Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47795896_47805709delCA658655622MSH6c.460_3646+2del
c.238-2715_3256+2del
c.163_3349+2del
c.169+2491_170-6451del (p.=)
c.*124+2290_*125-6451del (p.=)
c.458-2715_*2993+2del
c.-443_2740+2del
c.-279-2715_2740+2del
c.-2637_550+2del
c.277_3463+2del
2g.47799557_47804482dupCA10575504MSH6c.1574_3439-428dup
c.1184_3049-428dup
c.1277_3142-428dup
c.169+3714_169+8639dup (p.=)
c.*124+3513_*124+8438dup (p.=)
c.*921_*2786-428dup
c.668_2533-428dup
c.-1523_335-420dup
c.1391_3256-428dup
ClinVar
2g.47799688_47799689delCA009079MSH6c.1705_1706del (p.Phe569HisfsTer7)
c.1315_1316del (p.Phe439HisfsTer7)
c.1408_1409del (p.Phe470HisfsTer7)
c.169+8509_169+8510del (p.=)
c.*124+8308_*124+8309del (p.=)
c.*1052_*1053del (p.=)
c.799_800del (p.Phe267HisfsTer7)
c.1702_1703del (p.Phe568HisfsTer7)
c.-1392_-1391del (p.=)
c.1522_1523del (p.Phe508HisfsTer7)
ClinVar dbSNP gnomAD
2g.47799689T>ACA346748545MSH6c.1706T>A (p.Phe569Tyr)
c.1316T>A (p.Phe439Tyr)
c.1409T>A (p.Phe470Tyr)
c.169+8506A>T (p.=)
c.*124+8305A>T (p.=)
c.*1053T>A (p.=)
c.800T>A (p.Phe267Tyr)
c.1703T>A (p.Phe568Tyr)
c.-1391T>A (p.=)
c.1523T>A (p.Phe508Tyr)
2g.47799689T>CCA346748546MSH6c.1706T>C (p.Phe569Ser)
c.1316T>C (p.Phe439Ser)
c.1409T>C (p.Phe470Ser)
c.169+8506A>G (p.=)
c.*124+8305A>G (p.=)
c.*1053T>C (p.=)
c.800T>C (p.Phe267Ser)
c.1703T>C (p.Phe568Ser)
c.-1391T>C (p.=)
c.1523T>C (p.Phe508Ser)
ClinVar
2g.47799689T>GCA346748544MSH6c.1706T>G (p.Phe569Cys)
c.1316T>G (p.Phe439Cys)
c.1409T>G (p.Phe470Cys)
c.169+8506A>C (p.=)
c.*124+8305A>C (p.=)
c.*1053T>G (p.=)
c.800T>G (p.Phe267Cys)
c.1703T>G (p.Phe568Cys)
c.-1391T>G (p.=)
c.1523T>G (p.Phe508Cys)
2g.47799689T=CA2496048919MSH6c.1706T= (p.Phe569=)
c.1316T= (p.Phe439=)
c.1409T= (p.Phe470=)
c.169+8506A= (p.=)
c.*124+8305A= (p.=)
c.*1053T= (p.=)
c.800T= (p.Phe267=)
c.1703T= (p.Phe568=)
c.-1391T= (p.=)
c.1523T= (p.Phe508=)
2g.47799689_47799690delinsTCCA2496048920MSH6c.1706_1707delinsTC (p.Phe569=)
c.1316_1317delinsTC (p.Phe439=)
c.1409_1410delinsTC (p.Phe470=)
c.169+8505_169+8506delinsGA (p.=)
c.*124+8304_*124+8305delinsGA (p.=)
c.*1053_*1054delinsTC (p.=)
c.800_801delinsTC (p.Phe267=)
c.1703_1704delinsTC (p.Phe568=)
c.-1391_-1390delinsTC (p.=)
c.1523_1524delinsTC (p.Phe508=)
2g.47799690delCA916079933MSH6c.1707del (p.Phe569LeufsTer2)
c.1317del (p.Phe439LeufsTer2)
c.1410del (p.Phe470LeufsTer2)
c.169+8505del (p.=)
c.*124+8304del (p.=)
c.*1054del (p.=)
c.801del (p.Phe267LeufsTer2)
c.1704del (p.Phe568LeufsTer2)
c.-1390del (p.=)
c.1524del (p.Phe508LeufsTer2)
ClinVar dbSNP
2g.47799690C>ACA346748550MSH6c.1707C>A (p.Phe569Leu)
c.1317C>A (p.Phe439Leu)
c.1410C>A (p.Phe470Leu)
c.169+8505G>T (p.=)
c.*124+8304G>T (p.=)
c.*1054C>A (p.=)
c.801C>A (p.Phe267Leu)
c.1704C>A (p.Phe568Leu)
c.-1390C>A (p.=)
c.1524C>A (p.Phe508Leu)
2g.47799690C=CA2496048921MSH6c.1707C= (p.Phe569=)
c.1317C= (p.Phe439=)
c.1410C= (p.Phe470=)
c.169+8505G= (p.=)
c.*124+8304G= (p.=)
c.*1054C= (p.=)
c.801C= (p.Phe267=)
c.1704C= (p.Phe568=)
c.-1390C= (p.=)
c.1524C= (p.Phe508=)
2g.47799690C>GCA346748554MSH6c.1707C>G (p.Phe569Leu)
c.1317C>G (p.Phe439Leu)
c.1410C>G (p.Phe470Leu)
c.169+8505G>C (p.=)
c.*124+8304G>C (p.=)
c.*1054C>G (p.=)
c.801C>G (p.Phe267Leu)
c.1704C>G (p.Phe568Leu)
c.-1390C>G (p.=)
c.1524C>G (p.Phe508Leu)
2g.47799690C>TCA426120975MSH6c.1707C>T (p.Phe569=)
c.1317C>T (p.Phe439=)
c.1410C>T (p.Phe470=)
c.169+8505G>A (p.=)
c.*124+8304G>A (p.=)
c.*1054C>T (p.=)
c.801C>T (p.Phe267=)
c.1704C>T (p.Phe568=)
c.-1390C>T (p.=)
c.1524C>T (p.Phe508=)
ClinVar
2g.47799691A=CA2496048922MSH6c.1708A= (p.Ile570=)
c.1318A= (p.Ile440=)
c.1411A= (p.Ile471=)
c.169+8504T= (p.=)
c.*124+8303T= (p.=)
c.*1055A= (p.=)
c.802A= (p.Ile268=)
c.1705A= (p.Ile569=)
c.-1389A= (p.=)
c.1525A= (p.Ile509=)
2g.47799691A>CCA346748557MSH6c.1708A>C (p.Ile570Leu)
c.1318A>C (p.Ile440Leu)
c.1411A>C (p.Ile471Leu)
c.169+8504T>G (p.=)
c.*124+8303T>G (p.=)
c.*1055A>C (p.=)
c.802A>C (p.Ile268Leu)
c.1705A>C (p.Ile569Leu)
c.-1389A>C (p.=)
c.1525A>C (p.Ile509Leu)
2g.47799691A>GCA068049MSH6c.1708A>G (p.Ile570Val)
c.1318A>G (p.Ile440Val)
c.1411A>G (p.Ile471Val)
c.169+8504T>C (p.=)
c.*124+8303T>C (p.=)
c.*1055A>G (p.=)
c.802A>G (p.Ile268Val)
c.1705A>G (p.Ile569Val)
c.-1389A>G (p.=)
c.1525A>G (p.Ile509Val)
ClinVar dbSNP ExAC gnomAD
2g.47799691A>TCA346748563MSH6c.1708A>T (p.Ile570Leu)
c.1318A>T (p.Ile440Leu)
c.1411A>T (p.Ile471Leu)
c.169+8504T>A (p.=)
c.*124+8303T>A (p.=)
c.*1055A>T (p.=)
c.802A>T (p.Ile268Leu)
c.1705A>T (p.Ile569Leu)
c.-1389A>T (p.=)
c.1525A>T (p.Ile509Leu)
ClinVar
2g.47799692T>ACA346748566MSH6c.1709T>A (p.Ile570Lys)
c.1319T>A (p.Ile440Lys)
c.1412T>A (p.Ile471Lys)
c.169+8503A>T (p.=)
c.*124+8302A>T (p.=)
c.*1056T>A (p.=)
c.803T>A (p.Ile268Lys)
c.1706T>A (p.Ile569Lys)
c.-1388T>A (p.=)
c.1526T>A (p.Ile509Lys)
2g.47799692T>CCA346748567MSH6c.1709T>C (p.Ile570Thr)
c.1319T>C (p.Ile440Thr)
c.1412T>C (p.Ile471Thr)
c.169+8503A>G (p.=)
c.*124+8302A>G (p.=)
c.*1056T>C (p.=)
c.803T>C (p.Ile268Thr)
c.1706T>C (p.Ile569Thr)
c.-1388T>C (p.=)
c.1526T>C (p.Ile509Thr)
ClinVar
2g.47799692T>GCA346748568MSH6c.1709T>G (p.Ile570Arg)
c.1319T>G (p.Ile440Arg)
c.1412T>G (p.Ile471Arg)
c.169+8503A>C (p.=)
c.*124+8302A>C (p.=)
c.*1056T>G (p.=)
c.803T>G (p.Ile268Arg)
c.1706T>G (p.Ile569Arg)
c.-1388T>G (p.=)
c.1526T>G (p.Ile509Arg)
2g.47799693A=CA2496048923MSH6c.1710A= (p.Ile570=)
c.1320A= (p.Ile440=)
c.1413A= (p.Ile471=)
c.169+8502T= (p.=)
c.*124+8301T= (p.=)
c.*1057A= (p.=)
c.804A= (p.Ile268=)
c.1707A= (p.Ile569=)
c.-1387A= (p.=)
c.1527A= (p.Ile509=)
2g.47799693A>CCA426120978MSH6c.1710A>C (p.Ile570=)
c.1320A>C (p.Ile440=)
c.1413A>C (p.Ile471=)
c.169+8502T>G (p.=)
c.*124+8301T>G (p.=)
c.*1057A>C (p.=)
c.804A>C (p.Ile268=)
c.1707A>C (p.Ile569=)
c.-1387A>C (p.=)
c.1527A>C (p.Ile509=)
2g.47799693A>GCA346748569MSH6c.1710A>G (p.Ile570Met)
c.1320A>G (p.Ile440Met)
c.1413A>G (p.Ile471Met)
c.169+8502T>C (p.=)
c.*124+8301T>C (p.=)
c.*1057A>G (p.=)
c.804A>G (p.Ile268Met)
c.1707A>G (p.Ile569Met)
c.-1387A>G (p.=)
c.1527A>G (p.Ile509Met)
ClinVar
2g.47799693A>TCA426120981MSH6c.1710A>T (p.Ile570=)
c.1320A>T (p.Ile440=)
c.1413A>T (p.Ile471=)
c.169+8502T>A (p.=)
c.*124+8301T>A (p.=)
c.*1057A>T (p.=)
c.804A>T (p.Ile268=)
c.1707A>T (p.Ile569=)
c.-1387A>T (p.=)
c.1527A>T (p.Ile509=)
2g.47799694G>ACA346748571MSH6c.1711G>A (p.Gly571Ser)
c.1321G>A (p.Gly441Ser)
c.1414G>A (p.Gly472Ser)
c.169+8501C>T (p.=)
c.*124+8300C>T (p.=)
c.*1058G>A (p.=)
c.805G>A (p.Gly269Ser)
c.1708G>A (p.Gly570Ser)
c.-1386G>A (p.=)
c.1528G>A (p.Gly510Ser)
ClinVar
2g.47799694G>CCA068053MSH6c.1711G>C (p.Gly571Arg)
c.1321G>C (p.Gly441Arg)
c.1414G>C (p.Gly472Arg)
c.169+8501C>G (p.=)
c.*124+8300C>G (p.=)
c.*1058G>C (p.=)
c.805G>C (p.Gly269Arg)
c.1708G>C (p.Gly570Arg)
c.-1386G>C (p.=)
c.1528G>C (p.Gly510Arg)
dbSNP ExAC gnomAD
2g.47799694G=CA2496048924MSH6c.1711G= (p.Gly571=)
c.1321G= (p.Gly441=)
c.1414G= (p.Gly472=)
c.169+8501C= (p.=)
c.*124+8300C= (p.=)
c.*1058G= (p.=)
c.805G= (p.Gly269=)
c.1708G= (p.Gly570=)
c.-1386G= (p.=)
c.1528G= (p.Gly510=)
2g.47799694G>TCA346748576MSH6c.1711G>T (p.Gly571Cys)
c.1321G>T (p.Gly441Cys)
c.1414G>T (p.Gly472Cys)
c.169+8501C>A (p.=)
c.*124+8300C>A (p.=)
c.*1058G>T (p.=)
c.805G>T (p.Gly269Cys)
c.1708G>T (p.Gly570Cys)
c.-1386G>T (p.=)
c.1528G>T (p.Gly510Cys)
2g.47799695G>ACA337622MSH6c.1712G>A (p.Gly571Asp)
c.1322G>A (p.Gly441Asp)
c.1415G>A (p.Gly472Asp)
c.169+8500C>T (p.=)
c.*124+8299C>T (p.=)
c.*1059G>A (p.=)
c.806G>A (p.Gly269Asp)
c.1709G>A (p.Gly570Asp)
c.-1385G>A (p.=)
c.1529G>A (p.Gly510Asp)
ClinVar dbSNP
2g.47799695G>CCA346748588MSH6c.1712G>C (p.Gly571Ala)
c.1322G>C (p.Gly441Ala)
c.1415G>C (p.Gly472Ala)
c.169+8500C>G (p.=)
c.*124+8299C>G (p.=)
c.*1059G>C (p.=)
c.806G>C (p.Gly269Ala)
c.1709G>C (p.Gly570Ala)
c.-1385G>C (p.=)
c.1529G>C (p.Gly510Ala)
2g.47799695G=CA2496048925MSH6c.1712G= (p.Gly571=)
c.1322G= (p.Gly441=)
c.1415G= (p.Gly472=)
c.169+8500C= (p.=)
c.*124+8299C= (p.=)
c.*1059G= (p.=)
c.806G= (p.Gly269=)
c.1709G= (p.Gly570=)
c.-1385G= (p.=)
c.1529G= (p.Gly510=)
2g.47799695G>TCA346748583MSH6c.1712G>T (p.Gly571Val)
c.1322G>T (p.Gly441Val)
c.1415G>T (p.Gly472Val)
c.169+8500C>A (p.=)
c.*124+8299C>A (p.=)
c.*1059G>T (p.=)
c.806G>T (p.Gly269Val)
c.1709G>T (p.Gly570Val)
c.-1385G>T (p.=)
c.1529G>T (p.Gly510Val)
2g.47799696T>ACA426120984MSH6c.1713T>A (p.Gly571=)
c.1323T>A (p.Gly441=)
c.1416T>A (p.Gly472=)
c.169+8499A>T (p.=)
c.*124+8298A>T (p.=)
c.*1060T>A (p.=)
c.807T>A (p.Gly269=)
c.1710T>A (p.Gly570=)
c.-1384T>A (p.=)
c.1530T>A (p.Gly510=)
2g.47799696T>CCA10578076MSH6c.1713T>C (p.Gly571=)
c.1323T>C (p.Gly441=)
c.1416T>C (p.Gly472=)
c.169+8499A>G (p.=)
c.*124+8298A>G (p.=)
c.*1060T>C (p.=)
c.807T>C (p.Gly269=)
c.1710T>C (p.Gly570=)
c.-1384T>C (p.=)
c.1530T>C (p.Gly510=)
ClinVar dbSNP
2g.47799696T>GCA068061MSH6c.1713T>G (p.Gly571=)
c.1323T>G (p.Gly441=)
c.1416T>G (p.Gly472=)
c.169+8499A>C (p.=)
c.*124+8298A>C (p.=)
c.*1060T>G (p.=)
c.807T>G (p.Gly269=)
c.1710T>G (p.Gly570=)
c.-1384T>G (p.=)
c.1530T>G (p.Gly510=)
ClinVar dbSNP ExAC gnomAD
2g.47799696T=CA2496048926MSH6c.1713T= (p.Gly571=)
c.1323T= (p.Gly441=)
c.1416T= (p.Gly472=)
c.169+8499A= (p.=)
c.*124+8298A= (p.=)
c.*1060T= (p.=)
c.807T= (p.Gly269=)
c.1710T= (p.Gly570=)
c.-1384T= (p.=)
c.1530T= (p.Gly510=)
2g.47799697C>ACA346748595MSH6c.1714C>A (p.Gln572Lys)
c.1324C>A (p.Gln442Lys)
c.1417C>A (p.Gln473Lys)
c.169+8498G>T (p.=)
c.*124+8297G>T (p.=)
c.*1061C>A (p.=)
c.808C>A (p.Gln270Lys)
c.1711C>A (p.Gln571Lys)
c.-1383C>A (p.=)
c.1531C>A (p.Gln511Lys)
2g.47799697C=CA2496048927MSH6c.1714C= (p.Gln572=)
c.1324C= (p.Gln442=)
c.1417C= (p.Gln473=)
c.169+8498G= (p.=)
c.*124+8297G= (p.=)
c.*1061C= (p.=)
c.808C= (p.Gln270=)
c.1711C= (p.Gln571=)
c.-1383C= (p.=)
c.1531C= (p.Gln511=)
2g.47799697C>GCA346748599MSH6c.1714C>G (p.Gln572Glu)
c.1324C>G (p.Gln442Glu)
c.1417C>G (p.Gln473Glu)
c.169+8498G>C (p.=)
c.*124+8297G>C (p.=)
c.*1061C>G (p.=)
c.808C>G (p.Gln270Glu)
c.1711C>G (p.Gln571Glu)
c.-1383C>G (p.=)
c.1531C>G (p.Gln511Glu)
ClinVar
2g.47799697C>TCA16617658MSH6c.1714C>T (p.Gln572Ter)
c.1324C>T (p.Gln442Ter)
c.1417C>T (p.Gln473Ter)
c.169+8498G>A (p.=)
c.*124+8297G>A (p.=)
c.*1061C>T (p.=)
c.808C>T (p.Gln270Ter)
c.1711C>T (p.Gln571Ter)
c.-1383C>T (p.=)
c.1531C>T (p.Gln511Ter)
ClinVar COSMIC
2g.47799698A>CCA346748612MSH6c.1715A>C (p.Gln572Pro)
c.1325A>C (p.Gln442Pro)
c.1418A>C (p.Gln473Pro)
c.169+8497T>G (p.=)
c.*124+8296T>G (p.=)
c.*1062A>C (p.=)
c.809A>C (p.Gln270Pro)
c.1712A>C (p.Gln571Pro)
c.-1382A>C (p.=)
c.1532A>C (p.Gln511Pro)
2g.47799698A>GCA346748606MSH6c.1715A>G (p.Gln572Arg)
c.1325A>G (p.Gln442Arg)
c.1418A>G (p.Gln473Arg)
c.169+8497T>C (p.=)
c.*124+8296T>C (p.=)
c.*1062A>G (p.=)
c.809A>G (p.Gln270Arg)
c.1712A>G (p.Gln571Arg)
c.-1382A>G (p.=)
c.1532A>G (p.Gln511Arg)
2g.47799698A>TCA346748609MSH6c.1715A>T (p.Gln572Leu)
c.1325A>T (p.Gln442Leu)
c.1418A>T (p.Gln473Leu)
c.169+8497T>A (p.=)
c.*124+8296T>A (p.=)
c.*1062A>T (p.=)
c.809A>T (p.Gln270Leu)
c.1712A>T (p.Gln571Leu)
c.-1382A>T (p.=)
c.1532A>T (p.Gln511Leu)
2g.47799699G>ACA16610981MSH6c.1716G>A (p.Gln572=)
c.1326G>A (p.Gln442=)
c.1419G>A (p.Gln473=)
c.169+8496C>T (p.=)
c.*124+8295C>T (p.=)
c.*1063G>A (p.=)
c.810G>A (p.Gln270=)
c.1713G>A (p.Gln571=)
c.-1381G>A (p.=)
c.1533G>A (p.Gln511=)
ClinVar
2g.47799699G>CCA46709475MSH6c.1716G>C (p.Gln572His)
c.1326G>C (p.Gln442His)
c.1419G>C (p.Gln473His)
c.169+8496C>G (p.=)
c.*124+8295C>G (p.=)
c.*1063G>C (p.=)
c.810G>C (p.Gln270His)
c.1713G>C (p.Gln571His)
c.-1381G>C (p.=)
c.1533G>C (p.Gln511His)
ClinVar dbSNP
2g.47799699G=CA2496048928MSH6c.1716G= (p.Gln572=)
c.1326G= (p.Gln442=)
c.1419G= (p.Gln473=)
c.169+8496C= (p.=)
c.*124+8295C= (p.=)
c.*1063G= (p.=)
c.810G= (p.Gln270=)
c.1713G= (p.Gln571=)
c.-1381G= (p.=)
c.1533G= (p.Gln511=)
2g.47799699G>TCA068066MSH6c.1716G>T (p.Gln572His)
c.1326G>T (p.Gln442His)
c.1419G>T (p.Gln473His)
c.169+8496C>A (p.=)
c.*124+8295C>A (p.=)
c.*1063G>T (p.=)
c.810G>T (p.Gln270His)
c.1713G>T (p.Gln571His)
c.-1381G>T (p.=)
c.1533G>T (p.Gln511His)
ClinVar dbSNP ExAC gnomAD
2g.47799700T>ACA346748621MSH6c.1717T>A (p.Phe573Ile)
c.1327T>A (p.Phe443Ile)
c.1420T>A (p.Phe474Ile)
c.169+8495A>T (p.=)
c.*124+8294A>T (p.=)
c.*1064T>A (p.=)
c.811T>A (p.Phe271Ile)
c.1714T>A (p.Phe572Ile)
c.-1380T>A (p.=)
c.1534T>A (p.Phe512Ile)
2g.47799700T>CCA346748631MSH6c.1717T>C (p.Phe573Leu)
c.1327T>C (p.Phe443Leu)
c.1420T>C (p.Phe474Leu)
c.169+8495A>G (p.=)
c.*124+8294A>G (p.=)
c.*1064T>C (p.=)
c.811T>C (p.Phe271Leu)
c.1714T>C (p.Phe572Leu)
c.-1380T>C (p.=)
c.1534T>C (p.Phe512Leu)
2g.47799700T>GCA346748638MSH6c.1717T>G (p.Phe573Val)
c.1327T>G (p.Phe443Val)
c.1420T>G (p.Phe474Val)
c.169+8495A>C (p.=)
c.*124+8294A>C (p.=)
c.*1064T>G (p.=)
c.811T>G (p.Phe271Val)
c.1714T>G (p.Phe572Val)
c.-1380T>G (p.=)
c.1534T>G (p.Phe512Val)

Number of alleles fetched