Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.94988920C>ACA377676992CYP2C9c.1365C>A (p.Asn455Lys)
c.*374C>A (n.*374C>A)
dbSNP gnomAD v3 gnomAD v4
10g.94988920C=CA1929349676CYP2C9c.1365C= (p.Asn455=)
c.*374C= (n.*374C=)
10g.94988920C>GCA377676993CYP2C9c.1365C>G (p.Asn455Lys)
c.*374C>G (n.*374C>G)
10g.94988920C>TCA470837393CYP2C9c.1365C>T (p.Asn455=)
c.*374C>T (n.*374C>T)
dbSNP gnomAD v2 gnomAD v4
10g.94988921T>ACA377676994CYP2C9c.1366T>A (p.Phe456Ile)
c.*375T>A (n.*375T>A)
10g.94988921T>CCA377676995CYP2C9c.1366T>C (p.Phe456Leu)
c.*375T>C (n.*375T>C)
10g.94988921T>GCA377676996CYP2C9c.1366T>G (p.Phe456Val)
c.*375T>G (n.*375T>G)
10g.94988922T>ACA377676997CYP2C9c.1367T>A (p.Phe456Tyr)
c.*376T>A (n.*376T>A)
10g.94988922T>CCA377676998CYP2C9c.1367T>C (p.Phe456Ser)
c.*376T>C (n.*376T>C)
10g.94988922T>GCA377676999CYP2C9c.1367T>G (p.Phe456Cys)
c.*376T>G (n.*376T>G)
10g.94988923T>ACA377677000CYP2C9c.1368T>A (p.Phe456Leu)
c.*377T>A (n.*377T>A)
10g.94988923T>CCA470837394CYP2C9c.1368T>C (p.Phe456=)
c.*377T>C (n.*377T>C)
COSMIC
10g.94988923T>GCA377677001CYP2C9c.1368T>G (p.Phe456Leu)
c.*377T>G (n.*377T>G)
10g.94988923_94988924insGTTCATCA2545263425CYP2C9c.1368_1369insGTTCAT (p.Phe456_Asn457insValHis)
c.*377_*378insGTTCAT (n.*377_*378insGTTCAT)
10g.94988924A>CCA377677004CYP2C9c.1369A>C (p.Asn457His)
c.*378A>C (n.*378A>C)
10g.94988924A>GCA377677002CYP2C9c.1369A>G (p.Asn457Asp)
c.*378A>G (n.*378A>G)
10g.94988924A>TCA377677003CYP2C9c.1369A>T (p.Asn457Tyr)
c.*378A>T (n.*378A>T)
10g.94988925A=CA1929349681CYP2C9c.1370A= (p.Asn457=)
c.*379A= (n.*379A=)
10g.94988925A>CCA377677005CYP2C9c.1370A>C (p.Asn457Thr)
c.*379A>C (n.*379A>C)
10g.94988925A>GCA5617403CYP2C9c.1370A>G (p.Asn457Ser)
c.*379A>G (n.*379A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.94988925A>TCA377677006CYP2C9c.1370A>T (p.Asn457Ile)
c.*379A>T (n.*379A>T)
10g.94988926C>ACA377677007CYP2C9c.1371C>A (p.Asn457Lys)
c.*380C>A (n.*380C>A)
dbSNP
10g.94988926C=CA1929349686CYP2C9c.1371C= (p.Asn457=)
c.*380C= (n.*380C=)
10g.94988926C>GCA377677008CYP2C9c.1371C>G (p.Asn457Lys)
c.*380C>G (n.*380C>G)
10g.94988926C>TCA5617404CYP2C9c.1371C>T (p.Asn457=)
c.*380C>T (n.*380C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.94988926_94988927insTTACA2545944833CYP2C9c.1371_1372insTTA (p.Asn457_Leu458insLeu)
c.*380_*381insTTA (n.*380_*381insTTA)
10g.94988927C>ACA377677009CYP2C9c.1372C>A (p.Leu458Met)
c.*381C>A (n.*381C>A)
10g.94988927C=CA1929349694CYP2C9c.1372C= (p.Leu458=)
c.*381C= (n.*381C=)
10g.94988927C>GCA5617405CYP2C9c.1372C>G (p.Leu458Val)
c.*381C>G (n.*381C>G)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
10g.94988927C>TCA470837395CYP2C9c.1372C>T (p.Leu458=)
c.*381C>T (n.*381C>T)
COSMIC
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)

Number of alleles fetched