Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.97305277T>A | CA341375041 | DPYD,DPYD-AS1 | c.2281A>T (p.Thr761Ser) n.129-912T>A c.2065A>T (p.Thr689Ser) c.2170A>T (p.Thr724Ser) c.1786A>T (p.Thr596Ser) | |
1 | g.97305277T>C | CA27484629 | DPYD,DPYD-AS1 | c.2281A>G (p.Thr761Ala) n.129-912T>C c.2065A>G (p.Thr689Ala) c.2170A>G (p.Thr724Ala) c.1786A>G (p.Thr596Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.97305277T>G | CA341375042 | DPYD,DPYD-AS1 | c.2281A>C (p.Thr761Pro) n.129-912T>G c.2065A>C (p.Thr689Pro) c.2170A>C (p.Thr724Pro) c.1786A>C (p.Thr596Pro) | |
1 | g.97305277T= | CA1182808446 | DPYD,DPYD-AS1 | c.2281A= (p.Thr761=) n.129-912T= c.2065A= (p.Thr689=) c.2170A= (p.Thr724=) c.1786A= (p.Thr596=) | |
1 | g.97305278A>C | CA419137416 | DPYD,DPYD-AS1 | c.2280T>G (p.Thr760=) n.129-911A>C c.2064T>G (p.Thr688=) c.2169T>G (p.Thr723=) c.1785T>G (p.Thr595=) | |
1 | g.97305278A>G | CA419137417 | DPYD,DPYD-AS1 | c.2280T>C (p.Thr760=) n.129-911A>G c.2064T>C (p.Thr688=) c.2169T>C (p.Thr723=) c.1785T>C (p.Thr595=) | |
1 | g.97305278A>T | CA419137418 | DPYD,DPYD-AS1 | c.2280T>A (p.Thr760=) n.129-911A>T c.2064T>A (p.Thr688=) c.2169T>A (p.Thr723=) c.1785T>A (p.Thr595=) | dbSNP |
1 | g.97305279G>A | CA963080 | DPYD,DPYD-AS1 | c.2279C>T (p.Thr760Ile) n.129-910G>A c.2063C>T (p.Thr688Ile) c.2168C>T (p.Thr723Ile) c.1784C>T (p.Thr595Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.97305279G>C | CA963081 | DPYD,DPYD-AS1 | c.2279C>G (p.Thr760Ser) n.129-910G>C c.2063C>G (p.Thr688Ser) c.2168C>G (p.Thr723Ser) c.1784C>G (p.Thr595Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.97305279G= | CA1141291841 | DPYD,DPYD-AS1 | c.2279C= (p.Thr760=) n.129-910G= c.2063C= (p.Thr688=) c.2168C= (p.Thr723=) c.1784C= (p.Thr595=) | |
1 | g.97305279G>T | CA341375043 | DPYD,DPYD-AS1 | c.2279C>A (p.Thr760Asn) n.129-910G>T c.2063C>A (p.Thr688Asn) c.2168C>A (p.Thr723Asn) c.1784C>A (p.Thr595Asn) | dbSNP |
1 | g.97305280T>A | CA341375046 | DPYD,DPYD-AS1 | c.2278A>T (p.Thr760Ser) n.129-909T>A c.2062A>T (p.Thr688Ser) c.2167A>T (p.Thr723Ser) c.1783A>T (p.Thr595Ser) | dbSNP |
1 | g.97305280T>C | CA341375045 | DPYD,DPYD-AS1 | c.2278A>G (p.Thr760Ala) n.129-909T>C c.2062A>G (p.Thr688Ala) c.2167A>G (p.Thr723Ala) c.1783A>G (p.Thr595Ala) | dbSNP gnomAD v2 |
1 | g.97305280T>G | CA341375044 | DPYD,DPYD-AS1 | c.2278A>C (p.Thr760Pro) n.129-909T>G c.2062A>C (p.Thr688Pro) c.2167A>C (p.Thr723Pro) c.1783A>C (p.Thr595Pro) | |
1 | g.97305280T= | CA1182808447 | DPYD,DPYD-AS1 | c.2278A= (p.Thr760=) n.129-909T= c.2062A= (p.Thr688=) c.2167A= (p.Thr723=) c.1783A= (p.Thr595=) | |
1 | g.97305281T>A | CA419137419 | DPYD,DPYD-AS1 | c.2277A>T (p.Arg759=) n.129-908T>A c.2061A>T (p.Arg687=) c.2166A>T (p.Arg722=) c.1782A>T (p.Arg594=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.97305281T>C | CA419137420 | DPYD,DPYD-AS1 | c.2277A>G (p.Arg759=) n.129-908T>C c.2061A>G (p.Arg687=) c.2166A>G (p.Arg722=) c.1782A>G (p.Arg594=) | |
1 | g.97305281T>G | CA419137421 | DPYD,DPYD-AS1 | c.2277A>C (p.Arg759=) n.129-908T>G c.2061A>C (p.Arg687=) c.2166A>C (p.Arg722=) c.1782A>C (p.Arg594=) | |
1 | g.97305281T= | CA1182808448 | DPYD,DPYD-AS1 | c.2277A= (p.Arg759=) n.129-908T= c.2061A= (p.Arg687=) c.2166A= (p.Arg722=) c.1782A= (p.Arg594=) | |
1 | g.97305282C>A | CA341375047 | DPYD,DPYD-AS1 | c.2276G>T (p.Arg759Leu) n.129-907C>A c.2060G>T (p.Arg687Leu) c.2165G>T (p.Arg722Leu) c.1781G>T (p.Arg594Leu) | dbSNP |
1 | g.97305282C= | CA1143538183 | DPYD,DPYD-AS1 | c.2276G= (p.Arg759=) n.129-907C= c.2060G= (p.Arg687=) c.2165G= (p.Arg722=) c.1781G= (p.Arg594=) | |
1 | g.97305282C>G | CA341375048 | DPYD,DPYD-AS1 | c.2276G>C (p.Arg759Pro) n.129-907C>G c.2060G>C (p.Arg687Pro) c.2165G>C (p.Arg722Pro) c.1781G>C (p.Arg594Pro) | |
1 | g.97305282C>T | CA963082 | DPYD,DPYD-AS1 | c.2276G>A (p.Arg759Gln) n.129-907C>T c.2060G>A (p.Arg687Gln) c.2165G>A (p.Arg722Gln) c.1781G>A (p.Arg594Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.97305283G>A | CA963083 | DPYD,DPYD-AS1 | c.2275C>T (p.Arg759Ter) n.129-906G>A c.2059C>T (p.Arg687Ter) c.2164C>T (p.Arg722Ter) c.1780C>T (p.Arg594Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.97305283G>C | CA341375049 | DPYD,DPYD-AS1 | c.2275C>G (p.Arg759Gly) n.129-906G>C c.2059C>G (p.Arg687Gly) c.2164C>G (p.Arg722Gly) c.1780C>G (p.Arg594Gly) | dbSNP |
1 | g.97305283G= | CA1182808449 | DPYD,DPYD-AS1 | c.2275C= (p.Arg759=) n.129-906G= c.2059C= (p.Arg687=) c.2164C= (p.Arg722=) c.1780C= (p.Arg594=) | |
1 | g.97305283G>T | CA419137422 | DPYD,DPYD-AS1 | c.2275C>A (p.Arg759=) n.129-906G>T c.2059C>A (p.Arg687=) c.2164C>A (p.Arg722=) c.1780C>A (p.Arg594=) | dbSNP gnomAD v4 |
1 | g.97305284C>A | CA341375050 | DPYD,DPYD-AS1 | c.2274G>T (p.Lys758Asn) n.129-905C>A c.2058G>T (p.Lys686Asn) c.2163G>T (p.Lys721Asn) c.1779G>T (p.Lys593Asn) | dbSNP |
1 | g.97305284C>G | CA341375051 | DPYD,DPYD-AS1 | c.2274G>C (p.Lys758Asn) n.129-905C>G c.2058G>C (p.Lys686Asn) c.2163G>C (p.Lys721Asn) c.1779G>C (p.Lys593Asn) | |
1 | g.97305284C>T | CA419137423 | DPYD,DPYD-AS1 | c.2274G>A (p.Lys758=) n.129-905C>T c.2058G>A (p.Lys686=) c.2163G>A (p.Lys721=) c.1779G>A (p.Lys593=) | dbSNP gnomAD v4 |
1 | g.97305285T>A | CA341375052 | DPYD,DPYD-AS1 | c.2273A>T (p.Lys758Met) n.129-904T>A c.2057A>T (p.Lys686Met) c.2162A>T (p.Lys721Met) c.1778A>T (p.Lys593Met) | |
1 | g.97305285T>C | CA341375053 | DPYD,DPYD-AS1 | c.2273A>G (p.Lys758Arg) n.129-904T>C c.2057A>G (p.Lys686Arg) c.2162A>G (p.Lys721Arg) c.1778A>G (p.Lys593Arg) | gnomAD v4 |
1 | g.97305285T>G | CA341375054 | DPYD,DPYD-AS1 | c.2273A>C (p.Lys758Thr) n.129-904T>G c.2057A>C (p.Lys686Thr) c.2162A>C (p.Lys721Thr) c.1778A>C (p.Lys593Thr) | |
1 | g.97305286T>A | CA341375055 | DPYD,DPYD-AS1 | c.2272A>T (p.Lys758Ter) n.129-903T>A c.2056A>T (p.Lys686Ter) c.2161A>T (p.Lys721Ter) c.1777A>T (p.Lys593Ter) | |
1 | g.97305286T>C | CA341375056 | DPYD,DPYD-AS1 | c.2272A>G (p.Lys758Glu) n.129-903T>C c.2056A>G (p.Lys686Glu) c.2161A>G (p.Lys721Glu) c.1777A>G (p.Lys593Glu) | |
1 | g.97305286T>G | CA341375057 | DPYD,DPYD-AS1 | c.2272A>C (p.Lys758Gln) n.129-903T>G c.2056A>C (p.Lys686Gln) c.2161A>C (p.Lys721Gln) c.1777A>C (p.Lys593Gln) | |
1 | g.97305287T>A | CA419137426 | DPYD,DPYD-AS1 | c.2271A>T (p.Ala757=) n.129-902T>A c.2055A>T (p.Ala685=) c.2160A>T (p.Ala720=) c.1776A>T (p.Ala592=) | |
1 | g.97305287T>C | CA419137425 | DPYD,DPYD-AS1 | c.2271A>G (p.Ala757=) n.129-902T>C c.2055A>G (p.Ala685=) c.2160A>G (p.Ala720=) c.1776A>G (p.Ala592=) | |
1 | g.97305287T>G | CA419137424 | DPYD,DPYD-AS1 | c.2271A>C (p.Ala757=) n.129-902T>G c.2055A>C (p.Ala685=) c.2160A>C (p.Ala720=) c.1776A>C (p.Ala592=) | |
1 | g.97305288G>A | CA341375059 | DPYD,DPYD-AS1 | c.2270C>T (p.Ala757Val) n.129-901G>A c.2054C>T (p.Ala685Val) c.2159C>T (p.Ala720Val) c.1775C>T (p.Ala592Val) | dbSNP |
1 | g.97305288G>C | CA341375060 | DPYD,DPYD-AS1 | c.2270C>G (p.Ala757Gly) n.129-901G>C c.2054C>G (p.Ala685Gly) c.2159C>G (p.Ala720Gly) c.1775C>G (p.Ala592Gly) | dbSNP |
1 | g.97305288G>T | CA341375058 | DPYD,DPYD-AS1 | c.2270C>A (p.Ala757Glu) n.129-901G>T c.2054C>A (p.Ala685Glu) c.2159C>A (p.Ala720Glu) c.1775C>A (p.Ala592Glu) | |
1 | g.97305289C>A | CA341375061 | DPYD,DPYD-AS1 | c.2269G>T (p.Ala757Ser) n.129-900C>A c.2053G>T (p.Ala685Ser) c.2158G>T (p.Ala720Ser) c.1774G>T (p.Ala592Ser) | dbSNP |
1 | g.97305289C>G | CA341375063 | DPYD,DPYD-AS1 | c.2269G>C (p.Ala757Pro) n.129-900C>G c.2053G>C (p.Ala685Pro) c.2158G>C (p.Ala720Pro) c.1774G>C (p.Ala592Pro) | ClinVar dbSNP gnomAD v4 |
1 | g.97305289C>T | CA341375062 | DPYD,DPYD-AS1 | c.2269G>A (p.Ala757Thr) n.129-900C>T c.2053G>A (p.Ala685Thr) c.2158G>A (p.Ala720Thr) c.1774G>A (p.Ala592Thr) | dbSNP |
1 | g.97305290A>C | CA341375064 | DPYD,DPYD-AS1 | c.2268T>G (p.Ile756Met) n.129-899A>C c.2052T>G (p.Ile684Met) c.2157T>G (p.Ile719Met) c.1773T>G (p.Ile591Met) | |
1 | g.97305290A>G | CA419137428 | DPYD,DPYD-AS1 | c.2268T>C (p.Ile756=) n.129-899A>G c.2052T>C (p.Ile684=) c.2157T>C (p.Ile719=) c.1773T>C (p.Ile591=) | dbSNP |
1 | g.97305290A>T | CA419137427 | DPYD,DPYD-AS1 | c.2268T>A (p.Ile756=) n.129-899A>T c.2052T>A (p.Ile684=) c.2157T>A (p.Ile719=) c.1773T>A (p.Ile591=) | |
1 | g.97305291A= | CA1182808450 | DPYD,DPYD-AS1 | c.2267T= (p.Ile756=) n.129-898A= c.2051T= (p.Ile684=) c.2156T= (p.Ile719=) c.1772T= (p.Ile591=) | |
1 | g.97305291A>C | CA341375065 | DPYD,DPYD-AS1 | c.2267T>G (p.Ile756Ser) n.129-898A>C c.2051T>G (p.Ile684Ser) c.2156T>G (p.Ile719Ser) c.1772T>G (p.Ile591Ser) |