Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.94949124C>A | CA377673982 | CYP2C9 | c.659C>A (p.Ser220Tyr) n.430C>A | gnomAD v4 |
10 | g.94949124C>G | CA377673983 | CYP2C9 | c.659C>G (p.Ser220Cys) n.430C>G | |
10 | g.94949124C>T | CA377673984 | CYP2C9 | c.659C>T (p.Ser220Phe) n.430C>T | COSMIC |
10 | g.94949125T>A | CA470832620 | CYP2C9 | c.660T>A (p.Ser220=) n.431T>A | |
10 | g.94949125T>C | CA470832621 | CYP2C9 | c.660T>C (p.Ser220=) n.431T>C | gnomAD v4 |
10 | g.94949125T>G | CA470832622 | CYP2C9 | c.660T>G (p.Ser220=) n.431T>G | |
10 | g.94949126C>A | CA377673985 | CYP2C9 | c.661C>A (p.Pro221Thr) n.432C>A | gnomAD v4 |
10 | g.94949126C= | CA1929298277 | CYP2C9 | c.661C= (p.Pro221=) n.432C= | |
10 | g.94949126C>G | CA377673986 | CYP2C9 | c.661C>G (p.Pro221Ala) n.432C>G | |
10 | g.94949126C>T | CA377673987 | CYP2C9 | c.661C>T (p.Pro221Ser) n.432C>T | dbSNP gnomAD v2 gnomAD v4 |
10 | g.94949127del | CA2610265991 | CYP2C9 | c.662del (p.Pro221LeufsTer20) n.433del | gnomAD v4 |
10 | g.94949127C>A | CA377673988 | CYP2C9 | c.662C>A (p.Pro221His) n.433C>A | |
10 | g.94949127C>G | CA377673989 | CYP2C9 | c.662C>G (p.Pro221Arg) n.433C>G | gnomAD v4 |
10 | g.94949127C>T | CA377673990 | CYP2C9 | c.662C>T (p.Pro221Leu) n.433C>T | |
10 | g.94949128T>A | CA470832623 | CYP2C9 | c.663T>A (p.Pro221=) n.434T>A | |
10 | g.94949128T>C | CA470832624 | CYP2C9 | c.663T>C (p.Pro221=) n.434T>C | dbSNP gnomAD v4 |
10 | g.94949128T>G | CA470832625 | CYP2C9 | c.663T>G (p.Pro221=) n.434T>G | |
10 | g.94949128T= | CA1929298280 | CYP2C9 | c.663T= (p.Pro221=) n.434T= | |
10 | g.94949128_94949129delinsTA | CA1929298279 | CYP2C9 | c.663_664delinsTA (p.Pro221=) n.434_435delinsTA | |
10 | g.94949129del | CA595316252 | CYP2C9 | c.664del (p.Ile222SerfsTer19) n.435del | dbSNP gnomAD v2 gnomAD v4 |
10 | g.94949129A>C | CA377673991 | CYP2C9 | c.664A>C (p.Ile222Leu) n.435A>C | |
10 | g.94949129A>G | CA377673992 | CYP2C9 | c.664A>G (p.Ile222Val) n.435A>G | |
10 | g.94949129A>T | CA377673993 | CYP2C9 | c.664A>T (p.Ile222Phe) n.435A>T | gnomAD v4 |
10 | g.94949130T>A | CA377673994 | CYP2C9 | c.665T>A (p.Ile222Asn) n.436T>A | |
10 | g.94949130T>C | CA377673996 | CYP2C9 | c.665T>C (p.Ile222Thr) n.436T>C | gnomAD v4 |
10 | g.94949130T>G | CA377673995 | CYP2C9 | c.665T>G (p.Ile222Ser) n.436T>G | |
10 | g.94949131C>A | CA470832626 | CYP2C9 | c.666C>A (p.Ile222=) n.437C>A | gnomAD v4 |
10 | g.94949131C= | CA1929298286 | CYP2C9 | c.666C= (p.Ile222=) n.437C= | |
10 | g.94949131C>G | CA377673997 | CYP2C9 | c.666C>G (p.Ile222Met) n.437C>G | |
10 | g.94949131C>T | CA211700329 | CYP2C9 | c.666C>T (p.Ile222=) n.437C>T | dbSNP gnomAD v4 |
10 | g.94949132A= | CA1929298289 | CYP2C9 | c.667A= (p.Ile223=) n.438A= | |
10 | g.94949132A>C | CA377673998 | CYP2C9 | c.667A>C (p.Ile223Leu) n.438A>C | |
10 | g.94949132A>G | CA377673999 | CYP2C9 | c.667A>G (p.Ile223Val) n.438A>G | dbSNP gnomAD v2 gnomAD v4 |
10 | g.94949132A>T | CA377674000 | CYP2C9 | c.667A>T (p.Ile223Phe) n.438A>T | |
10 | g.94949133T>A | CA377674001 | CYP2C9 | c.668T>A (p.Ile223Asn) n.439T>A | |
10 | g.94949133T>C | CA377674002 | CYP2C9 | c.668T>C (p.Ile223Thr) n.439T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94949133T>G | CA377674003 | CYP2C9 | c.668T>G (p.Ile223Ser) n.439T>G | |
10 | g.94949133T= | CA1929298292 | CYP2C9 | c.668T= (p.Ile223=) n.439T= | |
10 | g.94949134T>A | CA470832627 | CYP2C9 | c.669T>A (p.Ile223=) n.440T>A | gnomAD v4 |
10 | g.94949134T>C | CA470832628 | CYP2C9 | c.669T>C (p.Ile223=) n.440T>C | gnomAD v4 |
10 | g.94949134T>G | CA377674004 | CYP2C9 | c.669T>G (p.Ile223Met) n.440T>G | |
10 | g.94949135G>A | CA377674005 | CYP2C9 | c.670G>A (p.Asp224Asn) n.441G>A | |
10 | g.94949135G>C | CA377674006 | CYP2C9 | c.670G>C (p.Asp224His) n.441G>C | |
10 | g.94949135G>T | CA377674007 | CYP2C9 | c.670G>T (p.Asp224Tyr) n.441G>T | gnomAD v4 |
10 | g.94949136A>C | CA377674010 | CYP2C9 | c.671A>C (p.Asp224Ala) n.442A>C | |
10 | g.94949136A>G | CA377674008 | CYP2C9 | c.671A>G (p.Asp224Gly) n.442A>G | |
10 | g.94949136A>T | CA377674009 | CYP2C9 | c.671A>T (p.Asp224Val) n.442A>T | |
10 | g.94949137T>A | CA377674011 | CYP2C9 | c.672T>A (p.Asp224Glu) n.443T>A | |
10 | g.94949137T>C | CA470832629 | CYP2C9 | c.672T>C (p.Asp224=) n.443T>C | |
10 | g.94949137T>G | CA377674012 | CYP2C9 | c.672T>G (p.Asp224Glu) n.443T>G |