| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.80674979_80674981del | CA2580613580 | MSH3 | c.1028-4_1028-2del (n.1028-4_1028-2del) c.860-4_860-2del (n.860-4_860-2del) | ClinVar dbSNP |
| 5 | g.80674981A= | CA1558493129 | MSH3 | c.1028-2A= (n.1028-2A=) c.860-2A= (n.860-2A=) | |
| 5 | g.80674981A>C | CA360267799 | MSH3 | c.1028-2A>C (n.1028-2A>C) c.860-2A>C (n.860-2A>C) | |
| 5 | g.80674981A>G | CA360267801 | MSH3 | c.1028-2A>G (n.1028-2A>G) c.860-2A>G (n.860-2A>G) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 5 | g.80674981A>T | CA360267803 | MSH3 | c.1028-2A>T (n.1028-2A>T) c.860-2A>T (n.860-2A>T) | ClinVar dbSNP |
| 5 | g.80674982A= | CA1558493137 | MSH3 | c.1028-1A= (n.1028-1A=) c.860-1A= (n.860-1A=) | |
| 5 | g.80674982A>C | CA360267805 | MSH3 | c.1028-1A>C (n.1028-1A>C) c.860-1A>C (n.860-1A>C) | ClinVar gnomAD v4 |
| 5 | g.80674982A>G | CA360267807 | MSH3 | c.1028-1A>G (n.1028-1A>G) c.860-1A>G (n.860-1A>G) | |
| 5 | g.80674982A>T | CA121295111 | MSH3 | c.1028-1A>T (n.1028-1A>T) c.860-1A>T (n.860-1A>T) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674983A= | CA1558493141 | MSH3 | c.1028A= (p.Asp343=) c.860A= (p.Asp287=) | |
| 5 | g.80674983A>C | CA360267810 | MSH3 | c.1028A>C (p.Asp343Ala) c.860A>C (p.Asp287Ala) | |
| 5 | g.80674983A>G | CA360267813 | MSH3 | c.1028A>G (p.Asp343Gly) c.860A>G (p.Asp287Gly) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80674983A>T | CA360267811 | MSH3 | c.1028A>T (p.Asp343Val) c.860A>T (p.Asp287Val) | |
| 5 | g.80674984T>A | CA360267814 | MSH3 | c.1029T>A (p.Asp343Glu) c.861T>A (p.Asp287Glu) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674984T>C | CA445159583 | MSH3 | c.1029T>C (p.Asp343=) c.861T>C (p.Asp287=) | ClinVar dbSNP |
| 5 | g.80674984T>G | CA360267815 | MSH3 | c.1029T>G (p.Asp343Glu) c.861T>G (p.Asp287Glu) | |
| 5 | g.80674985G>A | CA360267818 | MSH3 | c.1030G>A (p.Val344Met) c.862G>A (p.Val288Met) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80674985G>C | CA360267819 | MSH3 | c.1030G>C (p.Val344Leu) c.862G>C (p.Val288Leu) | |
| 5 | g.80674985G= | CA1558493147 | MSH3 | c.1030G= (p.Val344=) c.862G= (p.Val288=) | |
| 5 | g.80674985G>T | CA360267821 | MSH3 | c.1030G>T (p.Val344Leu) c.862G>T (p.Val288Leu) | ClinVar |
| 5 | g.80674986T>A | CA360267823 | MSH3 | c.1031T>A (p.Val344Glu) c.863T>A (p.Val288Glu) | |
| 5 | g.80674986T>C | CA360267825 | MSH3 | c.1031T>C (p.Val344Ala) c.863T>C (p.Val288Ala) | |
| 5 | g.80674986T>G | CA360267826 | MSH3 | c.1031T>G (p.Val344Gly) c.863T>G (p.Val288Gly) | |
| 5 | g.80674987G>A | CA445159590 | MSH3 | c.1032G>A (p.Val344=) c.864G>A (p.Val288=) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674987G>C | CA445159591 | MSH3 | c.1032G>C (p.Val344=) c.864G>C (p.Val288=) | |
| 5 | g.80674987G= | CA1558493157 | MSH3 | c.1032G= (p.Val344=) c.864G= (p.Val288=) | |
| 5 | g.80674987G>T | CA3327783 | MSH3 | c.1032G>T (p.Val344=) c.864G>T (p.Val288=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80674988A>C | CA360267829 | MSH3 | c.1033A>C (p.Asn345His) c.865A>C (p.Asn289His) | |
| 5 | g.80674988A>G | CA360267831 | MSH3 | c.1033A>G (p.Asn345Asp) c.865A>G (p.Asn289Asp) | |
| 5 | g.80674988A>T | CA360267832 | MSH3 | c.1033A>T (p.Asn345Tyr) c.865A>T (p.Asn289Tyr) | ClinVar |
| 5 | g.80674989A= | CA1558493163 | MSH3 | c.1034A= (p.Asn345=) c.866A= (p.Asn289=) | |
| 5 | g.80674989A>C | CA360267838 | MSH3 | c.1034A>C (p.Asn345Thr) c.866A>C (p.Asn289Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80674989A>G | CA360267837 | MSH3 | c.1034A>G (p.Asn345Ser) c.866A>G (p.Asn289Ser) | ClinVar dbSNP |
| 5 | g.80674989A>T | CA360267835 | MSH3 | c.1034A>T (p.Asn345Ile) c.866A>T (p.Asn289Ile) | |
| 5 | g.80674989_80674990delinsAT | CA1558493162 | MSH3 | c.1034_1035delinsAT (p.Asn345=) c.866_867delinsAT (p.Asn289=) | |
| 5 | g.80674990del | CA915943432 | MSH3 | c.1035del (p.Leu347Ter) c.867del (p.Leu291Ter) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674990T>A | CA360267841 | MSH3 | c.1035T>A (p.Asn345Lys) c.867T>A (p.Asn289Lys) | |
| 5 | g.80674990T>C | CA445159598 | MSH3 | c.1035T>C (p.Asn345=) c.867T>C (p.Asn289=) | |
| 5 | g.80674990T>G | CA360267842 | MSH3 | c.1035T>G (p.Asn345Lys) c.867T>G (p.Asn289Lys) | |
| 5 | g.80674991C>A | CA360267843 | MSH3 | c.1036C>A (p.Pro346Thr) c.868C>A (p.Pro290Thr) | dbSNP gnomAD v4 |
| 5 | g.80674991C= | CA1558493170 | MSH3 | c.1036C= (p.Pro346=) c.868C= (p.Pro290=) | |
| 5 | g.80674991C>G | CA360267845 | MSH3 | c.1036C>G (p.Pro346Ala) c.868C>G (p.Pro290Ala) | |
| 5 | g.80674991C>T | CA360267847 | MSH3 | c.1036C>T (p.Pro346Ser) c.868C>T (p.Pro290Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80674992C>A | CA360267848 | MSH3 | c.1037C>A (p.Pro346His) c.869C>A (p.Pro290His) | COSMIC COSMIC |
| 5 | g.80674992C= | CA1558493178 | MSH3 | c.1037C= (p.Pro346=) c.869C= (p.Pro290=) | |
| 5 | g.80674992C>G | CA3327784 | MSH3 | c.1037C>G (p.Pro346Arg) c.869C>G (p.Pro290Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80674992C>T | CA360267850 | MSH3 | c.1037C>T (p.Pro346Leu) c.869C>T (p.Pro290Leu) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674993C>A | CA445159607 | MSH3 | c.1038C>A (p.Pro346=) c.870C>A (p.Pro290=) | |
| 5 | g.80674993C>G | CA445159609 | MSH3 | c.1038C>G (p.Pro346=) c.870C>G (p.Pro290=) | |
| 5 | g.80674993C>T | CA445159611 | MSH3 | c.1038C>T (p.Pro346=) c.870C>T (p.Pro290=) | gnomAD v4 |
| 5 | g.80674994C>A | CA360267852 | MSH3 | c.1039C>A (p.Leu347Ile) c.871C>A (p.Leu291Ile) | gnomAD v4 |
| 5 | g.80674994C= | CA1558493189 | MSH3 | c.1039C= (p.Leu347=) c.871C= (p.Leu291=) | |
| 5 | g.80674994C>G | CA360267854 | MSH3 | c.1039C>G (p.Leu347Val) c.871C>G (p.Leu291Val) | |
| 5 | g.80674994C>T | CA445159614 | MSH3 | c.1039C>T (p.Leu347=) c.871C>T (p.Leu291=) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674994_80674995delinsCT | CA1558493190 | MSH3 | c.1039_1040delinsCT (p.Leu347=) c.871_872delinsCT (p.Leu291=) | |
| 5 | g.80674995del | CA915943433 | MSH3 | c.1040del (p.Leu347GlnfsTer8) c.872del (p.Leu291GlnfsTer8) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674995T>A | CA360267855 | MSH3 | c.1040T>A (p.Leu347Gln) c.872T>A (p.Leu291Gln) | |
| 5 | g.80674995T>C | CA360267858 | MSH3 | c.1040T>C (p.Leu347Pro) c.872T>C (p.Leu291Pro) | ClinVar gnomAD v4 |
| 5 | g.80674995T>G | CA360267860 | MSH3 | c.1040T>G (p.Leu347Arg) c.872T>G (p.Leu291Arg) | |
| 5 | g.80674996A= | CA1558493191 | MSH3 | c.1041A= (p.Leu347=) c.873A= (p.Leu291=) | |
| 5 | g.80674996A>C | CA445159618 | MSH3 | c.1041A>C (p.Leu347=) c.873A>C (p.Leu291=) | |
| 5 | g.80674996A>G | CA445159620 | MSH3 | c.1041A>G (p.Leu347=) c.873A>G (p.Leu291=) | |
| 5 | g.80674996A>T | CA3327785 | MSH3 | c.1041A>T (p.Leu347=) c.873A>T (p.Leu291=) | dbSNP ExAC |
| 5 | g.80674997A= | CA1558493192 | MSH3 | c.1042A= (p.Ile348=) c.874A= (p.Ile292=) | |
| 5 | g.80674997A>C | CA360267865 | MSH3 | c.1042A>C (p.Ile348Leu) c.874A>C (p.Ile292Leu) | ClinVar dbSNP |
| 5 | g.80674997A>G | CA360267863 | MSH3 | c.1042A>G (p.Ile348Val) c.874A>G (p.Ile292Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80674997A>T | CA360267866 | MSH3 | c.1042A>T (p.Ile348Phe) c.874A>T (p.Ile292Phe) | gnomAD v4 |
| 5 | g.80674998T>A | CA360267869 | MSH3 | c.1043T>A (p.Ile348Asn) c.875T>A (p.Ile292Asn) | dbSNP |
| 5 | g.80674998T>C | CA360267872 | MSH3 | c.1043T>C (p.Ile348Thr) c.875T>C (p.Ile292Thr) | |
| 5 | g.80674998T>G | CA360267870 | MSH3 | c.1043T>G (p.Ile348Ser) c.875T>G (p.Ile292Ser) | |
| 5 | g.80674999C>A | CA445159627 | MSH3 | c.1044C>A (p.Ile348=) c.876C>A (p.Ile292=) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674999C= | CA1558493193 | MSH3 | c.1044C= (p.Ile348=) c.876C= (p.Ile292=) | |
| 5 | g.80674999C>G | CA3327786 | MSH3 | c.1044C>G (p.Ile348Met) c.876C>G (p.Ile292Met) | ClinVar dbSNP ExAC gnomAD v2 |
| 5 | g.80674999C>T | CA445159629 | MSH3 | c.1044C>T (p.Ile348=) c.876C>T (p.Ile292=) | COSMIC COSMIC |
| 5 | g.80675000A>C | CA360267875 | MSH3 | c.1045A>C (p.Lys349Gln) c.877A>C (p.Lys293Gln) | |
| 5 | g.80675000A>G | CA360267877 | MSH3 | c.1045A>G (p.Lys349Glu) c.877A>G (p.Lys293Glu) | |
| 5 | g.80675000A>T | CA360267879 | MSH3 | c.1045A>T (p.Lys349Ter) c.877A>T (p.Lys293Ter) | gnomAD v4 |
| 5 | g.80675001A= | CA1558493194 | MSH3 | c.1046A= (p.Lys349=) c.878A= (p.Lys293=) | |
| 5 | g.80675001A>C | CA360267881 | MSH3 | c.1046A>C (p.Lys349Thr) c.878A>C (p.Lys293Thr) | |
| 5 | g.80675001A>G | CA3327787 | MSH3 | c.1046A>G (p.Lys349Arg) c.878A>G (p.Lys293Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675001A>T | CA360267883 | MSH3 | c.1046A>T (p.Lys349Met) c.878A>T (p.Lys293Met) | |
| 5 | g.80675002G>A | CA445159636 | MSH3 | c.1047G>A (p.Lys349=) c.879G>A (p.Lys293=) | ClinVar |
| 5 | g.80675002G>C | CA360267885 | MSH3 | c.1047G>C (p.Lys349Asn) c.879G>C (p.Lys293Asn) | |
| 5 | g.80675002G>T | CA360267887 | MSH3 | c.1047G>T (p.Lys349Asn) c.879G>T (p.Lys293Asn) | |
| 5 | g.80675003C>A | CA360267889 | MSH3 | c.1048C>A (p.Leu350Met) c.880C>A (p.Leu294Met) | |
| 5 | g.80675003C>G | CA360267891 | MSH3 | c.1048C>G (p.Leu350Val) c.880C>G (p.Leu294Val) | ClinVar dbSNP |
| 5 | g.80675003C>T | CA445159639 | MSH3 | c.1048C>T (p.Leu350=) c.880C>T (p.Leu294=) | |
| 5 | g.80675004T>A | CA360267895 | MSH3 | c.1049T>A (p.Leu350Gln) c.881T>A (p.Leu294Gln) | |
| 5 | g.80675004T>C | CA360267893 | MSH3 | c.1049T>C (p.Leu350Pro) c.881T>C (p.Leu294Pro) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80675004T>G | CA360267894 | MSH3 | c.1049T>G (p.Leu350Arg) c.881T>G (p.Leu294Arg) | |
| 5 | g.80675004T= | CA1558493195 | MSH3 | c.1049T= (p.Leu350=) c.881T= (p.Leu294=) | |
| 5 | g.80675005G>A | CA445159647 | MSH3 | c.1050G>A (p.Leu350=) c.882G>A (p.Leu294=) | ClinVar |
| 5 | g.80675005G>C | CA445159645 | MSH3 | c.1050G>C (p.Leu350=) c.882G>C (p.Leu294=) | |
| 5 | g.80675005G>T | CA445159644 | MSH3 | c.1050G>T (p.Leu350=) c.882G>T (p.Leu294=) | |
| 5 | g.80675006G>A | CA3327788 | MSH3 | c.1051G>A (p.Asp351Asn) c.883G>A (p.Asp295Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675006G>C | CA360267897 | MSH3 | c.1051G>C (p.Asp351His) c.883G>C (p.Asp295His) | |
| 5 | g.80675006G= | CA1558493196 | MSH3 | c.1051G= (p.Asp351=) c.883G= (p.Asp295=) | |
| 5 | g.80675006G>T | CA360267899 | MSH3 | c.1051G>T (p.Asp351Tyr) c.883G>T (p.Asp295Tyr) | COSMIC COSMIC |
| 5 | g.80675007A= | CA1558493204 | MSH3 | c.1052A= (p.Asp351=) c.884A= (p.Asp295=) | |
| 5 | g.80675007A>C | CA360267901 | MSH3 | c.1052A>C (p.Asp351Ala) c.884A>C (p.Asp295Ala) | |
| 5 | g.80675007A>G | CA3327789 | MSH3 | c.1052A>G (p.Asp351Gly) c.884A>G (p.Asp295Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675007A>T | CA360267903 | MSH3 | c.1052A>T (p.Asp351Val) c.884A>T (p.Asp295Val) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675008T>A | CA360267905 | MSH3 | c.1053T>A (p.Asp351Glu) c.885T>A (p.Asp295Glu) | |
| 5 | g.80675008T>C | CA445159656 | MSH3 | c.1053T>C (p.Asp351=) c.885T>C (p.Asp295=) | |
| 5 | g.80675008T>G | CA360267907 | MSH3 | c.1053T>G (p.Asp351Glu) c.885T>G (p.Asp295Glu) | |
| 5 | g.80675009G>A | CA360267909 | MSH3 | c.1054G>A (p.Asp352Asn) c.886G>A (p.Asp296Asn) | gnomAD v4 |
| 5 | g.80675009G>C | CA360267911 | MSH3 | c.1054G>C (p.Asp352His) c.886G>C (p.Asp296His) | ClinVar dbSNP |
| 5 | g.80675009G= | CA1558493209 | MSH3 | c.1054G= (p.Asp352=) c.886G= (p.Asp296=) | |
| 5 | g.80675009G>T | CA360267912 | MSH3 | c.1054G>T (p.Asp352Tyr) c.886G>T (p.Asp296Tyr) | |
| 5 | g.80675010A>C | CA360267915 | MSH3 | c.1055A>C (p.Asp352Ala) c.887A>C (p.Asp296Ala) | |
| 5 | g.80675010A>G | CA360267917 | MSH3 | c.1055A>G (p.Asp352Gly) c.887A>G (p.Asp296Gly) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675010A>T | CA360267914 | MSH3 | c.1055A>T (p.Asp352Val) c.887A>T (p.Asp296Val) | ClinVar gnomAD v4 |
| 5 | g.80675011T>A | CA360267919 | MSH3 | c.1056T>A (p.Asp352Glu) c.888T>A (p.Asp296Glu) | |
| 5 | g.80675011T>C | CA445159662 | MSH3 | c.1056T>C (p.Asp352=) c.888T>C (p.Asp296=) | |
| 5 | g.80675011T>G | CA360267921 | MSH3 | c.1056T>G (p.Asp352Glu) c.888T>G (p.Asp296Glu) | |
| 5 | g.80675012G>A | CA360267923 | MSH3 | c.1057G>A (p.Ala353Thr) c.889G>A (p.Ala297Thr) | ClinVar dbSNP |
| 5 | g.80675012G>C | CA360267924 | MSH3 | c.1057G>C (p.Ala353Pro) c.889G>C (p.Ala297Pro) | ClinVar |
| 5 | g.80675012G= | CA1558493213 | MSH3 | c.1057G= (p.Ala353=) c.889G= (p.Ala297=) | |
| 5 | g.80675012G>T | CA360267926 | MSH3 | c.1057G>T (p.Ala353Ser) c.889G>T (p.Ala297Ser) | |
| 5 | g.80675013C>A | CA360267932 | MSH3 | c.1058C>A (p.Ala353Asp) c.890C>A (p.Ala297Asp) | |
| 5 | g.80675013C>G | CA360267930 | MSH3 | c.1058C>G (p.Ala353Gly) c.890C>G (p.Ala297Gly) | ClinVar |
| 5 | g.80675013C>T | CA360267929 | MSH3 | c.1058C>T (p.Ala353Val) c.890C>T (p.Ala297Val) | ClinVar dbSNP |
| 5 | g.80675015_80675047dup | CA915943434 | MSH3 | c.1060_1092dup (p.Ser364_Thr365insValAsnValAspGluIleMetThrAspThrSer) c.892_924dup (p.Ser308_Thr309insValAsnValAspGluIleMetThrAspThrSer) | ClinVar dbSNP |
| 5 | g.80675014T>A | CA445159669 | MSH3 | c.1059T>A (p.Ala353=) c.891T>A (p.Ala297=) | |
| 5 | g.80675014T>C | CA445159671 | MSH3 | c.1059T>C (p.Ala353=) c.891T>C (p.Ala297=) | |
| 5 | g.80675014T>G | CA445159672 | MSH3 | c.1059T>G (p.Ala353=) c.891T>G (p.Ala297=) | ClinVar |
| 5 | g.80675014T= | CA1558493223 | MSH3 | c.1059T= (p.Ala353=) c.891T= (p.Ala297=) | |
| 5 | g.80675015_80675016del | CA2578350233 | MSH3 | c.1060_1061del (p.Val354LysfsTer3) c.892_893del (p.Val298LysfsTer3) | |
| 5 | g.80675017_80675022del | CA2580073614 | MSH3 | c.1062_1067del (p.Asn355_Val356del) c.894_899del (p.Asn299_Val300del) | ClinVar |
| 5 | g.80675015G>A | CA360267934 | MSH3 | c.1060G>A (p.Val354Ile) c.892G>A (p.Val298Ile) | dbSNP |
| 5 | g.80675015G>C | CA360267936 | MSH3 | c.1060G>C (p.Val354Leu) c.892G>C (p.Val298Leu) | |
| 5 | g.80675015G>T | CA360267937 | MSH3 | c.1060G>T (p.Val354Leu) c.892G>T (p.Val298Leu) | |
| 5 | g.80675015dup | CA915943435 | MSH3 | c.1060dup (p.Val354GlyfsTer4) c.892dup (p.Val298GlyfsTer4) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675016T>A | CA360267939 | MSH3 | c.1061T>A (p.Val354Glu) c.893T>A (p.Val298Glu) | |
| 5 | g.80675016T>C | CA360267940 | MSH3 | c.1061T>C (p.Val354Ala) c.893T>C (p.Val298Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80675016T>G | CA360267941 | MSH3 | c.1061T>G (p.Val354Gly) c.893T>G (p.Val298Gly) | |
| 5 | g.80675016T= | CA1558493234 | MSH3 | c.1061T= (p.Val354=) c.893T= (p.Val298=) | |
| 5 | g.80675016_80675017delinsTA | CA1558493233 | MSH3 | c.1061_1062delinsTA (p.Val354=) c.893_894delinsTA (p.Val298=) | |
| 5 | g.80675017A>C | CA445159678 | MSH3 | c.1062A>C (p.Val354=) c.894A>C (p.Val298=) | |
| 5 | g.80675017A>G | CA445159680 | MSH3 | c.1062A>G (p.Val354=) c.894A>G (p.Val298=) | |
| 5 | g.80675017A>T | CA445159681 | MSH3 | c.1062A>T (p.Val354=) c.894A>T (p.Val298=) | |
| 5 | g.80675019del | CA121295132 | MSH3 | c.1064del (p.Asn355MetfsTer5) c.896del (p.Asn299MetfsTer5) | dbSNP |
| 5 | g.80675018A= | CA1558493242 | MSH3 | c.1063A= (p.Asn355=) c.895A= (p.Asn299=) | |
| 5 | g.80675018A>C | CA360267942 | MSH3 | c.1063A>C (p.Asn355His) c.895A>C (p.Asn299His) | ClinVar dbSNP |
| 5 | g.80675018A>G | CA3327790 | MSH3 | c.1063A>G (p.Asn355Asp) c.895A>G (p.Asn299Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80675018A>T | CA360267943 | MSH3 | c.1063A>T (p.Asn355Tyr) c.895A>T (p.Asn299Tyr) | ClinVar dbSNP |
| 5 | g.80675019A>C | CA360267945 | MSH3 | c.1064A>C (p.Asn355Thr) c.896A>C (p.Asn299Thr) | |
| 5 | g.80675019A>G | CA360267946 | MSH3 | c.1064A>G (p.Asn355Ser) c.896A>G (p.Asn299Ser) | gnomAD v4 |
| 5 | g.80675019A>T | CA360267949 | MSH3 | c.1064A>T (p.Asn355Ile) c.896A>T (p.Asn299Ile) | |
| 5 | g.80675020T>A | CA360267953 | MSH3 | c.1065T>A (p.Asn355Lys) c.897T>A (p.Asn299Lys) | |
| 5 | g.80675020T>C | CA3327791 | MSH3 | c.1065T>C (p.Asn355=) c.897T>C (p.Asn299=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675020T>G | CA360267956 | MSH3 | c.1065T>G (p.Asn355Lys) c.897T>G (p.Asn299Lys) | ClinVar dbSNP |
| 5 | g.80675020T= | CA1558493246 | MSH3 | c.1065T= (p.Asn355=) c.897T= (p.Asn299=) | |
| 5 | g.80675021G>A | CA360267958 | MSH3 | c.1066G>A (p.Val356Ile) c.898G>A (p.Val300Ile) | ClinVar dbSNP |
| 5 | g.80675021G>C | CA360267960 | MSH3 | c.1066G>C (p.Val356Leu) c.898G>C (p.Val300Leu) | |
| 5 | g.80675021G>T | CA360267961 | MSH3 | c.1066G>T (p.Val356Phe) c.898G>T (p.Val300Phe) | gnomAD v4 |
| 5 | g.80675022T>A | CA360267963 | MSH3 | c.1067T>A (p.Val356Asp) c.899T>A (p.Val300Asp) | |
| 5 | g.80675022T>C | CA360267965 | MSH3 | c.1067T>C (p.Val356Ala) c.899T>C (p.Val300Ala) | |
| 5 | g.80675022T>G | CA360267967 | MSH3 | c.1067T>G (p.Val356Gly) c.899T>G (p.Val300Gly) | |
| 5 | g.80675023T>A | CA445159695 | MSH3 | c.1068T>A (p.Val356=) c.900T>A (p.Val300=) | |
| 5 | g.80675023T>C | CA445159696 | MSH3 | c.1068T>C (p.Val356=) c.900T>C (p.Val300=) | |
| 5 | g.80675023T>G | CA445159698 | MSH3 | c.1068T>G (p.Val356=) c.900T>G (p.Val300=) | |
| 5 | g.80675024G>A | CA360267972 | MSH3 | c.1069G>A (p.Asp357Asn) c.901G>A (p.Asp301Asn) | ClinVar |
| 5 | g.80675024G>C | CA360267971 | MSH3 | c.1069G>C (p.Asp357His) c.901G>C (p.Asp301His) | |
| 5 | g.80675024G>T | CA360267969 | MSH3 | c.1069G>T (p.Asp357Tyr) c.901G>T (p.Asp301Tyr) | |
| 5 | g.80675025A>C | CA360267973 | MSH3 | c.1070A>C (p.Asp357Ala) c.902A>C (p.Asp301Ala) | |
| 5 | g.80675025A>G | CA360267975 | MSH3 | c.1070A>G (p.Asp357Gly) c.902A>G (p.Asp301Gly) | |
| 5 | g.80675025A>T | CA360267977 | MSH3 | c.1070A>T (p.Asp357Val) c.902A>T (p.Asp301Val) | ClinVar |
| 5 | g.80675026T>A | CA360267978 | MSH3 | c.1071T>A (p.Asp357Glu) c.903T>A (p.Asp301Glu) | ClinVar dbSNP gnomAD v2 |
| 5 | g.80675026T>C | CA3327792 | MSH3 | c.1071T>C (p.Asp357=) c.903T>C (p.Asp301=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80675026T>G | CA360267980 | MSH3 | c.1071T>G (p.Asp357Glu) c.903T>G (p.Asp301Glu) | gnomAD v4 |
| 5 | g.80675026T= | CA1558493250 | MSH3 | c.1071T= (p.Asp357=) c.903T= (p.Asp301=) | |
| 5 | g.80675027G>A | CA360267986 | MSH3 | c.1072G>A (p.Glu358Lys) c.904G>A (p.Glu302Lys) | gnomAD v4 |
| 5 | g.80675027G>C | CA360267983 | MSH3 | c.1072G>C (p.Glu358Gln) c.904G>C (p.Glu302Gln) | |
| 5 | g.80675027G>T | CA360267985 | MSH3 | c.1072G>T (p.Glu358Ter) c.904G>T (p.Glu302Ter) | |
| 5 | g.80675028A= | CA1558493261 | MSH3 | c.1073A= (p.Glu358=) c.905A= (p.Glu302=) | |
| 5 | g.80675028A>C | CA360267988 | MSH3 | c.1073A>C (p.Glu358Ala) c.905A>C (p.Glu302Ala) | ClinVar dbSNP |
| 5 | g.80675028A>G | CA360267990 | MSH3 | c.1073A>G (p.Glu358Gly) c.905A>G (p.Glu302Gly) | ClinVar |
| 5 | g.80675028A>T | CA360267991 | MSH3 | c.1073A>T (p.Glu358Val) c.905A>T (p.Glu302Val) | |
| 5 | g.80675029G>A | CA445159710 | MSH3 | c.1074G>A (p.Glu358=) c.906G>A (p.Glu302=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80675029G>C | CA360267992 | MSH3 | c.1074G>C (p.Glu358Asp) c.906G>C (p.Glu302Asp) | ClinVar |
| 5 | g.80675029G= | CA1558493268 | MSH3 | c.1074G= (p.Glu358=) c.906G= (p.Glu302=) | |
| 5 | g.80675029G>T | CA360267993 | MSH3 | c.1074G>T (p.Glu358Asp) c.906G>T (p.Glu302Asp) | |
| 5 | g.80675030A= | CA1558493273 | MSH3 | c.1075A= (p.Ile359=) c.907A= (p.Ile303=) | |
| 5 | g.80675030A>C | CA360267996 | MSH3 | c.1075A>C (p.Ile359Leu) c.907A>C (p.Ile303Leu) | ClinVar dbSNP |
| 5 | g.80675030A>G | CA360267994 | MSH3 | c.1075A>G (p.Ile359Val) c.907A>G (p.Ile303Val) | ClinVar |
| 5 | g.80675030A>T | CA360267995 | MSH3 | c.1075A>T (p.Ile359Leu) c.907A>T (p.Ile303Leu) | |
| 5 | g.80675031T>A | CA360267997 | MSH3 | c.1076T>A (p.Ile359Lys) c.908T>A (p.Ile303Lys) | |
| 5 | g.80675031T>C | CA360267999 | MSH3 | c.1076T>C (p.Ile359Thr) c.908T>C (p.Ile303Thr) | |
| 5 | g.80675031T>G | CA360268000 | MSH3 | c.1076T>G (p.Ile359Arg) c.908T>G (p.Ile303Arg) | |
| 5 | g.80675032A>C | CA445159716 | MSH3 | c.1077A>C (p.Ile359=) c.909A>C (p.Ile303=) | |
| 5 | g.80675032A>G | CA360268002 | MSH3 | c.1077A>G (p.Ile359Met) c.909A>G (p.Ile303Met) | ClinVar |
| 5 | g.80675032A>T | CA445159718 | MSH3 | c.1077A>T (p.Ile359=) c.909A>T (p.Ile303=) | |
| 5 | g.80675033A= | CA1558493278 | MSH3 | c.1078A= (p.Met360=) c.910A= (p.Met304=) | |
| 5 | g.80675033A>C | CA360268004 | MSH3 | c.1078A>C (p.Met360Leu) c.910A>C (p.Met304Leu) | |
| 5 | g.80675033A>G | CA360268006 | MSH3 | c.1078A>G (p.Met360Val) c.910A>G (p.Met304Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80675033A>T | CA360268008 | MSH3 | c.1078A>T (p.Met360Leu) c.910A>T (p.Met304Leu) | |
| 5 | g.80675034T>A | CA360268010 | MSH3 | c.1079T>A (p.Met360Lys) c.911T>A (p.Met304Lys) | |
| 5 | g.80675034T>C | CA360268012 | MSH3 | c.1079T>C (p.Met360Thr) c.911T>C (p.Met304Thr) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675034T>G | CA360268014 | MSH3 | c.1079T>G (p.Met360Arg) c.911T>G (p.Met304Arg) | |
| 5 | g.80675034T= | CA1558493285 | MSH3 | c.1079T= (p.Met360=) c.911T= (p.Met304=) | |
| 5 | g.80675035G>A | CA360268017 | MSH3 | c.1080G>A (p.Met360Ile) c.912G>A (p.Met304Ile) | |
| 5 | g.80675035G>C | CA3327793 | MSH3 | c.1080G>C (p.Met360Ile) c.912G>C (p.Met304Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80675035G= | CA1558493289 | MSH3 | c.1080G= (p.Met360=) c.912G= (p.Met304=) | |
| 5 | g.80675035G>T | CA360268019 | MSH3 | c.1080G>T (p.Met360Ile) c.912G>T (p.Met304Ile) | |
| 5 | g.80675036A>C | CA360268020 | MSH3 | c.1081A>C (p.Thr361Pro) c.913A>C (p.Thr305Pro) | |
| 5 | g.80675036A>G | CA360268023 | MSH3 | c.1081A>G (p.Thr361Ala) c.913A>G (p.Thr305Ala) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675036A>T | CA360268022 | MSH3 | c.1081A>T (p.Thr361Ser) c.913A>T (p.Thr305Ser) | ClinVar |
| 5 | g.80675037C>A | CA360268025 | MSH3 | c.1082C>A (p.Thr361Asn) c.914C>A (p.Thr305Asn) | |
| 5 | g.80675037C>G | CA360268027 | MSH3 | c.1082C>G (p.Thr361Ser) c.914C>G (p.Thr305Ser) | |
| 5 | g.80675037C>T | CA360268028 | MSH3 | c.1082C>T (p.Thr361Ile) c.914C>T (p.Thr305Ile) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675037_80675038insG | CA2674443045 | MSH3 | c.1082_1083insG (p.Asp362Ter) c.914_915insG (p.Asp306Ter) | gnomAD v4 |
| 5 | g.80675038T>A | CA445159732 | MSH3 | c.1083T>A (p.Thr361=) c.915T>A (p.Thr305=) | |
| 5 | g.80675038T>C | CA445159733 | MSH3 | c.1083T>C (p.Thr361=) c.915T>C (p.Thr305=) | |
| 5 | g.80675038T>G | CA445159735 | MSH3 | c.1083T>G (p.Thr361=) c.915T>G (p.Thr305=) | |
| 5 | g.80675039G>A | CA360268030 | MSH3 | c.1084G>A (p.Asp362Asn) c.916G>A (p.Asp306Asn) | dbSNP |
| 5 | g.80675039G>C | CA360268031 | MSH3 | c.1084G>C (p.Asp362His) c.916G>C (p.Asp306His) | ClinVar dbSNP |
| 5 | g.80675039G>T | CA360268033 | MSH3 | c.1084G>T (p.Asp362Tyr) c.916G>T (p.Asp306Tyr) | |
| 5 | g.80675040A= | CA1558493294 | MSH3 | c.1085A= (p.Asp362=) c.917A= (p.Asp306=) | |
| 5 | g.80675040A>C | CA3327794 | MSH3 | c.1085A>C (p.Asp362Ala) c.917A>C (p.Asp306Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80675040A>G | CA360268035 | MSH3 | c.1085A>G (p.Asp362Gly) c.917A>G (p.Asp306Gly) | |
| 5 | g.80675040A>T | CA360268036 | MSH3 | c.1085A>T (p.Asp362Val) c.917A>T (p.Asp306Val) | ClinVar |
| 5 | g.80675041T>A | CA360268039 | MSH3 | c.1086T>A (p.Asp362Glu) c.918T>A (p.Asp306Glu) | |
| 5 | g.80675041T>C | CA445159744 | MSH3 | c.1086T>C (p.Asp362=) c.918T>C (p.Asp306=) | ClinVar dbSNP |
| 5 | g.80675041T>G | CA360268040 | MSH3 | c.1086T>G (p.Asp362Glu) c.918T>G (p.Asp306Glu) | |
| 5 | g.80675041T= | CA1558493306 | MSH3 | c.1086T= (p.Asp362=) c.918T= (p.Asp306=) | |
| 5 | g.80675042A>C | CA360268043 | MSH3 | c.1087A>C (p.Thr363Pro) c.919A>C (p.Thr307Pro) | |
| 5 | g.80675042A>G | CA360268045 | MSH3 | c.1087A>G (p.Thr363Ala) c.919A>G (p.Thr307Ala) | |
| 5 | g.80675042A>T | CA360268046 | MSH3 | c.1087A>T (p.Thr363Ser) c.919A>T (p.Thr307Ser) | |
| 5 | g.80675042dup | CA560552923 | MSH3 | c.1087dup (p.Thr363AsnfsTer11) c.919dup (p.Thr307AsnfsTer11) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80675043C>A | CA121295147 | MSH3 | c.1088C>A (p.Thr363Asn) c.920C>A (p.Thr307Asn) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675043C= | CA1558493324 | MSH3 | c.1088C= (p.Thr363=) c.920C= (p.Thr307=) | |
| 5 | g.80675043C>G | CA360268050 | MSH3 | c.1088C>G (p.Thr363Ser) c.920C>G (p.Thr307Ser) | |
| 5 | g.80675043C>T | CA3327795 | MSH3 | c.1088C>T (p.Thr363Ile) c.920C>T (p.Thr307Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675044T>A | CA445159751 | MSH3 | c.1089T>A (p.Thr363=) c.921T>A (p.Thr307=) | |
| 5 | g.80675044T>C | CA445159752 | MSH3 | c.1089T>C (p.Thr363=) c.921T>C (p.Thr307=) | ClinVar |
| 5 | g.80675044T>G | CA3327796 | MSH3 | c.1089T>G (p.Thr363=) c.921T>G (p.Thr307=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80675044T= | CA1558493333 | MSH3 | c.1089T= (p.Thr363=) c.921T= (p.Thr307=) | |
| 5 | g.80675045T>A | CA360268052 | MSH3 | c.1090T>A (p.Ser364Thr) c.922T>A (p.Ser308Thr) | |
| 5 | g.80675045T>C | CA360268054 | MSH3 | c.1090T>C (p.Ser364Pro) c.922T>C (p.Ser308Pro) | |
| 5 | g.80675045T>G | CA360268056 | MSH3 | c.1090T>G (p.Ser364Ala) c.922T>G (p.Ser308Ala) | |
| 5 | g.80675046C>A | CA360268057 | MSH3 | c.1091C>A (p.Ser364Tyr) c.923C>A (p.Ser308Tyr) | |
| 5 | g.80675046C>G | CA360268059 | MSH3 | c.1091C>G (p.Ser364Cys) c.923C>G (p.Ser308Cys) | |
| 5 | g.80675046C>T | CA360268061 | MSH3 | c.1091C>T (p.Ser364Phe) c.923C>T (p.Ser308Phe) | |
| 5 | g.80675047T>A | CA445159757 | MSH3 | c.1092T>A (p.Ser364=) c.924T>A (p.Ser308=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80675047T>C | CA445159759 | MSH3 | c.1092T>C (p.Ser364=) c.924T>C (p.Ser308=) | ClinVar dbSNP |
| 5 | g.80675047T>G | CA445159760 | MSH3 | c.1092T>G (p.Ser364=) c.924T>G (p.Ser308=) | |
| 5 | g.80675047T= | CA1558493338 | MSH3 | c.1092T= (p.Ser364=) c.924T= (p.Ser308=) | |
| 5 | g.80675048A= | CA1558493344 | MSH3 | c.1093A= (p.Thr365=) c.925A= (p.Thr309=) | |
| 5 | g.80675048A>C | CA360268063 | MSH3 | c.1093A>C (p.Thr365Pro) c.925A>C (p.Thr309Pro) | |
| 5 | g.80675048A>G | CA360268064 | MSH3 | c.1093A>G (p.Thr365Ala) c.925A>G (p.Thr309Ala) | ClinVar dbSNP |
| 5 | g.80675048A>T | CA360268066 | MSH3 | c.1093A>T (p.Thr365Ser) c.925A>T (p.Thr309Ser) | |
| 5 | g.80675049C>A | CA360268068 | MSH3 | c.1094C>A (p.Thr365Asn) c.926C>A (p.Thr309Asn) | |
| 5 | g.80675049C= | CA1558493349 | MSH3 | c.1094C= (p.Thr365=) c.926C= (p.Thr309=) | |
| 5 | g.80675049C>G | CA360268071 | MSH3 | c.1094C>G (p.Thr365Ser) c.926C>G (p.Thr309Ser) | |
| 5 | g.80675049C>T | CA360268070 | MSH3 | c.1094C>T (p.Thr365Ile) c.926C>T (p.Thr309Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675050C>A | CA445159770 | MSH3 | c.1095C>A (p.Thr365=) c.927C>A (p.Thr309=) | dbSNP |
| 5 | g.80675050C= | CA1558493356 | MSH3 | c.1095C= (p.Thr365=) c.927C= (p.Thr309=) | |
| 5 | g.80675050C>G | CA445159767 | MSH3 | c.1095C>G (p.Thr365=) c.927C>G (p.Thr309=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80675050C>T | CA445159768 | MSH3 | c.1095C>T (p.Thr365=) c.927C>T (p.Thr309=) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 5 | g.80675051A>C | CA360268072 | MSH3 | c.1096A>C (p.Ser366Arg) c.928A>C (p.Ser310Arg) | |
| 5 | g.80675051A>G | CA360268075 | MSH3 | c.1096A>G (p.Ser366Gly) c.928A>G (p.Ser310Gly) | |
| 5 | g.80675051A>T | CA360268073 | MSH3 | c.1096A>T (p.Ser366Cys) c.928A>T (p.Ser310Cys) | |
| 5 | g.80675052_80675055dup | CA2580073621 | MSH3 | c.1097_1100dup (p.Tyr367Ter) c.929_932dup (p.Tyr311Ter) | ClinVar |
| 5 | g.80675052G>A | CA360268077 | MSH3 | c.1097G>A (p.Ser366Asn) c.929G>A (p.Ser310Asn) | ClinVar dbSNP |
| 5 | g.80675052G>C | CA360268080 | MSH3 | c.1097G>C (p.Ser366Thr) c.929G>C (p.Ser310Thr) | ClinVar |
| 5 | g.80675052G= | CA1558493365 | MSH3 | c.1097G= (p.Ser366=) c.929G= (p.Ser310=) | |
| 5 | g.80675052G>T | CA360268079 | MSH3 | c.1097G>T (p.Ser366Ile) c.929G>T (p.Ser310Ile) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80675053C>A | CA360268083 | MSH3 | c.1098C>A (p.Ser366Arg) c.930C>A (p.Ser310Arg) | |
| 5 | g.80675053C>G | CA360268084 | MSH3 | c.1098C>G (p.Ser366Arg) c.930C>G (p.Ser310Arg) | |
| 5 | g.80675053C>T | CA445159778 | MSH3 | c.1098C>T (p.Ser366=) c.930C>T (p.Ser310=) | |
| 5 | g.80675054T>A | CA360268086 | MSH3 | c.1099T>A (p.Tyr367Asn) c.931T>A (p.Tyr311Asn) | |
| 5 | g.80675054T>C | CA360268088 | MSH3 | c.1099T>C (p.Tyr367His) c.931T>C (p.Tyr311His) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675054T>G | CA360268089 | MSH3 | c.1099T>G (p.Tyr367Asp) c.931T>G (p.Tyr311Asp) | |
| 5 | g.80675054T= | CA1558493368 | MSH3 | c.1099T= (p.Tyr367=) c.931T= (p.Tyr311=) | |
| 5 | g.80675055A= | CA1558493372 | MSH3 | c.1100A= (p.Tyr367=) c.932A= (p.Tyr311=) | |
| 5 | g.80675055A>C | CA360268090 | MSH3 | c.1100A>C (p.Tyr367Ser) c.932A>C (p.Tyr311Ser) | ClinVar |
| 5 | g.80675055A>G | CA360268092 | MSH3 | c.1100A>G (p.Tyr367Cys) c.932A>G (p.Tyr311Cys) | ClinVar dbSNP |
| 5 | g.80675055A>T | CA360268094 | MSH3 | c.1100A>T (p.Tyr367Phe) c.932A>T (p.Tyr311Phe) | |
| 5 | g.80675056T>A | CA360268096 | MSH3 | c.1101T>A (p.Tyr367Ter) c.933T>A (p.Tyr311Ter) | |
| 5 | g.80675056T>C | CA3327797 | MSH3 | c.1101T>C (p.Tyr367=) c.933T>C (p.Tyr311=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675056T>G | CA360268098 | MSH3 | c.1101T>G (p.Tyr367Ter) c.933T>G (p.Tyr311Ter) | |
| 5 | g.80675056T= | CA1558493376 | MSH3 | c.1101T= (p.Tyr367=) c.933T= (p.Tyr311=) | |
| 5 | g.80675057C>A | CA360268100 | MSH3 | c.1102C>A (p.Leu368Ile) c.934C>A (p.Leu312Ile) | |
| 5 | g.80675057C= | CA1558493390 | MSH3 | c.1102C= (p.Leu368=) c.934C= (p.Leu312=) | |
| 5 | g.80675057C>G | CA360268101 | MSH3 | c.1102C>G (p.Leu368Val) c.934C>G (p.Leu312Val) | ClinVar dbSNP |
| 5 | g.80675057C>T | CA3327798 | MSH3 | c.1102C>T (p.Leu368Phe) c.934C>T (p.Leu312Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80675058T>A | CA360268107 | MSH3 | c.1103T>A (p.Leu368His) c.935T>A (p.Leu312His) | |
| 5 | g.80675058T>C | CA360268103 | MSH3 | c.1103T>C (p.Leu368Pro) c.935T>C (p.Leu312Pro) | gnomAD v4 |
| 5 | g.80675058T>G | CA360268105 | MSH3 | c.1103T>G (p.Leu368Arg) c.935T>G (p.Leu312Arg) | ClinVar |
| 5 | g.80675059T>A | CA445159791 | MSH3 | c.1104T>A (p.Leu368=) c.936T>A (p.Leu312=) | |
| 5 | g.80675059T>C | CA445159793 | MSH3 | c.1104T>C (p.Leu368=) c.936T>C (p.Leu312=) | gnomAD v4 |
| 5 | g.80675059T>G | CA3327799 | MSH3 | c.1104T>G (p.Leu368=) c.936T>G (p.Leu312=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675059T= | CA1558493392 | MSH3 | c.1104T= (p.Leu368=) c.936T= (p.Leu312=) | |
| 5 | g.80675060C>A | CA360268110 | MSH3 | c.1105C>A (p.Leu369Met) c.937C>A (p.Leu313Met) | |
| 5 | g.80675060C>G | CA360268111 | MSH3 | c.1105C>G (p.Leu369Val) c.937C>G (p.Leu313Val) | ClinVar |
| 5 | g.80675060C>T | CA445159796 | MSH3 | c.1105C>T (p.Leu369=) c.937C>T (p.Leu313=) | |
| 5 | g.80675061T>A | CA360268113 | MSH3 | c.1106T>A (p.Leu369Gln) c.938T>A (p.Leu313Gln) | dbSNP |
| 5 | g.80675061T>C | CA360268115 | MSH3 | c.1106T>C (p.Leu369Pro) c.938T>C (p.Leu313Pro) | dbSNP |
| 5 | g.80675061T>G | CA360268116 | MSH3 | c.1106T>G (p.Leu369Arg) c.938T>G (p.Leu313Arg) | |
| 5 | g.80675061T= | CA1558493395 | MSH3 | c.1106T= (p.Leu369=) c.938T= (p.Leu313=) | |
| 5 | g.80675061dup | CA2580073623 | MSH3 | c.1106dup (p.Cys370ValfsTer4) c.938dup (p.Cys314ValfsTer4) | ClinVar |
| 5 | g.80675062G>A | CA121295178 | MSH3 | c.1107G>A (p.Leu369=) c.939G>A (p.Leu313=) | dbSNP gnomAD v4 |
| 5 | g.80675062G>C | CA445159801 | MSH3 | c.1107G>C (p.Leu369=) c.939G>C (p.Leu313=) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675062G= | CA1558493400 | MSH3 | c.1107G= (p.Leu369=) c.939G= (p.Leu313=) | |
| 5 | g.80675062G>T | CA445159802 | MSH3 | c.1107G>T (p.Leu369=) c.939G>T (p.Leu313=) | gnomAD v3 gnomAD v4 |
| 5 | g.80675063T>A | CA360268117 | MSH3 | c.1108T>A (p.Cys370Ser) c.940T>A (p.Cys314Ser) | |
| 5 | g.80675063T>C | CA360268118 | MSH3 | c.1108T>C (p.Cys370Arg) c.940T>C (p.Cys314Arg) | gnomAD v4 |
| 5 | g.80675063T>G | CA121295183 | MSH3 | c.1108T>G (p.Cys370Gly) c.940T>G (p.Cys314Gly) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80675063T= | CA1558493406 | MSH3 | c.1108T= (p.Cys370=) c.940T= (p.Cys314=) | |
| 5 | g.80675064G>A | CA360268120 | MSH3 | c.1109G>A (p.Cys370Tyr) c.941G>A (p.Cys314Tyr) | ClinVar gnomAD v4 |
| 5 | g.80675064G>C | CA360268121 | MSH3 | c.1109G>C (p.Cys370Ser) c.941G>C (p.Cys314Ser) | |
| 5 | g.80675064G>T | CA360268122 | MSH3 | c.1109G>T (p.Cys370Phe) c.941G>T (p.Cys314Phe) | |
| 5 | g.80675065C>A | CA360268123 | MSH3 | c.1110C>A (p.Cys370Ter) c.942C>A (p.Cys314Ter) | |
| 5 | g.80675065C>G | CA360268124 | MSH3 | c.1110C>G (p.Cys370Trp) c.942C>G (p.Cys314Trp) | |
| 5 | g.80675065C>T | CA445159809 | MSH3 | c.1110C>T (p.Cys370=) c.942C>T (p.Cys314=) | ClinVar |
| 5 | g.80675066A= | CA1558493415 | MSH3 | c.1111A= (p.Ile371=) c.943A= (p.Ile315=) | |
| 5 | g.80675066A>C | CA360268125 | MSH3 | c.1111A>C (p.Ile371Leu) c.943A>C (p.Ile315Leu) | |
| 5 | g.80675066A>G | CA360268126 | MSH3 | c.1111A>G (p.Ile371Val) c.943A>G (p.Ile315Val) | ClinVar dbSNP |
| 5 | g.80675066A>T | CA360268127 | MSH3 | c.1111A>T (p.Ile371Phe) c.943A>T (p.Ile315Phe) | |
| 5 | g.80675067T>A | CA360268129 | MSH3 | c.1112T>A (p.Ile371Asn) c.944T>A (p.Ile315Asn) | |
| 5 | g.80675067T>C | CA360268131 | MSH3 | c.1112T>C (p.Ile371Thr) c.944T>C (p.Ile315Thr) | gnomAD v4 COSMIC COSMIC |
| 5 | g.80675067T>G | CA360268133 | MSH3 | c.1112T>G (p.Ile371Ser) c.944T>G (p.Ile315Ser) | |
| 5 | g.80675070_80675071del | CA2674443046 | MSH3 | c.1115_1116del (p.Ser372Ter) c.947_948del (p.Ser316Ter) | gnomAD v4 |
| 5 | g.80675068C>A | CA445159816 | MSH3 | c.1113C>A (p.Ile371=) c.945C>A (p.Ile315=) | gnomAD v4 |
| 5 | g.80675068C= | CA1558493424 | MSH3 | c.1113C= (p.Ile371=) c.945C= (p.Ile315=) | |
| 5 | g.80675068C>G | CA360268135 | MSH3 | c.1113C>G (p.Ile371Met) c.945C>G (p.Ile315Met) | |
| 5 | g.80675068C>T | CA445159818 | MSH3 | c.1113C>T (p.Ile371=) c.945C>T (p.Ile315=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80675069T>A | CA360268137 | MSH3 | c.1114T>A (p.Ser372Thr) c.946T>A (p.Ser316Thr) | dbSNP |
| 5 | g.80675069T>C | CA360268139 | MSH3 | c.1114T>C (p.Ser372Pro) c.946T>C (p.Ser316Pro) | ClinVar dbSNP |
| 5 | g.80675069T>G | CA360268141 | MSH3 | c.1114T>G (p.Ser372Ala) c.946T>G (p.Ser316Ala) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80675069T= | CA1558493430 | MSH3 | c.1114T= (p.Ser372=) c.946T= (p.Ser316=) | |
| 5 | g.80675070C>A | CA360268143 | MSH3 | c.1115C>A (p.Ser372Tyr) c.947C>A (p.Ser316Tyr) | |
| 5 | g.80675070C>G | CA360268144 | MSH3 | c.1115C>G (p.Ser372Cys) c.947C>G (p.Ser316Cys) | |
| 5 | g.80675070C>T | CA360268146 | MSH3 | c.1115C>T (p.Ser372Phe) c.947C>T (p.Ser316Phe) | ClinVar |
| 5 | g.80675071del | CA2499217931 | MSH3 | c.1116del (p.Glu373LysfsTer?) c.948del (p.Glu317LysfsTer?) | ClinVar dbSNP |
| 5 | g.80675071T>A | CA445159825 | MSH3 | c.1116T>A (p.Ser372=) c.948T>A (p.Ser316=) | |
| 5 | g.80675071T>C | CA445159823 | MSH3 | c.1116T>C (p.Ser372=) c.948T>C (p.Ser316=) | |
| 5 | g.80675071T>G | CA445159822 | MSH3 | c.1116T>G (p.Ser372=) c.948T>G (p.Ser316=) | ClinVar dbSNP |
| 5 | g.80675072G>A | CA360268148 | MSH3 | c.1117G>A (p.Glu373Lys) c.949G>A (p.Glu317Lys) | gnomAD v4 |
| 5 | g.80675072G>C | CA360268150 | MSH3 | c.1117G>C (p.Glu373Gln) c.949G>C (p.Glu317Gln) | |
| 5 | g.80675072G>T | CA360268149 | MSH3 | c.1117G>T (p.Glu373Ter) c.949G>T (p.Glu317Ter) | |
| 5 | g.80675073A>C | CA360268152 | MSH3 | c.1118A>C (p.Glu373Ala) c.950A>C (p.Glu317Ala) | |
| 5 | g.80675073A>G | CA360268154 | MSH3 | c.1118A>G (p.Glu373Gly) c.950A>G (p.Glu317Gly) | |
| 5 | g.80675073A>T | CA360268155 | MSH3 | c.1118A>T (p.Glu373Val) c.950A>T (p.Glu317Val) | |
| 5 | g.80675074A>C | CA360268157 | MSH3 | c.1119A>C (p.Glu373Asp) c.951A>C (p.Glu317Asp) | |
| 5 | g.80675074A>G | CA445159832 | MSH3 | c.1119A>G (p.Glu373=) c.951A>G (p.Glu317=) | |
| 5 | g.80675074A>T | CA360268159 | MSH3 | c.1119A>T (p.Glu373Asp) c.951A>T (p.Glu317Asp) | |
| 5 | g.80675075A>C | CA360268161 | MSH3 | c.1120A>C (p.Asn374His) c.952A>C (p.Asn318His) | COSMIC COSMIC |
| 5 | g.80675075A>G | CA360268163 | MSH3 | c.1120A>G (p.Asn374Asp) c.952A>G (p.Asn318Asp) | gnomAD v4 |
| 5 | g.80675075A>T | CA360268165 | MSH3 | c.1120A>T (p.Asn374Tyr) c.952A>T (p.Asn318Tyr) | |
| 5 | g.80675076A= | CA1558493438 | MSH3 | c.1121A= (p.Asn374=) c.953A= (p.Asn318=) | |
| 5 | g.80675076A>C | CA360268167 | MSH3 | c.1121A>C (p.Asn374Thr) c.953A>C (p.Asn318Thr) | |
| 5 | g.80675076A>G | CA360268169 | MSH3 | c.1121A>G (p.Asn374Ser) c.953A>G (p.Asn318Ser) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675076A>T | CA360268171 | MSH3 | c.1121A>T (p.Asn374Ile) c.953A>T (p.Asn318Ile) | |
| 5 | g.80675077T>A | CA360268172 | MSH3 | c.1122T>A (p.Asn374Lys) c.954T>A (p.Asn318Lys) | |
| 5 | g.80675077T>C | CA445159838 | MSH3 | c.1122T>C (p.Asn374=) c.954T>C (p.Asn318=) | gnomAD v4 |
| 5 | g.80675077T>G | CA3327800 | MSH3 | c.1122T>G (p.Asn374Lys) c.954T>G (p.Asn318Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675077T= | CA1558493450 | MSH3 | c.1122T= (p.Asn374=) c.954T= (p.Asn318=) | |
| 5 | g.80675077_80675078delinsTA | CA1558493451 | MSH3 | c.1122_1123delinsTA (p.Asn374=) c.954_955delinsTA (p.Asn318=) | |
| 5 | g.80675078A= | CA1558493462 | MSH3 | c.1123A= (p.Lys375=) c.955A= (p.Lys319=) | |
| 5 | g.80675078A>C | CA360268175 | MSH3 | c.1123A>C (p.Lys375Gln) c.955A>C (p.Lys319Gln) | |
| 5 | g.80675078A>G | CA360268178 | MSH3 | c.1123A>G (p.Lys375Glu) c.955A>G (p.Lys319Glu) | |
| 5 | g.80675078A>T | CA360268177 | MSH3 | c.1123A>T (p.Lys375Ter) c.955A>T (p.Lys319Ter) | ClinVar dbSNP |
| 5 | g.80675079del | CA121295188 | MSH3 | c.1124del (p.Lys375ArgfsTer?) c.956del (p.Lys319ArgfsTer?) | dbSNP |
| 5 | g.80675079A= | CA1558493467 | MSH3 | c.1124A= (p.Lys375=) c.956A= (p.Lys319=) | |
| 5 | g.80675079A>C | CA360268180 | MSH3 | c.1124A>C (p.Lys375Thr) c.956A>C (p.Lys319Thr) | |
| 5 | g.80675079A>G | CA360268182 | MSH3 | c.1124A>G (p.Lys375Arg) c.956A>G (p.Lys319Arg) | ClinVar gnomAD v4 |
| 5 | g.80675079A>T | CA3327801 | MSH3 | c.1124A>T (p.Lys375Met) c.956A>T (p.Lys319Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80675080G>A | CA445159844 | MSH3 | c.1125G>A (p.Lys375=) c.957G>A (p.Lys319=) | |
| 5 | g.80675080G>C | CA360268185 | MSH3 | c.1125G>C (p.Lys375Asn) c.957G>C (p.Lys319Asn) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80675080G= | CA1558493469 | MSH3 | c.1125G= (p.Lys375=) c.957G= (p.Lys319=) | |
| 5 | g.80675080G>T | CA360268187 | MSH3 | c.1125G>T (p.Lys375Asn) c.957G>T (p.Lys319Asn) | |
| 5 | g.80675081G>A | CA360268189 | MSH3 | c.1126G>A (p.Glu376Lys) c.958G>A (p.Glu320Lys) | ClinVar gnomAD v4 |
| 5 | g.80675081G>C | CA360268191 | MSH3 | c.1126G>C (p.Glu376Gln) c.958G>C (p.Glu320Gln) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80675081G= | CA1558493472 | MSH3 | c.1126G= (p.Glu376=) c.958G= (p.Glu320=) | |
| 5 | g.80675081G>T | CA360268193 | MSH3 | c.1126G>T (p.Glu376Ter) c.958G>T (p.Glu320Ter) | ClinVar |
| 5 | g.80675081_80675082delinsGA | CA1558493474 | MSH3 | c.1126_1127delinsGA (p.Glu376=) c.958_959delinsGA (p.Glu320=) |