Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.18400672T>A | CA370636377 | NAT2 | c.669T>A (p.Cys223Ter) c.279T>A (p.Cys93Ter) | |
8 | g.18400672T>C | CA459881327 | NAT2 | c.669T>C (p.Cys223=) c.279T>C (p.Cys93=) | |
8 | g.18400672T>G | CA370636378 | NAT2 | c.669T>G (p.Cys223Trp) c.279T>G (p.Cys93Trp) | gnomAD |
8 | g.18400672T= | CA1768219093 | NAT2 | c.669T= (p.Cys223=) c.279T= (p.Cys93=) | |
8 | g.18400673T>A | CA370636379 | NAT2 | c.670T>A (p.Ser224Thr) c.280T>A (p.Ser94Thr) | |
8 | g.18400673T>C | CA370636380 | NAT2 | c.670T>C (p.Ser224Pro) c.280T>C (p.Ser94Pro) | |
8 | g.18400673T>G | CA370636381 | NAT2 | c.670T>G (p.Ser224Ala) c.280T>G (p.Ser94Ala) | |
8 | g.18400674C>A | CA370636382 | NAT2 | c.671C>A (p.Ser224Tyr) c.281C>A (p.Ser94Tyr) | |
8 | g.18400674C>G | CA370636383 | NAT2 | c.671C>G (p.Ser224Cys) c.281C>G (p.Ser94Cys) | |
8 | g.18400674C>T | CA370636384 | NAT2 | c.671C>T (p.Ser224Phe) c.281C>T (p.Ser94Phe) | |
8 | g.18400675C>A | CA459881328 | NAT2 | c.672C>A (p.Ser224=) c.282C>A (p.Ser94=) | |
8 | g.18400675C= | CA1768219094 | NAT2 | c.672C= (p.Ser224=) c.282C= (p.Ser94=) | |
8 | g.18400675C>G | CA459881329 | NAT2 | c.672C>G (p.Ser224=) c.282C>G (p.Ser94=) | |
8 | g.18400675C>T | CA4651673 | NAT2 | c.672C>T (p.Ser224=) c.282C>T (p.Ser94=) | dbSNP ExAC gnomAD |
8 | g.18400676T>A | CA370636385 | NAT2 | c.673T>A (p.Leu225Met) c.283T>A (p.Leu95Met) | |
8 | g.18400676T>C | CA459881330 | NAT2 | c.673T>C (p.Leu225=) c.283T>C (p.Leu95=) | |
8 | g.18400676T>G | CA370636386 | NAT2 | c.673T>G (p.Leu225Val) c.283T>G (p.Leu95Val) | |
8 | g.18400677T>A | CA4651674 | NAT2 | c.674T>A (p.Leu225Ter) c.284T>A (p.Leu95Ter) | dbSNP ExAC gnomAD |
8 | g.18400677T>C | CA370636387 | NAT2 | c.674T>C (p.Leu225Ser) c.284T>C (p.Leu95Ser) | COSMIC |
8 | g.18400677T>G | CA370636388 | NAT2 | c.674T>G (p.Leu225Trp) c.284T>G (p.Leu95Trp) | |
8 | g.18400677T= | CA1768219095 | NAT2 | c.674T= (p.Leu225=) c.284T= (p.Leu95=) | |
8 | g.18400678G>A | CA459881331 | NAT2 | c.675G>A (p.Leu225=) c.285G>A (p.Leu95=) | |
8 | g.18400678G>C | CA370636389 | NAT2 | c.675G>C (p.Leu225Phe) c.285G>C (p.Leu95Phe) | |
8 | g.18400678G>T | CA370636390 | NAT2 | c.675G>T (p.Leu225Phe) c.285G>T (p.Leu95Phe) | |
8 | g.18400679C>A | CA370636391 | NAT2 | c.676C>A (p.Gln226Lys) c.286C>A (p.Gln96Lys) | |
8 | g.18400679C>G | CA370636392 | NAT2 | c.676C>G (p.Gln226Glu) c.286C>G (p.Gln96Glu) | |
8 | g.18400679C>T | CA370636393 | NAT2 | c.676C>T (p.Gln226Ter) c.286C>T (p.Gln96Ter) | |
8 | g.18400680A>C | CA370636394 | NAT2 | c.677A>C (p.Gln226Pro) c.287A>C (p.Gln96Pro) | |
8 | g.18400680A>G | CA370636395 | NAT2 | c.677A>G (p.Gln226Arg) c.287A>G (p.Gln96Arg) | |
8 | g.18400680A>T | CA370636396 | NAT2 | c.677A>T (p.Gln226Leu) c.287A>T (p.Gln96Leu) | |
8 | g.18400681G>A | CA459881332 | NAT2 | c.678G>A (p.Gln226=) c.288G>A (p.Gln96=) | |
8 | g.18400681G>C | CA370636397 | NAT2 | c.678G>C (p.Gln226His) c.288G>C (p.Gln96His) | |
8 | g.18400681G>T | CA370636398 | NAT2 | c.678G>T (p.Gln226His) c.288G>T (p.Gln96His) | |
8 | g.18400682A>C | CA370636400 | NAT2 | c.679A>C (p.Thr227Pro) c.289A>C (p.Thr97Pro) | |
8 | g.18400682A>G | CA370636401 | NAT2 | c.679A>G (p.Thr227Ala) c.289A>G (p.Thr97Ala) | |
8 | g.18400682A>T | CA370636399 | NAT2 | c.679A>T (p.Thr227Ser) c.289A>T (p.Thr97Ser) | |
8 | g.18400683C>A | CA370636402 | NAT2 | c.680C>A (p.Thr227Asn) c.290C>A (p.Thr97Asn) | |
8 | g.18400683C>G | CA370636403 | NAT2 | c.680C>G (p.Thr227Ser) c.290C>G (p.Thr97Ser) | |
8 | g.18400683C>T | CA370636404 | NAT2 | c.680C>T (p.Thr227Ile) c.290C>T (p.Thr97Ile) | |
8 | g.18400684C>A | CA459881334 | NAT2 | c.681C>A (p.Thr227=) c.291C>A (p.Thr97=) | |
8 | g.18400684C= | CA1768219096 | NAT2 | c.681C= (p.Thr227=) c.291C= (p.Thr97=) | |
8 | g.18400684C>G | CA459881333 | NAT2 | c.681C>G (p.Thr227=) c.291C>G (p.Thr97=) | |
8 | g.18400684C>T | CA173519934 | NAT2 | c.681C>T (p.Thr227=) c.291C>T (p.Thr97=) | dbSNP |
8 | g.18400685C>A | CA370636405 | NAT2 | c.682C>A (p.Pro228Thr) c.292C>A (p.Pro98Thr) | |
8 | g.18400685C= | CA1768219097 | NAT2 | c.682C= (p.Pro228=) c.292C= (p.Pro98=) | |
8 | g.18400685C>G | CA370636406 | NAT2 | c.682C>G (p.Pro228Ala) c.292C>G (p.Pro98Ala) | |
8 | g.18400685C>T | CA4651675 | NAT2 | c.682C>T (p.Pro228Ser) c.292C>T (p.Pro98Ser) | dbSNP ExAC gnomAD |
8 | g.18400686C>A | CA370636407 | NAT2 | c.683C>A (p.Pro228Gln) c.293C>A (p.Pro98Gln) | |
8 | g.18400686C= | CA1768219098 | NAT2 | c.683C= (p.Pro228=) c.293C= (p.Pro98=) | |
8 | g.18400686C>G | CA370636408 | NAT2 | c.683C>G (p.Pro228Arg) c.293C>G (p.Pro98Arg) |