Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
10g.94988942G>TCA377677039CYP2C9c.1387G>T (p.Asp463Tyr)
c.*396G>T (n.*396G>T)
10g.94988943A>CCA377677040CYP2C9c.1388A>C (p.Asp463Ala)
c.*397A>C (n.*397A>C)
10g.94988943A>GCA377677042CYP2C9c.1388A>G (p.Asp463Gly)
c.*397A>G (n.*397A>G)
gnomAD v4
10g.94988943A>TCA377677041CYP2C9c.1388A>T (p.Asp463Val)
c.*397A>T (n.*397A>T)
10g.94988944C>ACA377677043CYP2C9c.1389C>A (p.Asp463Glu)
c.*398C>A (n.*398C>A)
10g.94988944C=CA1929349713CYP2C9c.1389C= (p.Asp463=)
c.*398C= (n.*398C=)
10g.94988944C>GCA377677044CYP2C9c.1389C>G (p.Asp463Glu)
c.*398C>G (n.*398C>G)
10g.94988944C>TCA5617406CYP2C9c.1389C>T (p.Asp463=)
c.*398C>T (n.*398C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.94988945C>ACA377677045CYP2C9c.1390C>A (p.Pro464Thr)
c.*399C>A (n.*399C>A)
10g.94988945C>GCA377677046CYP2C9c.1390C>G (p.Pro464Ala)
c.*399C>G (n.*399C>G)
10g.94988945C>TCA377677047CYP2C9c.1390C>T (p.Pro464Ser)
c.*399C>T (n.*399C>T)
COSMIC
10g.94988946C>ACA377677048CYP2C9c.1391C>A (p.Pro464Gln)
c.*400C>A (n.*400C>A)
10g.94988946C>GCA377677049CYP2C9c.1391C>G (p.Pro464Arg)
c.*400C>G (n.*400C>G)
10g.94988946C>TCA377677050CYP2C9c.1391C>T (p.Pro464Leu)
c.*400C>T (n.*400C>T)
COSMIC
10g.94988947A>CCA470837410CYP2C9c.1392A>C (p.Pro464=)
c.*401A>C (n.*401A>C)
10g.94988947A>GCA470837411CYP2C9c.1392A>G (p.Pro464=)
c.*401A>G (n.*401A>G)
10g.94988947A>TCA470837412CYP2C9c.1392A>T (p.Pro464=)
c.*401A>T (n.*401A>T)
10g.94988948A=CA1929349720CYP2C9c.1393A= (p.Lys465=)
c.*402A= (n.*402A=)
10g.94988948A>CCA377677052CYP2C9c.1393A>C (p.Lys465Gln)
c.*402A>C (n.*402A>C)
10g.94988948A>GCA377677053CYP2C9c.1393A>G (p.Lys465Glu)
c.*402A>G (n.*402A>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.94988948A>TCA377677051CYP2C9c.1393A>T (p.Lys465Ter)
c.*402A>T (n.*402A>T)
10g.94988949A>CCA377677054CYP2C9c.1394A>C (p.Lys465Thr)
c.*403A>C (n.*403A>C)
gnomAD v4
10g.94988949A>GCA377677055CYP2C9c.1394A>G (p.Lys465Arg)
c.*403A>G (n.*403A>G)
10g.94988949A>TCA377677056CYP2C9c.1394A>T (p.Lys465Met)
c.*403A>T (n.*403A>T)
10g.94988950delCA645547922CYP2C9c.1395del (p.Asn466ThrfsTer?)
c.*404del (n.*404del)
COSMIC
10g.94988950G>ACA470837413CYP2C9c.1395G>A (p.Lys465=)
c.*404G>A (n.*404G>A)
10g.94988950G>CCA377677057CYP2C9c.1395G>C (p.Lys465Asn)
c.*404G>C (n.*404G>C)
10g.94988950G>TCA377677058CYP2C9c.1395G>T (p.Lys465Asn)
c.*404G>T (n.*404G>T)
10g.94988951A>CCA377677061CYP2C9c.1396A>C (p.Asn466His)
c.*405A>C (n.*405A>C)
10g.94988951A>GCA377677059CYP2C9c.1396A>G (p.Asn466Asp)
c.*405A>G (n.*405A>G)
10g.94988951A>TCA377677060CYP2C9c.1396A>T (p.Asn466Tyr)
c.*405A>T (n.*405A>T)
10g.94988952A=CA1929349728CYP2C9c.1397A= (p.Asn466=)
c.*406A= (n.*406A=)
10g.94988952A>CCA377677062CYP2C9c.1397A>C (p.Asn466Thr)
c.*406A>C (n.*406A>C)
dbSNP gnomAD v4
10g.94988952A>GCA377677063CYP2C9c.1397A>G (p.Asn466Ser)
c.*406A>G (n.*406A>G)
COSMIC
10g.94988952A>TCA377677064CYP2C9c.1397A>T (p.Asn466Ile)
c.*406A>T (n.*406A>T)
10g.94988953C>ACA377677065CYP2C9c.1398C>A (p.Asn466Lys)
c.*407C>A (n.*407C>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.94988953C=CA1929349732CYP2C9c.1398C= (p.Asn466=)
c.*407C= (n.*407C=)
10g.94988953C>GCA377677066CYP2C9c.1398C>G (p.Asn466Lys)
c.*407C>G (n.*407C>G)
10g.94988953C>TCA470837414CYP2C9c.1398C>T (p.Asn466=)
c.*407C>T (n.*407C>T)
10g.94988954C>ACA377677067CYP2C9c.1399C>A (p.Leu467Ile)
c.*408C>A (n.*408C>A)
dbSNP COSMIC
10g.94988954C=CA1929349738CYP2C9c.1399C= (p.Leu467=)
c.*408C= (n.*408C=)
10g.94988954C>GCA377677068CYP2C9c.1399C>G (p.Leu467Val)
c.*408C>G (n.*408C>G)
gnomAD v4

Number of alleles fetched