Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.22120359del | CA2574257952 | WNT4 | c.749del (p.Gly250AlafsTer?) c.815del (p.Gly272AlafsTer?) c.584del (p.Gly195AlafsTer?) | |
1 | g.22120359C>A | CA416682277 | WNT4 | c.747G>T (p.Val249=) c.813G>T (p.Val271=) c.582G>T (p.Val194=) | dbSNP gnomAD v4 |
1 | g.22120359C= | CA1158256860 | WNT4 | c.747G= (p.Val249=) c.813G= (p.Val271=) c.582G= (p.Val194=) | |
1 | g.22120359C>G | CA416682278 | WNT4 | c.747G>C (p.Val249=) c.813G>C (p.Val271=) c.582G>C (p.Val194=) | |
1 | g.22120359C>T | CA675280 | WNT4 | c.747G>A (p.Val249=) c.813G>A (p.Val271=) c.582G>A (p.Val194=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.22120360A>C | CA338916586 | WNT4 | c.746T>G (p.Val249Gly) c.812T>G (p.Val271Gly) c.581T>G (p.Val194Gly) | |
1 | g.22120360A>G | CA338916587 | WNT4 | c.746T>C (p.Val249Ala) c.812T>C (p.Val271Ala) c.581T>C (p.Val194Ala) | |
1 | g.22120360A>T | CA338916589 | WNT4 | c.746T>A (p.Val249Glu) c.812T>A (p.Val271Glu) c.581T>A (p.Val194Glu) | |
1 | g.22120361C>A | CA338916594 | WNT4 | c.745G>T (p.Val249Leu) c.811G>T (p.Val271Leu) c.580G>T (p.Val194Leu) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.22120361C= | CA1158256861 | WNT4 | c.745G= (p.Val249=) c.811G= (p.Val271=) c.580G= (p.Val194=) | |
1 | g.22120361C>G | CA338916592 | WNT4 | c.745G>C (p.Val249Leu) c.811G>C (p.Val271Leu) c.580G>C (p.Val194Leu) | |
1 | g.22120361C>T | CA675281 | WNT4 | c.745G>A (p.Val249Met) c.811G>A (p.Val271Met) c.580G>A (p.Val194Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.22120362G>A | CA416682292 | WNT4 | c.744C>T (p.Arg248=) c.810C>T (p.Arg270=) c.579C>T (p.Arg193=) | dbSNP gnomAD v4 COSMIC |
1 | g.22120362G>C | CA416682288 | WNT4 | c.744C>G (p.Arg248=) c.810C>G (p.Arg270=) c.579C>G (p.Arg193=) | |
1 | g.22120362G= | CA1158256862 | WNT4 | c.744C= (p.Arg248=) c.810C= (p.Arg270=) c.579C= (p.Arg193=) | |
1 | g.22120362G>T | CA416682287 | WNT4 | c.744C>A (p.Arg248=) c.810C>A (p.Arg270=) c.579C>A (p.Arg193=) | |
1 | g.22120363C>A | CA338916596 | WNT4 | c.743G>T (p.Arg248Leu) c.809G>T (p.Arg270Leu) c.578G>T (p.Arg193Leu) | |
1 | g.22120363C= | CA1141891301 | WNT4 | c.743G= (p.Arg248=) c.809G= (p.Arg270=) c.578G= (p.Arg193=) | |
1 | g.22120363C>G | CA338916598 | WNT4 | c.743G>C (p.Arg248Pro) c.809G>C (p.Arg270Pro) c.578G>C (p.Arg193Pro) | |
1 | g.22120363C>T | CA675282 | WNT4 | c.743G>A (p.Arg248His) c.809G>A (p.Arg270His) c.578G>A (p.Arg193His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.22120364G>A | CA675283 | WNT4 | c.742C>T (p.Arg248Cys) c.808C>T (p.Arg270Cys) c.577C>T (p.Arg193Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.22120364G>C | CA338916601 | WNT4 | c.742C>G (p.Arg248Gly) c.808C>G (p.Arg270Gly) c.577C>G (p.Arg193Gly) | |
1 | g.22120364G= | CA1143685925 | WNT4 | c.742C= (p.Arg248=) c.808C= (p.Arg270=) c.577C= (p.Arg193=) | |
1 | g.22120364G>T | CA338916603 | WNT4 | c.742C>A (p.Arg248Ser) c.808C>A (p.Arg270Ser) c.577C>A (p.Arg193Ser) | |
1 | g.22120365G>A | CA416682307 | WNT4 | c.741C>T (p.Arg247=) c.807C>T (p.Arg269=) c.576C>T (p.Arg192=) | |
1 | g.22120365G>C | CA416682306 | WNT4 | c.741C>G (p.Arg247=) c.807C>G (p.Arg269=) c.576C>G (p.Arg192=) | |
1 | g.22120365G>T | CA416682308 | WNT4 | c.741C>A (p.Arg247=) c.807C>A (p.Arg269=) c.576C>A (p.Arg192=) | |
1 | g.22120366C>A | CA338916605 | WNT4 | c.740G>T (p.Arg247Leu) c.806G>T (p.Arg269Leu) c.575G>T (p.Arg192Leu) | |
1 | g.22120366C= | CA1144159212 | WNT4 | c.740G= (p.Arg247=) c.806G= (p.Arg269=) c.575G= (p.Arg192=) | |
1 | g.22120366C>G | CA338916607 | WNT4 | c.740G>C (p.Arg247Pro) c.806G>C (p.Arg269Pro) c.575G>C (p.Arg192Pro) | |
1 | g.22120366C>T | CA675284 | WNT4 | c.740G>A (p.Arg247His) c.806G>A (p.Arg269His) c.575G>A (p.Arg192His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.22120367G>A | CA675285 | WNT4 | c.739C>T (p.Arg247Cys) c.805C>T (p.Arg269Cys) c.574C>T (p.Arg192Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.22120367G>C | CA338916611 | WNT4 | c.739C>G (p.Arg247Gly) c.805C>G (p.Arg269Gly) c.574C>G (p.Arg192Gly) | |
1 | g.22120367G= | CA1141719604 | WNT4 | c.739C= (p.Arg247=) c.805C= (p.Arg269=) c.574C= (p.Arg192=) | |
1 | g.22120367G>T | CA338916613 | WNT4 | c.739C>A (p.Arg247Ser) c.805C>A (p.Arg269Ser) c.574C>A (p.Arg192Ser) | |
1 | g.22120368T>A | CA416682314 | WNT4 | c.738A>T (p.Pro246=) c.804A>T (p.Pro268=) c.573A>T (p.Pro191=) | |
1 | g.22120368T>C | CA416682315 | WNT4 | c.738A>G (p.Pro246=) c.804A>G (p.Pro268=) c.573A>G (p.Pro191=) | |
1 | g.22120368T>G | CA416682316 | WNT4 | c.738A>C (p.Pro246=) c.804A>C (p.Pro268=) c.573A>C (p.Pro191=) | |
1 | g.22120369G>A | CA338916617 | WNT4 | c.737C>T (p.Pro246Leu) c.803C>T (p.Pro268Leu) c.572C>T (p.Pro191Leu) | dbSNP gnomAD v4 |
1 | g.22120369G>C | CA338916619 | WNT4 | c.737C>G (p.Pro246Arg) c.803C>G (p.Pro268Arg) c.572C>G (p.Pro191Arg) | |
1 | g.22120369G= | CA1158256863 | WNT4 | c.737C= (p.Pro246=) c.803C= (p.Pro268=) c.572C= (p.Pro191=) | |
1 | g.22120369G>T | CA338916616 | WNT4 | c.737C>A (p.Pro246Gln) c.803C>A (p.Pro268Gln) c.572C>A (p.Pro191Gln) | |
1 | g.22120370dup | CA2574257953 | WNT4 | c.737dup (p.Arg247ThrfsTer22) c.803dup (p.Arg269ThrfsTer22) c.572dup (p.Arg192ThrfsTer22) | |
1 | g.22120370G>A | CA338916621 | WNT4 | c.736C>T (p.Pro246Ser) c.802C>T (p.Pro268Ser) c.571C>T (p.Pro191Ser) | |
1 | g.22120370G>C | CA338916623 | WNT4 | c.736C>G (p.Pro246Ala) c.802C>G (p.Pro268Ala) c.571C>G (p.Pro191Ala) | |
1 | g.22120370G= | CA1158256864 | WNT4 | c.736C= (p.Pro246=) c.802C= (p.Pro268=) c.571C= (p.Pro191=) | |
1 | g.22120370G>T | CA338916624 | WNT4 | c.736C>A (p.Pro246Thr) c.802C>A (p.Pro268Thr) c.571C>A (p.Pro191Thr) | dbSNP gnomAD v4 |
1 | g.22120371C>A | CA338916626 | WNT4 | c.735G>T (p.Glu245Asp) c.801G>T (p.Glu267Asp) c.570G>T (p.Glu190Asp) | |
1 | g.22120371C= | CA1142292440 | WNT4 | c.735G= (p.Glu245=) c.801G= (p.Glu267=) c.570G= (p.Glu190=) | |
1 | g.22120371C>G | CA338916628 | WNT4 | c.735G>C (p.Glu245Asp) c.801G>C (p.Glu267Asp) c.570G>C (p.Glu190Asp) |