Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
10g.94949130T>ACA377673994CYP2C9c.665T>A (p.Ile222Asn)
n.436T>A
10g.94949130T>CCA377673996CYP2C9c.665T>C (p.Ile222Thr)
n.436T>C
gnomAD v4
10g.94949130T>GCA377673995CYP2C9c.665T>G (p.Ile222Ser)
n.436T>G
10g.94949131C>ACA470832626CYP2C9c.666C>A (p.Ile222=)
n.437C>A
gnomAD v4
10g.94949131C=CA1929298286CYP2C9c.666C= (p.Ile222=)
n.437C=
10g.94949131C>GCA377673997CYP2C9c.666C>G (p.Ile222Met)
n.437C>G
10g.94949131C>TCA211700329CYP2C9c.666C>T (p.Ile222=)
n.437C>T
dbSNP gnomAD v4
10g.94949132A=CA1929298289CYP2C9c.667A= (p.Ile223=)
n.438A=
10g.94949132A>CCA377673998CYP2C9c.667A>C (p.Ile223Leu)
n.438A>C
10g.94949132A>GCA377673999CYP2C9c.667A>G (p.Ile223Val)
n.438A>G
dbSNP gnomAD v2 gnomAD v4
10g.94949132A>TCA377674000CYP2C9c.667A>T (p.Ile223Phe)
n.438A>T
10g.94949133T>ACA377674001CYP2C9c.668T>A (p.Ile223Asn)
n.439T>A
10g.94949133T>CCA377674002CYP2C9c.668T>C (p.Ile223Thr)
n.439T>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.94949133T>GCA377674003CYP2C9c.668T>G (p.Ile223Ser)
n.439T>G
10g.94949133T=CA1929298292CYP2C9c.668T= (p.Ile223=)
n.439T=
10g.94949134T>ACA470832627CYP2C9c.669T>A (p.Ile223=)
n.440T>A
gnomAD v4
10g.94949134T>CCA470832628CYP2C9c.669T>C (p.Ile223=)
n.440T>C
gnomAD v4
10g.94949134T>GCA377674004CYP2C9c.669T>G (p.Ile223Met)
n.440T>G
10g.94949135G>ACA377674005CYP2C9c.670G>A (p.Asp224Asn)
n.441G>A
10g.94949135G>CCA377674006CYP2C9c.670G>C (p.Asp224His)
n.441G>C
10g.94949135G>TCA377674007CYP2C9c.670G>T (p.Asp224Tyr)
n.441G>T
gnomAD v4
10g.94949136A>CCA377674010CYP2C9c.671A>C (p.Asp224Ala)
n.442A>C
10g.94949136A>GCA377674008CYP2C9c.671A>G (p.Asp224Gly)
n.442A>G
10g.94949136A>TCA377674009CYP2C9c.671A>T (p.Asp224Val)
n.442A>T
10g.94949137T>ACA377674011CYP2C9c.672T>A (p.Asp224Glu)
n.443T>A
10g.94949137T>CCA470832629CYP2C9c.672T>C (p.Asp224=)
n.443T>C
10g.94949137T>GCA377674012CYP2C9c.672T>G (p.Asp224Glu)
n.443T>G
10g.94949138T>ACA377674013CYP2C9c.673T>A (p.Tyr225Asn)
n.444T>A
10g.94949138T>CCA5617160CYP2C9c.673T>C (p.Tyr225His)
n.444T>C
dbSNP ExAC gnomAD v2 gnomAD v4
10g.94949138T>GCA377674014CYP2C9c.673T>G (p.Tyr225Asp)
n.444T>G
10g.94949138T=CA1929298295CYP2C9c.673T= (p.Tyr225=)
n.444T=
10g.94949139A>CCA377674015CYP2C9c.674A>C (p.Tyr225Ser)
n.445A>C
10g.94949139A>GCA377674016CYP2C9c.674A>G (p.Tyr225Cys)
n.445A>G
COSMIC
10g.94949139A>TCA377674017CYP2C9c.674A>T (p.Tyr225Phe)
n.445A>T
10g.94949140C>ACA377674018CYP2C9c.675C>A (p.Tyr225Ter)
n.446C>A
gnomAD v4
10g.94949140C=CA1929298299CYP2C9c.675C= (p.Tyr225=)
n.446C=
10g.94949140C>GCA377674019CYP2C9c.675C>G (p.Tyr225Ter)
n.446C>G
dbSNP
10g.94949140C>TCA5617161CYP2C9c.675C>T (p.Tyr225=)
n.446C>T
dbSNP ExAC gnomAD v2
10g.94949141T>ACA377674021CYP2C9c.676T>A (p.Phe226Ile)
n.447T>A
10g.94949141T>CCA377674022CYP2C9c.676T>C (p.Phe226Leu)
n.447T>C
10g.94949141T>GCA377674020CYP2C9c.676T>G (p.Phe226Val)
n.447T>G

Number of alleles fetched