Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.94981196A>CCA377676144CYP2C9c.975A>C (p.Glu325Asp)
c.833A>C (p.Lys278Thr)
10g.94981196A>GCA470836211CYP2C9c.975A>G (p.Glu325=)
c.833A>G (p.Lys278Arg)
10g.94981196A>TCA377676145CYP2C9c.975A>T (p.Glu325Asp)
c.833A>T (p.Lys278Met)
10g.94981197G>ACA377676146CYP2C9c.976G>A (p.Glu326Lys)
c.834G>A (p.Lys278=)
dbSNP
10g.94981197G>CCA377676147CYP2C9c.976G>C (p.Glu326Gln)
c.834G>C (p.Lys278Asn)
10g.94981197G=CA1929341897CYP2C9c.976G= (p.Glu326=)
c.834G= (p.Lys278=)
10g.94981197G>TCA377676148CYP2C9c.976G>T (p.Glu326Ter)
c.834G>T (p.Lys278Asn)
10g.94981198A=CA1929341899CYP2C9c.977A= (p.Glu326=)
c.835A= (p.Arg279=)
10g.94981198A>CCA377676150CYP2C9c.977A>C (p.Glu326Ala)
c.835A>C (p.Arg279=)
gnomAD v4
10g.94981198A>GCA377676151CYP2C9c.977A>G (p.Glu326Gly)
c.835A>G (p.Arg279Gly)
10g.94981198A>TCA377676149CYP2C9c.977A>T (p.Glu326Val)
c.835A>T (p.Arg279Ter)
dbSNP
10g.94981199G>ACA211729618CYP2C9c.978G>A (p.Glu326=)
c.836G>A (p.Arg279Lys)
dbSNP gnomAD v2 COSMIC
10g.94981199G>CCA377676152CYP2C9c.978G>C (p.Glu326Asp)
c.836G>C (p.Arg279Thr)
10g.94981199G=CA1929341902CYP2C9c.978G= (p.Glu326=)
c.836G= (p.Arg279=)
10g.94981199G>TCA377676153CYP2C9c.978G>T (p.Glu326Asp)
c.836G>T (p.Arg279Ile)
10g.94981200A>CCA377676154CYP2C9c.979A>C (p.Ile327Leu)
c.837A>C (p.Arg279Ser)
10g.94981200A>GCA377676155CYP2C9c.979A>G (p.Ile327Val)
c.837A>G (p.Arg279=)
gnomAD v4
10g.94981200A>TCA377676156CYP2C9c.979A>T (p.Ile327Phe)
c.837A>T (p.Arg279Ser)
10g.94981201T>ACA377676157CYP2C9c.980T>A (p.Ile327Asn)
c.838T>A (p.Leu280Met)
10g.94981201T>CCA5617272CYP2C9c.980T>C (p.Ile327Thr)
c.838T>C (p.Leu280=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.94981201T>GCA377676158CYP2C9c.980T>G (p.Ile327Ser)
c.838T>G (p.Leu280Val)
10g.94981201T=CA1929341905CYP2C9c.980T= (p.Ile327=)
c.838T= (p.Leu280=)
10g.94981202T>ACA470836233CYP2C9c.981T>A (p.Ile327=)
c.839T>A (p.Leu280Ter)
10g.94981202T>CCA470836235CYP2C9c.981T>C (p.Ile327=)
c.839T>C (p.Leu280Ser)
10g.94981202T>GCA377676160CYP2C9c.981T>G (p.Ile327Met)
c.839T>G (p.Leu280Trp)
10g.94981203G>ACA377676161CYP2C9c.982G>A (p.Glu328Lys)
c.840G>A (p.Leu280=)
gnomAD v4 COSMIC
10g.94981203G>CCA377676162CYP2C9c.982G>C (p.Glu328Gln)
c.840G>C (p.Leu280Phe)
10g.94981203G>TCA377676163CYP2C9c.982G>T (p.Glu328Ter)
c.840G>T (p.Leu280Phe)
10g.94981204A=CA1929341907CYP2C9c.983A= (p.Glu328=)
c.841A= (p.Asn281=)
10g.94981204A>CCA377676165CYP2C9c.983A>C (p.Glu328Ala)
c.841A>C (p.Asn281His)
10g.94981204A>GCA377676166CYP2C9c.983A>G (p.Glu328Gly)
c.841A>G (p.Asn281Asp)
dbSNP gnomAD v2 gnomAD v4
10g.94981204A>TCA377676164CYP2C9c.983A>T (p.Glu328Val)
c.841A>T (p.Asn281Tyr)
10g.94981205A>CCA377676167CYP2C9c.984A>C (p.Glu328Asp)
c.842A>C (p.Asn281Thr)
10g.94981205A>GCA470836236CYP2C9c.984A>G (p.Glu328=)
c.842A>G (p.Asn281Ser)
COSMIC
10g.94981205A>TCA377676168CYP2C9c.984A>T (p.Glu328Asp)
c.842A>T (p.Asn281Ile)
10g.94981206C>ACA377676169CYP2C9c.985C>A (p.Arg329Ser)
c.843C>A (p.Asn281Lys)
dbSNP gnomAD v3 gnomAD v4
10g.94981206C=CA1929341912CYP2C9c.985C= (p.Arg329=)
c.843C= (p.Asn281=)
10g.94981206C>GCA5617273CYP2C9c.985C>G (p.Arg329Gly)
c.843C>G (p.Asn281Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.94981206C>TCA5617274CYP2C9c.985C>T (p.Arg329Cys)
c.843C>T (p.Asn281=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.94981207G>ACA5617275CYP2C9c.986G>A (p.Arg329His)
c.844G>A (p.Val282Met)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.94981207G>CCA377676170CYP2C9c.986G>C (p.Arg329Pro)
c.844G>C (p.Val282Leu)
gnomAD v4
10g.94981207G=CA1929341918CYP2C9c.986G= (p.Arg329=)
c.844G= (p.Val282=)
10g.94981207G>TCA377676171CYP2C9c.986G>T (p.Arg329Leu)
c.844G>T (p.Val282Leu)
dbSNP
10g.94981208T>ACA470836250CYP2C9c.987T>A (p.Arg329=)
c.845T>A (p.Val282Glu)
10g.94981208T>CCA470836252CYP2C9c.987T>C (p.Arg329=)
c.845T>C (p.Val282Ala)
10g.94981208T>GCA470836254CYP2C9c.987T>G (p.Arg329=)
c.845T>G (p.Val282Gly)
10g.94981209G>ACA377676172CYP2C9c.988G>A (p.Val330Met)
c.846G>A (p.Val282=)
10g.94981209G>CCA377676173CYP2C9c.988G>C (p.Val330Leu)
c.846G>C (p.Val282=)
10g.94981209G>TCA377676174CYP2C9c.988G>T (p.Val330Leu)
c.846G>T (p.Val282=)
10g.94981210T>ACA377676175CYP2C9c.989T>A (p.Val330Glu)
c.847T>A (p.Ter283Arg)

Number of alleles fetched