Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.94988952A= | CA1929349728 | CYP2C9 | c.1397A= (p.Asn466=) c.*406A= (n.*406A=) | |
10 | g.94988952A>C | CA377677062 | CYP2C9 | c.1397A>C (p.Asn466Thr) c.*406A>C (n.*406A>C) | dbSNP gnomAD v4 |
10 | g.94988952A>G | CA377677063 | CYP2C9 | c.1397A>G (p.Asn466Ser) c.*406A>G (n.*406A>G) | COSMIC |
10 | g.94988952A>T | CA377677064 | CYP2C9 | c.1397A>T (p.Asn466Ile) c.*406A>T (n.*406A>T) | |
10 | g.94988953C>A | CA377677065 | CYP2C9 | c.1398C>A (p.Asn466Lys) c.*407C>A (n.*407C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94988953C= | CA1929349732 | CYP2C9 | c.1398C= (p.Asn466=) c.*407C= (n.*407C=) | |
10 | g.94988953C>G | CA377677066 | CYP2C9 | c.1398C>G (p.Asn466Lys) c.*407C>G (n.*407C>G) | |
10 | g.94988953C>T | CA470837414 | CYP2C9 | c.1398C>T (p.Asn466=) c.*407C>T (n.*407C>T) | |
10 | g.94988954C>A | CA377677067 | CYP2C9 | c.1399C>A (p.Leu467Ile) c.*408C>A (n.*408C>A) | dbSNP COSMIC |
10 | g.94988954C= | CA1929349738 | CYP2C9 | c.1399C= (p.Leu467=) c.*408C= (n.*408C=) | |
10 | g.94988954C>G | CA377677068 | CYP2C9 | c.1399C>G (p.Leu467Val) c.*408C>G (n.*408C>G) | gnomAD v4 |
10 | g.94988954C>T | CA5617407 | CYP2C9 | c.1399C>T (p.Leu467Phe) c.*408C>T (n.*408C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.94988955T>A | CA377677069 | CYP2C9 | c.1400T>A (p.Leu467His) c.*409T>A (n.*409T>A) | |
10 | g.94988955T>C | CA5617408 | CYP2C9 | c.1400T>C (p.Leu467Pro) c.*409T>C (n.*409T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94988955T>G | CA377677070 | CYP2C9 | c.1400T>G (p.Leu467Arg) c.*409T>G (n.*409T>G) | |
10 | g.94988955T= | CA1929349745 | CYP2C9 | c.1400T= (p.Leu467=) c.*409T= (n.*409T=) | |
10 | g.94988956T>A | CA470837417 | CYP2C9 | c.1401T>A (p.Leu467=) c.*410T>A (n.*410T>A) | |
10 | g.94988956T>C | CA470837415 | CYP2C9 | c.1401T>C (p.Leu467=) c.*410T>C (n.*410T>C) | |
10 | g.94988956T>G | CA470837416 | CYP2C9 | c.1401T>G (p.Leu467=) c.*410T>G (n.*410T>G) | |
10 | g.94988957G>A | CA377677071 | CYP2C9 | c.1402G>A (p.Asp468Asn) c.*411G>A (n.*411G>A) | |
10 | g.94988957G>C | CA377677072 | CYP2C9 | c.1402G>C (p.Asp468His) c.*411G>C (n.*411G>C) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
10 | g.94988957G= | CA1929349756 | CYP2C9 | c.1402G= (p.Asp468=) c.*411G= (n.*411G=) | |
10 | g.94988957G>T | CA377677073 | CYP2C9 | c.1402G>T (p.Asp468Tyr) c.*411G>T (n.*411G>T) | |
10 | g.94988958A>C | CA377677074 | CYP2C9 | c.1403A>C (p.Asp468Ala) c.*412A>C (n.*412A>C) | |
10 | g.94988958A>G | CA377677075 | CYP2C9 | c.1403A>G (p.Asp468Gly) c.*412A>G (n.*412A>G) | |
10 | g.94988958A>T | CA377677076 | CYP2C9 | c.1403A>T (p.Asp468Val) c.*412A>T (n.*412A>T) | |
10 | g.94988959C>A | CA377677077 | CYP2C9 | c.1404C>A (p.Asp468Glu) c.*413C>A (n.*413C>A) | |
10 | g.94988959C>G | CA377677078 | CYP2C9 | c.1404C>G (p.Asp468Glu) c.*413C>G (n.*413C>G) | |
10 | g.94988959C>T | CA470837418 | CYP2C9 | c.1404C>T (p.Asp468=) c.*413C>T (n.*413C>T) | |
10 | g.94988960A= | CA1929349760 | CYP2C9 | c.1405A= (p.Thr469=) c.*414A= (n.*414A=) | |
10 | g.94988960A>C | CA377677081 | CYP2C9 | c.1405A>C (p.Thr469Pro) c.*414A>C (n.*414A>C) | dbSNP |
10 | g.94988960A>G | CA377677080 | CYP2C9 | c.1405A>G (p.Thr469Ala) c.*414A>G (n.*414A>G) | |
10 | g.94988960A>T | CA377677079 | CYP2C9 | c.1405A>T (p.Thr469Ser) c.*414A>T (n.*414A>T) | |
10 | g.94988961C>A | CA377677082 | CYP2C9 | c.1406C>A (p.Thr469Asn) c.*415C>A (n.*415C>A) | dbSNP gnomAD v3 gnomAD v4 |
10 | g.94988961C= | CA1929349764 | CYP2C9 | c.1406C= (p.Thr469=) c.*415C= (n.*415C=) | |
10 | g.94988961C>G | CA377677084 | CYP2C9 | c.1406C>G (p.Thr469Ser) c.*415C>G (n.*415C>G) | |
10 | g.94988961C>T | CA377677083 | CYP2C9 | c.1406C>T (p.Thr469Ile) c.*415C>T (n.*415C>T) | |
10 | g.94988962C>A | CA470837419 | CYP2C9 | c.1407C>A (p.Thr469=) c.*416C>A (n.*416C>A) | |
10 | g.94988962C>G | CA470837420 | CYP2C9 | c.1407C>G (p.Thr469=) c.*416C>G (n.*416C>G) | |
10 | g.94988962C>T | CA470837421 | CYP2C9 | c.1407C>T (p.Thr469=) c.*416C>T (n.*416C>T) | |
10 | g.94988963A>C | CA377677085 | CYP2C9 | c.1408A>C (p.Thr470Pro) c.*417A>C (n.*417A>C) | |
10 | g.94988963A>G | CA377677086 | CYP2C9 | c.1408A>G (p.Thr470Ala) c.*417A>G (n.*417A>G) | |
10 | g.94988963A>T | CA377677087 | CYP2C9 | c.1408A>T (p.Thr470Ser) c.*417A>T (n.*417A>T) | |
10 | g.94988964C>A | CA377677088 | CYP2C9 | c.1409C>A (p.Thr470Asn) c.*418C>A (n.*418C>A) | |
10 | g.94988964C= | CA1929349770 | CYP2C9 | c.1409C= (p.Thr470=) c.*418C= (n.*418C=) | |
10 | g.94988964C>G | CA377677089 | CYP2C9 | c.1409C>G (p.Thr470Ser) c.*418C>G (n.*418C>G) | |
10 | g.94988964C>T | CA5617409 | CYP2C9 | c.1409C>T (p.Thr470Ile) c.*418C>T (n.*418C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.94988965T>A | CA470837422 | CYP2C9 | c.1410T>A (p.Thr470=) c.*419T>A (n.*419T>A) | |
10 | g.94988965T>C | CA5617410 | CYP2C9 | c.1410T>C (p.Thr470=) c.*419T>C (n.*419T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.94988965T>G | CA470837423 | CYP2C9 | c.1410T>G (p.Thr470=) c.*419T>G (n.*419T>G) |