Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.74752127_74752129delinsCTG | CA2187825705 | CYP1A2 | c.1046_1048delinsCTG (p.Thr349=) | |
15 | g.74752128T>A | CA491219679 | CYP1A2 | c.1047T>A (p.Thr349=) | |
15 | g.74752128T>C | CA7659971 | CYP1A2 | c.1047T>C (p.Thr349=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74752128T>G | CA491219680 | CYP1A2 | c.1047T>G (p.Thr349=) | |
15 | g.74752128T= | CA2187825706 | CYP1A2 | c.1047T= (p.Thr349=) | |
15 | g.74752130_74752131del | CA715675155 | CYP1A2 | c.1049_1050del (p.Val350AspfsTer11) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.74752129G>A | CA393165031 | CYP1A2 | c.1048G>A (p.Val350Met) | |
15 | g.74752129G>C | CA393165033 | CYP1A2 | c.1048G>C (p.Val350Leu) | gnomAD v4 |
15 | g.74752129G>T | CA393165037 | CYP1A2 | c.1048G>T (p.Val350Leu) | |
15 | g.74752130T>A | CA393165041 | CYP1A2 | c.1049T>A (p.Val350Glu) | |
15 | g.74752130T>C | CA393165039 | CYP1A2 | c.1049T>C (p.Val350Ala) | |
15 | g.74752130T>G | CA7659972 | CYP1A2 | c.1049T>G (p.Val350Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.74752130T= | CA2187825707 | CYP1A2 | c.1049T= (p.Val350=) | |
15 | g.74752131G>A | CA491219684 | CYP1A2 | c.1050G>A (p.Val350=) | dbSNP |
15 | g.74752131G>C | CA491219683 | CYP1A2 | c.1050G>C (p.Val350=) | |
15 | g.74752131G= | CA2187825708 | CYP1A2 | c.1050G= (p.Val350=) | |
15 | g.74752131G>T | CA491219682 | CYP1A2 | c.1050G>T (p.Val350=) | |
15 | g.74752132A>C | CA393165045 | CYP1A2 | c.1051A>C (p.Ile351Leu) | |
15 | g.74752132A>G | CA393165048 | CYP1A2 | c.1051A>G (p.Ile351Val) | |
15 | g.74752132A>T | CA393165052 | CYP1A2 | c.1051A>T (p.Ile351Phe) | |
15 | g.74752133T>A | CA393165055 | CYP1A2 | c.1052T>A (p.Ile351Asn) | |
15 | g.74752133T>C | CA393165057 | CYP1A2 | c.1052T>C (p.Ile351Thr) | dbSNP |
15 | g.74752133T>G | CA393165062 | CYP1A2 | c.1052T>G (p.Ile351Ser) | |
15 | g.74752133T= | CA2187825709 | CYP1A2 | c.1052T= (p.Ile351=) | |
15 | g.74752134T>A | CA491219686 | CYP1A2 | c.1053T>A (p.Ile351=) | |
15 | g.74752134T>C | CA491219687 | CYP1A2 | c.1053T>C (p.Ile351=) | dbSNP |
15 | g.74752134T>G | CA393165064 | CYP1A2 | c.1053T>G (p.Ile351Met) | dbSNP gnomAD v4 |
15 | g.74752134T= | CA2187825710 | CYP1A2 | c.1053T= (p.Ile351=) | |
15 | g.74752135G>A | CA393165065 | CYP1A2 | c.1054G>A (p.Gly352Ser) | dbSNP gnomAD v4 |
15 | g.74752135G>C | CA393165066 | CYP1A2 | c.1054G>C (p.Gly352Arg) | |
15 | g.74752135G= | CA2187825711 | CYP1A2 | c.1054G= (p.Gly352=) | |
15 | g.74752135G>T | CA393165068 | CYP1A2 | c.1054G>T (p.Gly352Cys) | dbSNP gnomAD v4 |
15 | g.74752136G>A | CA393165075 | CYP1A2 | c.1055G>A (p.Gly352Asp) | gnomAD v4 |
15 | g.74752136G>C | CA393165078 | CYP1A2 | c.1055G>C (p.Gly352Ala) | |
15 | g.74752136G>T | CA393165082 | CYP1A2 | c.1055G>T (p.Gly352Val) | |
15 | g.74752137C>A | CA491219689 | CYP1A2 | c.1056C>A (p.Gly352=) | |
15 | g.74752137C>G | CA491219690 | CYP1A2 | c.1056C>G (p.Gly352=) | |
15 | g.74752137C>T | CA491219691 | CYP1A2 | c.1056C>T (p.Gly352=) | |
15 | g.74752138A>C | CA491219692 | CYP1A2 | c.1057A>C (p.Arg353=) | |
15 | g.74752138A>G | CA393165089 | CYP1A2 | c.1057A>G (p.Arg353Gly) | |
15 | g.74752138A>T | CA393165086 | CYP1A2 | c.1057A>T (p.Arg353Trp) | |
15 | g.74752139G>A | CA393165093 | CYP1A2 | c.1058G>A (p.Arg353Lys) | |
15 | g.74752139G>C | CA393165096 | CYP1A2 | c.1058G>C (p.Arg353Thr) | |
15 | g.74752139G>T | CA393165099 | CYP1A2 | c.1058G>T (p.Arg353Met) | |
15 | g.74752140G>A | CA491219694 | CYP1A2 | c.1059G>A (p.Arg353=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74752140G>C | CA393165100 | CYP1A2 | c.1059G>C (p.Arg353Ser) | gnomAD v4 |
15 | g.74752140G= | CA2187825712 | CYP1A2 | c.1059G= (p.Arg353=) | |
15 | g.74752140G>T | CA393165101 | CYP1A2 | c.1059G>T (p.Arg353Ser) | |
15 | g.74752141G>A | CA272815269 | CYP1A2 | c.1060G>A (p.Glu354Lys) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.74752141G>C | CA393165103 | CYP1A2 | c.1060G>C (p.Glu354Gln) |