| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.40848628A= | CA2336179004 | CYP2A6 | c.479T= (p.Leu160=) n.330T= c.*291T= (n.*291T=) c.120-43363A= | |
| 19 | g.40848628A>C | CA405965602 | CYP2A6 | c.479T>G (p.Leu160Arg) n.330T>G c.*291T>G (n.*291T>G) c.120-43363A>C | |
| 19 | g.40848628A>G | CA405965603 | CYP2A6 | c.479T>C (p.Leu160Pro) n.330T>C c.*291T>C (n.*291T>C) c.120-43363A>G | |
| 19 | g.40848628A>T | CA215129 | CYP2A6 | c.479T>A (p.Leu160His) n.330T>A c.*291T>A (n.*291T>A) c.120-43363A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.40848629G>A | CA405965604 | CYP2A6 | c.478C>T (p.Leu160Phe) n.329C>T c.*290C>T (n.*290C>T) c.120-43362G>A | |
| 19 | g.40848629G>C | CA405965605 | CYP2A6 | c.478C>G (p.Leu160Val) n.329C>G c.*290C>G (n.*290C>G) c.120-43362G>C | |
| 19 | g.40848629G= | CA2336179005 | CYP2A6 | c.478C= (p.Leu160=) n.329C= c.*290C= (n.*290C=) c.120-43362G= | |
| 19 | g.40848629G>T | CA9453092 | CYP2A6 | c.478C>A (p.Leu160Ile) n.329C>A c.*290C>A (n.*290C>A) c.120-43362G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.40848629_40848633delinsTGGCC | CA2695228735 | CYP2A6 | c.474_478delinsGGCCA (p.Asp158_Leu160delinsGluAlaIle) n.325_329delinsGGCCA c.*286_*290delinsGGCCA (n.*286_*290delinsGGCCA) c.120-43362_120-43358delinsTGGCC | |
| 19 | g.40848630G>A | CA507688185 | CYP2A6 | c.477C>T (p.Ala159=) n.328C>T c.*289C>T (n.*289C>T) c.120-43361G>A | gnomAD v4 |
| 19 | g.40848630G>C | CA507688186 | CYP2A6 | c.477C>G (p.Ala159=) n.328C>G c.*289C>G (n.*289C>G) c.120-43361G>C | |
| 19 | g.40848630G>T | CA507688187 | CYP2A6 | c.477C>A (p.Ala159=) n.328C>A c.*289C>A (n.*289C>A) c.120-43361G>T | |
| 19 | g.40848631G>A | CA405965608 | CYP2A6 | c.476C>T (p.Ala159Val) n.327C>T c.*288C>T (n.*288C>T) c.120-43360G>A | dbSNP |
| 19 | g.40848631G>C | CA405965606 | CYP2A6 | c.476C>G (p.Ala159Gly) n.327C>G c.*288C>G (n.*288C>G) c.120-43360G>C | gnomAD v4 |
| 19 | g.40848631G= | CA2336179007 | CYP2A6 | c.476C= (p.Ala159=) n.327C= c.*288C= (n.*288C=) c.120-43360G= | |
| 19 | g.40848631G>T | CA405965607 | CYP2A6 | c.476C>A (p.Ala159Asp) n.327C>A c.*288C>A (n.*288C>A) c.120-43360G>T | |
| 19 | g.40848631_40848632delinsGC | CA2336179006 | CYP2A6 | c.475_476delinsGC (p.Ala159=) n.326_327delinsGC c.*287_*288delinsGC (n.*287_*288delinsGC) c.120-43360_120-43359delinsGC | |
| 19 | g.40848632del | CA9453093 | CYP2A6 | c.475del (p.Ala159ProfsTer16) n.326del c.*287del (n.*287del) c.120-43359del | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.40848632C>A | CA405965609 | CYP2A6 | c.475G>T (p.Ala159Ser) n.326G>T c.*287G>T (n.*287G>T) c.120-43359C>A | |
| 19 | g.40848632C>G | CA405965610 | CYP2A6 | c.475G>C (p.Ala159Pro) n.326G>C c.*287G>C (n.*287G>C) c.120-43359C>G | |
| 19 | g.40848632C>T | CA405965611 | CYP2A6 | c.475G>A (p.Ala159Thr) n.326G>A c.*287G>A (n.*287G>A) c.120-43359C>T | |
| 19 | g.40848633G>A | CA507688188 | CYP2A6 | c.474C>T (p.Asp158=) n.325C>T c.*286C>T (n.*286C>T) c.120-43358G>A | gnomAD v4 COSMIC |
| 19 | g.40848633G>C | CA9453094 | CYP2A6 | c.474C>G (p.Asp158Glu) n.325C>G c.*286C>G (n.*286C>G) c.120-43358G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 19 | g.40848633G= | CA2336179008 | CYP2A6 | c.474C= (p.Asp158=) n.325C= c.*286C= (n.*286C=) c.120-43358G= | |
| 19 | g.40848633G>T | CA9453095 | CYP2A6 | c.474C>A (p.Asp158Glu) n.325C>A c.*286C>A (n.*286C>A) c.120-43358G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.40848634T>A | CA405965612 | CYP2A6 | c.473A>T (p.Asp158Val) n.324A>T c.*285A>T (n.*285A>T) c.120-43357T>A | |
| 19 | g.40848634T>C | CA405965613 | CYP2A6 | c.473A>G (p.Asp158Gly) n.324A>G c.*285A>G (n.*285A>G) c.120-43357T>C | |
| 19 | g.40848634T>G | CA405965614 | CYP2A6 | c.473A>C (p.Asp158Ala) n.324A>C c.*285A>C (n.*285A>C) c.120-43357T>G | |
| 19 | g.40848635C>A | CA405965615 | CYP2A6 | c.472G>T (p.Asp158Tyr) n.323G>T c.*284G>T (n.*284G>T) c.120-43356C>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.40848635C= | CA2336179009 | CYP2A6 | c.472G= (p.Asp158=) n.323G= c.*284G= (n.*284G=) c.120-43356C= | |
| 19 | g.40848635C>G | CA405965616 | CYP2A6 | c.472G>C (p.Asp158His) n.323G>C c.*284G>C (n.*284G>C) c.120-43356C>G | |
| 19 | g.40848635C>T | CA9453096 | CYP2A6 | c.472G>A (p.Asp158Asn) n.323G>A c.*284G>A (n.*284G>A) c.120-43356C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.40848636G>A | CA507688189 | CYP2A6 | c.471C>T (p.Ile157=) n.322C>T c.*283C>T (n.*283C>T) c.120-43355G>A | dbSNP |
| 19 | g.40848636G>C | CA9453097 | CYP2A6 | c.471C>G (p.Ile157Met) n.322C>G c.*283C>G (n.*283C>G) c.120-43355G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.40848636G= | CA2336179010 | CYP2A6 | c.471C= (p.Ile157=) n.322C= c.*283C= (n.*283C=) c.120-43355G= | |
| 19 | g.40848636G>T | CA9453098 | CYP2A6 | c.471C>A (p.Ile157=) n.322C>A c.*283C>A (n.*283C>A) c.120-43355G>T | dbSNP ExAC gnomAD v2 |
| 19 | g.40848637A>C | CA405965617 | CYP2A6 | c.470T>G (p.Ile157Ser) n.321T>G c.*282T>G (n.*282T>G) c.120-43354A>C | |
| 19 | g.40848637A>G | CA405965618 | CYP2A6 | c.470T>C (p.Ile157Thr) n.321T>C c.*282T>C (n.*282T>C) c.120-43354A>G | |
| 19 | g.40848637A>T | CA405965619 | CYP2A6 | c.470T>A (p.Ile157Asn) n.321T>A c.*282T>A (n.*282T>A) c.120-43354A>T | |
| 19 | g.40848638T>A | CA405965620 | CYP2A6 | c.469A>T (p.Ile157Phe) n.320A>T c.*281A>T (n.*281A>T) c.120-43353T>A | dbSNP gnomAD v4 |
| 19 | g.40848638T>C | CA405965621 | CYP2A6 | c.469A>G (p.Ile157Val) n.320A>G c.*281A>G (n.*281A>G) c.120-43353T>C | gnomAD v4 |
| 19 | g.40848638T>G | CA405965622 | CYP2A6 | c.469A>C (p.Ile157Leu) n.320A>C c.*281A>C (n.*281A>C) c.120-43353T>G | |
| 19 | g.40848638T= | CA2336179011 | CYP2A6 | c.469A= (p.Ile157=) n.320A= c.*281A= (n.*281A=) c.120-43353T= | |
| 19 | g.40848639G>A | CA507688192 | CYP2A6 | c.468C>T (p.Leu156=) n.319C>T c.*280C>T (n.*280C>T) c.120-43352G>A | gnomAD v4 |
| 19 | g.40848639G>C | CA507688190 | CYP2A6 | c.468C>G (p.Leu156=) n.319C>G c.*280C>G (n.*280C>G) c.120-43352G>C | |
| 19 | g.40848639G>T | CA507688191 | CYP2A6 | c.468C>A (p.Leu156=) n.319C>A c.*280C>A (n.*280C>A) c.120-43352G>T | |
| 19 | g.40848640A= | CA2336179012 | CYP2A6 | c.467T= (p.Leu156=) n.318T= c.*279T= (n.*279T=) c.120-43351A= | |
| 19 | g.40848640A>C | CA405965625 | CYP2A6 | c.467T>G (p.Leu156Arg) n.318T>G c.*279T>G (n.*279T>G) c.120-43351A>C | |
| 19 | g.40848640A>G | CA405965623 | CYP2A6 | c.467T>C (p.Leu156Pro) n.318T>C c.*279T>C (n.*279T>C) c.120-43351A>G | |
| 19 | g.40848640A>T | CA405965624 | CYP2A6 | c.467T>A (p.Leu156His) n.318T>A c.*279T>A (n.*279T>A) c.120-43351A>T | dbSNP |