Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.4086C>A | CA337096785 | MT-ND1 | c.780C>A (p.Val260=) | |
MT | m.4086C= | CA2499563728 | MT-ND1 | c.780C= (p.Val260=) | |
MT | m.4086C>G | CA337096787 | MT-ND1 | c.780C>G (p.Val260=) | |
MT | m.4086C>T | CA913176903 | MT-ND1 | c.780C>T (p.Val260=) | dbSNP |
MT | m.4087A= | CA2573329231 | MT-ND1 | c.781A= (p.Thr261=) | |
MT | m.4087A>C | CA414774158 | MT-ND1 | c.781A>C (p.Thr261Pro) | |
MT | m.4087A>G | CA414774159 | MT-ND1 | c.781A>G (p.Thr261Ala) | |
MT | m.4087A>T | CA414774160 | MT-ND1 | c.781A>T (p.Thr261Ser) | |
MT | m.4088C>A | CA414774163 | MT-ND1 | c.782C>A (p.Thr261Asn) | |
MT | m.4088C= | CA2573329233 | MT-ND1 | c.782C= (p.Thr261=) | |
MT | m.4088C>G | CA414774161 | MT-ND1 | c.782C>G (p.Thr261Ser) | |
MT | m.4088C>T | CA414774162 | MT-ND1 | c.782C>T (p.Thr261Ile) | |
MT | m.4089C>A | CA913176909 | MT-ND1 | c.783C>A (p.Thr261=) | |
MT | m.4089C= | CA2573329235 | MT-ND1 | c.783C= (p.Thr261=) | |
MT | m.4089C>G | CA913176908 | MT-ND1 | c.783C>G (p.Thr261=) | |
MT | m.4089C>T | CA913176907 | MT-ND1 | c.783C>T (p.Thr261=) | dbSNP |
MT | m.4090A= | CA2573329237 | MT-ND1 | c.784A= (p.Lys262=) | |
MT | m.4090A>C | CA414774164 | MT-ND1 | c.784A>C (p.Lys262Gln) | |
MT | m.4090A>G | CA414774165 | MT-ND1 | c.784A>G (p.Lys262Glu) | |
MT | m.4090A>T | CA414774166 | MT-ND1 | c.784A>T (p.Lys262Ter) | |
MT | m.4091A= | CA2513225506 | MT-ND1 | c.785A= (p.Lys262=) | |
MT | m.4091A>C | CA414774167 | MT-ND1 | c.785A>C (p.Lys262Thr) | |
MT | m.4091A>G | CA414774168 | MT-ND1 | c.785A>G (p.Lys262Arg) | |
MT | m.4091A>T | CA414774169 | MT-ND1 | c.785A>T (p.Lys262Met) | |
MT | m.4092G>A | CA645608455 | MT-ND1 | c.786G>A (p.Lys262=) | dbSNP COSMIC COSMIC |
MT | m.4092G>C | CA414774170 | MT-ND1 | c.786G>C (p.Lys262Asn) | |
MT | m.4092G= | CA2499563729 | MT-ND1 | c.786G= (p.Lys262=) | |
MT | m.4092G>T | CA414774171 | MT-ND1 | c.786G>T (p.Lys262Asn) | |
MT | m.4093A= | CA2499563730 | MT-ND1 | c.787A= (p.Thr263=) | |
MT | m.4093A>C | CA414774172 | MT-ND1 | c.787A>C (p.Thr263Pro) | |
MT | m.4093A>G | CA337096789 | MT-ND1 | c.787A>G (p.Thr263Ala) | ClinVar dbSNP |
MT | m.4093A>T | CA414774173 | MT-ND1 | c.787A>T (p.Thr263Ser) | |
MT | m.4094C>A | CA414774176 | MT-ND1 | c.788C>A (p.Thr263Asn) | |
MT | m.4094C= | CA2499563731 | MT-ND1 | c.788C= (p.Thr263=) | |
MT | m.4094C>G | CA414774175 | MT-ND1 | c.788C>G (p.Thr263Ser) | |
MT | m.4094C>T | CA414774174 | MT-ND1 | c.788C>T (p.Thr263Ile) | ClinVar dbSNP |
MT | m.4095C>A | CA913176918 | MT-ND1 | c.789C>A (p.Thr263=) | |
MT | m.4095C= | CA2573329245 | MT-ND1 | c.789C= (p.Thr263=) | |
MT | m.4095C>G | CA913176919 | MT-ND1 | c.789C>G (p.Thr263=) | |
MT | m.4095C>T | CA913176920 | MT-ND1 | c.789C>T (p.Thr263=) | |
MT | m.4096C>A | CA414774178 | MT-ND1 | c.790C>A (p.Leu264Ile) | |
MT | m.4096C= | CA2573329247 | MT-ND1 | c.790C= (p.Leu264=) | |
MT | m.4096C>G | CA414774177 | MT-ND1 | c.790C>G (p.Leu264Val) | |
MT | m.4096C>T | CA913176921 | MT-ND1 | c.790C>T (p.Leu264=) | |
MT | m.4097T>A | CA414774179 | MT-ND1 | c.791T>A (p.Leu264Gln) | |
MT | m.4097T>C | CA414774180 | MT-ND1 | c.791T>C (p.Leu264Pro) | |
MT | m.4097T>G | CA414774181 | MT-ND1 | c.791T>G (p.Leu264Arg) | |
MT | m.4097T= | CA2573329250 | MT-ND1 | c.791T= (p.Leu264=) | |
MT | m.4098A= | CA2499563732 | MT-ND1 | c.792A= (p.Leu264=) | |
MT | m.4098A>C | CA913176924 | MT-ND1 | c.792A>C (p.Leu264=) |