| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.68810197_68810341del | CA645596626 | CDH1 | c.688_832del n.454+1349_455-1343del n.759_903del c.532_676del c.-48_97del c.-928_-784del c.-1132_-988del | COSMIC |
| 16 | g.68810205_68810206del | CA16614952 | CDH1 | c.696_697del (p.His233ArgfsTer10) n.454+1357_454+1358del n.767_768del c.540_541del (p.His181ArgfsTer10) c.-40_-39del (p.=) c.-920_-919del (p.=) c.-1124_-1123del (p.=) | ClinVar dbSNP COSMIC |
| 16 | g.68810205T>A | CA496152756 | CDH1 | c.696T>A (p.Ser232=) n.454+1357T>A n.767T>A c.540T>A (p.Ser180=) c.-40T>A (p.=) c.-920T>A (p.=) c.-1124T>A (p.=) | |
| 16 | g.68810205T>C | CA496152757 | CDH1 | c.696T>C (p.Ser232=) n.454+1357T>C n.767T>C c.540T>C (p.Ser180=) c.-40T>C (p.=) c.-920T>C (p.=) c.-1124T>C (p.=) | |
| 16 | g.68810205T>G | CA496152758 | CDH1 | c.696T>G (p.Ser232=) n.454+1357T>G n.767T>G c.540T>G (p.Ser180=) c.-40T>G (p.=) c.-920T>G (p.=) c.-1124T>G (p.=) | |
| 16 | g.68810206C>A | CA396458385 | CDH1 | c.697C>A (p.His233Asn) n.454+1358C>A n.768C>A c.541C>A (p.His181Asn) c.-39C>A (p.=) c.-919C>A (p.=) c.-1123C>A (p.=) | |
| 16 | g.68810206C= | CA2229966873 | CDH1 | c.697C= (p.His233=) n.454+1358C= n.768C= c.541C= (p.His181=) c.-39C= (p.=) c.-919C= (p.=) c.-1123C= (p.=) | |
| 16 | g.68810206C>G | CA396458387 | CDH1 | c.697C>G (p.His233Asp) n.454+1358C>G n.768C>G c.541C>G (p.His181Asp) c.-39C>G (p.=) c.-919C>G (p.=) c.-1123C>G (p.=) | |
| 16 | g.68810206C>T | CA396458386 | CDH1 | c.697C>T (p.His233Tyr) n.454+1358C>T n.768C>T c.541C>T (p.His181Tyr) c.-39C>T (p.=) c.-919C>T (p.=) c.-1123C>T (p.=) | ClinVar gnomAD |
| 16 | g.68810207A>C | CA396458388 | CDH1 | c.698A>C (p.His233Pro) n.454+1359A>C n.769A>C c.542A>C (p.His181Pro) c.-38A>C (p.=) c.-918A>C (p.=) c.-1122A>C (p.=) | |
| 16 | g.68810207A>G | CA396458389 | CDH1 | c.698A>G (p.His233Arg) n.454+1359A>G n.769A>G c.542A>G (p.His181Arg) c.-38A>G (p.=) c.-918A>G (p.=) c.-1122A>G (p.=) | |
| 16 | g.68810207A>T | CA396458390 | CDH1 | c.698A>T (p.His233Leu) n.454+1359A>T n.769A>T c.542A>T (p.His181Leu) c.-38A>T (p.=) c.-918A>T (p.=) c.-1122A>T (p.=) | |
| 16 | g.68810208C>A | CA396458392 | CDH1 | c.699C>A (p.His233Gln) n.454+1360C>A n.770C>A c.543C>A (p.His181Gln) c.-37C>A (p.=) c.-917C>A (p.=) c.-1121C>A (p.=) | |
| 16 | g.68810208C= | CA2229966878 | CDH1 | c.699C= (p.His233=) n.454+1360C= n.770C= c.543C= (p.His181=) c.-37C= (p.=) c.-917C= (p.=) c.-1121C= (p.=) | |
| 16 | g.68810208C>G | CA10580090 | CDH1 | c.699C>G (p.His233Gln) n.454+1360C>G n.770C>G c.543C>G (p.His181Gln) c.-37C>G (p.=) c.-917C>G (p.=) c.-1121C>G (p.=) | ClinVar dbSNP COSMIC |
| 16 | g.68810208C>T | CA290003 | CDH1 | c.699C>T (p.His233=) n.454+1360C>T n.770C>T c.543C>T (p.His181=) c.-37C>T (p.=) c.-917C>T (p.=) c.-1121C>T (p.=) | ClinVar dbSNP ExAC gnomAD COSMIC |
| 16 | g.68810209G>A | CA10583410 | CDH1 | c.700G>A (p.Ala234Thr) n.454+1361G>A n.771G>A c.544G>A (p.Ala182Thr) c.-36G>A (p.=) c.-916G>A (p.=) c.-1120G>A (p.=) | ClinVar dbSNP COSMIC |
| 16 | g.68810209G>C | CA396458396 | CDH1 | c.700G>C (p.Ala234Pro) n.454+1361G>C n.771G>C c.544G>C (p.Ala182Pro) c.-36G>C (p.=) c.-916G>C (p.=) c.-1120G>C (p.=) | |
| 16 | g.68810209G= | CA2229966888 | CDH1 | c.700G= (p.Ala234=) n.454+1361G= n.771G= c.544G= (p.Ala182=) c.-36G= (p.=) c.-916G= (p.=) c.-1120G= (p.=) | |
| 16 | g.68810209G>T | CA396458398 | CDH1 | c.700G>T (p.Ala234Ser) n.454+1361G>T n.771G>T c.544G>T (p.Ala182Ser) c.-36G>T (p.=) c.-916G>T (p.=) c.-1120G>T (p.=) | |
| 16 | g.68810210C>A | CA396458400 | CDH1 | c.701C>A (p.Ala234Asp) n.454+1362C>A n.772C>A c.545C>A (p.Ala182Asp) c.-35C>A (p.=) c.-915C>A (p.=) c.-1119C>A (p.=) | |
| 16 | g.68810210C= | CA2229966893 | CDH1 | c.701C= (p.Ala234=) n.454+1362C= n.772C= c.545C= (p.Ala182=) c.-35C= (p.=) c.-915C= (p.=) c.-1119C= (p.=) | |
| 16 | g.68810210C>G | CA396458401 | CDH1 | c.701C>G (p.Ala234Gly) n.454+1362C>G n.772C>G c.545C>G (p.Ala182Gly) c.-35C>G (p.=) c.-915C>G (p.=) c.-1119C>G (p.=) | |
| 16 | g.68810210C>T | CA396458403 | CDH1 | c.701C>T (p.Ala234Val) n.454+1362C>T n.772C>T c.545C>T (p.Ala182Val) c.-35C>T (p.=) c.-915C>T (p.=) c.-1119C>T (p.=) | |
| 16 | g.68810211T>A | CA496152759 | CDH1 | c.702T>A (p.Ala234=) n.454+1363T>A n.773T>A c.546T>A (p.Ala182=) c.-34T>A (p.=) c.-914T>A (p.=) c.-1118T>A (p.=) | |
| 16 | g.68810211T>C | CA496152760 | CDH1 | c.702T>C (p.Ala234=) n.454+1363T>C n.773T>C c.546T>C (p.Ala182=) c.-34T>C (p.=) c.-914T>C (p.=) c.-1118T>C (p.=) | |
| 16 | g.68810211T>G | CA496152761 | CDH1 | c.702T>G (p.Ala234=) n.454+1363T>G n.773T>G c.546T>G (p.Ala182=) c.-34T>G (p.=) c.-914T>G (p.=) c.-1118T>G (p.=) | ClinVar |
| 16 | g.68810211T= | CA2229966896 | CDH1 | c.702T= (p.Ala234=) n.454+1363T= n.773T= c.546T= (p.Ala182=) c.-34T= (p.=) c.-914T= (p.=) c.-1118T= (p.=) | |
| 16 | g.68810212G>A | CA396458408 | CDH1 | c.703G>A (p.Val235Met) n.454+1364G>A n.774G>A c.547G>A (p.Val183Met) c.-33G>A (p.=) c.-913G>A (p.=) c.-1117G>A (p.=) | ClinVar |
| 16 | g.68810212G>C | CA396458406 | CDH1 | c.703G>C (p.Val235Leu) n.454+1364G>C n.774G>C c.547G>C (p.Val183Leu) c.-33G>C (p.=) c.-913G>C (p.=) c.-1117G>C (p.=) | |
| 16 | g.68810212G= | CA2229966898 | CDH1 | c.703G= (p.Val235=) n.454+1364G= n.774G= c.547G= (p.Val183=) c.-33G= (p.=) c.-913G= (p.=) c.-1117G= (p.=) | |
| 16 | g.68810212G>T | CA396458405 | CDH1 | c.703G>T (p.Val235Leu) n.454+1364G>T n.774G>T c.547G>T (p.Val183Leu) c.-33G>T (p.=) c.-913G>T (p.=) c.-1117G>T (p.=) | |
| 16 | g.68810213T>A | CA396458410 | CDH1 | c.704T>A (p.Val235Glu) n.454+1365T>A n.775T>A c.548T>A (p.Val183Glu) c.-32T>A (p.=) c.-912T>A (p.=) c.-1116T>A (p.=) | |
| 16 | g.68810213T>C | CA396458411 | CDH1 | c.704T>C (p.Val235Ala) n.454+1365T>C n.775T>C c.548T>C (p.Val183Ala) c.-32T>C (p.=) c.-912T>C (p.=) c.-1116T>C (p.=) | |
| 16 | g.68810213T>G | CA396458413 | CDH1 | c.704T>G (p.Val235Gly) n.454+1365T>G n.775T>G c.548T>G (p.Val183Gly) c.-32T>G (p.=) c.-912T>G (p.=) c.-1116T>G (p.=) | |
| 16 | g.68810214G>A | CA496152762 | CDH1 | c.705G>A (p.Val235=) n.454+1366G>A n.776G>A c.549G>A (p.Val183=) c.-31G>A (p.=) c.-911G>A (p.=) c.-1115G>A (p.=) | |
| 16 | g.68810214G>C | CA496152763 | CDH1 | c.705G>C (p.Val235=) n.454+1366G>C n.776G>C c.549G>C (p.Val183=) c.-31G>C (p.=) c.-911G>C (p.=) c.-1115G>C (p.=) | |
| 16 | g.68810214G>T | CA496152764 | CDH1 | c.705G>T (p.Val235=) n.454+1366G>T n.776G>T c.549G>T (p.Val183=) c.-31G>T (p.=) c.-911G>T (p.=) c.-1115G>T (p.=) | |
| 16 | g.68810215T>A | CA396458415 | CDH1 | c.706T>A (p.Ser236Thr) n.454+1367T>A n.777T>A c.550T>A (p.Ser184Thr) c.-30T>A (p.=) c.-910T>A (p.=) c.-1114T>A (p.=) | |
| 16 | g.68810215T>C | CA396458417 | CDH1 | c.706T>C (p.Ser236Pro) n.454+1367T>C n.777T>C c.550T>C (p.Ser184Pro) c.-30T>C (p.=) c.-910T>C (p.=) c.-1114T>C (p.=) | |
| 16 | g.68810215T>G | CA396458418 | CDH1 | c.706T>G (p.Ser236Ala) n.454+1367T>G n.777T>G c.550T>G (p.Ser184Ala) c.-30T>G (p.=) c.-910T>G (p.=) c.-1114T>G (p.=) | |
| 16 | g.68810216C>A | CA298974 | CDH1 | c.707C>A (p.Ser236Ter) n.454+1368C>A n.778C>A c.551C>A (p.Ser184Ter) c.-29C>A (p.=) c.-909C>A (p.=) c.-1113C>A (p.=) | ClinVar dbSNP |
| 16 | g.68810216C= | CA2229966902 | CDH1 | c.707C= (p.Ser236=) n.454+1368C= n.778C= c.551C= (p.Ser184=) c.-29C= (p.=) c.-909C= (p.=) c.-1113C= (p.=) | |
| 16 | g.68810216C>G | CA396458421 | CDH1 | c.707C>G (p.Ser236Ter) n.454+1368C>G n.778C>G c.551C>G (p.Ser184Ter) c.-29C>G (p.=) c.-909C>G (p.=) c.-1113C>G (p.=) | |
| 16 | g.68810216C>T | CA396458423 | CDH1 | c.707C>T (p.Ser236Leu) n.454+1368C>T n.778C>T c.551C>T (p.Ser184Leu) c.-29C>T (p.=) c.-909C>T (p.=) c.-1113C>T (p.=) | |
| 16 | g.68810217A= | CA2229966903 | CDH1 | c.708A= (p.Ser236=) n.454+1369A= n.779A= c.552A= (p.Ser184=) c.-28A= (p.=) c.-908A= (p.=) c.-1112A= (p.=) | |
| 16 | g.68810217A>C | CA338203 | CDH1 | c.708A>C (p.Ser236=) n.454+1369A>C n.779A>C c.552A>C (p.Ser184=) c.-28A>C (p.=) c.-908A>C (p.=) c.-1112A>C (p.=) | ClinVar dbSNP |
| 16 | g.68810217A>G | CA496152766 | CDH1 | c.708A>G (p.Ser236=) n.454+1369A>G n.779A>G c.552A>G (p.Ser184=) c.-28A>G (p.=) c.-908A>G (p.=) c.-1112A>G (p.=) | |
| 16 | g.68810217A>T | CA496152765 | CDH1 | c.708A>T (p.Ser236=) n.454+1369A>T n.779A>T c.552A>T (p.Ser184=) c.-28A>T (p.=) c.-908A>T (p.=) c.-1112A>T (p.=) | |
| 16 | g.68810218T>A | CA396458425 | CDH1 | c.709T>A (p.Ser237Thr) n.454+1370T>A n.780T>A c.553T>A (p.Ser185Thr) c.-27T>A (p.=) c.-907T>A (p.=) c.-1111T>A (p.=) |