Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.3902_3967del | CA2740098101 | MT-ND1 | c.596_661del (p.Asp199_Phe220del) | |
MT | m.3921C>A | CA913176144 | MT-ND1 | c.615C>A (p.Ser205=) | ClinVar dbSNP |
MT | m.3921C= | CA2499563652 | MT-ND1 | c.615C= (p.Ser205=) | |
MT | m.3921C>G | CA913176149 | MT-ND1 | c.615C>G (p.Ser205=) | |
MT | m.3921C>T | CA337096724 | MT-ND1 | c.615C>T (p.Ser205=) | dbSNP |
MT | m.3921_3922insTCCTTCTCCTCCTTCAGCCTGGCTTG | CA2740098102 | MT-ND1 | c.615_616insTCCTTCTCCTCCTTCAGCCTGGCTTG (p.Glu206SerfsTer11) | |
MT | m.3922G>A | CA414773806 | MT-ND1 | c.616G>A (p.Glu206Lys) | |
MT | m.3922G>C | CA414773807 | MT-ND1 | c.616G>C (p.Glu206Gln) | |
MT | m.3922G= | CA2573328882 | MT-ND1 | c.616G= (p.Glu206=) | |
MT | m.3922G>T | CA414773808 | MT-ND1 | c.616G>T (p.Glu206Ter) | |
MT | m.3923A= | CA2573328885 | MT-ND1 | c.617A= (p.Glu206=) | |
MT | m.3923A>C | CA414773809 | MT-ND1 | c.617A>C (p.Glu206Ala) | |
MT | m.3923A>G | CA414773810 | MT-ND1 | c.617A>G (p.Glu206Gly) | |
MT | m.3923A>T | CA414773811 | MT-ND1 | c.617A>T (p.Glu206Val) | |
MT | m.3924A= | CA2573328887 | MT-ND1 | c.618A= (p.Glu206=) | |
MT | m.3924A>C | CA414773813 | MT-ND1 | c.618A>C (p.Glu206Asp) | |
MT | m.3924A>G | CA913176172 | MT-ND1 | c.618A>G (p.Glu206=) | dbSNP |
MT | m.3924A>T | CA414773812 | MT-ND1 | c.618A>T (p.Glu206Asp) | |
MT | m.3925C>A | CA414773814 | MT-ND1 | c.619C>A (p.Leu207Ile) | |
MT | m.3925C= | CA2573328890 | MT-ND1 | c.619C= (p.Leu207=) | |
MT | m.3925C>G | CA414773815 | MT-ND1 | c.619C>G (p.Leu207Val) | |
MT | m.3925C>T | CA913176180 | MT-ND1 | c.619C>T (p.Leu207=) | |
MT | m.3926T>A | CA414773816 | MT-ND1 | c.620T>A (p.Leu207Gln) | |
MT | m.3926T>C | CA414773817 | MT-ND1 | c.620T>C (p.Leu207Pro) | |
MT | m.3926T>G | CA414773818 | MT-ND1 | c.620T>G (p.Leu207Arg) | |
MT | m.3926T= | CA2573328894 | MT-ND1 | c.620T= (p.Leu207=) | |
MT | m.3927A= | CA2499563653 | MT-ND1 | c.621A= (p.Leu207=) | |
MT | m.3927A>C | CA913176193 | MT-ND1 | c.621A>C (p.Leu207=) | |
MT | m.3927A>G | CA337096726 | MT-ND1 | c.621A>G (p.Leu207=) | dbSNP |
MT | m.3927A>T | CA913176190 | MT-ND1 | c.621A>T (p.Leu207=) | |
MT | m.3928G>A | CA414773819 | MT-ND1 | c.622G>A (p.Val208Ile) | COSMIC COSMIC |
MT | m.3928G>C | CA345920 | MT-ND1 | c.622G>C (p.Val208Leu) | ClinVar dbSNP |
MT | m.3928G= | CA2499563654 | MT-ND1 | c.622G= (p.Val208=) | |
MT | m.3928G>T | CA414773820 | MT-ND1 | c.622G>T (p.Val208Phe) | |
MT | m.3929T>A | CA414773821 | MT-ND1 | c.623T>A (p.Val208Asp) | |
MT | m.3929T>C | CA414773822 | MT-ND1 | c.623T>C (p.Val208Ala) | |
MT | m.3929T>G | CA414773823 | MT-ND1 | c.623T>G (p.Val208Gly) | |
MT | m.3929T= | CA2573328902 | MT-ND1 | c.623T= (p.Val208=) | |
MT | m.3930C>A | CA913176226 | MT-ND1 | c.624C>A (p.Val208=) | dbSNP |
MT | m.3930C= | CA2573328905 | MT-ND1 | c.624C= (p.Val208=) | |
MT | m.3930C>G | CA913176223 | MT-ND1 | c.624C>G (p.Val208=) | |
MT | m.3930C>T | CA913176225 | MT-ND1 | c.624C>T (p.Val208=) | |
MT | m.3931T>A | CA414773824 | MT-ND1 | c.625T>A (p.Ser209Thr) | |
MT | m.3931T>C | CA414773826 | MT-ND1 | c.625T>C (p.Ser209Pro) | |
MT | m.3931T>G | CA414773825 | MT-ND1 | c.625T>G (p.Ser209Ala) | |
MT | m.3931T= | CA2573328908 | MT-ND1 | c.625T= (p.Ser209=) | |
MT | m.3932C>A | CA414773827 | MT-ND1 | c.626C>A (p.Ser209Ter) | |
MT | m.3932C= | CA2573328910 | MT-ND1 | c.626C= (p.Ser209=) | |
MT | m.3932C>G | CA414773828 | MT-ND1 | c.626C>G (p.Ser209Ter) | |
MT | m.3932C>T | CA414773829 | MT-ND1 | c.626C>T (p.Ser209Leu) |