Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 |
5 | g.80675106G>A | CA121295214 | MSH3 | c.1151G>A (p.Gly384Asp) c.983G>A (p.Gly328Asp) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
5 | g.80675106G>C | CA360268307 | MSH3 | c.1151G>C (p.Gly384Ala) c.983G>C (p.Gly328Ala) | |
5 | g.80675106G= | CA1558493608 | MSH3 | c.1151G= (p.Gly384=) c.983G= (p.Gly328=) | |
5 | g.80675106G>T | CA360268343 | MSH3 | c.1151G>T (p.Gly384Val) c.983G>T (p.Gly328Val) | |
5 | g.80675107C>A | CA445159903 | MSH3 | c.1152C>A (p.Gly384=) c.984C>A (p.Gly328=) | dbSNP |
5 | g.80675107C>G | CA445159901 | MSH3 | c.1152C>G (p.Gly384=) c.984C>G (p.Gly328=) | |
5 | g.80675107C>T | CA445159899 | MSH3 | c.1152C>T (p.Gly384=) c.984C>T (p.Gly328=) | |
5 | g.80675107_80675108delinsCA | CA1558493617 | MSH3 | c.1152_1153delinsCA (p.Gly384=) c.984_985delinsCA (p.Gly328=) | |
5 | g.80675108A>C | CA360268348 | MSH3 | c.1153A>C (p.Asn385His) c.985A>C (p.Asn329His) | ClinVar |
5 | g.80675108A>G | CA360268345 | MSH3 | c.1153A>G (p.Asn385Asp) c.985A>G (p.Asn329Asp) | |
5 | g.80675108A>T | CA360268347 | MSH3 | c.1153A>T (p.Asn385Tyr) c.985A>T (p.Asn329Tyr) | |
5 | g.80675109del | CA121295220 | MSH3 | c.1154del (p.Asn385ThrfsTer30) c.986del (p.Asn329ThrfsTer30) | dbSNP |
5 | g.80675109A= | CA1558493628 | MSH3 | c.1154A= (p.Asn385=) c.986A= (p.Asn329=) | |
5 | g.80675109A>C | CA360268350 | MSH3 | c.1154A>C (p.Asn385Thr) c.986A>C (p.Asn329Thr) | gnomAD v4 |
5 | g.80675109A>G | CA360268352 | MSH3 | c.1154A>G (p.Asn385Ser) c.986A>G (p.Asn329Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.80675109A>T | CA360268353 | MSH3 | c.1154A>T (p.Asn385Ile) c.986A>T (p.Asn329Ile) | ClinVar COSMIC COSMIC |
5 | g.80675110C>A | CA360268355 | MSH3 | c.1155C>A (p.Asn385Lys) c.987C>A (p.Asn329Lys) | |
5 | g.80675110C= | CA1558493638 | MSH3 | c.1155C= (p.Asn385=) c.987C= (p.Asn329=) | |
5 | g.80675110C>G | CA3327807 | MSH3 | c.1155C>G (p.Asn385Lys) c.987C>G (p.Asn329Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.80675110C>T | CA445159911 | MSH3 | c.1155C>T (p.Asn385=) c.987C>T (p.Asn329=) | |
5 | g.80675111A= | CA1558493649 | MSH3 | c.1156A= (p.Ile386=) c.988A= (p.Ile330=) | |
5 | g.80675111A>C | CA360268358 | MSH3 | c.1156A>C (p.Ile386Leu) c.988A>C (p.Ile330Leu) | |
5 | g.80675111A>G | CA3327808 | MSH3 | c.1156A>G (p.Ile386Val) c.988A>G (p.Ile330Val) | ClinVar dbSNP ExAC gnomAD v2 |
5 | g.80675111A>T | CA360268360 | MSH3 | c.1156A>T (p.Ile386Phe) c.988A>T (p.Ile330Phe) | |
5 | g.80675111_80675112delinsAT | CA1558493651 | MSH3 | c.1156_1157delinsAT (p.Ile386=) c.988_989delinsAT (p.Ile330=) | |
5 | g.80675112T>A | CA360268362 | MSH3 | c.1157T>A (p.Ile386Asn) c.989T>A (p.Ile330Asn) | ClinVar |
5 | g.80675112T>C | CA360268363 | MSH3 | c.1157T>C (p.Ile386Thr) c.989T>C (p.Ile330Thr) | ClinVar |
5 | g.80675112T>G | CA360268365 | MSH3 | c.1157T>G (p.Ile386Ser) c.989T>G (p.Ile330Ser) | |
5 | g.80675116del | CA121295233 | MSH3 | c.1161del (p.Phe387LeufsTer28) c.993del (p.Phe331LeufsTer28) | ClinVar dbSNP |
5 | g.80675113T>A | CA445159917 | MSH3 | c.1158T>A (p.Ile386=) c.990T>A (p.Ile330=) | |
5 | g.80675113T>C | CA445159919 | MSH3 | c.1158T>C (p.Ile386=) c.990T>C (p.Ile330=) | ClinVar |
5 | g.80675113T>G | CA360268368 | MSH3 | c.1158T>G (p.Ile386Met) c.990T>G (p.Ile330Met) | |
5 | g.80675114T>A | CA360268374 | MSH3 | c.1159T>A (p.Phe387Ile) c.991T>A (p.Phe331Ile) | |
5 | g.80675114T>C | CA360268370 | MSH3 | c.1159T>C (p.Phe387Leu) c.991T>C (p.Phe331Leu) | |
5 | g.80675114T>G | CA360268372 | MSH3 | c.1159T>G (p.Phe387Val) c.991T>G (p.Phe331Val) | |
5 | g.80675115T>A | CA3327809 | MSH3 | c.1160T>A (p.Phe387Tyr) c.992T>A (p.Phe331Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.80675115T>C | CA360268375 | MSH3 | c.1160T>C (p.Phe387Ser) c.992T>C (p.Phe331Ser) | |
5 | g.80675115T>G | CA360268377 | MSH3 | c.1160T>G (p.Phe387Cys) c.992T>G (p.Phe331Cys) | |
5 | g.80675115T= | CA1558493663 | MSH3 | c.1160T= (p.Phe387=) c.992T= (p.Phe331=) | |
5 | g.80675116T>A | CA360268380 | MSH3 | c.1161T>A (p.Phe387Leu) c.993T>A (p.Phe331Leu) | |
5 | g.80675116T>C | CA445159931 | MSH3 | c.1161T>C (p.Phe387=) c.993T>C (p.Phe331=) | gnomAD v4 |
5 | g.80675116T>G | CA360268381 | MSH3 | c.1161T>G (p.Phe387Leu) c.993T>G (p.Phe331Leu) | |
5 | g.80675117A= | CA1558493668 | MSH3 | c.1162A= (p.Ile388=) c.994A= (p.Ile332=) | |
5 | g.80675117A>C | CA360268384 | MSH3 | c.1162A>C (p.Ile388Leu) c.994A>C (p.Ile332Leu) | |
5 | g.80675117A>G | CA360268387 | MSH3 | c.1162A>G (p.Ile388Val) c.994A>G (p.Ile332Val) | gnomAD v4 |
5 | g.80675117A>T | CA360268385 | MSH3 | c.1162A>T (p.Ile388Phe) c.994A>T (p.Ile332Phe) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.80675118T>A | CA360268389 | MSH3 | c.1163T>A (p.Ile388Asn) c.995T>A (p.Ile332Asn) | |
5 | g.80675118T>C | CA121295259 | MSH3 | c.1163T>C (p.Ile388Thr) c.995T>C (p.Ile332Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
5 | g.80675118T>G | CA360268391 | MSH3 | c.1163T>G (p.Ile388Ser) c.995T>G (p.Ile332Ser) | ClinVar |
5 | g.80675118T= | CA1558493672 | MSH3 | c.1163T= (p.Ile388=) c.995T= (p.Ile332=) | |
5 | g.80675119T>A | CA445159941 | MSH3 | c.1164T>A (p.Ile388=) c.996T>A (p.Ile332=) | |
5 | g.80675119T>C | CA445159944 | MSH3 | c.1164T>C (p.Ile388=) c.996T>C (p.Ile332=) | ClinVar dbSNP COSMIC COSMIC |
5 | g.80675119T>G | CA360268392 | MSH3 | c.1164T>G (p.Ile388Met) c.996T>G (p.Ile332Met) | |
5 | g.80675120G>A | CA360268395 | MSH3 | c.1165G>A (p.Gly389Ser) c.997G>A (p.Gly333Ser) | |
5 | g.80675120G>C | CA360268398 | MSH3 | c.1165G>C (p.Gly389Arg) c.997G>C (p.Gly333Arg) | |
5 | g.80675120G>T | CA360268397 | MSH3 | c.1165G>T (p.Gly389Cys) c.997G>T (p.Gly333Cys) | |
5 | g.80675121G>A | CA360268401 | MSH3 | c.1166G>A (p.Gly389Asp) c.998G>A (p.Gly333Asp) | ClinVar dbSNP |
5 | g.80675121G>C | CA360268402 | MSH3 | c.1166G>C (p.Gly389Ala) c.998G>C (p.Gly333Ala) | ClinVar |
5 | g.80675121G= | CA1558493682 | MSH3 | c.1166G= (p.Gly389=) c.998G= (p.Gly333=) | |
5 | g.80675121G>T | CA360268404 | MSH3 | c.1166G>T (p.Gly389Val) c.998G>T (p.Gly333Val) | ClinVar dbSNP |
5 | g.80675122C>A | CA445159952 | MSH3 | c.1167C>A (p.Gly389=) c.999C>A (p.Gly333=) | dbSNP |
5 | g.80675122C>G | CA445159955 | MSH3 | c.1167C>G (p.Gly389=) c.999C>G (p.Gly333=) | |
5 | g.80675122C>T | CA445159957 | MSH3 | c.1167C>T (p.Gly389=) c.999C>T (p.Gly333=) | ClinVar |
5 | g.80675123A= | CA1558493692 | MSH3 | c.1168A= (p.Ile390=) c.1000A= (p.Ile334=) | |
5 | g.80675123A>C | CA360268406 | MSH3 | c.1168A>C (p.Ile390Leu) c.1000A>C (p.Ile334Leu) | |
5 | g.80675123A>G | CA360268408 | MSH3 | c.1168A>G (p.Ile390Val) c.1000A>G (p.Ile334Val) | ClinVar dbSNP gnomAD v2 |
5 | g.80675123A>T | CA360268410 | MSH3 | c.1168A>T (p.Ile390Phe) c.1000A>T (p.Ile334Phe) | |
5 | g.80675124T>A | CA360268413 | MSH3 | c.1169T>A (p.Ile390Asn) c.1001T>A (p.Ile334Asn) | |
5 | g.80675124T>C | CA360268414 | MSH3 | c.1169T>C (p.Ile390Thr) c.1001T>C (p.Ile334Thr) | ClinVar |
5 | g.80675124T>G | CA360268416 | MSH3 | c.1169T>G (p.Ile390Ser) c.1001T>G (p.Ile334Ser) | |
5 | g.80675125T>A | CA445159964 | MSH3 | c.1170T>A (p.Ile390=) c.1002T>A (p.Ile334=) | |
5 | g.80675125T>C | CA445159965 | MSH3 | c.1170T>C (p.Ile390=) c.1002T>C (p.Ile334=) | |
5 | g.80675125T>G | CA360268418 | MSH3 | c.1170T>G (p.Ile390Met) c.1002T>G (p.Ile334Met) | |
5 | g.80675126G>A | CA360268427 | MSH3 | c.1171G>A (p.Val391Met) c.1003G>A (p.Val335Met) | COSMIC COSMIC |
5 | g.80675126G>C | CA360268423 | MSH3 | c.1171G>C (p.Val391Leu) c.1003G>C (p.Val335Leu) | |
5 | g.80675126G= | CA1558493703 | MSH3 | c.1171G= (p.Val391=) c.1003G= (p.Val335=) | |
5 | g.80675126G>T | CA360268420 | MSH3 | c.1171G>T (p.Val391Leu) c.1003G>T (p.Val335Leu) | ClinVar dbSNP |
5 | g.80675127T>A | CA360268428 | MSH3 | c.1172T>A (p.Val391Glu) c.1004T>A (p.Val335Glu) | |
5 | g.80675127T>C | CA360268431 | MSH3 | c.1172T>C (p.Val391Ala) c.1004T>C (p.Val335Ala) | |
5 | g.80675127T>G | CA360268430 | MSH3 | c.1172T>G (p.Val391Gly) c.1004T>G (p.Val335Gly) | |
5 | g.80675128G>A | CA445159973 | MSH3 | c.1173G>A (p.Val391=) c.1005G>A (p.Val335=) | ClinVar dbSNP |
5 | g.80675128G>C | CA445159975 | MSH3 | c.1173G>C (p.Val391=) c.1005G>C (p.Val335=) | |
5 | g.80675128G= | CA1558493708 | MSH3 | c.1173G= (p.Val391=) c.1005G= (p.Val335=) | |
5 | g.80675128G>T | CA445159972 | MSH3 | c.1173G>T (p.Val391=) c.1005G>T (p.Val335=) | |
5 | g.80675129_80675133del | CA2695198653 | MSH3 | c.1173+1_1173+5del c.1005+1_1005+5del | ClinVar |
5 | g.80675128_80675129insA | CA121295270 | MSH3 | c.1173_1173+1insA (n.1173_1173+1insA) c.1005_1005+1insA (n.1005_1005+1insA) | dbSNP |
5 | g.80675129G>A | CA121295266 | MSH3 | c.1173+1G>A (n.1173+1G>A) c.1005+1G>A (n.1005+1G>A) | ClinVar dbSNP |
5 | g.80675129G>C | CA360268434 | MSH3 | c.1173+1G>C (n.1173+1G>C) c.1005+1G>C (n.1005+1G>C) | |
5 | g.80675129G= | CA1558493723 | MSH3 | c.1173+1G= (n.1173+1G=) c.1005+1G= (n.1005+1G=) | |
5 | g.80675129G>T | CA360268435 | MSH3 | c.1173+1G>T (n.1173+1G>T) c.1005+1G>T (n.1005+1G>T) | |
5 | g.80675130T>A | CA360268437 | MSH3 | c.1173+2T>A (n.1173+2T>A) c.1005+2T>A (n.1005+2T>A) | |
5 | g.80675130T>C | CA360268439 | MSH3 | c.1173+2T>C (n.1173+2T>C) c.1005+2T>C (n.1005+2T>C) | |
5 | g.80675130T>G | CA360268440 | MSH3 | c.1173+2T>G (n.1173+2T>G) c.1005+2T>G (n.1005+2T>G) | ClinVar dbSNP |
5 | g.80675133G>A | CA3327810 | MSH3 | c.1173+5G>A (n.1173+5G>A) c.1005+5G>A (n.1005+5G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.80675133G= | CA1558493731 | MSH3 | c.1173+5G= (n.1173+5G=) c.1005+5G= (n.1005+5G=) | |
5 | g.80675134T>C | CA1558493736 | MSH3 | c.1173+6T>C (n.1173+6T>C) c.1005+6T>C (n.1005+6T>C) | dbSNP gnomAD v4 |
5 | g.80675134T= | CA1558493735 | MSH3 | c.1173+6T= (n.1173+6T=) c.1005+6T= (n.1005+6T=) | |
5 | g.80675136_80675137delinsCT | CA1558493739 | MSH3 | c.1173+8_1173+9delinsCT (n.1173+8_1173+9delinsCT) c.1005+8_1005+9delinsCT (n.1005+8_1005+9delinsCT) | |
5 | g.80675137T>C | CA2580073642 | MSH3 | c.1173+9T>C (n.1173+9T>C) c.1005+9T>C (n.1005+9T>C) | ClinVar |
5 | g.80675137T>G | CA2580073643 | MSH3 | c.1173+9T>G (n.1173+9T>G) c.1005+9T>G (n.1005+9T>G) | ClinVar |
5 | g.80675139del | CA3327811 | MSH3 | c.1173+11del (n.1173+11del) c.1005+11del (n.1005+11del) | dbSNP ExAC gnomAD v3 gnomAD v4 |
5 | g.80675138T>G | CA2674443048 | MSH3 | c.1173+10T>G (n.1173+10T>G) c.1005+10T>G (n.1005+10T>G) | gnomAD v4 |
5 | g.80675139T>C | CA3327812 | MSH3 | c.1173+11T>C (n.1173+11T>C) c.1005+11T>C (n.1005+11T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.80675139T= | CA1558493745 | MSH3 | c.1173+11T= (n.1173+11T=) c.1005+11T= (n.1005+11T=) | |
5 | g.80675140G>A | CA3327813 | MSH3 | c.1173+12G>A (n.1173+12G>A) c.1005+12G>A (n.1005+12G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.80675140G= | CA1558493750 | MSH3 | c.1173+12G= (n.1173+12G=) c.1005+12G= (n.1005+12G=) | |
5 | g.80675141C= | CA1558493754 | MSH3 | c.1173+13C= (n.1173+13C=) c.1005+13C= (n.1005+13C=) | |
5 | g.80675141C>T | CA1077959084 | MSH3 | c.1173+13C>T (n.1173+13C>T) c.1005+13C>T (n.1005+13C>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
5 | g.80675144G>A | CA2739274814 | MSH3 | c.1173+16G>A (n.1173+16G>A) c.1005+16G>A (n.1005+16G>A) | ClinVar |
5 | g.80675145T>G | CA2578350234 | MSH3 | c.1173+17T>G (n.1173+17T>G) c.1005+17T>G (n.1005+17T>G) | ClinVar |
5 | g.80675146G>A | CA560552984 | MSH3 | c.1173+18G>A (n.1173+18G>A) c.1005+18G>A (n.1005+18G>A) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.80675146G= | CA1558493758 | MSH3 | c.1173+18G= (n.1173+18G=) c.1005+18G= (n.1005+18G=) | |
5 | g.80675147A= | CA1558493761 | MSH3 | c.1173+19A= (n.1173+19A=) c.1005+19A= (n.1005+19A=) | |
5 | g.80675147A>T | CA1558493763 | MSH3 | c.1173+19A>T (n.1173+19A>T) c.1005+19A>T (n.1005+19A>T) | dbSNP gnomAD v4 |
5 | g.80675148G>A | CA2740091764 | MSH3 | c.1173+20G>A (n.1173+20G>A) c.1005+20G>A (n.1005+20G>A) | ClinVar |
5 | g.80675149G>A | CA1558493768 | MSH3 | c.1173+21G>A (n.1173+21G>A) c.1005+21G>A (n.1005+21G>A) | dbSNP gnomAD v4 |
5 | g.80675149G>C | CA1558493770 | MSH3 | c.1173+21G>C (n.1173+21G>C) c.1005+21G>C (n.1005+21G>C) | dbSNP |
5 | g.80675149G= | CA1558493767 | MSH3 | c.1173+21G= (n.1173+21G=) c.1005+21G= (n.1005+21G=) | |
5 | g.80675151A>G | CA2674443049 | MSH3 | c.1173+23A>G (n.1173+23A>G) c.1005+23A>G (n.1005+23A>G) | gnomAD v4 |
5 | g.80675152C= | CA1558493772 | MSH3 | c.1173+24C= (n.1173+24C=) c.1005+24C= (n.1005+24C=) | |
5 | g.80675152C>T | CA3327814 | MSH3 | c.1173+24C>T (n.1173+24C>T) c.1005+24C>T (n.1005+24C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.80675154A= | CA1558493806 | MSH3 | c.1173+26A= (n.1173+26A=) c.1005+26A= (n.1005+26A=) | |
5 | g.80675154A>G | CA560552985 | MSH3 | c.1173+26A>G (n.1173+26A>G) c.1005+26A>G (n.1005+26A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.80675154_80675161delinsAATGTTAG | CA1558493775 | MSH3 | c.1173+26_1173+33delinsAATGTTAG (n.1173+26_1173+33delinsAATGTTAG) c.1005+26_1005+33delinsAATGTTAG (n.1005+26_1005+33delinsAATGTTAG) | |
5 | g.80675155A= | CA1558493811 | MSH3 | c.1173+27A= (n.1173+27A=) c.1005+27A= (n.1005+27A=) | |
5 | g.80675155A>G | CA3327815 | MSH3 | c.1173+27A>G (n.1173+27A>G) c.1005+27A>G (n.1005+27A>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.80675160_80675166del | CA1558493810 | MSH3 | c.1173+32_1173+38del (n.1173+32_1173+38del) c.1005+32_1005+38del (n.1005+32_1005+38del) | dbSNP |
5 | g.80675157G>A | CA2674443050 | MSH3 | c.1173+29G>A (n.1173+29G>A) c.1005+29G>A (n.1005+29G>A) | gnomAD v4 |
5 | g.80675158T>C | CA560552988 | MSH3 | c.1173+30T>C (n.1173+30T>C) c.1005+30T>C (n.1005+30T>C) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.80675158T>G | CA3327816 | MSH3 | c.1173+30T>G (n.1173+30T>G) c.1005+30T>G (n.1005+30T>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.80675158T= | CA1558493819 | MSH3 | c.1173+30T= (n.1173+30T=) c.1005+30T= (n.1005+30T=) | |
5 | g.80675161G>A | CA1077959086 | MSH3 | c.1173+33G>A (n.1173+33G>A) c.1005+33G>A (n.1005+33G>A) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.80675161G= | CA1558493826 | MSH3 | c.1173+33G= (n.1173+33G=) c.1005+33G= (n.1005+33G=) | |
5 | g.80675162A= | CA1558493830 | MSH3 | c.1173+34A= (n.1173+34A=) c.1005+34A= (n.1005+34A=) | |
5 | g.80675162A>G | CA560552991 | MSH3 | c.1173+34A>G (n.1173+34A>G) c.1005+34A>G (n.1005+34A>G) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.80675163T>A | CA814453967 | MSH3 | c.1173+35T>A (n.1173+35T>A) c.1005+35T>A (n.1005+35T>A) | dbSNP |
5 | g.80675163T= | CA1558493833 | MSH3 | c.1173+35T= (n.1173+35T=) c.1005+35T= (n.1005+35T=) | |
5 | g.80675167C>A | CA649966194 | MSH3 | c.1173+39C>A (n.1173+39C>A) c.1005+39C>A (n.1005+39C>A) | COSMIC |
5 | g.80675167C>T | CA2674443051 | MSH3 | c.1173+39C>T (n.1173+39C>T) c.1005+39C>T (n.1005+39C>T) | gnomAD v4 |
5 | g.80675168A= | CA1558493835 | MSH3 | c.1173+40A= (n.1173+40A=) c.1005+40A= (n.1005+40A=) | |
5 | g.80675168A>C | CA560552992 | MSH3 | c.1173+40A>C (n.1173+40A>C) c.1005+40A>C (n.1005+40A>C) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.80675168A>G | CA1558493836 | MSH3 | c.1173+40A>G (n.1173+40A>G) c.1005+40A>G (n.1005+40A>G) | dbSNP gnomAD v4 |
5 | g.80675169T>C | CA3327817 | MSH3 | c.1173+41T>C (n.1173+41T>C) c.1005+41T>C (n.1005+41T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.80675169T= | CA1558493840 | MSH3 | c.1173+41T= (n.1173+41T=) c.1005+41T= (n.1005+41T=) | |
5 | g.80675170G>A | CA2674443052 | MSH3 | c.1173+42G>A (n.1173+42G>A) c.1005+42G>A (n.1005+42G>A) | gnomAD v4 |
5 | g.80675171G>A | CA3327819 | MSH3 | c.1173+43G>A (n.1173+43G>A) c.1005+43G>A (n.1005+43G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.80675171G= | CA1558493862 | MSH3 | c.1173+43G= (n.1173+43G=) c.1005+43G= (n.1005+43G=) | |
5 | g.80675171_80675173delinsGTA | CA1558493863 | MSH3 | c.1173+43_1173+45delinsGTA (n.1173+43_1173+45delinsGTA) c.1005+43_1005+45delinsGTA (n.1005+43_1005+45delinsGTA) | |
5 | g.80675172T>C | CA560552994 | MSH3 | c.1173+44T>C (n.1173+44T>C) c.1005+44T>C (n.1005+44T>C) | dbSNP gnomAD v2 |
5 | g.80675172T= | CA1558493865 | MSH3 | c.1173+44T= (n.1173+44T=) c.1005+44T= (n.1005+44T=) | |
5 | g.80675173_80675174del | CA3327818 | MSH3 | c.1173+45_1173+46del (n.1173+45_1173+46del) c.1005+45_1005+46del (n.1005+45_1005+46del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.80675173A= | CA1558493870 | MSH3 | c.1173+45A= (n.1173+45A=) c.1005+45A= (n.1005+45A=) | |
5 | g.80675173A>G | CA814453985 | MSH3 | c.1173+45A>G (n.1173+45A>G) c.1005+45A>G (n.1005+45A>G) | dbSNP |
5 | g.80675177_80675178del | CA2578350235 | MSH3 | c.1173+49_1173+50del (n.1173+49_1173+50del) c.1005+49_1005+50del (n.1005+49_1005+50del) | |
5 | g.80675175C>A | CA2674443053 | MSH3 | c.1173+47C>A (n.1173+47C>A) c.1005+47C>A (n.1005+47C>A) | gnomAD v4 |
5 | g.80675175C>G | CA2674443054 | MSH3 | c.1173+47C>G (n.1173+47C>G) c.1005+47C>G (n.1005+47C>G) | gnomAD v4 |