Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.74752120A= | CA2187825699 | CYP1A2 | c.1043-4A= (n.1043-4A=) | |
15 | g.74752120A>G | CA272815256 | CYP1A2 | c.1043-4A>G (n.1043-4A>G) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.74752121_74752122del | CA2629509784 | CYP1A2 | c.1043-3_1043-2del (n.1043-3_1043-2del) | gnomAD v4 |
15 | g.74752121C= | CA2187825700 | CYP1A2 | c.1043-3C= (n.1043-3C=) | |
15 | g.74752121C>T | CA2187825701 | CYP1A2 | c.1043-3C>T (n.1043-3C>T) | dbSNP gnomAD v4 |
15 | g.74752122A>C | CA393164920 | CYP1A2 | c.1043-2A>C (n.1043-2A>C) | |
15 | g.74752122A>G | CA393164929 | CYP1A2 | c.1043-2A>G (n.1043-2A>G) | gnomAD v4 |
15 | g.74752122A>T | CA393164932 | CYP1A2 | c.1043-2A>T (n.1043-2A>T) | |
15 | g.74752123G>A | CA272815259 | CYP1A2 | c.1043-1G>A (n.1043-1G>A) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.74752123G>C | CA393164938 | CYP1A2 | c.1043-1G>C (n.1043-1G>C) | |
15 | g.74752123G= | CA2187825702 | CYP1A2 | c.1043-1G= (n.1043-1G=) | |
15 | g.74752123G>T | CA393164941 | CYP1A2 | c.1043-1G>T (n.1043-1G>T) | COSMIC |
15 | g.74752123_74752125delinsGAC | CA2187825703 | CYP1A2 | c.1043-1_1044delinsGAC | |
15 | g.74752124A>C | CA393164959 | CYP1A2 | c.1043A>C (p.Asp348Ala) | |
15 | g.74752124A>G | CA393164957 | CYP1A2 | c.1043A>G (p.Asp348Gly) | |
15 | g.74752124A>T | CA393164962 | CYP1A2 | c.1043A>T (p.Asp348Val) | |
15 | g.74752126_74752127del | CA7659969 | CYP1A2 | c.1045_1046del (p.Thr349CysfsTer12) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74752125C>A | CA393164970 | CYP1A2 | c.1044C>A (p.Asp348Glu) | |
15 | g.74752125C>G | CA393164966 | CYP1A2 | c.1044C>G (p.Asp348Glu) | |
15 | g.74752125C>T | CA491219677 | CYP1A2 | c.1044C>T (p.Asp348=) | gnomAD v4 |
15 | g.74752126A>C | CA393164974 | CYP1A2 | c.1045A>C (p.Thr349Pro) | |
15 | g.74752126A>G | CA393164977 | CYP1A2 | c.1045A>G (p.Thr349Ala) | |
15 | g.74752126A>T | CA393164997 | CYP1A2 | c.1045A>T (p.Thr349Ser) | dbSNP |
15 | g.74752127C>A | CA393165009 | CYP1A2 | c.1046C>A (p.Thr349Asn) | |
15 | g.74752127C= | CA2187825704 | CYP1A2 | c.1046C= (p.Thr349=) | |
15 | g.74752127C>G | CA393165016 | CYP1A2 | c.1046C>G (p.Thr349Ser) | |
15 | g.74752127C>T | CA7659970 | CYP1A2 | c.1046C>T (p.Thr349Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
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) |