Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
10g.94981210T>CCA5617276CYP2C9c.989T>C (p.Val330Ala)
c.847T>C (p.Ter283Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.94981210T>GCA377676176CYP2C9c.989T>G (p.Val330Gly)
c.847T>G (p.Ter283Gly)
10g.94981210T=CA1929341921CYP2C9c.989T= (p.Val330=)
c.847T= (p.Ter283=)
10g.94981211G>ACA5617277CYP2C9c.990G>A (p.Val330=)
c.848G>A (p.Ter283=)
dbSNP ExAC gnomAD v2
10g.94981211G>CCA470836266CYP2C9c.990G>C (p.Val330=)
c.848G>C (p.Ter283Ser)
10g.94981211G=CA1929341924CYP2C9c.990G= (p.Val330=)
c.848G= (p.Ter283=)
10g.94981211G>TCA470836268CYP2C9c.990G>T (p.Val330=)
c.848G>T (p.Ter283Leu)
10g.94981212A>CCA377676179CYP2C9c.991A>C (p.Ile331Leu)
c.849A>C (p.Ter283Cys)
10g.94981212A>GCA377676177CYP2C9c.991A>G (p.Ile331Val)
c.849A>G (p.Ter283Trp)
10g.94981212A>TCA377676178CYP2C9c.991A>T (p.Ile331Phe)
c.849A>T (p.Ter283Cys)
COSMIC
10g.94981213T>ACA377676180CYP2C9c.992T>A (p.Ile331Asn)
c.*1T>A (n.*1T>A)
10g.94981213T>CCA377676181CYP2C9c.992T>C (p.Ile331Thr)
c.*1T>C (n.*1T>C)
dbSNP gnomAD v4
10g.94981213T>GCA377676182CYP2C9c.992T>G (p.Ile331Ser)
c.*1T>G (n.*1T>G)
10g.94981213T=CA1929341926CYP2C9c.992T= (p.Ile331=)
c.*1T= (n.*1T=)
10g.94981214T>ACA470836279CYP2C9c.993T>A (p.Ile331=)
c.*2T>A (n.*2T>A)
10g.94981214T>CCA470836281CYP2C9c.993T>C (p.Ile331=)
c.*2T>C (n.*2T>C)
10g.94981214T>GCA377676183CYP2C9c.993T>G (p.Ile331Met)
c.*2T>G (n.*2T>G)
10g.94981215G>ACA377676186CYP2C9c.994G>A (p.Gly332Ser)
c.*3G>A (n.*3G>A)

Number of alleles fetched