Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.4768_4769delinsCG | CA915952201 | MT-ND2 | c.299_300delinsCG (p.Ile100Thr) | ClinVar dbSNP |
MT | m.4768_4769delinsTA | CA2499564013 | MT-ND2 | c.299_300delinsTA (p.Ile100=) | |
MT | m.4769A= | CA2499564014 | MT-ND2 | c.300A= (p.Ile100=) | |
MT | m.4769A>C | CA913178684 | MT-ND2 | c.300A>C (p.Ile100=) | |
MT | m.4769A>G | CA337096951 | MT-ND2 | c.300A>G (p.Ile100Met) | ClinVar dbSNP |
MT | m.4769A>T | CA913178685 | MT-ND2 | c.300A>T (p.Ile100=) | |
MT | m.4770G>A | CA414775706 | MT-ND2 | c.301G>A (p.Ala101Thr) | ClinVar dbSNP |
MT | m.4770G>C | CA414775708 | MT-ND2 | c.301G>C (p.Ala101Pro) | |
MT | m.4770G= | CA2499564015 | MT-ND2 | c.301G= (p.Ala101=) | |
MT | m.4770G>T | CA414775710 | MT-ND2 | c.301G>T (p.Ala101Ser) | |
MT | m.4771C>A | CA414775716 | MT-ND2 | c.302C>A (p.Ala101Asp) | |
MT | m.4771C= | CA2573330449 | MT-ND2 | c.302C= (p.Ala101=) | |
MT | m.4771C>G | CA414775712 | MT-ND2 | c.302C>G (p.Ala101Gly) | |
MT | m.4771C>T | CA414775714 | MT-ND2 | c.302C>T (p.Ala101Val) | |
MT | m.4772T>A | CA337096953 | MT-ND2 | c.303T>A (p.Ala101=) | |
MT | m.4772T>C | CA913178687 | MT-ND2 | c.303T>C (p.Ala101=) | dbSNP |
MT | m.4772T>G | CA337096955 | MT-ND2 | c.303T>G (p.Ala101=) | |
MT | m.4772T= | CA2499564016 | MT-ND2 | c.303T= (p.Ala101=) | |
MT | m.4773A= | CA2573330463 | MT-ND2 | c.304A= (p.Ile102=) | |
MT | m.4773A>C | CA414775720 | MT-ND2 | c.304A>C (p.Ile102Leu) | |
MT | m.4773A>G | CA414775724 | MT-ND2 | c.304A>G (p.Ile102Val) | |
MT | m.4773A>T | CA414775722 | MT-ND2 | c.304A>T (p.Ile102Leu) | |
MT | m.4774T>A | CA414775726 | MT-ND2 | c.305T>A (p.Ile102Lys) | |
MT | m.4774T>C | CA414775729 | MT-ND2 | c.305T>C (p.Ile102Thr) | |
MT | m.4774T>G | CA414775727 | MT-ND2 | c.305T>G (p.Ile102Arg) | |
MT | m.4774T= | CA2573330469 | MT-ND2 | c.305T= (p.Ile102=) | |
MT | m.4775A= | CA2499564017 | MT-ND2 | c.306A= (p.Ile102=) | |
MT | m.4775A>C | CA913178688 | MT-ND2 | c.306A>C (p.Ile102=) | |
MT | m.4775A>G | CA414775732 | MT-ND2 | c.306A>G (p.Ile102Met) | dbSNP |
MT | m.4775A>T | CA913178689 | MT-ND2 | c.306A>T (p.Ile102=) | |
MT | m.4776G>A | CA414775733 | MT-ND2 | c.307G>A (p.Ala103Thr) | ClinVar dbSNP |
MT | m.4776G>C | CA414775735 | MT-ND2 | c.307G>C (p.Ala103Pro) | |
MT | m.4776G= | CA2499564018 | MT-ND2 | c.307G= (p.Ala103=) | |
MT | m.4776G>T | CA414775737 | MT-ND2 | c.307G>T (p.Ala103Ser) | |
MT | m.4777C>A | CA414775739 | MT-ND2 | c.308C>A (p.Ala103Glu) | |
MT | m.4777C= | CA2573330476 | MT-ND2 | c.308C= (p.Ala103=) | |
MT | m.4777C>G | CA414775740 | MT-ND2 | c.308C>G (p.Ala103Gly) | |
MT | m.4777C>T | CA414775742 | MT-ND2 | c.308C>T (p.Ala103Val) | |
MT | m.4778A= | CA2499564019 | MT-ND2 | c.309A= (p.Ala103=) | |
MT | m.4778A>C | CA913178692 | MT-ND2 | c.309A>C (p.Ala103=) | |
MT | m.4778A>G | CA913178693 | MT-ND2 | c.309A>G (p.Ala103=) | dbSNP |
MT | m.4778A>T | CA913178694 | MT-ND2 | c.309A>T (p.Ala103=) | |
MT | m.4779A= | CA2573330480 | MT-ND2 | c.310A= (p.Ile104=) | |
MT | m.4779A>C | CA414775744 | MT-ND2 | c.310A>C (p.Ile104Leu) | |
MT | m.4779A>G | CA414775746 | MT-ND2 | c.310A>G (p.Ile104Val) | |
MT | m.4779A>T | CA414775747 | MT-ND2 | c.310A>T (p.Ile104Leu) | |
MT | m.4780T>A | CA414775753 | MT-ND2 | c.311T>A (p.Ile104Lys) | |
MT | m.4780T>C | CA414775749 | MT-ND2 | c.311T>C (p.Ile104Thr) | dbSNP |
MT | m.4780T>G | CA414775751 | MT-ND2 | c.311T>G (p.Ile104Arg) | |
MT | m.4780T= | CA2499564020 | MT-ND2 | c.311T= (p.Ile104=) |