Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.94988928T>ACA377677010CYP2C9c.1373T>A (p.Leu458Gln)
c.*382T>A (n.*382T>A)
10g.94988928T>CCA377677011CYP2C9c.1373T>C (p.Leu458Pro)
c.*382T>C (n.*382T>C)
10g.94988928T>GCA377677012CYP2C9c.1373T>G (p.Leu458Arg)
c.*382T>G (n.*382T>G)
gnomAD v4
10g.94988928_94988929insATACA2538430215CYP2C9c.1373_1374insATA (p.Leu459Ter)
c.*382_*383insATA (n.*382_*383insATA)
10g.94988929G>ACA470837396CYP2C9c.1374G>A (p.Leu458=)
c.*383G>A (n.*383G>A)
10g.94988929G>CCA470837397CYP2C9c.1374G>C (p.Leu458=)
c.*383G>C (n.*383G>C)
gnomAD v4
10g.94988929G>TCA470837398CYP2C9c.1374G>T (p.Leu458=)
c.*383G>T (n.*383G>T)
10g.94988929_94988930insCATTTACCTTGTTCCA2530743839CYP2C9c.1374_1375insCATTTACCTTGTTC (p.Lys459HisfsTer?)
c.*383_*384insCATTTACCTTGTTC (n.*383_*384insCATTTACCTTGTTC)
10g.94988930A>CCA377677013CYP2C9c.1375A>C (p.Lys459Gln)
c.*384A>C (n.*384A>C)
10g.94988930A>GCA377677015CYP2C9c.1375A>G (p.Lys459Glu)
c.*384A>G (n.*384A>G)
gnomAD v4
10g.94988930A>TCA377677014CYP2C9c.1375A>T (p.Lys459Ter)
c.*384A>T (n.*384A>T)
10g.94988931A=CA1929349698CYP2C9c.1376A= (p.Lys459=)
c.*385A= (n.*385A=)
10g.94988931A>CCA211735572CYP2C9c.1376A>C (p.Lys459Thr)
c.*385A>C (n.*385A>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.94988931A>GCA377677017CYP2C9c.1376A>G (p.Lys459Arg)
c.*385A>G (n.*385A>G)
10g.94988931A>TCA377677016CYP2C9c.1376A>T (p.Lys459Ile)
c.*385A>T (n.*385A>T)
10g.94988932A=CA1929349703CYP2C9c.1377A= (p.Lys459=)
c.*386A= (n.*386A=)
10g.94988932A>CCA377677018CYP2C9c.1377A>C (p.Lys459Asn)
c.*386A>C (n.*386A>C)
10g.94988932A>GCA470837399CYP2C9c.1377A>G (p.Lys459=)
c.*386A>G (n.*386A>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.94988932A>TCA377677019CYP2C9c.1377A>T (p.Lys459Asn)
c.*386A>T (n.*386A>T)
10g.94988933T>ACA377677020CYP2C9c.1378T>A (p.Ser460Thr)
c.*387T>A (n.*387T>A)
10g.94988933T>CCA377677022CYP2C9c.1378T>C (p.Ser460Pro)
c.*387T>C (n.*387T>C)
10g.94988933T>GCA377677021CYP2C9c.1378T>G (p.Ser460Ala)
c.*387T>G (n.*387T>G)
10g.94988933_94988934insTATGTGTTTATATATATTTCTCTCATTAGATCATGAGCTTGAAGGCA2502214426CYP2C9c.1378_1379insTATGTGTTTATATATATTTCTCTCATTAGATCATGAGCTTGAAGG (p.Ser460LeufsTer10)
c.*387_*388insTATGTGTTTATATATATTTCTCTCATTAGATCATGAGCTTGAAGG (n.*387_*388insTATGTGTTTATATATATTTCTCTCATTAGATCATGAGCTTGAAGG)
10g.94988934C>ACA377677023CYP2C9c.1379C>A (p.Ser460Tyr)
c.*388C>A (n.*388C>A)
gnomAD v4 COSMIC
10g.94988934C>GCA377677025CYP2C9c.1379C>G (p.Ser460Cys)
c.*388C>G (n.*388C>G)
10g.94988934C>TCA377677024CYP2C9c.1379C>T (p.Ser460Phe)
c.*388C>T (n.*388C>T)
COSMIC
10g.94988935T>ACA470837402CYP2C9c.1380T>A (p.Ser460=)
c.*389T>A (n.*389T>A)
10g.94988935T>CCA470837400CYP2C9c.1380T>C (p.Ser460=)
c.*389T>C (n.*389T>C)
10g.94988935T>GCA470837401CYP2C9c.1380T>G (p.Ser460=)
c.*389T>G (n.*389T>G)
10g.94988936C>ACA377677026CYP2C9c.1381C>A (p.Leu461Met)
c.*390C>A (n.*390C>A)
10g.94988936C=CA1929349708CYP2C9c.1381C= (p.Leu461=)
c.*390C= (n.*390C=)
10g.94988936C>GCA377677027CYP2C9c.1381C>G (p.Leu461Val)
c.*390C>G (n.*390C>G)
dbSNP gnomAD v2 gnomAD v4
10g.94988936C>TCA470837403CYP2C9c.1381C>T (p.Leu461=)
c.*390C>T (n.*390C>T)
COSMIC
10g.94988937T>ACA377677028CYP2C9c.1382T>A (p.Leu461Gln)
c.*391T>A (n.*391T>A)
10g.94988937T>CCA377677029CYP2C9c.1382T>C (p.Leu461Pro)
c.*391T>C (n.*391T>C)
10g.94988937T>GCA377677030CYP2C9c.1382T>G (p.Leu461Arg)
c.*391T>G (n.*391T>G)
10g.94988938G>ACA470837404CYP2C9c.1383G>A (p.Leu461=)
c.*392G>A (n.*392G>A)
gnomAD v4
10g.94988938G>CCA470837405CYP2C9c.1383G>C (p.Leu461=)
c.*392G>C (n.*392G>C)
10g.94988938G>TCA470837406CYP2C9c.1383G>T (p.Leu461=)
c.*392G>T (n.*392G>T)
10g.94988939G>ACA377677031CYP2C9c.1384G>A (p.Val462Ile)
c.*393G>A (n.*393G>A)
10g.94988939G>CCA377677032CYP2C9c.1384G>C (p.Val462Leu)
c.*393G>C (n.*393G>C)
10g.94988939G>TCA377677033CYP2C9c.1384G>T (p.Val462Phe)
c.*393G>T (n.*393G>T)
10g.94988940T>ACA377677034CYP2C9c.1385T>A (p.Val462Asp)
c.*394T>A (n.*394T>A)
10g.94988940T>CCA377677035CYP2C9c.1385T>C (p.Val462Ala)
c.*394T>C (n.*394T>C)
gnomAD v4
10g.94988940T>GCA377677036CYP2C9c.1385T>G (p.Val462Gly)
c.*394T>G (n.*394T>G)
10g.94988941T>ACA470837409CYP2C9c.1386T>A (p.Val462=)
c.*395T>A (n.*395T>A)
10g.94988941T>CCA470837407CYP2C9c.1386T>C (p.Val462=)
c.*395T>C (n.*395T>C)
10g.94988941T>GCA470837408CYP2C9c.1386T>G (p.Val462=)
c.*395T>G (n.*395T>G)
10g.94988942G>ACA377677037CYP2C9c.1387G>A (p.Asp463Asn)
c.*396G>A (n.*396G>A)
10g.94988942G>CCA377677038CYP2C9c.1387G>C (p.Asp463His)
c.*396G>C (n.*396G>C)

Number of alleles fetched