Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.68810197_68810341delCA645596626CDH1c.688_832del
n.454+1349_455-1343del
n.759_903del
c.532_676del
c.-48_97del
c.-928_-784del
c.-1132_-988del
COSMIC
16g.68810205_68810206delCA16614952CDH1c.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
16g.68810205T>ACA496152756CDH1c.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.=)
16g.68810205T>CCA496152757CDH1c.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.=)
16g.68810205T>GCA496152758CDH1c.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.=)
16g.68810206C>ACA396458385CDH1c.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.=)
16g.68810206C=CA2229966873CDH1c.697C= (p.His233=)
n.454+1358C=
n.768C=
c.541C= (p.His181=)
c.-39C= (p.=)
c.-919C= (p.=)
c.-1123C= (p.=)
16g.68810206C>GCA396458387CDH1c.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.=)
16g.68810206C>TCA396458386CDH1c.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
16g.68810207A>CCA396458388CDH1c.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.=)
16g.68810207A>GCA396458389CDH1c.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.=)
16g.68810207A>TCA396458390CDH1c.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.=)
16g.68810208C>ACA396458392CDH1c.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.=)
16g.68810208C=CA2229966878CDH1c.699C= (p.His233=)
n.454+1360C=
n.770C=
c.543C= (p.His181=)
c.-37C= (p.=)
c.-917C= (p.=)
c.-1121C= (p.=)
16g.68810208C>GCA10580090CDH1c.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
16g.68810208C>TCA290003CDH1c.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
16g.68810209G>ACA10583410CDH1c.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
16g.68810209G>CCA396458396CDH1c.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.=)
16g.68810209G=CA2229966888CDH1c.700G= (p.Ala234=)
n.454+1361G=
n.771G=
c.544G= (p.Ala182=)
c.-36G= (p.=)
c.-916G= (p.=)
c.-1120G= (p.=)
16g.68810209G>TCA396458398CDH1c.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.=)
16g.68810210C>ACA396458400CDH1c.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.=)
16g.68810210C=CA2229966893CDH1c.701C= (p.Ala234=)
n.454+1362C=
n.772C=
c.545C= (p.Ala182=)
c.-35C= (p.=)
c.-915C= (p.=)
c.-1119C= (p.=)
16g.68810210C>GCA396458401CDH1c.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.=)
16g.68810210C>TCA396458403CDH1c.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.=)
16g.68810211T>ACA496152759CDH1c.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.=)
16g.68810211T>CCA496152760CDH1c.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.=)
16g.68810211T>GCA496152761CDH1c.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
16g.68810211T=CA2229966896CDH1c.702T= (p.Ala234=)
n.454+1363T=
n.773T=
c.546T= (p.Ala182=)
c.-34T= (p.=)
c.-914T= (p.=)
c.-1118T= (p.=)
16g.68810212G>ACA396458408CDH1c.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
16g.68810212G>CCA396458406CDH1c.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.=)
16g.68810212G=CA2229966898CDH1c.703G= (p.Val235=)
n.454+1364G=
n.774G=
c.547G= (p.Val183=)
c.-33G= (p.=)
c.-913G= (p.=)
c.-1117G= (p.=)
16g.68810212G>TCA396458405CDH1c.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.=)
16g.68810213T>ACA396458410CDH1c.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.=)
16g.68810213T>CCA396458411CDH1c.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.=)
16g.68810213T>GCA396458413CDH1c.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.=)
16g.68810214G>ACA496152762CDH1c.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.=)
16g.68810214G>CCA496152763CDH1c.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.=)
16g.68810214G>TCA496152764CDH1c.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.=)
16g.68810215T>ACA396458415CDH1c.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.=)
16g.68810215T>CCA396458417CDH1c.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.=)
16g.68810215T>GCA396458418CDH1c.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.=)
16g.68810216C>ACA298974CDH1c.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
16g.68810216C=CA2229966902CDH1c.707C= (p.Ser236=)
n.454+1368C=
n.778C=
c.551C= (p.Ser184=)
c.-29C= (p.=)
c.-909C= (p.=)
c.-1113C= (p.=)
16g.68810216C>GCA396458421CDH1c.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.=)
16g.68810216C>TCA396458423CDH1c.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.=)
16g.68810217A=CA2229966903CDH1c.708A= (p.Ser236=)
n.454+1369A=
n.779A=
c.552A= (p.Ser184=)
c.-28A= (p.=)
c.-908A= (p.=)
c.-1112A= (p.=)
16g.68810217A>CCA338203CDH1c.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
16g.68810217A>GCA496152766CDH1c.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.=)
16g.68810217A>TCA496152765CDH1c.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.=)
16g.68810218T>ACA396458425CDH1c.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.=)

Number of alleles fetched