| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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=) | |
| 5 | g.80675082A= | CA1558493478 | MSH3 | c.1127A= (p.Glu376=) c.959A= (p.Glu320=) | |
| 5 | g.80675082A>C | CA360268195 | MSH3 | c.1127A>C (p.Glu376Ala) c.959A>C (p.Glu320Ala) | dbSNP |
| 5 | g.80675082A>G | CA121295192 | MSH3 | c.1127A>G (p.Glu376Gly) c.959A>G (p.Glu320Gly) | dbSNP |
| 5 | g.80675082A>T | CA360268197 | MSH3 | c.1127A>T (p.Glu376Val) c.959A>T (p.Glu320Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80675085del | CA560552943 | MSH3 | c.1130del (p.Asn377MetfsTer?) c.962del (p.Asn321MetfsTer?) | dbSNP gnomAD v2 |
| 5 | g.80675083A= | CA1558493491 | MSH3 | c.1128A= (p.Glu376=) c.960A= (p.Glu320=) | |
| 5 | g.80675083A>C | CA360268200 | MSH3 | c.1128A>C (p.Glu376Asp) c.960A>C (p.Glu320Asp) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80675083A>G | CA445159853 | MSH3 | c.1128A>G (p.Glu376=) c.960A>G (p.Glu320=) | |
| 5 | g.80675083A>T | CA360268199 | MSH3 | c.1128A>T (p.Glu376Asp) c.960A>T (p.Glu320Asp) | |
| 5 | g.80675084A>C | CA360268202 | MSH3 | c.1129A>C (p.Asn377His) c.961A>C (p.Asn321His) | |
| 5 | g.80675084A>G | CA360268203 | MSH3 | c.1129A>G (p.Asn377Asp) c.961A>G (p.Asn321Asp) | |
| 5 | g.80675084A>T | CA360268205 | MSH3 | c.1129A>T (p.Asn377Tyr) c.961A>T (p.Asn321Tyr) | |
| 5 | g.80675084_80675086delinsCAA | CA2695198652 | MSH3 | c.1129_1131delinsCAA (p.Asn377Gln) c.961_963delinsCAA (p.Asn321Gln) | ClinVar |
| 5 | g.80675085A>C | CA360268207 | MSH3 | c.1130A>C (p.Asn377Thr) c.962A>C (p.Asn321Thr) | |
| 5 | g.80675085A>G | CA360268209 | MSH3 | c.1130A>G (p.Asn377Ser) c.962A>G (p.Asn321Ser) | |
| 5 | g.80675085A>T | CA360268211 | MSH3 | c.1130A>T (p.Asn377Ile) c.962A>T (p.Asn321Ile) | |
| 5 | g.80675085_80675087delinsTT | CA2580073628 | MSH3 | c.1130_1132delinsTT (p.Asn377IlefsTer?) c.962_964delinsTT (p.Asn321IlefsTer?) | ClinVar |
| 5 | g.80675085_80675093delinsATGTTAGGG | CA1558493496 | MSH3 | c.1130_1138delinsATGTTAGGG (p.Asn377=) c.962_970delinsATGTTAGGG (p.Asn321=) | |
| 5 | g.80675086T>A | CA360268213 | MSH3 | c.1131T>A (p.Asn377Lys) c.963T>A (p.Asn321Lys) | |
| 5 | g.80675086T>C | CA445159855 | MSH3 | c.1131T>C (p.Asn377=) c.963T>C (p.Asn321=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80675086T>G | CA360268214 | MSH3 | c.1131T>G (p.Asn377Lys) c.963T>G (p.Asn321Lys) | ClinVar |
| 5 | g.80675086T= | CA1558493501 | MSH3 | c.1131T= (p.Asn377=) c.963T= (p.Asn321=) | |
| 5 | g.80675086_80675089del | CA2580073630 | MSH3 | c.1131_1134del (p.Asn377LysfsTer?) c.963_966del (p.Asn321LysfsTer?) | ClinVar gnomAD v4 |
| 5 | g.80675086_80675093del | CA560552945 | MSH3 | c.1131_1138del (p.Asn377LysfsTer24) c.963_970del (p.Asn321LysfsTer24) | dbSNP gnomAD v2 |
| 5 | g.80675087G>A | CA360268216 | MSH3 | c.1132G>A (p.Val378Ile) c.964G>A (p.Val322Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675087G>C | CA360268218 | MSH3 | c.1132G>C (p.Val378Leu) c.964G>C (p.Val322Leu) | |
| 5 | g.80675087G= | CA1558493507 | MSH3 | c.1132G= (p.Val378=) c.964G= (p.Val322=) | |
| 5 | g.80675087G>T | CA360268219 | MSH3 | c.1132G>T (p.Val378Phe) c.964G>T (p.Val322Phe) | ClinVar dbSNP gnomAD v2 |
| 5 | g.80675088T>A | CA360268222 | MSH3 | c.1133T>A (p.Val378Asp) c.965T>A (p.Val322Asp) | gnomAD v4 |
| 5 | g.80675088T>C | CA360268224 | MSH3 | c.1133T>C (p.Val378Ala) c.965T>C (p.Val322Ala) | gnomAD v4 |
| 5 | g.80675088T>G | CA121295197 | MSH3 | c.1133T>G (p.Val378Gly) c.965T>G (p.Val322Gly) | dbSNP |
| 5 | g.80675088T= | CA1558493511 | MSH3 | c.1133T= (p.Val378=) c.965T= (p.Val322=) | |
| 5 | g.80675089T>A | CA445159856 | MSH3 | c.1134T>A (p.Val378=) c.966T>A (p.Val322=) | gnomAD v4 |
| 5 | g.80675089T>C | CA445159857 | MSH3 | c.1134T>C (p.Val378=) c.966T>C (p.Val322=) | |
| 5 | g.80675089T>G | CA445159858 | MSH3 | c.1134T>G (p.Val378=) c.966T>G (p.Val322=) | |
| 5 | g.80675090A>C | CA445159859 | MSH3 | c.1135A>C (p.Arg379=) c.967A>C (p.Arg323=) | |
| 5 | g.80675090A>G | CA360268226 | MSH3 | c.1135A>G (p.Arg379Gly) c.967A>G (p.Arg323Gly) | |
| 5 | g.80675090A>T | CA360268227 | MSH3 | c.1135A>T (p.Arg379Trp) c.967A>T (p.Arg323Trp) | |
| 5 | g.80675091G>A | CA360268229 | MSH3 | c.1136G>A (p.Arg379Lys) c.968G>A (p.Arg323Lys) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675091G>C | CA360268231 | MSH3 | c.1136G>C (p.Arg379Thr) c.968G>C (p.Arg323Thr) | gnomAD v4 |
| 5 | g.80675091G= | CA1558493518 | MSH3 | c.1136G= (p.Arg379=) c.968G= (p.Arg323=) | |
| 5 | g.80675091G>T | CA360268233 | MSH3 | c.1136G>T (p.Arg379Met) c.968G>T (p.Arg323Met) | |
| 5 | g.80675092G>A | CA445159860 | MSH3 | c.1137G>A (p.Arg379=) c.969G>A (p.Arg323=) | gnomAD v3 gnomAD v4 |
| 5 | g.80675092G>C | CA360268234 | MSH3 | c.1137G>C (p.Arg379Ser) c.969G>C (p.Arg323Ser) | |
| 5 | g.80675092G>T | CA360268235 | MSH3 | c.1137G>T (p.Arg379Ser) c.969G>T (p.Arg323Ser) | dbSNP |
| 5 | g.80675093G>A | CA360268238 | MSH3 | c.1138G>A (p.Asp380Asn) c.970G>A (p.Asp324Asn) | gnomAD v3 gnomAD v4 |
| 5 | g.80675093G>C | CA360268240 | MSH3 | c.1138G>C (p.Asp380His) c.970G>C (p.Asp324His) | ClinVar |
| 5 | g.80675093G= | CA1558493524 | MSH3 | c.1138G= (p.Asp380=) c.970G= (p.Asp324=) | |
| 5 | g.80675093G>T | CA360268241 | MSH3 | c.1138G>T (p.Asp380Tyr) c.970G>T (p.Asp324Tyr) | |
| 5 | g.80675094A>C | CA360268244 | MSH3 | c.1139A>C (p.Asp380Ala) c.971A>C (p.Asp324Ala) | |
| 5 | g.80675094A>G | CA360268246 | MSH3 | c.1139A>G (p.Asp380Gly) c.971A>G (p.Asp324Gly) | |
| 5 | g.80675094A>T | CA360268247 | MSH3 | c.1139A>T (p.Asp380Val) c.971A>T (p.Asp324Val) | |
| 5 | g.80675094_80675095insAAAAAAAA | CA560552950 | MSH3 | c.1139_1140insAAAAAAAA (p.Asp380GlufsTer?) c.971_972insAAAAAAAA (p.Asp324GlufsTer?) | gnomAD v2 |
| 5 | g.80675094dup | CA3327802 | MSH3 | c.1139dup (p.Asp380GlufsTer24) c.971dup (p.Asp324GlufsTer24) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80675095C>A | CA3327803 | MSH3 | c.1140C>A (p.Asp380Glu) c.972C>A (p.Asp324Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 5 | g.80675095C= | CA1558493533 | MSH3 | c.1140C= (p.Asp380=) c.972C= (p.Asp324=) | |
| 5 | g.80675095C>G | CA360268248 | MSH3 | c.1140C>G (p.Asp380Glu) c.972C>G (p.Asp324Glu) | ClinVar dbSNP |
| 5 | g.80675095C>T | CA445159868 | MSH3 | c.1140C>T (p.Asp380=) c.972C>T (p.Asp324=) | |
| 5 | g.80675095_80675096delinsCA | CA1558493535 | MSH3 | c.1140_1141delinsCA (p.Asp380=) c.972_973delinsCA (p.Asp324=) | |
| 5 | g.80675096A= | CA1558493563 | MSH3 | c.1141A= (p.Lys381=) c.973A= (p.Lys325=) | |
| 5 | g.80675096A>C | CA3327804 | MSH3 | c.1141A>C (p.Lys381Gln) c.973A>C (p.Lys325Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80675096A>G | CA360268251 | MSH3 | c.1141A>G (p.Lys381Glu) c.973A>G (p.Lys325Glu) | ClinVar |
| 5 | g.80675096A>T | CA360268253 | MSH3 | c.1141A>T (p.Lys381Ter) c.973A>T (p.Lys325Ter) | |
| 5 | g.80675103dup | CA445159870 | MSH3 | c.1148dup (p.Asn385GlnfsTer19) c.980dup (p.Asn329GlnfsTer19) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
| 5 | g.80675103del | CA119871 | MSH3 | c.1148del (p.Lys383ArgfsTer?) c.980del (p.Lys327ArgfsTer?) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 5 | g.80675102_80675103del | CA645547809 | MSH3 | c.1147_1148del (p.Lys383GlyfsTer20) c.979_980del (p.Lys327GlyfsTer20) | COSMIC COSMIC |
| 5 | g.80675100_80675103del | CA2739274813 | MSH3 | c.1145_1148del (p.Lys382ArgfsTer?) c.977_980del (p.Lys326ArgfsTer?) | ClinVar |
| 5 | g.80675097A= | CA1558493578 | MSH3 | c.1142A= (p.Lys381=) c.974A= (p.Lys325=) | |
| 5 | g.80675097A>C | CA360268257 | MSH3 | c.1142A>C (p.Lys381Thr) c.974A>C (p.Lys325Thr) | |
| 5 | g.80675097A>G | CA360268259 | MSH3 | c.1142A>G (p.Lys381Arg) c.974A>G (p.Lys325Arg) | |
| 5 | g.80675097A>T | CA360268261 | MSH3 | c.1142A>T (p.Lys381Ile) c.974A>T (p.Lys325Ile) | ClinVar dbSNP |
| 5 | g.80675098A= | CA1558493581 | MSH3 | c.1143A= (p.Lys381=) c.975A= (p.Lys325=) | |
| 5 | g.80675098A>C | CA360268263 | MSH3 | c.1143A>C (p.Lys381Asn) c.975A>C (p.Lys325Asn) | |
| 5 | g.80675098A>G | CA445159879 | MSH3 | c.1143A>G (p.Lys381=) c.975A>G (p.Lys325=) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80675098A>T | CA360268265 | MSH3 | c.1143A>T (p.Lys381Asn) c.975A>T (p.Lys325Asn) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675099A= | CA1558493584 | MSH3 | c.1144A= (p.Lys382=) c.976A= (p.Lys326=) | |
| 5 | g.80675099A>C | CA360268266 | MSH3 | c.1144A>C (p.Lys382Gln) c.976A>C (p.Lys326Gln) | |
| 5 | g.80675099A>G | CA360268269 | MSH3 | c.1144A>G (p.Lys382Glu) c.976A>G (p.Lys326Glu) | ClinVar |
| 5 | g.80675099A>T | CA3327805 | MSH3 | c.1144A>T (p.Lys382Ter) c.976A>T (p.Lys326Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675100A= | CA1558493589 | MSH3 | c.1145A= (p.Lys382=) c.977A= (p.Lys326=) | |
| 5 | g.80675100A>C | CA360268275 | MSH3 | c.1145A>C (p.Lys382Thr) c.977A>C (p.Lys326Thr) | |
| 5 | g.80675100A>G | CA360268272 | MSH3 | c.1145A>G (p.Lys382Arg) c.977A>G (p.Lys326Arg) | ClinVar |
| 5 | g.80675100A>T | CA360268273 | MSH3 | c.1145A>T (p.Lys382Ile) c.977A>T (p.Lys326Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675101A>C | CA360268276 | MSH3 | c.1146A>C (p.Lys382Asn) c.978A>C (p.Lys326Asn) | |
| 5 | g.80675101A>G | CA445159886 | MSH3 | c.1146A>G (p.Lys382=) c.978A>G (p.Lys326=) | ClinVar dbSNP |
| 5 | g.80675101A>T | CA360268277 | MSH3 | c.1146A>T (p.Lys382Asn) c.978A>T (p.Lys326Asn) | |
| 5 | g.80675101_80675102insCC | CA2767180110 | MSH3 | c.1146_1147insCC (p.Lys383ProfsTer?) c.978_979insCC (p.Lys327ProfsTer?) | |
| 5 | g.80675101_80675102insCCCCAAACACACCCAACAC | CA2767180111 | MSH3 | c.1146_1147insCCCCAAACACACCCAACAC (p.Lys383ProfsTer27) c.978_979insCCCCAAACACACCCAACAC (p.Lys327ProfsTer27) | |
| 5 | g.80675102A>C | CA360268281 | MSH3 | c.1147A>C (p.Lys383Gln) c.979A>C (p.Lys327Gln) | ClinVar dbSNP |
| 5 | g.80675102A>G | CA360268280 | MSH3 | c.1147A>G (p.Lys383Glu) c.979A>G (p.Lys327Glu) | |
| 5 | g.80675102A>T | CA360268283 | MSH3 | c.1147A>T (p.Lys383Ter) c.979A>T (p.Lys327Ter) | |
| 5 | g.80675103A= | CA1558493595 | MSH3 | c.1148A= (p.Lys383=) c.980A= (p.Lys327=) | |
| 5 | g.80675103A>C | CA360268287 | MSH3 | c.1148A>C (p.Lys383Thr) c.980A>C (p.Lys327Thr) | ClinVar dbSNP |
| 5 | g.80675103A>G | CA121295206 | MSH3 | c.1148A>G (p.Lys383Arg) c.980A>G (p.Lys327Arg) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675103A>T | CA360268286 | MSH3 | c.1148A>T (p.Lys383Met) c.980A>T (p.Lys327Met) | |
| 5 | g.80675103_80675104del | CA2580073638 | MSH3 | c.1148_1149del (p.Lys383ArgfsTer20) c.980_981del (p.Lys327ArgfsTer20) | ClinVar gnomAD v4 |
| 5 | g.80675103_80675104insC | CA2674443047 | MSH3 | c.1148_1149insC (p.Lys383AsnfsTer21) c.980_981insC (p.Lys327AsnfsTer21) | gnomAD v4 |
| 5 | g.80675104G>A | CA3327806 | MSH3 | c.1149G>A (p.Lys383=) c.981G>A (p.Lys327=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675104G>C | CA360268296 | MSH3 | c.1149G>C (p.Lys383Asn) c.981G>C (p.Lys327Asn) | |
| 5 | g.80675104G= | CA1558493600 | MSH3 | c.1149G= (p.Lys383=) c.981G= (p.Lys327=) | |
| 5 | g.80675104G>T | CA360268297 | MSH3 | c.1149G>T (p.Lys383Asn) c.981G>T (p.Lys327Asn) | |
| 5 | g.80675105G>A | CA360268299 | MSH3 | c.1150G>A (p.Gly384Ser) c.982G>A (p.Gly328Ser) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675105G>C | CA360268301 | MSH3 | c.1150G>C (p.Gly384Arg) c.982G>C (p.Gly328Arg) | |
| 5 | g.80675105G= | CA1558493604 | MSH3 | c.1150G= (p.Gly384=) c.982G= (p.Gly328=) | |
| 5 | g.80675105G>T | CA360268303 | MSH3 | c.1150G>T (p.Gly384Cys) c.982G>T (p.Gly328Cys) | dbSNP |