| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.40845362C>A | CA405962100 | CYP2A6 | c.1093G>T (p.Val365Leu) n.944G>T c.119+43947C>A | gnomAD v4 |
| 19 | g.40845362C= | CA2336177282 | CYP2A6 | c.1093G= (p.Val365=) n.944G= c.119+43947C= | |
| 19 | g.40845362C>G | CA405962104 | CYP2A6 | c.1093G>C (p.Val365Leu) n.944G>C c.119+43947C>G | |
| 19 | g.40845362C>T | CA9452789 | CYP2A6 | c.1093G>A (p.Val365Met) n.944G>A c.119+43947C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.40845363G>A | CA9452790 | CYP2A6 | c.1092C>T (p.Asp364=) n.943C>T c.119+43948G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.40845363G>C | CA405962117 | CYP2A6 | c.1092C>G (p.Asp364Glu) n.943C>G c.119+43948G>C | |
| 19 | g.40845363G= | CA2336177283 | CYP2A6 | c.1092C= (p.Asp364=) n.943C= c.119+43948G= | |
| 19 | g.40845363G>T | CA405962118 | CYP2A6 | c.1092C>A (p.Asp364Glu) n.943C>A c.119+43948G>T | dbSNP gnomAD v4 |
| 19 | g.40845364T>A | CA405962120 | CYP2A6 | c.1091A>T (p.Asp364Val) n.942A>T c.119+43949T>A | |
| 19 | g.40845364T>C | CA405962123 | CYP2A6 | c.1091A>G (p.Asp364Gly) n.942A>G c.119+43949T>C | |
| 19 | g.40845364T>G | CA405962125 | CYP2A6 | c.1091A>C (p.Asp364Ala) n.942A>C c.119+43949T>G | COSMIC |
| 19 | g.40845365C>A | CA405962131 | CYP2A6 | c.1090G>T (p.Asp364Tyr) n.941G>T c.119+43950C>A | |
| 19 | g.40845365C= | CA2336177284 | CYP2A6 | c.1090G= (p.Asp364=) n.941G= c.119+43950C= | |
| 19 | g.40845365C>G | CA405962133 | CYP2A6 | c.1090G>C (p.Asp364His) n.941G>C c.119+43950C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.40845365C>T | CA9452791 | CYP2A6 | c.1090G>A (p.Asp364Asn) n.941G>A c.119+43950C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.40845366T>A | CA507688327 | CYP2A6 | c.1089A>T (p.Gly363=) n.940A>T c.119+43951T>A | |
| 19 | g.40845366T>C | CA507688326 | CYP2A6 | c.1089A>G (p.Gly363=) n.940A>G c.119+43951T>C | |
| 19 | g.40845366T>G | CA507688325 | CYP2A6 | c.1089A>C (p.Gly363=) n.940A>C c.119+43951T>G | |
| 19 | g.40845367C>A | CA405962144 | CYP2A6 | c.1088G>T (p.Gly363Val) n.939G>T c.119+43952C>A | |
| 19 | g.40845367C>G | CA405962140 | CYP2A6 | c.1088G>C (p.Gly363Ala) n.939G>C c.119+43952C>G | |
| 19 | g.40845367C>T | CA405962143 | CYP2A6 | c.1088G>A (p.Gly363Glu) n.939G>A c.119+43952C>T | |
| 19 | g.40845368C>A | CA405962145 | CYP2A6 | c.1087G>T (p.Gly363Ter) n.938G>T c.119+43953C>A | |
| 19 | g.40845368C>G | CA405962146 | CYP2A6 | c.1087G>C (p.Gly363Arg) n.938G>C c.119+43953C>G | |
| 19 | g.40845368C>T | CA405962148 | CYP2A6 | c.1087G>A (p.Gly363Arg) n.938G>A c.119+43953C>T | gnomAD v4 |
| 19 | g.40845369A>C | CA405962152 | CYP2A6 | c.1086T>G (p.Phe362Leu) n.937T>G c.119+43954A>C | |
| 19 | g.40845369A>G | CA507688334 | CYP2A6 | c.1086T>C (p.Phe362=) n.937T>C c.119+43954A>G | |
| 19 | g.40845369A>T | CA405962154 | CYP2A6 | c.1086T>A (p.Phe362Leu) n.937T>A c.119+43954A>T | |
| 19 | g.40845370A= | CA2336177285 | CYP2A6 | c.1085T= (p.Phe362=) n.936T= c.119+43955A= | |
| 19 | g.40845370A>C | CA405962158 | CYP2A6 | c.1085T>G (p.Phe362Cys) n.936T>G c.119+43955A>C | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.40845370A>G | CA9452792 | CYP2A6 | c.1085T>C (p.Phe362Ser) n.936T>C c.119+43955A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.40845370A>T | CA405962165 | CYP2A6 | c.1085T>A (p.Phe362Tyr) n.936T>A c.119+43955A>T | |
| 19 | g.40845371A>C | CA405962168 | CYP2A6 | c.1084T>G (p.Phe362Val) n.935T>G c.119+43956A>C | |
| 19 | g.40845371A>G | CA405962169 | CYP2A6 | c.1084T>C (p.Phe362Leu) n.935T>C c.119+43956A>G | |
| 19 | g.40845371A>T | CA405962171 | CYP2A6 | c.1084T>A (p.Phe362Ile) n.935T>A c.119+43956A>T | |
| 19 | g.40845372T>A | CA405962174 | CYP2A6 | c.1083A>T (p.Arg361Ser) n.934A>T c.119+43957T>A | gnomAD v4 |
| 19 | g.40845372T>C | CA507688344 | CYP2A6 | c.1083A>G (p.Arg361=) n.934A>G c.119+43957T>C | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.40845372T>G | CA405962172 | CYP2A6 | c.1083A>C (p.Arg361Ser) n.934A>C c.119+43957T>G | |
| 19 | g.40845372T= | CA2336177286 | CYP2A6 | c.1083A= (p.Arg361=) n.934A= c.119+43957T= | |
| 19 | g.40845373C>A | CA405962176 | CYP2A6 | c.1082G>T (p.Arg361Ile) n.933G>T c.119+43958C>A | dbSNP |
| 19 | g.40845373C= | CA2336177287 | CYP2A6 | c.1082G= (p.Arg361=) n.933G= c.119+43958C= | |
| 19 | g.40845373C>G | CA405962178 | CYP2A6 | c.1082G>C (p.Arg361Thr) n.933G>C c.119+43958C>G | |
| 19 | g.40845373C>T | CA405962177 | CYP2A6 | c.1082G>A (p.Arg361Lys) n.933G>A c.119+43958C>T | |
| 19 | g.40845374T>A | CA405962179 | CYP2A6 | c.1081A>T (p.Arg361Ter) n.932A>T c.119+43959T>A | |
| 19 | g.40845374T>C | CA405962180 | CYP2A6 | c.1081A>G (p.Arg361Gly) n.932A>G c.119+43959T>C | |
| 19 | g.40845374T>G | CA507688347 | CYP2A6 | c.1081A>C (p.Arg361=) n.932A>C c.119+43959T>G | |
| 19 | g.40845375T>A | CA405962183 | CYP2A6 | c.1080A>T (p.Gln360His) n.931A>T c.119+43960T>A | |
| 19 | g.40845375T>C | CA507688351 | CYP2A6 | c.1080A>G (p.Gln360=) n.931A>G c.119+43960T>C | |
| 19 | g.40845375T>G | CA405962185 | CYP2A6 | c.1080A>C (p.Gln360His) n.931A>C c.119+43960T>G | |
| 19 | g.40845376T>A | CA405962188 | CYP2A6 | c.1079A>T (p.Gln360Leu) n.930A>T c.119+43961T>A | |
| 19 | g.40845376T>C | CA405962189 | CYP2A6 | c.1079A>G (p.Gln360Arg) n.930A>G c.119+43961T>C |