Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
10g.94988954C>TCA5617407CYP2C9c.1399C>T (p.Leu467Phe)
c.*408C>T (n.*408C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.94988955T>ACA377677069CYP2C9c.1400T>A (p.Leu467His)
c.*409T>A (n.*409T>A)
10g.94988955T>CCA5617408CYP2C9c.1400T>C (p.Leu467Pro)
c.*409T>C (n.*409T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.94988955T>GCA377677070CYP2C9c.1400T>G (p.Leu467Arg)
c.*409T>G (n.*409T>G)
10g.94988955T=CA1929349745CYP2C9c.1400T= (p.Leu467=)
c.*409T= (n.*409T=)
10g.94988956T>ACA470837417CYP2C9c.1401T>A (p.Leu467=)
c.*410T>A (n.*410T>A)
10g.94988956T>CCA470837415CYP2C9c.1401T>C (p.Leu467=)
c.*410T>C (n.*410T>C)
10g.94988956T>GCA470837416CYP2C9c.1401T>G (p.Leu467=)
c.*410T>G (n.*410T>G)
10g.94988957G>ACA377677071CYP2C9c.1402G>A (p.Asp468Asn)
c.*411G>A (n.*411G>A)
10g.94988957G>CCA377677072CYP2C9c.1402G>C (p.Asp468His)
c.*411G>C (n.*411G>C)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.94988957G=CA1929349756CYP2C9c.1402G= (p.Asp468=)
c.*411G= (n.*411G=)
10g.94988957G>TCA377677073CYP2C9c.1402G>T (p.Asp468Tyr)
c.*411G>T (n.*411G>T)
10g.94988958A>CCA377677074CYP2C9c.1403A>C (p.Asp468Ala)
c.*412A>C (n.*412A>C)
10g.94988958A>GCA377677075CYP2C9c.1403A>G (p.Asp468Gly)
c.*412A>G (n.*412A>G)
10g.94988958A>TCA377677076CYP2C9c.1403A>T (p.Asp468Val)
c.*412A>T (n.*412A>T)
10g.94988959C>ACA377677077CYP2C9c.1404C>A (p.Asp468Glu)
c.*413C>A (n.*413C>A)
10g.94988959C>GCA377677078CYP2C9c.1404C>G (p.Asp468Glu)
c.*413C>G (n.*413C>G)
10g.94988959C>TCA470837418CYP2C9c.1404C>T (p.Asp468=)
c.*413C>T (n.*413C>T)
10g.94988960A=CA1929349760CYP2C9c.1405A= (p.Thr469=)
c.*414A= (n.*414A=)
10g.94988960A>CCA377677081CYP2C9c.1405A>C (p.Thr469Pro)
c.*414A>C (n.*414A>C)
dbSNP
10g.94988960A>GCA377677080CYP2C9c.1405A>G (p.Thr469Ala)
c.*414A>G (n.*414A>G)
10g.94988960A>TCA377677079CYP2C9c.1405A>T (p.Thr469Ser)
c.*414A>T (n.*414A>T)
10g.94988961C>ACA377677082CYP2C9c.1406C>A (p.Thr469Asn)
c.*415C>A (n.*415C>A)
dbSNP gnomAD v3 gnomAD v4
10g.94988961C=CA1929349764CYP2C9c.1406C= (p.Thr469=)
c.*415C= (n.*415C=)
10g.94988961C>GCA377677084CYP2C9c.1406C>G (p.Thr469Ser)
c.*415C>G (n.*415C>G)
10g.94988961C>TCA377677083CYP2C9c.1406C>T (p.Thr469Ile)
c.*415C>T (n.*415C>T)
10g.94988962C>ACA470837419CYP2C9c.1407C>A (p.Thr469=)
c.*416C>A (n.*416C>A)
10g.94988962C>GCA470837420CYP2C9c.1407C>G (p.Thr469=)
c.*416C>G (n.*416C>G)
10g.94988962C>TCA470837421CYP2C9c.1407C>T (p.Thr469=)
c.*416C>T (n.*416C>T)
10g.94988963A>CCA377677085CYP2C9c.1408A>C (p.Thr470Pro)
c.*417A>C (n.*417A>C)
10g.94988963A>GCA377677086CYP2C9c.1408A>G (p.Thr470Ala)
c.*417A>G (n.*417A>G)
10g.94988963A>TCA377677087CYP2C9c.1408A>T (p.Thr470Ser)
c.*417A>T (n.*417A>T)
10g.94988964C>ACA377677088CYP2C9c.1409C>A (p.Thr470Asn)
c.*418C>A (n.*418C>A)
10g.94988964C=CA1929349770CYP2C9c.1409C= (p.Thr470=)
c.*418C= (n.*418C=)
10g.94988964C>GCA377677089CYP2C9c.1409C>G (p.Thr470Ser)
c.*418C>G (n.*418C>G)
10g.94988964C>TCA5617409CYP2C9c.1409C>T (p.Thr470Ile)
c.*418C>T (n.*418C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.94988965T>ACA470837422CYP2C9c.1410T>A (p.Thr470=)
c.*419T>A (n.*419T>A)
10g.94988965T>CCA5617410CYP2C9c.1410T>C (p.Thr470=)
c.*419T>C (n.*419T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.94988965T>GCA470837423CYP2C9c.1410T>G (p.Thr470=)
c.*419T>G (n.*419T>G)

Number of alleles fetched