| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.48981500T>A | CA384637701 | WNT1 | c.973T>A (p.Cys325Ser) c.940T>A (p.Cys314Ser) | |
| 12 | g.48981500T>C | CA384637704 | WNT1 | c.973T>C (p.Cys325Arg) c.940T>C (p.Cys314Arg) | gnomAD v4 |
| 12 | g.48981500T>G | CA384637712 | WNT1 | c.973T>G (p.Cys325Gly) c.940T>G (p.Cys314Gly) | |
| 12 | g.48981501G>A | CA384637719 | WNT1 | c.974G>A (p.Cys325Tyr) c.941G>A (p.Cys314Tyr) | gnomAD v4 |
| 12 | g.48981501G>C | CA384637724 | WNT1 | c.974G>C (p.Cys325Ser) c.941G>C (p.Cys314Ser) | |
| 12 | g.48981501G>T | CA384637727 | WNT1 | c.974G>T (p.Cys325Phe) c.941G>T (p.Cys314Phe) | |
| 12 | g.48981502C>A | CA384637729 | WNT1 | c.975C>A (p.Cys325Ter) c.942C>A (p.Cys314Ter) | gnomAD v4 COSMIC |
| 12 | g.48981502C= | CA2034926253 | WNT1 | c.975C= (p.Cys325=) c.942C= (p.Cys314=) | |
| 12 | g.48981502C>G | CA384637730 | WNT1 | c.975C>G (p.Cys325Trp) c.942C>G (p.Cys314Trp) | |
| 12 | g.48981502C>T | CA6544494 | WNT1 | c.975C>T (p.Cys325=) c.942C>T (p.Cys314=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 12 | g.48981503G>A | CA384637767 | WNT1 | c.976G>A (p.Glu326Lys) c.943G>A (p.Glu315Lys) | ClinVar gnomAD v4 |
| 12 | g.48981503G>C | CA384637780 | WNT1 | c.976G>C (p.Glu326Gln) c.943G>C (p.Glu315Gln) | |
| 12 | g.48981503G>T | CA384637785 | WNT1 | c.976G>T (p.Glu326Ter) c.943G>T (p.Glu315Ter) | gnomAD v4 |
| 12 | g.48981504A>C | CA384637821 | WNT1 | c.977A>C (p.Glu326Ala) c.944A>C (p.Glu315Ala) | |
| 12 | g.48981504A>G | CA384637826 | WNT1 | c.977A>G (p.Glu326Gly) c.944A>G (p.Glu315Gly) | |
| 12 | g.48981504A>T | CA384637817 | WNT1 | c.977A>T (p.Glu326Val) c.944A>T (p.Glu315Val) | |
| 12 | g.48981505G>A | CA479704387 | WNT1 | c.978G>A (p.Glu326=) c.945G>A (p.Glu315=) | |
| 12 | g.48981505G>C | CA384637827 | WNT1 | c.978G>C (p.Glu326Asp) c.945G>C (p.Glu315Asp) | |
| 12 | g.48981505G>T | CA384637828 | WNT1 | c.978G>T (p.Glu326Asp) c.945G>T (p.Glu315Asp) | gnomAD v4 |
| 12 | g.48981506C>A | CA384637830 | WNT1 | c.979C>A (p.Leu327Met) c.946C>A (p.Leu316Met) | |
| 12 | g.48981506C>G | CA384637835 | WNT1 | c.979C>G (p.Leu327Val) c.946C>G (p.Leu316Val) | |
| 12 | g.48981506C>T | CA479704392 | WNT1 | c.979C>T (p.Leu327=) c.946C>T (p.Leu316=) | gnomAD v4 |
| 12 | g.48981507T>A | CA384637859 | WNT1 | c.980T>A (p.Leu327Gln) c.947T>A (p.Leu316Gln) | |
| 12 | g.48981507T>C | CA384637849 | WNT1 | c.980T>C (p.Leu327Pro) c.947T>C (p.Leu316Pro) | gnomAD v4 |
| 12 | g.48981507T>G | CA384637848 | WNT1 | c.980T>G (p.Leu327Arg) c.947T>G (p.Leu316Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48981507T= | CA2034926256 | WNT1 | c.980T= (p.Leu327=) c.947T= (p.Leu316=) | |
| 12 | g.48981508G>A | CA479704393 | WNT1 | c.981G>A (p.Leu327=) c.948G>A (p.Leu316=) | gnomAD v4 |
| 12 | g.48981508G>C | CA479704394 | WNT1 | c.981G>C (p.Leu327=) c.948G>C (p.Leu316=) | |
| 12 | g.48981508G>T | CA479704395 | WNT1 | c.981G>T (p.Leu327=) c.948G>T (p.Leu316=) | gnomAD v4 |
| 12 | g.48981509C>A | CA384637862 | WNT1 | c.982C>A (p.Leu328Ile) c.949C>A (p.Leu317Ile) | gnomAD v4 |
| 12 | g.48981509C= | CA2034926260 | WNT1 | c.982C= (p.Leu328=) c.949C= (p.Leu317=) | |
| 12 | g.48981509C>G | CA384637870 | WNT1 | c.982C>G (p.Leu328Val) c.949C>G (p.Leu317Val) | |
| 12 | g.48981509C>T | CA236608806 | WNT1 | c.982C>T (p.Leu328Phe) c.949C>T (p.Leu317Phe) | dbSNP |
| 12 | g.48981510T>A | CA384637899 | WNT1 | c.983T>A (p.Leu328His) c.950T>A (p.Leu317His) | |
| 12 | g.48981510T>C | CA384637909 | WNT1 | c.983T>C (p.Leu328Pro) c.950T>C (p.Leu317Pro) | gnomAD v4 |
| 12 | g.48981510T>G | CA384637914 | WNT1 | c.983T>G (p.Leu328Arg) c.950T>G (p.Leu317Arg) | dbSNP |
| 12 | g.48981510T= | CA2034926262 | WNT1 | c.983T= (p.Leu328=) c.950T= (p.Leu317=) | |
| 12 | g.48981511C>A | CA479704397 | WNT1 | c.984C>A (p.Leu328=) c.951C>A (p.Leu317=) | |
| 12 | g.48981511C>G | CA479704398 | WNT1 | c.984C>G (p.Leu328=) c.951C>G (p.Leu317=) | |
| 12 | g.48981511C>T | CA479704399 | WNT1 | c.984C>T (p.Leu328=) c.951C>T (p.Leu317=) | |
| 12 | g.48981512T>A | CA384637921 | WNT1 | c.985T>A (p.Cys329Ser) c.952T>A (p.Cys318Ser) | |
| 12 | g.48981512T>C | CA384637919 | WNT1 | c.985T>C (p.Cys329Arg) c.952T>C (p.Cys318Arg) | |
| 12 | g.48981512T>G | CA384637917 | WNT1 | c.985T>G (p.Cys329Gly) c.952T>G (p.Cys318Gly) | |
| 12 | g.48981513G>A | CA384637926 | WNT1 | c.986G>A (p.Cys329Tyr) c.953G>A (p.Cys318Tyr) | |
| 12 | g.48981513G>C | CA384637943 | WNT1 | c.986G>C (p.Cys329Ser) c.953G>C (p.Cys318Ser) | |
| 12 | g.48981513G>T | CA384637930 | WNT1 | c.986G>T (p.Cys329Phe) c.953G>T (p.Cys318Phe) | gnomAD v4 |
| 12 | g.48981514C>A | CA384637950 | WNT1 | c.987C>A (p.Cys329Ter) c.954C>A (p.Cys318Ter) | gnomAD v4 |
| 12 | g.48981514C= | CA2034926266 | WNT1 | c.987C= (p.Cys329=) c.954C= (p.Cys318=) | |
| 12 | g.48981514C>G | CA384637952 | WNT1 | c.987C>G (p.Cys329Trp) c.954C>G (p.Cys318Trp) | |
| 12 | g.48981514C>T | CA479704403 | WNT1 | c.987C>T (p.Cys329=) c.954C>T (p.Cys318=) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48981515T>A | CA384637957 | WNT1 | c.988T>A (p.Cys330Ser) c.955T>A (p.Cys319Ser) | |
| 12 | g.48981515T>C | CA384637965 | WNT1 | c.988T>C (p.Cys330Arg) c.955T>C (p.Cys319Arg) | ClinVar dbSNP gnomAD v4 |
| 12 | g.48981515T>G | CA384637969 | WNT1 | c.988T>G (p.Cys330Gly) c.955T>G (p.Cys319Gly) | |
| 12 | g.48981515T= | CA2034926268 | WNT1 | c.988T= (p.Cys330=) c.955T= (p.Cys319=) | |
| 12 | g.48981516G>A | CA384637990 | WNT1 | c.989G>A (p.Cys330Tyr) c.956G>A (p.Cys319Tyr) | ClinVar dbSNP gnomAD v4 |
| 12 | g.48981516G>C | CA384638017 | WNT1 | c.989G>C (p.Cys330Ser) c.956G>C (p.Cys319Ser) | |
| 12 | g.48981516G= | CA2034926271 | WNT1 | c.989G= (p.Cys330=) c.956G= (p.Cys319=) | |
| 12 | g.48981516G>T | CA384638024 | WNT1 | c.989G>T (p.Cys330Phe) c.956G>T (p.Cys319Phe) | gnomAD v4 |
| 12 | g.48981517C>A | CA236608808 | WNT1 | c.990C>A (p.Cys330Ter) c.957C>A (p.Cys319Ter) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48981517C= | CA2034926277 | WNT1 | c.990C= (p.Cys330=) c.957C= (p.Cys319=) | |
| 12 | g.48981517C>G | CA384638028 | WNT1 | c.990C>G (p.Cys330Trp) c.957C>G (p.Cys319Trp) | |
| 12 | g.48981517C>T | CA479704408 | WNT1 | c.990C>T (p.Cys330=) c.957C>T (p.Cys319=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48981518G>A | CA384638029 | WNT1 | c.991G>A (p.Gly331Ser) c.958G>A (p.Gly320Ser) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 12 | g.48981518G>C | CA384638031 | WNT1 | c.991G>C (p.Gly331Arg) c.958G>C (p.Gly320Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48981518G= | CA2034926280 | WNT1 | c.991G= (p.Gly331=) c.958G= (p.Gly320=) | |
| 12 | g.48981518G>T | CA384638035 | WNT1 | c.991G>T (p.Gly331Cys) c.958G>T (p.Gly320Cys) | gnomAD v4 |
| 12 | g.48981519G>A | CA384638052 | WNT1 | c.992G>A (p.Gly331Asp) c.959G>A (p.Gly320Asp) | gnomAD v4 |
| 12 | g.48981519G>C | CA384638046 | WNT1 | c.992G>C (p.Gly331Ala) c.959G>C (p.Gly320Ala) | |
| 12 | g.48981519G>T | CA384638041 | WNT1 | c.992G>T (p.Gly331Val) c.959G>T (p.Gly320Val) | gnomAD v4 |
| 12 | g.48981520C>A | CA479704413 | WNT1 | c.993C>A (p.Gly331=) c.960C>A (p.Gly320=) | |
| 12 | g.48981520C= | CA2034902072 | WNT1 | c.993C= (p.Gly331=) c.960C= (p.Gly320=) | |
| 12 | g.48981520C>G | CA479704414 | WNT1 | c.993C>G (p.Gly331=) c.960C>G (p.Gly320=) | |
| 12 | g.48981520C>T | CA236608810 | WNT1 | c.993C>T (p.Gly331=) c.960C>T (p.Gly320=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48981521A= | CA2034902073 | WNT1 | c.994A= (p.Arg332=) c.961A= (p.Arg321=) | |
| 12 | g.48981521A>C | CA6544495 | WNT1 | c.994A>C (p.Arg332=) c.961A>C (p.Arg321=) | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
| 12 | g.48981521A>G | CA384638058 | WNT1 | c.994A>G (p.Arg332Gly) c.961A>G (p.Arg321Gly) | COSMIC |
| 12 | g.48981521A>T | CA384638061 | WNT1 | c.994A>T (p.Arg332Trp) c.961A>T (p.Arg321Trp) | |
| 12 | g.48981522G>A | CA384638095 | WNT1 | c.995G>A (p.Arg332Lys) c.962G>A (p.Arg321Lys) | |
| 12 | g.48981522G>C | CA384638100 | WNT1 | c.995G>C (p.Arg332Thr) c.962G>C (p.Arg321Thr) | gnomAD v4 |
| 12 | g.48981522G>T | CA384638104 | WNT1 | c.995G>T (p.Arg332Met) c.962G>T (p.Arg321Met) | gnomAD v4 |
| 12 | g.48981525dup | CA2618599448 | WNT1 | c.998dup (p.His334ProfsTer?) c.965dup (p.His323ProfsTer?) | gnomAD v4 |
| 12 | g.48981525del | CA2618599454 | WNT1 | c.998del (p.Gly333AlafsTer?) c.965del (p.Gly322AlafsTer?) | gnomAD v4 |
| 12 | g.48981523G>A | CA236608814 | WNT1 | c.996G>A (p.Arg332=) c.963G>A (p.Arg321=) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48981523G>C | CA384638119 | WNT1 | c.996G>C (p.Arg332Ser) c.963G>C (p.Arg321Ser) | |
| 12 | g.48981523G= | CA2034902074 | WNT1 | c.996G= (p.Arg332=) c.963G= (p.Arg321=) | |
| 12 | g.48981523G>T | CA384638121 | WNT1 | c.996G>T (p.Arg332Ser) c.963G>T (p.Arg321Ser) | gnomAD v4 |
| 12 | g.48981524G>A | CA384638122 | WNT1 | c.997G>A (p.Gly333Ser) c.964G>A (p.Gly322Ser) | gnomAD v4 |
| 12 | g.48981524G>C | CA384638123 | WNT1 | c.997G>C (p.Gly333Arg) c.964G>C (p.Gly322Arg) | |
| 12 | g.48981524G>T | CA384638125 | WNT1 | c.997G>T (p.Gly333Cys) c.964G>T (p.Gly322Cys) | |
| 12 | g.48981524_48981547delinsGGCCACCGCACGCGCACGCAGCGC | CA2034902075 | WNT1 | c.997_1020delinsGGCCACCGCACGCGCACGCAGCGC (p.Gly333=) c.964_987delinsGGCCACCGCACGCGCACGCAGCGC (p.Gly322=) | |
| 12 | g.48981525G>A | CA384638139 | WNT1 | c.998G>A (p.Gly333Asp) c.965G>A (p.Gly322Asp) | gnomAD v4 |
| 12 | g.48981525G>C | CA384638133 | WNT1 | c.998G>C (p.Gly333Ala) c.965G>C (p.Gly322Ala) | |
| 12 | g.48981525G>T | CA384638131 | WNT1 | c.998G>T (p.Gly333Val) c.965G>T (p.Gly322Val) | gnomAD v4 |
| 12 | g.48981526_48981548del | CA947424479 | WNT1 | c.999_1021del (p.Thr336AlafsTer?) c.966_988del (p.Thr325AlafsTer?) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.48981526C>A | CA479704422 | WNT1 | c.999C>A (p.Gly333=) c.966C>A (p.Gly322=) | gnomAD v4 |
| 12 | g.48981526C>G | CA479704424 | WNT1 | c.999C>G (p.Gly333=) c.966C>G (p.Gly322=) | |
| 12 | g.48981526C>T | CA479704421 | WNT1 | c.999C>T (p.Gly333=) c.966C>T (p.Gly322=) | gnomAD v4 |
| 12 | g.48981526_48981549delinsCCACCGCACGCGCACGCAGCGCGT | CA2034902076 | WNT1 | c.999_1022delinsCCACCGCACGCGCACGCAGCGCGT (p.Gly333=) c.966_989delinsCCACCGCACGCGCACGCAGCGCGT (p.Gly322=) | |
| 12 | g.48981527C>A | CA384638166 | WNT1 | c.1000C>A (p.His334Asn) c.967C>A (p.His323Asn) | |
| 12 | g.48981527C>G | CA384638153 | WNT1 | c.1000C>G (p.His334Asp) c.967C>G (p.His323Asp) | |
| 12 | g.48981527C>T | CA384638165 | WNT1 | c.1000C>T (p.His334Tyr) c.967C>T (p.His323Tyr) | dbSNP |
| 12 | g.48981532_48981554del | CA605233429 | WNT1 | c.1005_1027del (p.Thr336AlafsTer?) c.972_994del (p.Thr325AlafsTer?) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48981528A>C | CA384638167 | WNT1 | c.1001A>C (p.His334Pro) c.968A>C (p.His323Pro) | |
| 12 | g.48981528A>G | CA384638168 | WNT1 | c.1001A>G (p.His334Arg) c.968A>G (p.His323Arg) | |
| 12 | g.48981528A>T | CA384638170 | WNT1 | c.1001A>T (p.His334Leu) c.968A>T (p.His323Leu) | |
| 12 | g.48981529C>A | CA384638175 | WNT1 | c.1002C>A (p.His334Gln) c.969C>A (p.His323Gln) | |
| 12 | g.48981529C>G | CA384638177 | WNT1 | c.1002C>G (p.His334Gln) c.969C>G (p.His323Gln) | |
| 12 | g.48981529C>T | CA479704426 | WNT1 | c.1002C>T (p.His334=) c.969C>T (p.His323=) | gnomAD v4 |
| 12 | g.48981530C>A | CA384638180 | WNT1 | c.1003C>A (p.Arg335Ser) c.970C>A (p.Arg324Ser) | |
| 12 | g.48981530C= | CA2034902077 | WNT1 | c.1003C= (p.Arg335=) c.970C= (p.Arg324=) | |
| 12 | g.48981530C>G | CA384638185 | WNT1 | c.1003C>G (p.Arg335Gly) c.970C>G (p.Arg324Gly) | dbSNP |
| 12 | g.48981530C>T | CA384638189 | WNT1 | c.1003C>T (p.Arg335Cys) c.970C>T (p.Arg324Cys) | gnomAD v4 |
| 12 | g.48981531G>A | CA384638194 | WNT1 | c.1004G>A (p.Arg335His) c.971G>A (p.Arg324His) | gnomAD v4 |
| 12 | g.48981531G>C | CA384638200 | WNT1 | c.1004G>C (p.Arg335Pro) c.971G>C (p.Arg324Pro) | |
| 12 | g.48981531G= | CA2034902078 | WNT1 | c.1004G= (p.Arg335=) c.971G= (p.Arg324=) | |
| 12 | g.48981531G>T | CA384638202 | WNT1 | c.1004G>T (p.Arg335Leu) c.971G>T (p.Arg324Leu) | dbSNP gnomAD v4 |
| 12 | g.48981532C>A | CA479704431 | WNT1 | c.1005C>A (p.Arg335=) c.972C>A (p.Arg324=) | gnomAD v4 |
| 12 | g.48981532C>G | CA479704433 | WNT1 | c.1005C>G (p.Arg335=) c.972C>G (p.Arg324=) | gnomAD v4 |
| 12 | g.48981532C>T | CA479704432 | WNT1 | c.1005C>T (p.Arg335=) c.972C>T (p.Arg324=) | |
| 12 | g.48981533A= | CA2034902079 | WNT1 | c.1006A= (p.Thr336=) c.973A= (p.Thr325=) | |
| 12 | g.48981533A>C | CA384638216 | WNT1 | c.1006A>C (p.Thr336Pro) c.973A>C (p.Thr325Pro) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.48981533A>G | CA384638206 | WNT1 | c.1006A>G (p.Thr336Ala) c.973A>G (p.Thr325Ala) | |
| 12 | g.48981533A>T | CA384638209 | WNT1 | c.1006A>T (p.Thr336Ser) c.973A>T (p.Thr325Ser) | |
| 12 | g.48981534C>A | CA384638232 | WNT1 | c.1007C>A (p.Thr336Lys) c.974C>A (p.Thr325Lys) | gnomAD v4 |
| 12 | g.48981534C= | CA2034902080 | WNT1 | c.1007C= (p.Thr336=) c.974C= (p.Thr325=) | |
| 12 | g.48981534C>G | CA384638233 | WNT1 | c.1007C>G (p.Thr336Arg) c.974C>G (p.Thr325Arg) | |
| 12 | g.48981534C>T | CA6544496 | WNT1 | c.1007C>T (p.Thr336Met) c.974C>T (p.Thr325Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48981535G>A | CA479704440 | WNT1 | c.1008G>A (p.Thr336=) c.975G>A (p.Thr325=) | gnomAD v4 |
| 12 | g.48981535G>C | CA479704441 | WNT1 | c.1008G>C (p.Thr336=) c.975G>C (p.Thr325=) | |
| 12 | g.48981535G>T | CA479704442 | WNT1 | c.1008G>T (p.Thr336=) c.975G>T (p.Thr325=) | gnomAD v4 |
| 12 | g.48981536C>A | CA384638234 | WNT1 | c.1009C>A (p.Arg337Ser) c.976C>A (p.Arg326Ser) | |
| 12 | g.48981536C>G | CA384638255 | WNT1 | c.1009C>G (p.Arg337Gly) c.976C>G (p.Arg326Gly) | |
| 12 | g.48981536C>T | CA384638256 | WNT1 | c.1009C>T (p.Arg337Cys) c.976C>T (p.Arg326Cys) | |
| 12 | g.48981537G>A | CA384638276 | WNT1 | c.1010G>A (p.Arg337His) c.977G>A (p.Arg326His) | gnomAD v4 |
| 12 | g.48981537G>C | CA384638281 | WNT1 | c.1010G>C (p.Arg337Pro) c.977G>C (p.Arg326Pro) | |
| 12 | g.48981537G>T | CA384638287 | WNT1 | c.1010G>T (p.Arg337Leu) c.977G>T (p.Arg326Leu) | gnomAD v4 |
| 12 | g.48981538C>A | CA479704447 | WNT1 | c.1011C>A (p.Arg337=) c.978C>A (p.Arg326=) | gnomAD v4 |
| 12 | g.48981538C>G | CA479704448 | WNT1 | c.1011C>G (p.Arg337=) c.978C>G (p.Arg326=) | |
| 12 | g.48981538C>T | CA479704449 | WNT1 | c.1011C>T (p.Arg337=) c.978C>T (p.Arg326=) | |
| 12 | g.48981539A>C | CA384638288 | WNT1 | c.1012A>C (p.Thr338Pro) c.979A>C (p.Thr327Pro) | |
| 12 | g.48981539A>G | CA384638289 | WNT1 | c.1012A>G (p.Thr338Ala) c.979A>G (p.Thr327Ala) | gnomAD v4 |
| 12 | g.48981539A>T | CA384638290 | WNT1 | c.1012A>T (p.Thr338Ser) c.979A>T (p.Thr327Ser) | |
| 12 | g.48981540C>A | CA384638299 | WNT1 | c.1013C>A (p.Thr338Lys) c.980C>A (p.Thr327Lys) | gnomAD v4 |
| 12 | g.48981540C= | CA2034902081 | WNT1 | c.1013C= (p.Thr338=) c.980C= (p.Thr327=) | |
| 12 | g.48981540C>G | CA384638295 | WNT1 | c.1013C>G (p.Thr338Arg) c.980C>G (p.Thr327Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.48981540C>T | CA384638292 | WNT1 | c.1013C>T (p.Thr338Met) c.980C>T (p.Thr327Met) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48981541G>A | CA479704453 | WNT1 | c.1014G>A (p.Thr338=) c.981G>A (p.Thr327=) | gnomAD v4 |
| 12 | g.48981541G>C | CA479704454 | WNT1 | c.1014G>C (p.Thr338=) c.981G>C (p.Thr327=) | |
| 12 | g.48981541G>T | CA479704455 | WNT1 | c.1014G>T (p.Thr338=) c.981G>T (p.Thr327=) | gnomAD v4 |
| 12 | g.48981542C>A | CA384638302 | WNT1 | c.1015C>A (p.Gln339Lys) c.982C>A (p.Gln328Lys) | gnomAD v4 |
| 12 | g.48981542C>G | CA384638304 | WNT1 | c.1015C>G (p.Gln339Glu) c.982C>G (p.Gln328Glu) | gnomAD v4 |
| 12 | g.48981542C>T | CA384638306 | WNT1 | c.1015C>T (p.Gln339Ter) c.982C>T (p.Gln328Ter) | |
| 12 | g.48981543A>C | CA384638332 | WNT1 | c.1016A>C (p.Gln339Pro) c.983A>C (p.Gln328Pro) | gnomAD v4 |
| 12 | g.48981543A>G | CA384638335 | WNT1 | c.1016A>G (p.Gln339Arg) c.983A>G (p.Gln328Arg) | |
| 12 | g.48981543A>T | CA384638337 | WNT1 | c.1016A>T (p.Gln339Leu) c.983A>T (p.Gln328Leu) | gnomAD v4 |
| 12 | g.48981544G>A | CA479704459 | WNT1 | c.1017G>A (p.Gln339=) c.984G>A (p.Gln328=) | |
| 12 | g.48981544G>C | CA384638349 | WNT1 | c.1017G>C (p.Gln339His) c.984G>C (p.Gln328His) | |
| 12 | g.48981544G>T | CA384638342 | WNT1 | c.1017G>T (p.Gln339His) c.984G>T (p.Gln328His) | gnomAD v4 |
| 12 | g.48981545C>A | CA384638355 | WNT1 | c.1018C>A (p.Arg340Ser) c.985C>A (p.Arg329Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48981545C= | CA2034902082 | WNT1 | c.1018C= (p.Arg340=) c.985C= (p.Arg329=) | |
| 12 | g.48981545C>G | CA384638378 | WNT1 | c.1018C>G (p.Arg340Gly) c.985C>G (p.Arg329Gly) | |
| 12 | g.48981545C>T | CA384638386 | WNT1 | c.1018C>T (p.Arg340Cys) c.985C>T (p.Arg329Cys) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48981546G>A | CA384638400 | WNT1 | c.1019G>A (p.Arg340His) c.986G>A (p.Arg329His) | |
| 12 | g.48981546G>C | CA6544497 | WNT1 | c.1019G>C (p.Arg340Pro) c.986G>C (p.Arg329Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.48981546G= | CA2034902083 | WNT1 | c.1019G= (p.Arg340=) c.986G= (p.Arg329=) | |
| 12 | g.48981546G>T | CA384638420 | WNT1 | c.1019G>T (p.Arg340Leu) c.986G>T (p.Arg329Leu) | |
| 12 | g.48981547C>A | CA479704466 | WNT1 | c.1020C>A (p.Arg340=) c.987C>A (p.Arg329=) | gnomAD v4 |
| 12 | g.48981547C>G | CA479704464 | WNT1 | c.1020C>G (p.Arg340=) c.987C>G (p.Arg329=) | |
| 12 | g.48981547C>T | CA479704465 | WNT1 | c.1020C>T (p.Arg340=) c.987C>T (p.Arg329=) | gnomAD v4 |
| 12 | g.48981548G>A | CA384638455 | WNT1 | c.1021G>A (p.Val341Ile) c.988G>A (p.Val330Ile) | gnomAD v4 |
| 12 | g.48981548G>C | CA384638428 | WNT1 | c.1021G>C (p.Val341Leu) c.988G>C (p.Val330Leu) | |
| 12 | g.48981548G>T | CA384638446 | WNT1 | c.1021G>T (p.Val341Phe) c.988G>T (p.Val330Phe) | |
| 12 | g.48981549T>A | CA384638465 | WNT1 | c.1022T>A (p.Val341Asp) c.989T>A (p.Val330Asp) | |
| 12 | g.48981549T>C | CA384638469 | WNT1 | c.1022T>C (p.Val341Ala) c.989T>C (p.Val330Ala) | dbSNP gnomAD v4 |
| 12 | g.48981549T>G | CA384638474 | WNT1 | c.1022T>G (p.Val341Gly) c.989T>G (p.Val330Gly) | |
| 12 | g.48981549T= | CA2034902084 | WNT1 | c.1022T= (p.Val341=) c.989T= (p.Val330=) | |
| 12 | g.48981550C>A | CA479704471 | WNT1 | c.1023C>A (p.Val341=) c.990C>A (p.Val330=) | gnomAD v4 |
| 12 | g.48981550C= | CA2034902085 | WNT1 | c.1023C= (p.Val341=) c.990C= (p.Val330=) | |
| 12 | g.48981550C>G | CA479704470 | WNT1 | c.1023C>G (p.Val341=) c.990C>G (p.Val330=) | |
| 12 | g.48981550C>T | CA479704469 | WNT1 | c.1023C>T (p.Val341=) c.990C>T (p.Val330=) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48981551A>C | CA384638480 | WNT1 | c.1024A>C (p.Thr342Pro) c.991A>C (p.Thr331Pro) | |
| 12 | g.48981551A>G | CA384638481 | WNT1 | c.1024A>G (p.Thr342Ala) c.991A>G (p.Thr331Ala) | gnomAD v4 |
| 12 | g.48981551A>T | CA384638482 | WNT1 | c.1024A>T (p.Thr342Ser) c.991A>T (p.Thr331Ser) | |
| 12 | g.48981551_48981552delinsAC | CA2034902086 | WNT1 | c.1024_1025delinsAC (p.Thr342=) c.991_992delinsAC (p.Thr331=) | |
| 12 | g.48981552C>A | CA384638486 | WNT1 | c.1025C>A (p.Thr342Asn) c.992C>A (p.Thr331Asn) | gnomAD v4 |
| 12 | g.48981552C= | CA2034902087 | WNT1 | c.1025C= (p.Thr342=) c.992C= (p.Thr331=) | |
| 12 | g.48981552C>G | CA6544498 | WNT1 | c.1025C>G (p.Thr342Ser) c.992C>G (p.Thr331Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48981552C>T | CA384638493 | WNT1 | c.1025C>T (p.Thr342Ile) c.992C>T (p.Thr331Ile) | |
| 12 | g.48981553del | CA185909 | WNT1 | c.1026del (p.Glu343SerfsTer?) c.993del (p.Glu332SerfsTer?) | ClinVar dbSNP gnomAD v4 |
| 12 | g.48981553C>A | CA479704478 | WNT1 | c.1026C>A (p.Thr342=) c.993C>A (p.Thr331=) | gnomAD v4 |
| 12 | g.48981553C>G | CA479704480 | WNT1 | c.1026C>G (p.Thr342=) c.993C>G (p.Thr331=) | |
| 12 | g.48981553C>T | CA479704479 | WNT1 | c.1026C>T (p.Thr342=) c.993C>T (p.Thr331=) | |
| 12 | g.48981554G>A | CA384638502 | WNT1 | c.1027G>A (p.Glu343Lys) c.994G>A (p.Glu332Lys) | gnomAD v4 |
| 12 | g.48981554G>C | CA6544499 | WNT1 | c.1027G>C (p.Glu343Gln) c.994G>C (p.Glu332Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48981554G= | CA2034902088 | WNT1 | c.1027G= (p.Glu343=) c.994G= (p.Glu332=) | |
| 12 | g.48981554G>T | CA384638511 | WNT1 | c.1027G>T (p.Glu343Ter) c.994G>T (p.Glu332Ter) | gnomAD v4 |
| 12 | g.48981555A>C | CA384638524 | WNT1 | c.1028A>C (p.Glu343Ala) c.995A>C (p.Glu332Ala) | |
| 12 | g.48981555A>G | CA384638538 | WNT1 | c.1028A>G (p.Glu343Gly) c.995A>G (p.Glu332Gly) | |
| 12 | g.48981555A>T | CA384638528 | WNT1 | c.1028A>T (p.Glu343Val) c.995A>T (p.Glu332Val) | |
| 12 | g.48981556G>A | CA479704487 | WNT1 | c.1029G>A (p.Glu343=) c.996G>A (p.Glu332=) | |
| 12 | g.48981556G>C | CA384638555 | WNT1 | c.1029G>C (p.Glu343Asp) c.996G>C (p.Glu332Asp) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.48981556G= | CA2034902089 | WNT1 | c.1029G= (p.Glu343=) c.996G= (p.Glu332=) | |
| 12 | g.48981556G>T | CA384638567 | WNT1 | c.1029G>T (p.Glu343Asp) c.996G>T (p.Glu332Asp) | |
| 12 | g.48981557C>A | CA384638575 | WNT1 | c.1030C>A (p.Arg344Ser) c.997C>A (p.Arg333Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48981557C= | CA2034902090 | WNT1 | c.1030C= (p.Arg344=) c.997C= (p.Arg333=) | |
| 12 | g.48981557C>G | CA384638580 | WNT1 | c.1030C>G (p.Arg344Gly) c.997C>G (p.Arg333Gly) | gnomAD v4 |
| 12 | g.48981557C>T | CA384638594 | WNT1 | c.1030C>T (p.Arg344Cys) c.997C>T (p.Arg333Cys) | gnomAD v4 |
| 12 | g.48981558G>A | CA384638609 | WNT1 | c.1031G>A (p.Arg344His) c.998G>A (p.Arg333His) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48981558G>C | CA384638611 | WNT1 | c.1031G>C (p.Arg344Pro) c.998G>C (p.Arg333Pro) | |
| 12 | g.48981558G= | CA2034902091 | WNT1 | c.1031G= (p.Arg344=) c.998G= (p.Arg333=) | |
| 12 | g.48981558G>T | CA384638612 | WNT1 | c.1031G>T (p.Arg344Leu) c.998G>T (p.Arg333Leu) | gnomAD v4 |
| 12 | g.48981559C>A | CA479704490 | WNT1 | c.1032C>A (p.Arg344=) c.999C>A (p.Arg333=) | |
| 12 | g.48981559C>G | CA479704491 | WNT1 | c.1032C>G (p.Arg344=) c.999C>G (p.Arg333=) | |
| 12 | g.48981559C>T | CA479704492 | WNT1 | c.1032C>T (p.Arg344=) c.999C>T (p.Arg333=) | gnomAD v4 |
| 12 | g.48981560del | CA2618599574 | WNT1 | c.1033del (p.Cys345AlafsTer?) c.1000del (p.Cys334AlafsTer?) | gnomAD v4 |
| 12 | g.48981560T>A | CA384638614 | WNT1 | c.1033T>A (p.Cys345Ser) c.1000T>A (p.Cys334Ser) | |
| 12 | g.48981560T>C | CA236608820 | WNT1 | c.1033T>C (p.Cys345Arg) c.1000T>C (p.Cys334Arg) | dbSNP gnomAD v4 |
| 12 | g.48981560T>G | CA384638628 | WNT1 | c.1033T>G (p.Cys345Gly) c.1000T>G (p.Cys334Gly) | dbSNP |
| 12 | g.48981560T= | CA2034902092 | WNT1 | c.1033T= (p.Cys345=) c.1000T= (p.Cys334=) | |
| 12 | g.48981561G>A | CA384638633 | WNT1 | c.1034G>A (p.Cys345Tyr) c.1001G>A (p.Cys334Tyr) | gnomAD v4 |
| 12 | g.48981561G>C | CA384638635 | WNT1 | c.1034G>C (p.Cys345Ser) c.1001G>C (p.Cys334Ser) | |
| 12 | g.48981561G>T | CA384638639 | WNT1 | c.1034G>T (p.Cys345Phe) c.1001G>T (p.Cys334Phe) | |
| 12 | g.48981562C>A | CA384638643 | WNT1 | c.1035C>A (p.Cys345Ter) c.1002C>A (p.Cys334Ter) | gnomAD v4 |
| 12 | g.48981562C>G | CA384638647 | WNT1 | c.1035C>G (p.Cys345Trp) c.1002C>G (p.Cys334Trp) | |
| 12 | g.48981562C>T | CA479704495 | WNT1 | c.1035C>T (p.Cys345=) c.1002C>T (p.Cys334=) | gnomAD v4 |
| 12 | g.48981563A>C | CA384638669 | WNT1 | c.1036A>C (p.Asn346His) c.1003A>C (p.Asn335His) | |
| 12 | g.48981563A>G | CA384638671 | WNT1 | c.1036A>G (p.Asn346Asp) c.1003A>G (p.Asn335Asp) | |
| 12 | g.48981563A>T | CA384638680 | WNT1 | c.1036A>T (p.Asn346Tyr) c.1003A>T (p.Asn335Tyr) | gnomAD v4 |
| 12 | g.48981564A>C | CA384638685 | WNT1 | c.1037A>C (p.Asn346Thr) c.1004A>C (p.Asn335Thr) | ClinVar dbSNP |
| 12 | g.48981564A>G | CA384638688 | WNT1 | c.1037A>G (p.Asn346Ser) c.1004A>G (p.Asn335Ser) | |
| 12 | g.48981564A>T | CA384638691 | WNT1 | c.1037A>T (p.Asn346Ile) c.1004A>T (p.Asn335Ile) | |
| 12 | g.48981565C>A | CA384638703 | WNT1 | c.1038C>A (p.Asn346Lys) c.1005C>A (p.Asn335Lys) | gnomAD v4 |
| 12 | g.48981565C>G | CA384638704 | WNT1 | c.1038C>G (p.Asn346Lys) c.1005C>G (p.Asn335Lys) | |
| 12 | g.48981565C>T | CA479704501 | WNT1 | c.1038C>T (p.Asn346=) c.1005C>T (p.Asn335=) | |
| 12 | g.48981566T>A | CA384638705 | WNT1 | c.1039T>A (p.Cys347Ser) c.1006T>A (p.Cys336Ser) | |
| 12 | g.48981566T>C | CA384638706 | WNT1 | c.1039T>C (p.Cys347Arg) c.1006T>C (p.Cys336Arg) | gnomAD v4 |
| 12 | g.48981566T>G | CA384638713 | WNT1 | c.1039T>G (p.Cys347Gly) c.1006T>G (p.Cys336Gly) | gnomAD v4 |
| 12 | g.48981567G>A | CA384638717 | WNT1 | c.1040G>A (p.Cys347Tyr) c.1007G>A (p.Cys336Tyr) | gnomAD v4 |
| 12 | g.48981567G>C | CA384638720 | WNT1 | c.1040G>C (p.Cys347Ser) c.1007G>C (p.Cys336Ser) | |
| 12 | g.48981567G>T | CA384638718 | WNT1 | c.1040G>T (p.Cys347Phe) c.1007G>T (p.Cys336Phe) | |
| 12 | g.48981568C>A | CA384638724 | WNT1 | c.1041C>A (p.Cys347Ter) c.1008C>A (p.Cys336Ter) | gnomAD v4 |
| 12 | g.48981568C= | CA2034902093 | WNT1 | c.1041C= (p.Cys347=) c.1008C= (p.Cys336=) | |
| 12 | g.48981568C>G | CA384638732 | WNT1 | c.1041C>G (p.Cys347Trp) c.1008C>G (p.Cys336Trp) | |
| 12 | g.48981568C>T | CA479704506 | WNT1 | c.1041C>T (p.Cys347=) c.1008C>T (p.Cys336=) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48981569A= | CA2034902094 | WNT1 | c.1042A= (p.Thr348=) c.1009A= (p.Thr337=) | |
| 12 | g.48981569A>C | CA6544500 | WNT1 | c.1042A>C (p.Thr348Pro) c.1009A>C (p.Thr337Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.48981569A>G | CA384638738 | WNT1 | c.1042A>G (p.Thr348Ala) c.1009A>G (p.Thr337Ala) | dbSNP gnomAD v4 |
| 12 | g.48981569A>T | CA384638750 | WNT1 | c.1042A>T (p.Thr348Ser) c.1009A>T (p.Thr337Ser) | |
| 12 | g.48981570C>A | CA384638754 | WNT1 | c.1043C>A (p.Thr348Asn) c.1010C>A (p.Thr337Asn) | gnomAD v4 |
| 12 | g.48981570C= | CA2034902095 | WNT1 | c.1043C= (p.Thr348=) c.1010C= (p.Thr337=) | |
| 12 | g.48981570C>G | CA384638758 | WNT1 | c.1043C>G (p.Thr348Ser) c.1010C>G (p.Thr337Ser) | |
| 12 | g.48981570C>T | CA384638760 | WNT1 | c.1043C>T (p.Thr348Ile) c.1010C>T (p.Thr337Ile) | dbSNP gnomAD v2 |
| 12 | g.48981572_48981575del | CA2575143759 | WNT1 | c.1045_1048del (p.Phe349ThrfsTer?) c.1012_1015del (p.Phe338ThrfsTer?) | |
| 12 | g.48981571C>A | CA479704516 | WNT1 | c.1044C>A (p.Thr348=) c.1011C>A (p.Thr337=) | gnomAD v4 |
| 12 | g.48981571C= | CA2034902096 | WNT1 | c.1044C= (p.Thr348=) c.1011C= (p.Thr337=) | |
| 12 | g.48981571C>G | CA479704513 | WNT1 | c.1044C>G (p.Thr348=) c.1011C>G (p.Thr337=) | |
| 12 | g.48981571C>T | CA479704511 | WNT1 | c.1044C>T (p.Thr348=) c.1011C>T (p.Thr337=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48981572T>A | CA384638764 | WNT1 | c.1045T>A (p.Phe349Ile) c.1012T>A (p.Phe338Ile) | |
| 12 | g.48981572T>C | CA384638770 | WNT1 | c.1045T>C (p.Phe349Leu) c.1012T>C (p.Phe338Leu) | |
| 12 | g.48981572T>G | CA384638775 | WNT1 | c.1045T>G (p.Phe349Val) c.1012T>G (p.Phe338Val) | |
| 12 | g.48981573T>A | CA384638778 | WNT1 | c.1046T>A (p.Phe349Tyr) c.1013T>A (p.Phe338Tyr) | |
| 12 | g.48981573T>C | CA384638782 | WNT1 | c.1046T>C (p.Phe349Ser) c.1013T>C (p.Phe338Ser) | |
| 12 | g.48981573T>G | CA384638793 | WNT1 | c.1046T>G (p.Phe349Cys) c.1013T>G (p.Phe338Cys) | |
| 12 | g.48981574C>A | CA384638804 | WNT1 | c.1047C>A (p.Phe349Leu) c.1014C>A (p.Phe338Leu) | gnomAD v4 |
| 12 | g.48981574C= | CA2034902097 | WNT1 | c.1047C= (p.Phe349=) c.1014C= (p.Phe338=) | |
| 12 | g.48981574C>G | CA384638803 | WNT1 | c.1047C>G (p.Phe349Leu) c.1014C>G (p.Phe338Leu) | |
| 12 | g.48981574C>T | CA479704522 | WNT1 | c.1047C>T (p.Phe349=) c.1014C>T (p.Phe338=) | dbSNP gnomAD v2 |
| 12 | g.48981575C>A | CA384638806 | WNT1 | c.1048C>A (p.His350Asn) c.1015C>A (p.His339Asn) | gnomAD v4 |
| 12 | g.48981575C= | CA2034902098 | WNT1 | c.1048C= (p.His350=) c.1015C= (p.His339=) | |
| 12 | g.48981575C>G | CA384638809 | WNT1 | c.1048C>G (p.His350Asp) c.1015C>G (p.His339Asp) | gnomAD v4 |
| 12 | g.48981575C>T | CA384638811 | WNT1 | c.1048C>T (p.His350Tyr) c.1015C>T (p.His339Tyr) | dbSNP gnomAD v4 |
| 12 | g.48981576A>C | CA384638815 | WNT1 | c.1049A>C (p.His350Pro) c.1016A>C (p.His339Pro) | |
| 12 | g.48981576A>G | CA384638820 | WNT1 | c.1049A>G (p.His350Arg) c.1016A>G (p.His339Arg) | gnomAD v4 |
| 12 | g.48981576A>T | CA384638835 | WNT1 | c.1049A>T (p.His350Leu) c.1016A>T (p.His339Leu) | |
| 12 | g.48981577C>A | CA384638855 | WNT1 | c.1050C>A (p.His350Gln) c.1017C>A (p.His339Gln) | gnomAD v4 |
| 12 | g.48981577C>G | CA384638854 | WNT1 | c.1050C>G (p.His350Gln) c.1017C>G (p.His339Gln) | |
| 12 | g.48981577C>T | CA479704526 | WNT1 | c.1050C>T (p.His350=) c.1017C>T (p.His339=) | gnomAD v4 |
| 12 | g.48981578T>A | CA384638856 | WNT1 | c.1051T>A (p.Trp351Arg) c.1018T>A (p.Trp340Arg) | gnomAD v4 |
| 12 | g.48981578T>C | CA384638857 | WNT1 | c.1051T>C (p.Trp351Arg) c.1018T>C (p.Trp340Arg) | gnomAD v4 |
| 12 | g.48981578T>G | CA16607302 | WNT1 | c.1051T>G (p.Trp351Gly) c.1018T>G (p.Trp340Gly) | ClinVar dbSNP |
| 12 | g.48981578T= | CA2034902099 | WNT1 | c.1051T= (p.Trp351=) c.1018T= (p.Trp340=) | |
| 12 | g.48981579G>A | CA384638893 | WNT1 | c.1052G>A (p.Trp351Ter) c.1019G>A (p.Trp340Ter) | gnomAD v4 |
| 12 | g.48981579G>C | CA384638896 | WNT1 | c.1052G>C (p.Trp351Ser) c.1019G>C (p.Trp340Ser) | |
| 12 | g.48981579G>T | CA384638916 | WNT1 | c.1052G>T (p.Trp351Leu) c.1019G>T (p.Trp340Leu) | gnomAD v4 |
| 12 | g.48981580G>A | CA384638931 | WNT1 | c.1053G>A (p.Trp351Ter) c.1020G>A (p.Trp340Ter) | |
| 12 | g.48981580G>C | CA384638923 | WNT1 | c.1053G>C (p.Trp351Cys) c.1020G>C (p.Trp340Cys) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48981580G= | CA2034902100 | WNT1 | c.1053G= (p.Trp351=) c.1020G= (p.Trp340=) | |
| 12 | g.48981580G>T | CA384638929 | WNT1 | c.1053G>T (p.Trp351Cys) c.1020G>T (p.Trp340Cys) | gnomAD v4 |
| 12 | g.48981581T>A | CA384638935 | WNT1 | c.1054T>A (p.Cys352Ser) c.1021T>A (p.Cys341Ser) | |
| 12 | g.48981581T>C | CA384638947 | WNT1 | c.1054T>C (p.Cys352Arg) c.1021T>C (p.Cys341Arg) | |
| 12 | g.48981581T>G | CA384638953 | WNT1 | c.1054T>G (p.Cys352Gly) c.1021T>G (p.Cys341Gly) | |
| 12 | g.48981582G>A | CA384638957 | WNT1 | c.1055G>A (p.Cys352Tyr) c.1022G>A (p.Cys341Tyr) | gnomAD v4 |
| 12 | g.48981582G>C | CA384638962 | WNT1 | c.1055G>C (p.Cys352Ser) c.1022G>C (p.Cys341Ser) | |
| 12 | g.48981582G>T | CA384638966 | WNT1 | c.1055G>T (p.Cys352Phe) c.1022G>T (p.Cys341Phe) | dbSNP gnomAD v4 |
| 12 | g.48981583C>A | CA384638973 | WNT1 | c.1056C>A (p.Cys352Ter) c.1023C>A (p.Cys341Ter) | gnomAD v4 |
| 12 | g.48981583C>G | CA384638971 | WNT1 | c.1056C>G (p.Cys352Trp) c.1023C>G (p.Cys341Trp) | |
| 12 | g.48981583C>T | CA479704533 | WNT1 | c.1056C>T (p.Cys352=) c.1023C>T (p.Cys341=) | gnomAD v4 |
| 12 | g.48981584T>A | CA384638976 | WNT1 | c.1057T>A (p.Cys353Ser) c.1024T>A (p.Cys342Ser) | |
| 12 | g.48981584T>C | CA384638977 | WNT1 | c.1057T>C (p.Cys353Arg) c.1024T>C (p.Cys342Arg) | gnomAD v4 |
| 12 | g.48981584T>G | CA384638978 | WNT1 | c.1057T>G (p.Cys353Gly) c.1024T>G (p.Cys342Gly) | |
| 12 | g.48981585G>A | CA384638979 | WNT1 | c.1058G>A (p.Cys353Tyr) c.1025G>A (p.Cys342Tyr) | gnomAD v4 |
| 12 | g.48981585G>C | CA384638983 | WNT1 | c.1058G>C (p.Cys353Ser) c.1025G>C (p.Cys342Ser) | |
| 12 | g.48981585G>T | CA384639001 | WNT1 | c.1058G>T (p.Cys353Phe) c.1025G>T (p.Cys342Phe) | gnomAD v4 |
| 12 | g.48981585_48981586delinsGC | CA2034902101 | WNT1 | c.1058_1059delinsGC (p.Cys353=) c.1025_1026delinsGC (p.Cys342=) | |
| 12 | g.48981586C>A | CA384639007 | WNT1 | c.1059C>A (p.Cys353Ter) c.1026C>A (p.Cys342Ter) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48981586C= | CA2034902102 | WNT1 | c.1059C= (p.Cys353=) c.1026C= (p.Cys342=) | |
| 12 | g.48981586C>G | CA384639014 | WNT1 | c.1059C>G (p.Cys353Trp) c.1026C>G (p.Cys342Trp) | ClinVar |
| 12 | g.48981586C>T | CA6544501 | WNT1 | c.1059C>T (p.Cys353=) c.1026C>T (p.Cys342=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48981587del | CA605233430 | WNT1 | c.1060del (p.His354ThrfsTer?) c.1027del (p.His343ThrfsTer?) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48981586_48981588delinsCCA | CA2034902103 | WNT1 | c.1059_1061delinsCCA (p.Cys353=) c.1026_1028delinsCCA (p.Cys342=) | |
| 12 | g.48981587C>A | CA384639019 | WNT1 | c.1060C>A (p.His354Asn) c.1027C>A (p.His343Asn) | gnomAD v4 |
| 12 | g.48981587C>G | CA384639023 | WNT1 | c.1060C>G (p.His354Asp) c.1027C>G (p.His343Asp) | |
| 12 | g.48981587C>T | CA384639034 | WNT1 | c.1060C>T (p.His354Tyr) c.1027C>T (p.His343Tyr) | gnomAD v4 |
| 12 | g.48981587_48981588delinsG | CA658797896 | WNT1 | c.1060_1061delinsG (p.His354AlafsTer?) c.1027_1028delinsG (p.His343AlafsTer?) | ClinVar dbSNP |
| 12 | g.48981588A= | CA2034902104 | WNT1 | c.1061A= (p.His354=) c.1028A= (p.His343=) | |
| 12 | g.48981588A>C | CA384639041 | WNT1 | c.1061A>C (p.His354Pro) c.1028A>C (p.His343Pro) | |
| 12 | g.48981588A>G | CA384639046 | WNT1 | c.1061A>G (p.His354Arg) c.1028A>G (p.His343Arg) | dbSNP gnomAD v4 |
| 12 | g.48981588A>T | CA384639050 | WNT1 | c.1061A>T (p.His354Leu) c.1028A>T (p.His343Leu) | ClinVar dbSNP gnomAD v4 |
| 12 | g.48981589C>A | CA384639062 | WNT1 | c.1062C>A (p.His354Gln) c.1029C>A (p.His343Gln) | gnomAD v4 |
| 12 | g.48981589C>G | CA384639065 | WNT1 | c.1062C>G (p.His354Gln) c.1029C>G (p.His343Gln) | |
| 12 | g.48981589C>T | CA479704538 | WNT1 | c.1062C>T (p.His354=) c.1029C>T (p.His343=) | gnomAD v4 |
| 12 | g.48981590G>A | CA384639070 | WNT1 | c.1063G>A (p.Val355Ile) c.1030G>A (p.Val344Ile) | gnomAD v4 |
| 12 | g.48981590G>C | CA384639074 | WNT1 | c.1063G>C (p.Val355Leu) c.1030G>C (p.Val344Leu) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.48981590G= | CA2034902105 | WNT1 | c.1063G= (p.Val355=) c.1030G= (p.Val344=) | |
| 12 | g.48981590G>T | CA143728 | WNT1 | c.1063G>T (p.Val355Phe) c.1030G>T (p.Val344Phe) | ClinVar dbSNP gnomAD v4 |
| 12 | g.48981591T>A | CA384639077 | WNT1 | c.1064T>A (p.Val355Asp) c.1031T>A (p.Val344Asp) | |
| 12 | g.48981591T>C | CA236608826 | WNT1 | c.1064T>C (p.Val355Ala) c.1031T>C (p.Val344Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48981591T>G | CA384639078 | WNT1 | c.1064T>G (p.Val355Gly) c.1031T>G (p.Val344Gly) | ClinVar |
| 12 | g.48981591T= | CA2034902106 | WNT1 | c.1064T= (p.Val355=) c.1031T= (p.Val344=) | |
| 12 | g.48981592C>A | CA479704542 | WNT1 | c.1065C>A (p.Val355=) c.1032C>A (p.Val344=) | gnomAD v4 |
| 12 | g.48981592C>G | CA479704543 | WNT1 | c.1065C>G (p.Val355=) c.1032C>G (p.Val344=) | gnomAD v4 |
| 12 | g.48981592C>T | CA479704544 | WNT1 | c.1065C>T (p.Val355=) c.1032C>T (p.Val344=) | gnomAD v4 |
| 12 | g.48981593A>C | CA384639081 | WNT1 | c.1066A>C (p.Ser356Arg) c.1033A>C (p.Ser345Arg) | |
| 12 | g.48981593A>G | CA384639083 | WNT1 | c.1066A>G (p.Ser356Gly) c.1033A>G (p.Ser345Gly) | |
| 12 | g.48981593A>T | CA384639082 | WNT1 | c.1066A>T (p.Ser356Cys) c.1033A>T (p.Ser345Cys) | |
| 12 | g.48981594G>A | CA384639084 | WNT1 | c.1067G>A (p.Ser356Asn) c.1034G>A (p.Ser345Asn) | gnomAD v4 |
| 12 | g.48981594G>C | CA384639087 | WNT1 | c.1067G>C (p.Ser356Thr) c.1034G>C (p.Ser345Thr) | |
| 12 | g.48981594G>T | CA384639091 | WNT1 | c.1067G>T (p.Ser356Ile) c.1034G>T (p.Ser345Ile) | gnomAD v4 |
| 12 | g.48981595C>A | CA384639100 | WNT1 | c.1068C>A (p.Ser356Arg) c.1035C>A (p.Ser345Arg) | gnomAD v4 |
| 12 | g.48981595C>G | CA384639103 | WNT1 | c.1068C>G (p.Ser356Arg) c.1035C>G (p.Ser345Arg) | |
| 12 | g.48981595C>T | CA479704550 | WNT1 | c.1068C>T (p.Ser356=) c.1035C>T (p.Ser345=) | |
| 12 | g.48981596T>A | CA384639108 | WNT1 | c.1069T>A (p.Cys357Ser) c.1036T>A (p.Cys346Ser) | |
| 12 | g.48981596T>C | CA384639111 | WNT1 | c.1069T>C (p.Cys357Arg) c.1036T>C (p.Cys346Arg) | |
| 12 | g.48981596T>G | CA384639112 | WNT1 | c.1069T>G (p.Cys357Gly) c.1036T>G (p.Cys346Gly) | |
| 12 | g.48981597G>A | CA384639116 | WNT1 | c.1070G>A (p.Cys357Tyr) c.1037G>A (p.Cys346Tyr) | gnomAD v4 |
| 12 | g.48981597G>C | CA384639119 | WNT1 | c.1070G>C (p.Cys357Ser) c.1037G>C (p.Cys346Ser) | |
| 12 | g.48981597G>T | CA384639123 | WNT1 | c.1070G>T (p.Cys357Phe) c.1037G>T (p.Cys346Phe) | gnomAD v4 |
| 12 | g.48981598C>A | CA384639128 | WNT1 | c.1071C>A (p.Cys357Ter) c.1038C>A (p.Cys346Ter) | gnomAD v4 |
| 12 | g.48981598C>G | CA384639126 | WNT1 | c.1071C>G (p.Cys357Trp) c.1038C>G (p.Cys346Trp) | |
| 12 | g.48981598C>T | CA479704554 | WNT1 | c.1071C>T (p.Cys357=) c.1038C>T (p.Cys346=) | gnomAD v4 |
| 12 | g.48981599C>A | CA384639132 | WNT1 | c.1072C>A (p.Arg358Ser) c.1039C>A (p.Arg347Ser) | gnomAD v4 |
| 12 | g.48981599C= | CA2034902107 | WNT1 | c.1072C= (p.Arg358=) c.1039C= (p.Arg347=) | |
| 12 | g.48981599C>G | CA384639134 | WNT1 | c.1072C>G (p.Arg358Gly) c.1039C>G (p.Arg347Gly) | |
| 12 | g.48981599C>T | CA384639135 | WNT1 | c.1072C>T (p.Arg358Cys) c.1039C>T (p.Arg347Cys) | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.48981600_48981601del | CA2618599708 | WNT1 | c.1073_1074del (p.Arg358GlnfsTer?) c.1040_1041del (p.Arg347GlnfsTer?) | gnomAD v4 |
| 12 | g.48981600G>A | CA6544502 | WNT1 | c.1073G>A (p.Arg358His) c.1040G>A (p.Arg347His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48981600G>C | CA384639136 | WNT1 | c.1073G>C (p.Arg358Pro) c.1040G>C (p.Arg347Pro) | |
| 12 | g.48981600G= | CA2034902108 | WNT1 | c.1073G= (p.Arg358=) c.1040G= (p.Arg347=) | |
| 12 | g.48981600G>T | CA384639137 | WNT1 | c.1073G>T (p.Arg358Leu) c.1040G>T (p.Arg347Leu) |