| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.94988933T>A | CA377677020 | CYP2C9 | c.1378T>A (p.Ser460Thr) c.*387T>A (n.*387T>A) | |
| 10 | g.94988933T>C | CA377677022 | CYP2C9 | c.1378T>C (p.Ser460Pro) c.*387T>C (n.*387T>C) | |
| 10 | g.94988933T>G | CA377677021 | CYP2C9 | c.1378T>G (p.Ser460Ala) c.*387T>G (n.*387T>G) | |
| 10 | g.94988933_94988934insTATGTGTTTATATATATTTCTCTCATTAGATCATGAGCTTGAAGG | CA2502214426 | CYP2C9 | c.1378_1379insTATGTGTTTATATATATTTCTCTCATTAGATCATGAGCTTGAAGG (p.Ser460LeufsTer10) c.*387_*388insTATGTGTTTATATATATTTCTCTCATTAGATCATGAGCTTGAAGG (n.*387_*388insTATGTGTTTATATATATTTCTCTCATTAGATCATGAGCTTGAAGG) | |
| 10 | g.94988934C>A | CA377677023 | CYP2C9 | c.1379C>A (p.Ser460Tyr) c.*388C>A (n.*388C>A) | gnomAD v4 COSMIC |
| 10 | g.94988934C>G | CA377677025 | CYP2C9 | c.1379C>G (p.Ser460Cys) c.*388C>G (n.*388C>G) | |
| 10 | g.94988934C>T | CA377677024 | CYP2C9 | c.1379C>T (p.Ser460Phe) c.*388C>T (n.*388C>T) | COSMIC |
| 10 | g.94988935T>A | CA470837402 | CYP2C9 | c.1380T>A (p.Ser460=) c.*389T>A (n.*389T>A) | |
| 10 | g.94988935T>C | CA470837400 | CYP2C9 | c.1380T>C (p.Ser460=) c.*389T>C (n.*389T>C) | |
| 10 | g.94988935T>G | CA470837401 | CYP2C9 | c.1380T>G (p.Ser460=) c.*389T>G (n.*389T>G) | |
| 10 | g.94988936C>A | CA377677026 | CYP2C9 | c.1381C>A (p.Leu461Met) c.*390C>A (n.*390C>A) | |
| 10 | g.94988936C= | CA1929349708 | CYP2C9 | c.1381C= (p.Leu461=) c.*390C= (n.*390C=) | |
| 10 | g.94988936C>G | CA377677027 | CYP2C9 | c.1381C>G (p.Leu461Val) c.*390C>G (n.*390C>G) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.94988936C>T | CA470837403 | CYP2C9 | c.1381C>T (p.Leu461=) c.*390C>T (n.*390C>T) | COSMIC |
| 10 | g.94988937T>A | CA377677028 | CYP2C9 | c.1382T>A (p.Leu461Gln) c.*391T>A (n.*391T>A) | |
| 10 | g.94988937T>C | CA377677029 | CYP2C9 | c.1382T>C (p.Leu461Pro) c.*391T>C (n.*391T>C) | |
| 10 | g.94988937T>G | CA377677030 | CYP2C9 | c.1382T>G (p.Leu461Arg) c.*391T>G (n.*391T>G) | |
| 10 | g.94988938G>A | CA470837404 | CYP2C9 | c.1383G>A (p.Leu461=) c.*392G>A (n.*392G>A) | gnomAD v4 |
| 10 | g.94988938G>C | CA470837405 | CYP2C9 | c.1383G>C (p.Leu461=) c.*392G>C (n.*392G>C) | |
| 10 | g.94988938G>T | CA470837406 | CYP2C9 | c.1383G>T (p.Leu461=) c.*392G>T (n.*392G>T) | |
| 10 | g.94988939G>A | CA377677031 | CYP2C9 | c.1384G>A (p.Val462Ile) c.*393G>A (n.*393G>A) | |
| 10 | g.94988939G>C | CA377677032 | CYP2C9 | c.1384G>C (p.Val462Leu) c.*393G>C (n.*393G>C) | |
| 10 | g.94988939G>T | CA377677033 | CYP2C9 | c.1384G>T (p.Val462Phe) c.*393G>T (n.*393G>T) | |
| 10 | g.94988940T>A | CA377677034 | CYP2C9 | c.1385T>A (p.Val462Asp) c.*394T>A (n.*394T>A) | |
| 10 | g.94988940T>C | CA377677035 | CYP2C9 | c.1385T>C (p.Val462Ala) c.*394T>C (n.*394T>C) | gnomAD v4 |
| 10 | g.94988940T>G | CA377677036 | CYP2C9 | c.1385T>G (p.Val462Gly) c.*394T>G (n.*394T>G) | |
| 10 | g.94988941T>A | CA470837409 | CYP2C9 | c.1386T>A (p.Val462=) c.*395T>A (n.*395T>A) | |
| 10 | g.94988941T>C | CA470837407 | CYP2C9 | c.1386T>C (p.Val462=) c.*395T>C (n.*395T>C) | |
| 10 | g.94988941T>G | CA470837408 | CYP2C9 | c.1386T>G (p.Val462=) c.*395T>G (n.*395T>G) | |
| 10 | g.94988942G>A | CA377677037 | CYP2C9 | c.1387G>A (p.Asp463Asn) c.*396G>A (n.*396G>A) | |
| 10 | g.94988942G>C | CA377677038 | CYP2C9 | c.1387G>C (p.Asp463His) c.*396G>C (n.*396G>C) | |
| 10 | g.94988942G>T | CA377677039 | CYP2C9 | c.1387G>T (p.Asp463Tyr) c.*396G>T (n.*396G>T) | |
| 10 | g.94988943A>C | CA377677040 | CYP2C9 | c.1388A>C (p.Asp463Ala) c.*397A>C (n.*397A>C) | |
| 10 | g.94988943A>G | CA377677042 | CYP2C9 | c.1388A>G (p.Asp463Gly) c.*397A>G (n.*397A>G) | gnomAD v4 |
| 10 | g.94988943A>T | CA377677041 | CYP2C9 | c.1388A>T (p.Asp463Val) c.*397A>T (n.*397A>T) | |
| 10 | g.94988944C>A | CA377677043 | CYP2C9 | c.1389C>A (p.Asp463Glu) c.*398C>A (n.*398C>A) | |
| 10 | g.94988944C= | CA1929349713 | CYP2C9 | c.1389C= (p.Asp463=) c.*398C= (n.*398C=) | |
| 10 | g.94988944C>G | CA377677044 | CYP2C9 | c.1389C>G (p.Asp463Glu) c.*398C>G (n.*398C>G) | |
| 10 | g.94988944C>T | CA5617406 | CYP2C9 | c.1389C>T (p.Asp463=) c.*398C>T (n.*398C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.94988945C>A | CA377677045 | CYP2C9 | c.1390C>A (p.Pro464Thr) c.*399C>A (n.*399C>A) | |
| 10 | g.94988945C>G | CA377677046 | CYP2C9 | c.1390C>G (p.Pro464Ala) c.*399C>G (n.*399C>G) | |
| 10 | g.94988945C>T | CA377677047 | CYP2C9 | c.1390C>T (p.Pro464Ser) c.*399C>T (n.*399C>T) | COSMIC |
| 10 | g.94988946C>A | CA377677048 | CYP2C9 | c.1391C>A (p.Pro464Gln) c.*400C>A (n.*400C>A) | |
| 10 | g.94988946C>G | CA377677049 | CYP2C9 | c.1391C>G (p.Pro464Arg) c.*400C>G (n.*400C>G) | |
| 10 | g.94988946C>T | CA377677050 | CYP2C9 | c.1391C>T (p.Pro464Leu) c.*400C>T (n.*400C>T) | COSMIC |
| 10 | g.94988947A>C | CA470837410 | CYP2C9 | c.1392A>C (p.Pro464=) c.*401A>C (n.*401A>C) | |
| 10 | g.94988947A>G | CA470837411 | CYP2C9 | c.1392A>G (p.Pro464=) c.*401A>G (n.*401A>G) | |
| 10 | g.94988947A>T | CA470837412 | CYP2C9 | c.1392A>T (p.Pro464=) c.*401A>T (n.*401A>T) | |
| 10 | g.94988948A= | CA1929349720 | CYP2C9 | c.1393A= (p.Lys465=) c.*402A= (n.*402A=) | |
| 10 | g.94988948A>C | CA377677052 | CYP2C9 | c.1393A>C (p.Lys465Gln) c.*402A>C (n.*402A>C) |