A>G (p.Thr8=) | |
MT | m.10783A>T | CA913164668 | MT-ND4 | c.24A>T (p.Thr8=) | |
MT | m.10784A= | CA2573326759 | MT-ND4 | c.25A= (p.Ile9=) | |
MT | m.10784A>C | CA414806838 | MT-ND4 | c.25A>C (p.Ile9Leu) | |
MT | m.10784A>G | CA414806840 | MT-ND4 | c.25A>G (p.Ile9Val) | |
MT | m.10784A>T | CA414806842 | MT-ND4 | c.25A>T (p.Ile9Phe) | |
MT | m.10785T>A | CA414806845 | MT-ND4 | c.26T>A (p.Ile9Asn) | |
MT | m.10785T>C | CA414806852 | MT-ND4 | c.26T>C (p.Ile9Thr) | ClinVar dbSNP |
MT | m.10785T>G | CA414806854 | MT-ND4 | c.26T>G (p.Ile9Ser) | |
MT | m.10785T= | CA2499566959 | MT-ND4 | c.26T= (p.Ile9=) | |
MT | m.10786T>A | CA913164685 | MT-ND4 | c.27T>A (p.Ile9=) | |
MT | m.10786T>C | CA913164686 | MT-ND4 | c.27T>C (p.Ile9=) | dbSNP |
MT | m.10786T>G | CA414806856 | MT-ND4 | c.27T>G (p.Ile9Met) |