Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.3902_3967del | CA2740098101 | MT-ND1 | c.596_661del (p.Asp199_Phe220del) | |
MT | m.3936C>A | CA337096729 | MT-ND1 | c.630C>A (p.Gly210=) | dbSNP |
MT | m.3936C= | CA2499563656 | MT-ND1 | c.630C= (p.Gly210=) | |
MT | m.3936C>G | CA913176269 | MT-ND1 | c.630C>G (p.Gly210=) | |
MT | m.3936C>T | CA913176267 | MT-ND1 | c.630C>T (p.Gly210=) | |
MT | m.3937T>A | CA414773838 | MT-ND1 | c.631T>A (p.Phe211Ile) | |
MT | m.3937T>C | CA414773837 | MT-ND1 | c.631T>C (p.Phe211Leu) | ClinVar dbSNP |
MT | m.3937T>G | CA414773836 | MT-ND1 | c.631T>G (p.Phe211Val) | |
MT | m.3937T= | CA2499563657 | MT-ND1 | c.631T= (p.Phe211=) | |
MT | m.3938T>A | CA414773839 | MT-ND1 | c.632T>A (p.Phe211Tyr) | |
MT | m.3938T>C | CA414773840 | MT-ND1 | c.632T>C (p.Phe211Ser) | |
MT | m.3938T>G | CA414773841 | MT-ND1 | c.632T>G (p.Phe211Cys) | |
MT | m.3938T= | CA2573328924 | MT-ND1 | c.632T= (p.Phe211=) | |
MT | m.3939C>A | CA414773842 | MT-ND1 | c.633C>A (p.Phe211Leu) | |
MT | m.3939C= | CA2499563658 | MT-ND1 | c.633C= (p.Phe211=) | |
MT | m.3939C>G | CA414773843 | MT-ND1 | c.633C>G (p.Phe211Leu) | |
MT | m.3939C>T | CA913176284 | MT-ND1 | c.633C>T (p.Phe211=) | dbSNP |
MT | m.3940A= | CA2573328929 | MT-ND1 | c.634A= (p.Asn212=) | |
MT | m.3940A>C | CA414773844 | MT-ND1 | c.634A>C (p.Asn212His) | |
MT | m.3940A>G | CA414773845 | MT-ND1 | c.634A>G (p.Asn212Asp) | |
MT | m.3940A>T | CA414773846 | MT-ND1 | c.634A>T (p.Asn212Tyr) | |
MT | m.3941A= | CA2573328931 | MT-ND1 | c.635A= (p.Asn212=) | |
MT | m.3941A>C | CA414773847 | MT-ND1 | c.635A>C (p.Asn212Thr) | |
MT | m.3941A>G | CA414773848 | MT-ND1 | c.635A>G (p.Asn212Ser) | |
MT | m.3941A>T | CA414773849 | MT-ND1 | c.635A>T (p.Asn212Ile) | |
MT | m.3942C>A | CA414773851 | MT-ND1 | c.636C>A (p.Asn212Lys) | |
MT | m.3942C= | CA2573328935 | MT-ND1 | c.636C= (p.Asn212=) | |
MT | m.3942C>G | CA414773850 | MT-ND1 | c.636C>G (p.Asn212Lys) | |
MT | m.3942C>T | CA913176295 | MT-ND1 | c.636C>T (p.Asn212=) | |
MT | m.3943A= | CA2499563659 | MT-ND1 | c.637A= (p.Ile213=) | |
MT | m.3943A>C | CA414773852 | MT-ND1 | c.637A>C (p.Ile213Leu) | |
MT | m.3943A>G | CA337096731 | MT-ND1 | c.637A>G (p.Ile213Val) | ClinVar dbSNP |
MT | m.3943A>T | CA414773853 | MT-ND1 | c.637A>T (p.Ile213Phe) | |
MT | m.3944T>A | CA414773854 | MT-ND1 | c.638T>A (p.Ile213Asn) | |
MT | m.3944T>C | CA414773855 | MT-ND1 | c.638T>C (p.Ile213Thr) | dbSNP |
MT | m.3944T>G | CA414773856 | MT-ND1 | c.638T>G (p.Ile213Ser) | |
MT | m.3944T= | CA2499563660 | MT-ND1 | c.638T= (p.Ile213=) | |
MT | m.3945C>A | CA913176322 | MT-ND1 | c.639C>A (p.Ile213=) | |
MT | m.3945C= | CA2499563661 | MT-ND1 | c.639C= (p.Ile213=) | |
MT | m.3945C>G | CA414773857 | MT-ND1 | c.639C>G (p.Ile213Met) | |
MT | m.3945C>T | CA913176319 | MT-ND1 | c.639C>T (p.Ile213=) | dbSNP |
MT | m.3946G>A | CA254862 | MT-ND1 | c.640G>A (p.Glu214Lys) | ClinVar dbSNP COSMIC COSMIC |
MT | m.3946G>C | CA414773858 | MT-ND1 | c.640G>C (p.Glu214Gln) | |
MT | m.3946G= | CA2499563662 | MT-ND1 | c.640G= (p.Glu214=) | |
MT | m.3946G>T | CA414773859 | MT-ND1 | c.640G>T (p.Glu214Ter) | |
MT | m.3947A= | CA2573328944 | MT-ND1 | c.641A= (p.Glu214=) | |
MT | m.3947A>C | CA414773860 | MT-ND1 | c.641A>C (p.Glu214Ala) | |
MT | m.3947A>G | CA414773861 | MT-ND1 | c.641A>G (p.Glu214Gly) | |
MT | m.3947A>T | CA414773862 | MT-ND1 | c.641A>T (p.Glu214Val) | |
MT | m.3948A= | CA2499563663 | MT-ND1 | c.642A= (p.Glu214=) |