Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.94988975A= | CA1929349805 | CYP2C9 | c.1420A= (p.Asn474=) c.*429A= (n.*429A=) | |
10 | g.94988975A>C | CA377677108 | CYP2C9 | c.1420A>C (p.Asn474His) c.*429A>C (n.*429A>C) | dbSNP |
10 | g.94988975A>G | CA377677106 | CYP2C9 | c.1420A>G (p.Asn474Asp) c.*429A>G (n.*429A>G) | |
10 | g.94988975A>T | CA377677107 | CYP2C9 | c.1420A>T (p.Asn474Tyr) c.*429A>T (n.*429A>T) | |
10 | g.94988975_94988976del | CA2610266833 | CYP2C9 | c.1420_1421del (p.Asn474TrpfsTer?) c.*429_*430del (n.*429_*430del) | gnomAD v4 |
10 | g.94988976A= | CA1929349810 | CYP2C9 | c.1421A= (p.Asn474=) c.*430A= (n.*430A=) | |
10 | g.94988976A>C | CA377677109 | CYP2C9 | c.1421A>C (p.Asn474Thr) c.*430A>C (n.*430A>C) | |
10 | g.94988976A>G | CA5617414 | CYP2C9 | c.1421A>G (p.Asn474Ser) c.*430A>G (n.*430A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94988976A>T | CA377677110 | CYP2C9 | c.1421A>T (p.Asn474Ile) c.*430A>T (n.*430A>T) | |
10 | g.94988977T>A | CA377677111 | CYP2C9 | c.1422T>A (p.Asn474Lys) c.*431T>A (n.*431T>A) | |
10 | g.94988977T>C | CA5617416 | CYP2C9 | c.1422T>C (p.Asn474=) c.*431T>C (n.*431T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.94988977T>G | CA377677112 | CYP2C9 | c.1422T>G (p.Asn474Lys) c.*431T>G (n.*431T>G) | |
10 | g.94988977T= | CA1929349811 | CYP2C9 | c.1422T= (p.Asn474=) c.*431T= (n.*431T=) | |
10 | g.94988977_94988978delinsTG | CA1929349812 | CYP2C9 | c.1422_1423delinsTG (p.Asn474=) c.*431_*432delinsTG (n.*431_*432delinsTG) | |
10 | g.94988978G>A | CA377677113 | CYP2C9 | c.1423G>A (p.Gly475Arg) c.*432G>A (n.*432G>A) | |
10 | g.94988978G>C | CA377677114 | CYP2C9 | c.1423G>C (p.Gly475Arg) c.*432G>C (n.*432G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94988978G= | CA1929349813 | CYP2C9 | c.1423G= (p.Gly475=) c.*432G= (n.*432G=) | |
10 | g.94988978G>T | CA377677115 | CYP2C9 | c.1423G>T (p.Gly475Ter) c.*432G>T (n.*432G>T) | |
10 | g.94988979del | CA5617415 | CYP2C9 | c.1424del (p.Gly475AspfsTer?) c.*433del (n.*433del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.94988979G>A | CA377677118 | CYP2C9 | c.1424G>A (p.Gly475Glu) c.*433G>A (n.*433G>A) | |
10 | g.94988979G>C | CA377677116 | CYP2C9 | c.1424G>C (p.Gly475Ala) c.*433G>C (n.*433G>C) | |
10 | g.94988979G= | CA1929349814 | CYP2C9 | c.1424G= (p.Gly475=) c.*433G= (n.*433G=) | |
10 | g.94988979G>T | CA377677117 | CYP2C9 | c.1424G>T (p.Gly475Val) c.*433G>T (n.*433G>T) | dbSNP |
10 | g.94988979_94988982del | CA2610266834 | CYP2C9 | c.1424_1427del (p.Gly475ValfsTer?) c.*433_*436del (n.*433_*436del) | gnomAD v4 |
10 | g.94988980A= | CA1929349815 | CYP2C9 | c.1425A= (p.Gly475=) c.*434A= (n.*434A=) | |
10 | g.94988980A>C | CA470837431 | CYP2C9 | c.1425A>C (p.Gly475=) c.*434A>C (n.*434A>C) | |
10 | g.94988980A>G | CA470837432 | CYP2C9 | c.1425A>G (p.Gly475=) c.*434A>G (n.*434A>G) | |
10 | g.94988980A>T | CA5617417 | CYP2C9 | c.1425A>T (p.Gly475=) c.*434A>T (n.*434A>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94988981T>A | CA377677119 | CYP2C9 | c.1426T>A (p.Phe476Ile) c.*435T>A (n.*435T>A) | |
10 | g.94988981T>C | CA377677120 | CYP2C9 | c.1426T>C (p.Phe476Leu) c.*435T>C (n.*435T>C) | dbSNP gnomAD v2 |
10 | g.94988981T>G | CA377677121 | CYP2C9 | c.1426T>G (p.Phe476Val) c.*435T>G (n.*435T>G) | |
10 | g.94988981T= | CA1929349816 | CYP2C9 | c.1426T= (p.Phe476=) c.*435T= (n.*435T=) | |
10 | g.94988982T>A | CA377677122 | CYP2C9 | c.1427T>A (p.Phe476Tyr) c.*436T>A (n.*436T>A) | |
10 | g.94988982T>C | CA377677123 | CYP2C9 | c.1427T>C (p.Phe476Ser) c.*436T>C (n.*436T>C) | |
10 | g.94988982T>G | CA377677124 | CYP2C9 | c.1427T>G (p.Phe476Cys) c.*436T>G (n.*436T>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94988982T= | CA1929349817 | CYP2C9 | c.1427T= (p.Phe476=) c.*436T= (n.*436T=) | |
10 | g.94988983T>A | CA377677125 | CYP2C9 | c.1428T>A (p.Phe476Leu) c.*437T>A (n.*437T>A) | |
10 | g.94988983T>C | CA470837433 | CYP2C9 | c.1428T>C (p.Phe476=) c.*437T>C (n.*437T>C) | |
10 | g.94988983T>G | CA377677126 | CYP2C9 | c.1428T>G (p.Phe476Leu) c.*437T>G (n.*437T>G) | |
10 | g.94988984G>A | CA5617418 | CYP2C9 | c.1429G>A (p.Ala477Thr) c.*438G>A (n.*438G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94988984G>C | CA377677127 | CYP2C9 | c.1429G>C (p.Ala477Pro) c.*438G>C (n.*438G>C) | |
10 | g.94988984G= | CA1929349818 | CYP2C9 | c.1429G= (p.Ala477=) c.*438G= (n.*438G=) | |
10 | g.94988984G>T | CA377677128 | CYP2C9 | c.1429G>T (p.Ala477Ser) c.*438G>T (n.*438G>T) | |
10 | g.94988984_94988986dup | CA2610266835 | CYP2C9 | c.1429_1431dup (p.Ala477_Ser478insAla) c.*438_*440dup (n.*438_*440dup) | gnomAD v4 |
10 | g.94988985C>A | CA377677129 | CYP2C9 | c.1430C>A (p.Ala477Asp) c.*439C>A (n.*439C>A) | |
10 | g.94988985C= | CA1929349819 | CYP2C9 | c.1430C= (p.Ala477=) c.*439C= (n.*439C=) | |
10 | g.94988985C>G | CA377677130 | CYP2C9 | c.1430C>G (p.Ala477Gly) c.*439C>G (n.*439C>G) | |
10 | g.94988985C>T | CA211735620 | CYP2C9 | c.1430C>T (p.Ala477Val) c.*439C>T (n.*439C>T) | dbSNP gnomAD v2 gnomAD v4 |
10 | g.94988986C>A | CA470837434 | CYP2C9 | c.1431C>A (p.Ala477=) c.*440C>A (n.*440C>A) | |
10 | g.94988986C>G | CA470837435 | CYP2C9 | c.1431C>G (p.Ala477=) c.*440C>G (n.*440C>G) |