Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.94949117_94949119del | CA2574620272 | CYP2C9 | c.652_654del (p.Asn218del) n.423_425del | |
10 | g.94949117A>C | CA377673964 | CYP2C9 | c.652A>C (p.Asn218His) n.423A>C | |
10 | g.94949117A>G | CA377673966 | CYP2C9 | c.652A>G (p.Asn218Asp) n.423A>G | |
10 | g.94949117A>T | CA377673965 | CYP2C9 | c.652A>T (p.Asn218Tyr) n.423A>T | gnomAD v4 |
10 | g.94949118A= | CA1929298272 | CYP2C9 | c.653A= (p.Asn218=) n.424A= | |
10 | g.94949118A>C | CA377673967 | CYP2C9 | c.653A>C (p.Asn218Thr) n.424A>C | dbSNP gnomAD v3 gnomAD v4 |
10 | g.94949118A>G | CA377673968 | CYP2C9 | c.653A>G (p.Asn218Ser) n.424A>G | dbSNP |
10 | g.94949118A>T | CA5617159 | CYP2C9 | c.653A>T (p.Asn218Ile) n.424A>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94949118_94949119insG | CA645557375 | CYP2C9 | c.653_654insG (p.Asn218LysfsTer7) n.424_425insG | COSMIC |
10 | g.94949119T>A | CA377673969 | CYP2C9 | c.654T>A (p.Asn218Lys) n.425T>A | |
10 | g.94949119T>C | CA470832617 | CYP2C9 | c.654T>C (p.Asn218=) n.425T>C | gnomAD v4 |
10 | g.94949119T>G | CA377673970 | CYP2C9 | c.654T>G (p.Asn218Lys) n.425T>G | |
10 | g.94949123del | CA2610265990 | CYP2C9 | c.658del (p.Ser220LeufsTer21) n.429del | gnomAD v4 |
10 | g.94949119_94949120insG | CA470832618 | CYP2C9 | c.654_655insG (p.Phe219ValfsTer6) n.425_426insG | |
10 | g.94949120T>A | CA377673971 | CYP2C9 | c.655T>A (p.Phe219Ile) n.426T>A | |
10 | g.94949120T>C | CA377673972 | CYP2C9 | c.655T>C (p.Phe219Leu) n.426T>C | |
10 | g.94949120T>G | CA377673973 | CYP2C9 | c.655T>G (p.Phe219Val) n.426T>G | |
10 | g.94949121T>A | CA377673974 | CYP2C9 | c.656T>A (p.Phe219Tyr) n.427T>A | |
10 | g.94949121T>C | CA377673975 | CYP2C9 | c.656T>C (p.Phe219Ser) n.427T>C | |
10 | g.94949121T>G | CA377673976 | CYP2C9 | c.656T>G (p.Phe219Cys) n.427T>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94949121T= | CA1929298274 | CYP2C9 | c.656T= (p.Phe219=) n.427T= | |
10 | g.94949122T>A | CA377673977 | CYP2C9 | c.657T>A (p.Phe219Leu) n.428T>A | |
10 | g.94949122T>C | CA470832619 | CYP2C9 | c.657T>C (p.Phe219=) n.428T>C | |
10 | g.94949122T>G | CA377673978 | CYP2C9 | c.657T>G (p.Phe219Leu) n.428T>G | |
10 | g.94949123T>A | CA377673981 | CYP2C9 | c.658T>A (p.Ser220Thr) n.429T>A | |
10 | g.94949123T>C | CA377673979 | CYP2C9 | c.658T>C (p.Ser220Pro) n.429T>C | gnomAD v4 |
10 | g.94949123T>G | CA377673980 | CYP2C9 | c.658T>G (p.Ser220Ala) n.429T>G | |
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 |