Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.94949117_94949119delCA2574620272CYP2C9c.652_654del (p.Asn218del)
n.423_425del
10g.94949117A>CCA377673964CYP2C9c.652A>C (p.Asn218His)
n.423A>C
10g.94949117A>GCA377673966CYP2C9c.652A>G (p.Asn218Asp)
n.423A>G
10g.94949117A>TCA377673965CYP2C9c.652A>T (p.Asn218Tyr)
n.423A>T
gnomAD v4
10g.94949118A=CA1929298272CYP2C9c.653A= (p.Asn218=)
n.424A=
10g.94949118A>CCA377673967CYP2C9c.653A>C (p.Asn218Thr)
n.424A>C
dbSNP gnomAD v3 gnomAD v4
10g.94949118A>GCA377673968CYP2C9c.653A>G (p.Asn218Ser)
n.424A>G
dbSNP
10g.94949118A>TCA5617159CYP2C9c.653A>T (p.Asn218Ile)
n.424A>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.94949118_94949119insGCA645557375CYP2C9c.653_654insG (p.Asn218LysfsTer7)
n.424_425insG
COSMIC
10g.94949119T>ACA377673969CYP2C9c.654T>A (p.Asn218Lys)
n.425T>A
10g.94949119T>CCA470832617CYP2C9c.654T>C (p.Asn218=)
n.425T>C
gnomAD v4
10g.94949119T>GCA377673970CYP2C9c.654T>G (p.Asn218Lys)
n.425T>G
10g.94949123delCA2610265990CYP2C9c.658del (p.Ser220LeufsTer21)
n.429del
gnomAD v4
10g.94949119_94949120insGCA470832618CYP2C9c.654_655insG (p.Phe219ValfsTer6)
n.425_426insG
10g.94949120T>ACA377673971CYP2C9c.655T>A (p.Phe219Ile)
n.426T>A
10g.94949120T>CCA377673972CYP2C9c.655T>C (p.Phe219Leu)
n.426T>C
10g.94949120T>GCA377673973CYP2C9c.655T>G (p.Phe219Val)
n.426T>G
10g.94949121T>ACA377673974CYP2C9c.656T>A (p.Phe219Tyr)
n.427T>A
10g.94949121T>CCA377673975CYP2C9c.656T>C (p.Phe219Ser)
n.427T>C
10g.94949121T>GCA377673976CYP2C9c.656T>G (p.Phe219Cys)
n.427T>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.94949121T=CA1929298274CYP2C9c.656T= (p.Phe219=)
n.427T=
10g.94949122T>ACA377673977CYP2C9c.657T>A (p.Phe219Leu)
n.428T>A
10g.94949122T>CCA470832619CYP2C9c.657T>C (p.Phe219=)
n.428T>C
10g.94949122T>GCA377673978CYP2C9c.657T>G (p.Phe219Leu)
n.428T>G
10g.94949123T>ACA377673981CYP2C9c.658T>A (p.Ser220Thr)
n.429T>A
10g.94949123T>CCA377673979CYP2C9c.658T>C (p.Ser220Pro)
n.429T>C
gnomAD v4
10g.94949123T>GCA377673980CYP2C9c.658T>G (p.Ser220Ala)
n.429T>G
10g.94949124C>ACA377673982CYP2C9c.659C>A (p.Ser220Tyr)
n.430C>A
gnomAD v4
10g.94949124C>GCA377673983CYP2C9c.659C>G (p.Ser220Cys)
n.430C>G
10g.94949124C>TCA377673984CYP2C9c.659C>T (p.Ser220Phe)
n.430C>T
COSMIC
10g.94949125T>ACA470832620CYP2C9c.660T>A (p.Ser220=)
n.431T>A
10g.94949125T>CCA470832621CYP2C9c.660T>C (p.Ser220=)
n.431T>C
gnomAD v4
10g.94949125T>GCA470832622CYP2C9c.660T>G (p.Ser220=)
n.431T>G
10g.94949126C>ACA377673985CYP2C9c.661C>A (p.Pro221Thr)
n.432C>A
gnomAD v4
10g.94949126C=CA1929298277CYP2C9c.661C= (p.Pro221=)
n.432C=
10g.94949126C>GCA377673986CYP2C9c.661C>G (p.Pro221Ala)
n.432C>G
10g.94949126C>TCA377673987CYP2C9c.661C>T (p.Pro221Ser)
n.432C>T
dbSNP gnomAD v2 gnomAD v4
10g.94949127delCA2610265991CYP2C9c.662del (p.Pro221LeufsTer20)
n.433del
gnomAD v4
10g.94949127C>ACA377673988CYP2C9c.662C>A (p.Pro221His)
n.433C>A
10g.94949127C>GCA377673989CYP2C9c.662C>G (p.Pro221Arg)
n.433C>G
gnomAD v4
10g.94949127C>TCA377673990CYP2C9c.662C>T (p.Pro221Leu)
n.433C>T
10g.94949128T>ACA470832623CYP2C9c.663T>A (p.Pro221=)
n.434T>A
10g.94949128T>CCA470832624CYP2C9c.663T>C (p.Pro221=)
n.434T>C
dbSNP gnomAD v4
10g.94949128T>GCA470832625CYP2C9c.663T>G (p.Pro221=)
n.434T>G
10g.94949128T=CA1929298280CYP2C9c.663T= (p.Pro221=)
n.434T=
10g.94949128_94949129delinsTACA1929298279CYP2C9c.663_664delinsTA (p.Pro221=)
n.434_435delinsTA
10g.94949129delCA595316252CYP2C9c.664del (p.Ile222SerfsTer19)
n.435del
dbSNP gnomAD v2 gnomAD v4
10g.94949129A>CCA377673991CYP2C9c.664A>C (p.Ile222Leu)
n.435A>C
10g.94949129A>GCA377673992CYP2C9c.664A>G (p.Ile222Val)
n.435A>G
10g.94949129A>TCA377673993CYP2C9c.664A>T (p.Ile222Phe)
n.435A>T
gnomAD v4

Number of alleles fetched