Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.94949182T>A | CA377674106 | CYP2C9 | c.717T>A (p.Phe239Leu) n.488T>A | |
10 | g.94949182T>C | CA470832659 | CYP2C9 | c.717T>C (p.Phe239=) n.488T>C | |
10 | g.94949182T>G | CA377674107 | CYP2C9 | c.717T>G (p.Phe239Leu) n.488T>G | |
10 | g.94949183A= | CA1929298367 | CYP2C9 | c.718A= (p.Met240=) n.489A= | |
10 | g.94949183A>C | CA377674108 | CYP2C9 | c.718A>C (p.Met240Leu) n.489A>C | |
10 | g.94949183A>G | CA377674109 | CYP2C9 | c.718A>G (p.Met240Val) n.489A>G | dbSNP gnomAD v4 |
10 | g.94949183A>T | CA377674110 | CYP2C9 | c.718A>T (p.Met240Leu) n.489A>T | gnomAD v4 |
10 | g.94949184T>A | CA377674111 | CYP2C9 | c.719T>A (p.Met240Lys) n.490T>A | |
10 | g.94949184T>C | CA5617175 | CYP2C9 | c.719T>C (p.Met240Thr) n.490T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94949184T>G | CA377674112 | CYP2C9 | c.719T>G (p.Met240Arg) n.490T>G | |
10 | g.94949184T= | CA1929298369 | CYP2C9 | c.719T= (p.Met240=) n.490T= | |
10 | g.94949185G>A | CA377674113 | CYP2C9 | c.720G>A (p.Met240Ile) n.491G>A | |
10 | g.94949185G>C | CA377674114 | CYP2C9 | c.720G>C (p.Met240Ile) n.491G>C | |
10 | g.94949185G>T | CA377674115 | CYP2C9 | c.720G>T (p.Met240Ile) n.491G>T | |
10 | g.94949186A= | CA1929298375 | CYP2C9 | c.721A= (p.Lys241=) n.492A= | |
10 | g.94949186A>C | CA377674116 | CYP2C9 | c.721A>C (p.Lys241Gln) n.492A>C | |
10 | g.94949186A>G | CA211700407 | CYP2C9 | c.721A>G (p.Lys241Glu) n.492A>G | dbSNP gnomAD v2 gnomAD v4 |
10 | g.94949186A>T | CA377674117 | CYP2C9 | c.721A>T (p.Lys241Ter) n.492A>T | |
10 | g.94949188_94949189del | CA2610265992 | CYP2C9 | c.723_724del (p.Ser242LeufsTer23) n.494_495del | gnomAD v4 |
10 | g.94949187A>C | CA377674118 | CYP2C9 | c.722A>C (p.Lys241Thr) n.493A>C | |
10 | g.94949187A>G | CA377674119 | CYP2C9 | c.722A>G (p.Lys241Arg) n.493A>G | |
10 | g.94949187A>T | CA377674120 | CYP2C9 | c.722A>T (p.Lys241Ile) n.493A>T | |
10 | g.94949188A>C | CA377674121 | CYP2C9 | c.723A>C (p.Lys241Asn) n.494A>C | |
10 | g.94949188A>G | CA470832660 | CYP2C9 | c.723A>G (p.Lys241=) n.494A>G | gnomAD v4 |
10 | g.94949188A>T | CA377674122 | CYP2C9 | c.723A>T (p.Lys241Asn) n.494A>T | |
10 | g.94949189A= | CA1929298379 | CYP2C9 | c.724A= (p.Ser242=) n.495A= | |
10 | g.94949189A>C | CA377674125 | CYP2C9 | c.724A>C (p.Ser242Arg) n.495A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94949189A>G | CA377674123 | CYP2C9 | c.724A>G (p.Ser242Gly) n.495A>G | |
10 | g.94949189A>T | CA377674124 | CYP2C9 | c.724A>T (p.Ser242Cys) n.495A>T | |
10 | g.94949190del | CA2610265993 | CYP2C9 | c.725del (p.Ser242IlefsTer7) n.496del | gnomAD v4 |
10 | g.94949190G>A | CA377674126 | CYP2C9 | c.725G>A (p.Ser242Asn) n.496G>A | |
10 | g.94949190G>C | CA377674127 | CYP2C9 | c.725G>C (p.Ser242Thr) n.496G>C | |
10 | g.94949190G>T | CA377674128 | CYP2C9 | c.725G>T (p.Ser242Ile) n.496G>T | COSMIC |
10 | g.94949191T>A | CA377674129 | CYP2C9 | c.726T>A (p.Ser242Arg) n.497T>A | dbSNP gnomAD v2 gnomAD v4 |
10 | g.94949191T>C | CA470832661 | CYP2C9 | c.726T>C (p.Ser242=) n.497T>C | dbSNP |
10 | g.94949191T>G | CA377674130 | CYP2C9 | c.726T>G (p.Ser242Arg) n.497T>G | gnomAD v4 |
10 | g.94949191T= | CA1929298382 | CYP2C9 | c.726T= (p.Ser242=) n.497T= | |
10 | g.94949192T>A | CA377674131 | CYP2C9 | c.727T>A (p.Tyr243Asn) n.498T>A | |
10 | g.94949192T>C | CA377674132 | CYP2C9 | c.727T>C (p.Tyr243His) n.498T>C | |
10 | g.94949192T>G | CA377674133 | CYP2C9 | c.727T>G (p.Tyr243Asp) n.498T>G | gnomAD v4 |
10 | g.94949193A>C | CA377674134 | CYP2C9 | c.728A>C (p.Tyr243Ser) n.499A>C | |
10 | g.94949193A>G | CA377674135 | CYP2C9 | c.728A>G (p.Tyr243Cys) n.499A>G | |
10 | g.94949193A>T | CA377674136 | CYP2C9 | c.728A>T (p.Tyr243Phe) n.499A>T | COSMIC |
10 | g.94949194T>A | CA377674138 | CYP2C9 | c.729T>A (p.Tyr243Ter) n.500T>A | gnomAD v4 |
10 | g.94949194T>C | CA470832662 | CYP2C9 | c.729T>C (p.Tyr243=) n.500T>C | dbSNP gnomAD v2 gnomAD v4 |
10 | g.94949194T>G | CA377674137 | CYP2C9 | c.729T>G (p.Tyr243Ter) n.500T>G | |
10 | g.94949194T= | CA1929298387 | CYP2C9 | c.729T= (p.Tyr243=) n.500T= | |
10 | g.94949195A= | CA1929298392 | CYP2C9 | c.730A= (p.Ile244=) n.501A= | |
10 | g.94949195A>C | CA377674139 | CYP2C9 | c.730A>C (p.Ile244Leu) n.501A>C | |
10 | g.94949195A>G | CA211700415 | CYP2C9 | c.730A>G (p.Ile244Val) n.501A>G | dbSNP |