Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.18222518A>C | CA459877889 | NAT1 | c.471A>C (p.Gly157=) c.657A>C (p.Gly219=) n.823A>C | |
8 | g.18222518A>G | CA459877891 | NAT1 | c.471A>G (p.Gly157=) c.657A>G (p.Gly219=) n.823A>G | |
8 | g.18222518A>T | CA459877892 | NAT1 | c.471A>T (p.Gly157=) c.657A>T (p.Gly219=) n.823A>T | |
8 | g.18222519T>A | CA370445374 | NAT1 | c.472T>A (p.Phe158Ile) c.658T>A (p.Phe220Ile) n.824T>A | |
8 | g.18222519T>C | CA4651420 | NAT1 | c.472T>C (p.Phe158Leu) c.658T>C (p.Phe220Leu) n.824T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.18222519T>G | CA370445375 | NAT1 | c.472T>G (p.Phe158Val) c.658T>G (p.Phe220Val) n.824T>G | |
8 | g.18222519T= | CA1768101192 | NAT1 | c.472T= (p.Phe158=) c.658T= (p.Phe220=) n.824T= | |
8 | g.18222520T>A | CA370445376 | NAT1 | c.473T>A (p.Phe158Tyr) c.659T>A (p.Phe220Tyr) n.825T>A | dbSNP gnomAD v4 |
8 | g.18222520T>C | CA370445377 | NAT1 | c.473T>C (p.Phe158Ser) c.659T>C (p.Phe220Ser) n.825T>C | |
8 | g.18222520T>G | CA370445378 | NAT1 | c.473T>G (p.Phe158Cys) c.659T>G (p.Phe220Cys) n.825T>G | |
8 | g.18222520T= | CA1768101193 | NAT1 | c.473T= (p.Phe158=) c.659T= (p.Phe220=) n.825T= | |
8 | g.18222521C>A | CA370445379 | NAT1 | c.474C>A (p.Phe158Leu) c.660C>A (p.Phe220Leu) n.826C>A | |
8 | g.18222521C= | CA1768101194 | NAT1 | c.474C= (p.Phe158=) c.660C= (p.Phe220=) n.826C= | |
8 | g.18222521C>G | CA370445380 | NAT1 | c.474C>G (p.Phe158Leu) c.660C>G (p.Phe220Leu) n.826C>G | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18222521C>T | CA459877898 | NAT1 | c.474C>T (p.Phe158=) c.660C>T (p.Phe220=) n.826C>T | |
8 | g.18222522T>A | CA370445381 | NAT1 | c.475T>A (p.Trp159Arg) c.661T>A (p.Trp221Arg) n.827T>A | |
8 | g.18222522T>C | CA370445382 | NAT1 | c.475T>C (p.Trp159Arg) c.661T>C (p.Trp221Arg) n.827T>C | dbSNP |
8 | g.18222522T>G | CA370445383 | NAT1 | c.475T>G (p.Trp159Gly) c.661T>G (p.Trp221Gly) n.827T>G | |
8 | g.18222522T= | CA1768101195 | NAT1 | c.475T= (p.Trp159=) c.661T= (p.Trp221=) n.827T= | |
8 | g.18222523G>A | CA370445386 | NAT1 | c.476G>A (p.Trp159Ter) c.662G>A (p.Trp221Ter) n.828G>A | |
8 | g.18222523G>C | CA370445384 | NAT1 | c.476G>C (p.Trp159Ser) c.662G>C (p.Trp221Ser) n.828G>C | |
8 | g.18222523G= | CA1768101196 | NAT1 | c.476G= (p.Trp159=) c.662G= (p.Trp221=) n.828G= | |
8 | g.18222523G>T | CA370445385 | NAT1 | c.476G>T (p.Trp159Leu) c.662G>T (p.Trp221Leu) n.828G>T | dbSNP gnomAD v3 gnomAD v4 |
8 | g.18222524G>A | CA370445387 | NAT1 | c.477G>A (p.Trp159Ter) c.663G>A (p.Trp221Ter) n.829G>A | dbSNP |
8 | g.18222524G>C | CA4651421 | NAT1 | c.477G>C (p.Trp159Cys) c.663G>C (p.Trp221Cys) n.829G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18222524G= | CA1768101197 | NAT1 | c.477G= (p.Trp159=) c.663G= (p.Trp221=) n.829G= | |
8 | g.18222524G>T | CA4651422 | NAT1 | c.477G>T (p.Trp159Cys) c.663G>T (p.Trp221Cys) n.829G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.18222525T>A | CA370445388 | NAT1 | c.478T>A (p.Tyr160Asn) c.664T>A (p.Tyr222Asn) n.830T>A | |
8 | g.18222525T>C | CA370445389 | NAT1 | c.478T>C (p.Tyr160His) c.664T>C (p.Tyr222His) n.830T>C | |
8 | g.18222525T>G | CA370445390 | NAT1 | c.478T>G (p.Tyr160Asp) c.664T>G (p.Tyr222Asp) n.830T>G | |
8 | g.18222526A= | CA1768101198 | NAT1 | c.479A= (p.Tyr160=) c.665A= (p.Tyr222=) n.831A= | |
8 | g.18222526A>C | CA370445391 | NAT1 | c.479A>C (p.Tyr160Ser) c.665A>C (p.Tyr222Ser) n.831A>C | |
8 | g.18222526A>G | CA370445392 | NAT1 | c.479A>G (p.Tyr160Cys) c.665A>G (p.Tyr222Cys) n.831A>G | dbSNP gnomAD v4 |
8 | g.18222526A>T | CA370445393 | NAT1 | c.479A>T (p.Tyr160Phe) c.665A>T (p.Tyr222Phe) n.831A>T | |
8 | g.18222527T>A | CA370445394 | NAT1 | c.480T>A (p.Tyr160Ter) c.666T>A (p.Tyr222Ter) n.832T>A | |
8 | g.18222527T>C | CA459877601 | NAT1 | c.480T>C (p.Tyr160=) c.666T>C (p.Tyr222=) n.832T>C | gnomAD v4 |
8 | g.18222527T>G | CA370445395 | NAT1 | c.480T>G (p.Tyr160Ter) c.666T>G (p.Tyr222Ter) n.832T>G | |
8 | g.18222528C>A | CA370445396 | NAT1 | c.481C>A (p.Leu161Ile) c.667C>A (p.Leu223Ile) n.833C>A | |
8 | g.18222528C>G | CA370445397 | NAT1 | c.481C>G (p.Leu161Val) c.667C>G (p.Leu223Val) n.833C>G | |
8 | g.18222528C>T | CA459877603 | NAT1 | c.481C>T (p.Leu161=) c.667C>T (p.Leu223=) n.833C>T | |
8 | g.18222529T>A | CA370445398 | NAT1 | c.482T>A (p.Leu161Gln) c.668T>A (p.Leu223Gln) n.834T>A | |
8 | g.18222529T>C | CA4651423 | NAT1 | c.482T>C (p.Leu161Pro) c.668T>C (p.Leu223Pro) n.834T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18222529T>G | CA370445399 | NAT1 | c.482T>G (p.Leu161Arg) c.668T>G (p.Leu223Arg) n.834T>G | |
8 | g.18222529T= | CA1768101199 | NAT1 | c.482T= (p.Leu161=) c.668T= (p.Leu223=) n.834T= | |
8 | g.18222530A= | CA1768101200 | NAT1 | c.483A= (p.Leu161=) c.669A= (p.Leu223=) n.835A= | |
8 | g.18222530A>C | CA173180397 | NAT1 | c.483A>C (p.Leu161=) c.669A>C (p.Leu223=) n.835A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18222530A>G | CA459877606 | NAT1 | c.483A>G (p.Leu161=) c.669A>G (p.Leu223=) n.835A>G | |
8 | g.18222530A>T | CA459877605 | NAT1 | c.483A>T (p.Leu161=) c.669A>T (p.Leu223=) n.835A>T | |
8 | g.18222531G>A | CA370445400 | NAT1 | c.484G>A (p.Asp162Asn) c.670G>A (p.Asp224Asn) n.836G>A | |
8 | g.18222531G>C | CA173180399 | NAT1 | c.484G>C (p.Asp162His) c.670G>C (p.Asp224His) n.836G>C | dbSNP |