| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.48966106C>A | CA384670731 | WNT10B | c.1159G>T (p.Val387Leu) c.*441G>T (n.*441G>T) c.793G>T (p.Val265Leu) | |
| 12 | g.48966106C>G | CA384670734 | WNT10B | c.1159G>C (p.Val387Leu) c.*441G>C (n.*441G>C) c.793G>C (p.Val265Leu) | |
| 12 | g.48966106C>T | CA384670738 | WNT10B | c.1159G>A (p.Val387Met) c.*441G>A (n.*441G>A) c.793G>A (p.Val265Met) | |
| 12 | g.48966107A>C | CA384670741 | WNT10B | c.1158T>G (p.Asn386Lys) c.*440T>G (n.*440T>G) c.792T>G (p.Asn264Lys) | |
| 12 | g.48966107A>G | CA479703451 | WNT10B | c.1158T>C (p.Asn386=) c.*440T>C (n.*440T>C) c.792T>C (p.Asn264=) | dbSNP |
| 12 | g.48966107A>T | CA384670744 | WNT10B | c.1158T>A (p.Asn386Lys) c.*440T>A (n.*440T>A) c.792T>A (p.Asn264Lys) | |
| 12 | g.48966108T>A | CA384670754 | WNT10B | c.1157A>T (p.Asn386Ile) c.*439A>T (n.*439A>T) c.791A>T (p.Asn264Ile) | dbSNP |
| 12 | g.48966108T>C | CA384670751 | WNT10B | c.1157A>G (p.Asn386Ser) c.*439A>G (n.*439A>G) c.791A>G (p.Asn264Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966108T>G | CA384670748 | WNT10B | c.1157A>C (p.Asn386Thr) c.*439A>C (n.*439A>C) c.791A>C (p.Asn264Thr) | |
| 12 | g.48966108T= | CA2034911772 | WNT10B | c.1157A= (p.Asn386=) c.*439A= (n.*439A=) c.791A= (p.Asn264=) | |
| 12 | g.48966109T>A | CA384670757 | WNT10B | c.1156A>T (p.Asn386Tyr) c.*438A>T (n.*438A>T) c.790A>T (p.Asn264Tyr) | |
| 12 | g.48966109T>C | CA384670759 | WNT10B | c.1156A>G (p.Asn386Asp) c.*438A>G (n.*438A>G) c.790A>G (p.Asn264Asp) | |
| 12 | g.48966109T>G | CA384670762 | WNT10B | c.1156A>C (p.Asn386His) c.*438A>C (n.*438A>C) c.790A>C (p.Asn264His) | |
| 12 | g.48966110C>A | CA479703455 | WNT10B | c.1155G>T (p.Val385=) c.*437G>T (n.*437G>T) c.789G>T (p.Val263=) | |
| 12 | g.48966110C= | CA2034911774 | WNT10B | c.1155G= (p.Val385=) c.*437G= (n.*437G=) c.789G= (p.Val263=) | |
| 12 | g.48966110C>G | CA6544026 | WNT10B | c.1155G>C (p.Val385=) c.*437G>C (n.*437G>C) c.789G>C (p.Val263=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.48966110C>T | CA6544025 | WNT10B | c.1155G>A (p.Val385=) c.*437G>A (n.*437G>A) c.789G>A (p.Val263=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966111A>C | CA384670779 | WNT10B | c.1154T>G (p.Val385Gly) c.*436T>G (n.*436T>G) c.788T>G (p.Val263Gly) | |
| 12 | g.48966111A>G | CA384670776 | WNT10B | c.1154T>C (p.Val385Ala) c.*436T>C (n.*436T>C) c.788T>C (p.Val263Ala) | |
| 12 | g.48966111A>T | CA384670772 | WNT10B | c.1154T>A (p.Val385Glu) c.*436T>A (n.*436T>A) c.788T>A (p.Val263Glu) | |
| 12 | g.48966112C>A | CA384670781 | WNT10B | c.1153G>T (p.Val385Leu) c.*435G>T (n.*435G>T) c.787G>T (p.Val263Leu) | |
| 12 | g.48966112C>G | CA384670784 | WNT10B | c.1153G>C (p.Val385Leu) c.*435G>C (n.*435G>C) c.787G>C (p.Val263Leu) | |
| 12 | g.48966112C>T | CA384670788 | WNT10B | c.1153G>A (p.Val385Met) c.*435G>A (n.*435G>A) c.787G>A (p.Val263Met) | gnomAD v4 |
| 12 | g.48966113C>A | CA384670792 | WNT10B | c.1152G>T (p.Trp384Cys) c.*434G>T (n.*434G>T) c.786G>T (p.Trp262Cys) | |
| 12 | g.48966113C= | CA2034911777 | WNT10B | c.1152G= (p.Trp384=) c.*434G= (n.*434G=) c.786G= (p.Trp262=) | |
| 12 | g.48966113C>G | CA384670795 | WNT10B | c.1152G>C (p.Trp384Cys) c.*434G>C (n.*434G>C) c.786G>C (p.Trp262Cys) | dbSNP gnomAD v4 |
| 12 | g.48966113C>T | CA384670797 | WNT10B | c.1152G>A (p.Trp384Ter) c.*434G>A (n.*434G>A) c.786G>A (p.Trp262Ter) | |
| 12 | g.48966114C>A | CA384670802 | WNT10B | c.1151G>T (p.Trp384Leu) c.*433G>T (n.*433G>T) c.785G>T (p.Trp262Leu) | |
| 12 | g.48966114C= | CA2034911778 | WNT10B | c.1151G= (p.Trp384=) c.*433G= (n.*433G=) c.785G= (p.Trp262=) | |
| 12 | g.48966114C>G | CA384670808 | WNT10B | c.1151G>C (p.Trp384Ser) c.*433G>C (n.*433G>C) c.785G>C (p.Trp262Ser) | |
| 12 | g.48966114C>T | CA384670806 | WNT10B | c.1151G>A (p.Trp384Ter) c.*433G>A (n.*433G>A) c.785G>A (p.Trp262Ter) | dbSNP gnomAD v4 COSMIC |
| 12 | g.48966115A>C | CA384670812 | WNT10B | c.1150T>G (p.Trp384Gly) c.*432T>G (n.*432T>G) c.784T>G (p.Trp262Gly) | |
| 12 | g.48966115A>G | CA384670814 | WNT10B | c.1150T>C (p.Trp384Arg) c.*432T>C (n.*432T>C) c.784T>C (p.Trp262Arg) | gnomAD v4 |
| 12 | g.48966115A>T | CA384670816 | WNT10B | c.1150T>A (p.Trp384Arg) c.*432T>A (n.*432T>A) c.784T>A (p.Trp262Arg) | |
| 12 | g.48966116C>A | CA384670819 | WNT10B | c.1149G>T (p.Glu383Asp) c.*431G>T (n.*431G>T) c.783G>T (p.Glu261Asp) | |
| 12 | g.48966116C>G | CA384670820 | WNT10B | c.1149G>C (p.Glu383Asp) c.*431G>C (n.*431G>C) c.783G>C (p.Glu261Asp) | |
| 12 | g.48966116C>T | CA479703460 | WNT10B | c.1149G>A (p.Glu383=) c.*431G>A (n.*431G>A) c.783G>A (p.Glu261=) | |
| 12 | g.48966117T>A | CA384670824 | WNT10B | c.1148A>T (p.Glu383Val) c.*430A>T (n.*430A>T) c.782A>T (p.Glu261Val) | |
| 12 | g.48966117T>C | CA6544027 | WNT10B | c.1148A>G (p.Glu383Gly) c.*430A>G (n.*430A>G) c.782A>G (p.Glu261Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966117T>G | CA384670830 | WNT10B | c.1148A>C (p.Glu383Ala) c.*430A>C (n.*430A>C) c.782A>C (p.Glu261Ala) | |
| 12 | g.48966117T= | CA2034911780 | WNT10B | c.1148A= (p.Glu383=) c.*430A= (n.*430A=) c.782A= (p.Glu261=) | |
| 12 | g.48966118C>A | CA384670834 | WNT10B | c.1147G>T (p.Glu383Ter) c.*429G>T (n.*429G>T) c.781G>T (p.Glu261Ter) | |
| 12 | g.48966118C>G | CA384670837 | WNT10B | c.1147G>C (p.Glu383Gln) c.*429G>C (n.*429G>C) c.781G>C (p.Glu261Gln) | |
| 12 | g.48966118C>T | CA384670840 | WNT10B | c.1147G>A (p.Glu383Lys) c.*429G>A (n.*429G>A) c.781G>A (p.Glu261Lys) | |
| 12 | g.48966119T>A | CA479703462 | WNT10B | c.1146A>T (p.Thr382=) c.*428A>T (n.*428A>T) c.780A>T (p.Thr260=) c.*424A>T (n.*424A>T) | |
| 12 | g.48966119T>C | CA6544028 | WNT10B | c.1146A>G (p.Thr382=) c.*428A>G (n.*428A>G) c.780A>G (p.Thr260=) c.*424A>G (n.*424A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.48966119T>G | CA479703461 | WNT10B | c.1146A>C (p.Thr382=) c.*428A>C (n.*428A>C) c.780A>C (p.Thr260=) c.*424A>C (n.*424A>C) | |
| 12 | g.48966119T= | CA2034911782 | WNT10B | c.1146A= (p.Thr382=) c.*428A= (n.*428A=) c.780A= (p.Thr260=) c.*424A= (n.*424A=) | |
| 12 | g.48966120G>A | CA384670850 | WNT10B | c.1145C>T (p.Thr382Ile) c.*427C>T (n.*427C>T) c.779C>T (p.Thr260Ile) c.*423C>T (n.*423C>T) | |
| 12 | g.48966120G>C | CA384670847 | WNT10B | c.1145C>G (p.Thr382Arg) c.*427C>G (n.*427C>G) c.779C>G (p.Thr260Arg) c.*423C>G (n.*423C>G) |