Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.97691781T>A | CA341379318 | DPYD | c.698A>T (p.Gln233Leu) n.462A>T c.587A>T (p.Gln196Leu) c.203A>T (p.Gln68Leu) | |
1 | g.97691781T>C | CA341379319 | DPYD | c.698A>G (p.Gln233Arg) n.462A>G c.587A>G (p.Gln196Arg) c.203A>G (p.Gln68Arg) | dbSNP |
1 | g.97691781T>G | CA341379320 | DPYD | c.698A>C (p.Gln233Pro) n.462A>C c.587A>C (p.Gln196Pro) c.203A>C (p.Gln68Pro) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.97691781T= | CA1182979322 | DPYD | c.698A= (p.Gln233=) n.462A= c.587A= (p.Gln196=) c.203A= (p.Gln68=) | |
1 | g.97691782G>A | CA341379321 | DPYD | c.697C>T (p.Gln233Ter) n.461C>T c.586C>T (p.Gln196Ter) c.202C>T (p.Gln68Ter) | ClinVar |
1 | g.97691782G>C | CA341379322 | DPYD | c.697C>G (p.Gln233Glu) n.461C>G c.586C>G (p.Gln196Glu) c.202C>G (p.Gln68Glu) | |
1 | g.97691782G>T | CA341379323 | DPYD | c.697C>A (p.Gln233Lys) n.461C>A c.586C>A (p.Gln196Lys) c.202C>A (p.Gln68Lys) | |
1 | g.97691783A>C | CA419147907 | DPYD | c.696T>G (p.Pro232=) n.460T>G c.585T>G (p.Pro195=) c.201T>G (p.Pro67=) | |
1 | g.97691783A>G | CA419147906 | DPYD | c.696T>C (p.Pro232=) n.460T>C c.585T>C (p.Pro195=) c.201T>C (p.Pro67=) | |
1 | g.97691783A>T | CA419147905 | DPYD | c.696T>A (p.Pro232=) n.460T>A c.585T>A (p.Pro195=) c.201T>A (p.Pro67=) | |
1 | g.97691784G>A | CA341379324 | DPYD | c.695C>T (p.Pro232Leu) n.459C>T c.584C>T (p.Pro195Leu) c.200C>T (p.Pro67Leu) | COSMIC |
1 | g.97691784G>C | CA341379325 | DPYD | c.695C>G (p.Pro232Arg) n.459C>G c.584C>G (p.Pro195Arg) c.200C>G (p.Pro67Arg) | |
1 | g.97691784G>T | CA341379326 | DPYD | c.695C>A (p.Pro232His) n.459C>A c.584C>A (p.Pro195His) c.200C>A (p.Pro67His) | |
1 | g.97691785G>A | CA341379328 | DPYD | c.694C>T (p.Pro232Ser) n.458C>T c.583C>T (p.Pro195Ser) c.199C>T (p.Pro67Ser) | |
1 | g.97691785G>C | CA341379327 | DPYD | c.694C>G (p.Pro232Ala) n.458C>G c.583C>G (p.Pro195Ala) c.199C>G (p.Pro67Ala) | |
1 | g.97691785G= | CA1182979323 | DPYD | c.694C= (p.Pro232=) n.458C= c.583C= (p.Pro195=) c.199C= (p.Pro67=) | |
1 | g.97691785G>T | CA27624759 | DPYD | c.694C>A (p.Pro232Thr) n.458C>A c.583C>A (p.Pro195Thr) c.199C>A (p.Pro67Thr) | dbSNP gnomAD v4 |
1 | g.97691786A>C | CA341379329 | DPYD | c.693T>G (p.Ile231Met) n.457T>G c.582T>G (p.Ile194Met) c.198T>G (p.Ile66Met) | |
1 | g.97691786A>G | CA419147908 | DPYD | c.693T>C (p.Ile231=) n.457T>C c.582T>C (p.Ile194=) c.198T>C (p.Ile66=) | |
1 | g.97691786A>T | CA419147909 | DPYD | c.693T>A (p.Ile231=) n.457T>A c.582T>A (p.Ile194=) c.198T>A (p.Ile66=) | |
1 | g.97691787A>C | CA341379332 | DPYD | c.692T>G (p.Ile231Ser) n.456T>G c.581T>G (p.Ile194Ser) c.197T>G (p.Ile66Ser) | |
1 | g.97691787A>G | CA341379330 | DPYD | c.692T>C (p.Ile231Thr) n.456T>C c.581T>C (p.Ile194Thr) c.197T>C (p.Ile66Thr) | |
1 | g.97691787A>T | CA341379331 | DPYD | c.692T>A (p.Ile231Asn) n.456T>A c.581T>A (p.Ile194Asn) c.197T>A (p.Ile66Asn) | |
1 | g.97691788T>A | CA341379333 | DPYD | c.691A>T (p.Ile231Phe) n.455A>T c.580A>T (p.Ile194Phe) c.196A>T (p.Ile66Phe) | |
1 | g.97691788T>C | CA341379334 | DPYD | c.691A>G (p.Ile231Val) n.455A>G c.580A>G (p.Ile194Val) c.196A>G (p.Ile66Val) | |
1 | g.97691788T>G | CA341379335 | DPYD | c.691A>C (p.Ile231Leu) n.455A>C c.580A>C (p.Ile194Leu) c.196A>C (p.Ile66Leu) | |
1 | g.97691789T>A | CA341379336 | DPYD | c.690A>T (p.Glu230Asp) n.454A>T c.579A>T (p.Glu193Asp) c.195A>T (p.Glu65Asp) | |
1 | g.97691789T>C | CA419147910 | DPYD | c.690A>G (p.Glu230=) n.454A>G c.579A>G (p.Glu193=) c.195A>G (p.Glu65=) | |
1 | g.97691789T>G | CA341379337 | DPYD | c.690A>C (p.Glu230Asp) n.454A>C c.579A>C (p.Glu193Asp) c.195A>C (p.Glu65Asp) | |
1 | g.97691790T>A | CA341379338 | DPYD | c.689A>T (p.Glu230Val) n.453A>T c.578A>T (p.Glu193Val) c.194A>T (p.Glu65Val) | |
1 | g.97691790T>C | CA341379339 | DPYD | c.689A>G (p.Glu230Gly) n.453A>G c.578A>G (p.Glu193Gly) c.194A>G (p.Glu65Gly) | |
1 | g.97691790T>G | CA341379340 | DPYD | c.689A>C (p.Glu230Ala) n.453A>C c.578A>C (p.Glu193Ala) c.194A>C (p.Glu65Ala) | |
1 | g.97691791C>A | CA341379341 | DPYD | c.688G>T (p.Glu230Ter) n.452G>T c.577G>T (p.Glu193Ter) c.193G>T (p.Glu65Ter) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.97691791C>G | CA341379342 | DPYD | c.688G>C (p.Glu230Gln) n.452G>C c.577G>C (p.Glu193Gln) c.193G>C (p.Glu65Gln) | |
1 | g.97691791C>T | CA341379343 | DPYD | c.688G>A (p.Glu230Lys) n.452G>A c.577G>A (p.Glu193Lys) c.193G>A (p.Glu65Lys) | |
1 | g.97691792A= | CA1182979324 | DPYD | c.687T= (p.Ser229=) n.451T= c.576T= (p.Ser192=) c.192T= (p.Ser64=) | |
1 | g.97691792A>C | CA419147911 | DPYD | c.687T>G (p.Ser229=) n.451T>G c.576T>G (p.Ser192=) c.192T>G (p.Ser64=) | |
1 | g.97691792A>G | CA419147913 | DPYD | c.687T>C (p.Ser229=) n.451T>C c.576T>C (p.Ser192=) c.192T>C (p.Ser64=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.97691792A>T | CA419147912 | DPYD | c.687T>A (p.Ser229=) n.451T>A c.576T>A (p.Ser192=) c.192T>A (p.Ser64=) | |
1 | g.97691793G>A | CA341379346 | DPYD | c.686C>T (p.Ser229Phe) n.450C>T c.575C>T (p.Ser192Phe) c.191C>T (p.Ser64Phe) | |
1 | g.97691793G>C | CA341379345 | DPYD | c.686C>G (p.Ser229Cys) n.450C>G c.575C>G (p.Ser192Cys) c.191C>G (p.Ser64Cys) | |
1 | g.97691793G>T | CA341379344 | DPYD | c.686C>A (p.Ser229Tyr) n.450C>A c.575C>A (p.Ser192Tyr) c.191C>A (p.Ser64Tyr) | |
1 | g.97691794A>C | CA341379347 | DPYD | c.685T>G (p.Ser229Ala) n.449T>G c.574T>G (p.Ser192Ala) c.190T>G (p.Ser64Ala) | |
1 | g.97691794A>G | CA341379348 | DPYD | c.685T>C (p.Ser229Pro) n.449T>C c.574T>C (p.Ser192Pro) c.190T>C (p.Ser64Pro) | |
1 | g.97691794A>T | CA341379349 | DPYD | c.685T>A (p.Ser229Thr) n.449T>A c.574T>A (p.Ser192Thr) c.190T>A (p.Ser64Thr) | |
1 | g.97691795A= | CA1182979325 | DPYD | c.684T= (p.Thr228=) n.448T= c.573T= (p.Thr191=) c.189T= (p.Thr63=) | |
1 | g.97691795A>C | CA419147914 | DPYD | c.684T>G (p.Thr228=) n.448T>G c.573T>G (p.Thr191=) c.189T>G (p.Thr63=) | |
1 | g.97691795A>G | CA27624769 | DPYD | c.684T>C (p.Thr228=) n.448T>C c.573T>C (p.Thr191=) c.189T>C (p.Thr63=) | dbSNP |
1 | g.97691795A>T | CA419147915 | DPYD | c.684T>A (p.Thr228=) n.448T>A c.573T>A (p.Thr191=) c.189T>A (p.Thr63=) | |
1 | g.97691796G>A | CA341379350 | DPYD | c.683C>T (p.Thr228Ile) n.447C>T c.572C>T (p.Thr191Ile) c.188C>T (p.Thr63Ile) | dbSNP gnomAD v4 |