UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.44265096_44265125del | CA2613210123 | ALX4 | c.967_996del (p.Val323_Met332del) c.445_474del (p.Val149_Met158del) | gnomAD v4 |
| 11 | g.44265104_44265114delinsGGCACCGGGTC | CA1967914980 | ALX4 | c.976_986delinsGACCCGGTGCC (p.Asp326=) c.454_464delinsGACCCGGTGCC (p.Asp152=) | |
| 11 | g.44265105_44265114delinsAGTTGCCATCTCTGTTGAGATCTTAG | CA270670 | ALX4 | c.976_985delinsCTAAGATCTCAACAGAGATGGCAACT (p.Asp326LeufsTer?) c.454_463delinsCTAAGATCTCAACAGAGATGGCAACT (p.Asp152LeufsTer?) | ClinVar dbSNP |
| 11 | g.44265111_44265113dup | CA2613210124 | ALX4 | c.977_979dup (p.Asp326_Pro327insHis) c.455_457dup (p.Asp152_Pro153insHis) | gnomAD v4 |
| 11 | g.44265112G>A | CA474035380 | ALX4 | c.978C>T (p.Asp326=) c.456C>T (p.Asp152=) | |
| 11 | g.44265112G>C | CA380181673 | ALX4 | c.978C>G (p.Asp326Glu) c.456C>G (p.Asp152Glu) | |
| 11 | g.44265112G>T | CA380181674 | ALX4 | c.978C>A (p.Asp326Glu) c.456C>A (p.Asp152Glu) | |
| 11 | g.44265113T>A | CA380181675 | ALX4 | c.977A>T (p.Asp326Val) c.455A>T (p.Asp152Val) | |
| 11 | g.44265113T>C | CA380181676 | ALX4 | c.977A>G (p.Asp326Gly) c.455A>G (p.Asp152Gly) | |
| 11 | g.44265113T>G | CA380181677 | ALX4 | c.977A>C (p.Asp326Ala) c.455A>C (p.Asp152Ala) | |
| 11 | g.44265114C>A | CA380181678 | ALX4 | c.976G>T (p.Asp326Tyr) c.454G>T (p.Asp152Tyr) | dbSNP gnomAD v2 |
| 11 | g.44265114C= | CA1967915052 | ALX4 | c.976G= (p.Asp326=) c.454G= (p.Asp152=) | |
| 11 | g.44265114C>G | CA380181679 | ALX4 | c.976G>C (p.Asp326His) c.454G>C (p.Asp152His) | |
| 11 | g.44265114C>T | CA5955560 | ALX4 | c.976G>A (p.Asp326Asn) c.454G>A (p.Asp152Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265115G>A | CA221487758 | ALX4 | c.975C>T (p.Cys325=) c.453C>T (p.Cys151=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.44265115G>C | CA380181680 | ALX4 | c.975C>G (p.Cys325Trp) c.453C>G (p.Cys151Trp) | |
| 11 | g.44265115G= | CA1967915056 | ALX4 | c.975C= (p.Cys325=) c.453C= (p.Cys151=) | |
| 11 | g.44265115G>T | CA380181681 | ALX4 | c.975C>A (p.Cys325Ter) c.453C>A (p.Cys151Ter) | |
| 11 | g.44265116C>A | CA380181682 | ALX4 | c.974G>T (p.Cys325Phe) c.452G>T (p.Cys151Phe) | |
| 11 | g.44265116C>G | CA380181684 | ALX4 | c.974G>C (p.Cys325Ser) c.452G>C (p.Cys151Ser) | |
| 11 | g.44265116C>T | CA380181683 | ALX4 | c.974G>A (p.Cys325Tyr) c.452G>A (p.Cys151Tyr) | |
| 11 | g.44265117A>C | CA380181685 | ALX4 | c.973T>G (p.Cys325Gly) c.451T>G (p.Cys151Gly) | |
| 11 | g.44265117A>G | CA380181686 | ALX4 | c.973T>C (p.Cys325Arg) c.451T>C (p.Cys151Arg) | |
| 11 | g.44265117A>T | CA380181687 | ALX4 | c.973T>A (p.Cys325Ser) c.451T>A (p.Cys151Ser) | gnomAD v4 |
| 11 | g.44265118G>A | CA5955561 | ALX4 | c.972C>T (p.Pro324=) c.450C>T (p.Pro150=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265118G>C | CA474035385 | ALX4 | c.972C>G (p.Pro324=) c.450C>G (p.Pro150=) | |
| 11 | g.44265118G= | CA1967915061 | ALX4 | c.972C= (p.Pro324=) c.450C= (p.Pro150=) | |
| 11 | g.44265118G>T | CA474035386 | ALX4 | c.972C>A (p.Pro324=) c.450C>A (p.Pro150=) | |
| 11 | g.44265119G>A | CA380181688 | ALX4 | c.971C>T (p.Pro324Leu) c.449C>T (p.Pro150Leu) | gnomAD v4 |
| 11 | g.44265119G>C | CA380181689 | ALX4 | c.971C>G (p.Pro324Arg) c.449C>G (p.Pro150Arg) | |
| 11 | g.44265119G>T | CA380181690 | ALX4 | c.971C>A (p.Pro324His) c.449C>A (p.Pro150His) | |
| 11 | g.44265120G>A | CA380181691 | ALX4 | c.970C>T (p.Pro324Ser) c.448C>T (p.Pro150Ser) | |
| 11 | g.44265120G>C | CA380181692 | ALX4 | c.970C>G (p.Pro324Ala) c.448C>G (p.Pro150Ala) | |
| 11 | g.44265120G>T | CA380181693 | ALX4 | c.970C>A (p.Pro324Thr) c.448C>A (p.Pro150Thr) | |
| 11 | g.44265121G>A | CA474035387 | ALX4 | c.969C>T (p.Val323=) c.447C>T (p.Val149=) | |
| 11 | g.44265121G>C | CA474035388 | ALX4 | c.969C>G (p.Val323=) c.447C>G (p.Val149=) | gnomAD v4 |
| 11 | g.44265121G>T | CA474035390 | ALX4 | c.969C>A (p.Val323=) c.447C>A (p.Val149=) | |
| 11 | g.44265122A= | CA1967915075 | ALX4 | c.968T= (p.Val323=) c.446T= (p.Val149=) | |
| 11 | g.44265122A>C | CA380181695 | ALX4 | c.968T>G (p.Val323Gly) c.446T>G (p.Val149Gly) | |
| 11 | g.44265122A>G | CA221487765 | ALX4 | c.968T>C (p.Val323Ala) c.446T>C (p.Val149Ala) | dbSNP gnomAD v4 |
| 11 | g.44265122A>T | CA380181694 | ALX4 | c.968T>A (p.Val323Asp) c.446T>A (p.Val149Asp) | |
| 11 | g.44265123C>A | CA380181696 | ALX4 | c.967G>T (p.Val323Phe) c.445G>T (p.Val149Phe) | gnomAD v4 |
| 11 | g.44265123C>G | CA380181698 | ALX4 | c.967G>C (p.Val323Leu) c.445G>C (p.Val149Leu) | |
| 11 | g.44265123C>T | CA380181697 | ALX4 | c.967G>A (p.Val323Ile) c.445G>A (p.Val149Ile) | |
| 11 | g.44265124C>A | CA474035397 | ALX4 | c.966G>T (p.Val322=) c.444G>T (p.Val148=) | |
| 11 | g.44265124C>G | CA474035395 | ALX4 | c.966G>C (p.Val322=) c.444G>C (p.Val148=) | |
| 11 | g.44265124C>T | CA474035394 | ALX4 | c.966G>A (p.Val322=) c.444G>A (p.Val148=) | |
| 11 | g.44265125A>C | CA380181699 | ALX4 | c.965T>G (p.Val322Gly) c.443T>G (p.Val148Gly) | |
| 11 | g.44265125A>G | CA380181700 | ALX4 | c.965T>C (p.Val322Ala) c.443T>C (p.Val148Ala) | |
| 11 | g.44265125A>T | CA380181701 | ALX4 | c.965T>A (p.Val322Glu) c.443T>A (p.Val148Glu) | |
| 11 | g.44265126C>A | CA5955562 | ALX4 | c.964G>T (p.Val322Leu) c.442G>T (p.Val148Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44265126C= | CA1967915087 | ALX4 | c.964G= (p.Val322=) c.442G= (p.Val148=) | |
| 11 | g.44265126C>G | CA380181702 | ALX4 | c.964G>C (p.Val322Leu) c.442G>C (p.Val148Leu) | |
| 11 | g.44265126C>T | CA5955563 | ALX4 | c.964G>A (p.Val322Met) c.442G>A (p.Val148Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.44265127G>A | CA5955564 | ALX4 | c.963C>T (p.Cys321=) c.441C>T (p.Cys147=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265127G>C | CA380181703 | ALX4 | c.963C>G (p.Cys321Trp) c.441C>G (p.Cys147Trp) | |
| 11 | g.44265127G= | CA1967915093 | ALX4 | c.963C= (p.Cys321=) c.441C= (p.Cys147=) | |
| 11 | g.44265127G>T | CA380181704 | ALX4 | c.963C>A (p.Cys321Ter) c.441C>A (p.Cys147Ter) | COSMIC |
| 11 | g.44265128C>A | CA380181705 | ALX4 | c.962G>T (p.Cys321Phe) c.440G>T (p.Cys147Phe) | |
| 11 | g.44265128C>G | CA380181706 | ALX4 | c.962G>C (p.Cys321Ser) c.440G>C (p.Cys147Ser) | |
| 11 | g.44265128C>T | CA380181707 | ALX4 | c.962G>A (p.Cys321Tyr) c.440G>A (p.Cys147Tyr) | |
| 11 | g.44265129A>C | CA380181708 | ALX4 | c.961T>G (p.Cys321Gly) c.439T>G (p.Cys147Gly) | |
| 11 | g.44265129A>G | CA380181710 | ALX4 | c.961T>C (p.Cys321Arg) c.439T>C (p.Cys147Arg) | |
| 11 | g.44265129A>T | CA380181709 | ALX4 | c.961T>A (p.Cys321Ser) c.439T>A (p.Cys147Ser) | |
| 11 | g.44265130G>A | CA221487797 | ALX4 | c.960C>T (p.Ala320=) c.438C>T (p.Ala146=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265130G>C | CA474035403 | ALX4 | c.960C>G (p.Ala320=) c.438C>G (p.Ala146=) | |
| 11 | g.44265130G= | CA1967915097 | ALX4 | c.960C= (p.Ala320=) c.438C= (p.Ala146=) | |
| 11 | g.44265130G>T | CA474035405 | ALX4 | c.960C>A (p.Ala320=) c.438C>A (p.Ala146=) | |
| 11 | g.44265133_44265136del | CA2613210125 | ALX4 | c.957_960del (p.Cys321TrpfsTer?) c.435_438del (p.Cys147TrpfsTer?) | gnomAD v4 |
| 11 | g.44265131G>A | CA380181711 | ALX4 | c.959C>T (p.Ala320Val) c.437C>T (p.Ala146Val) | COSMIC |
| 11 | g.44265131G>C | CA5955565 | ALX4 | c.959C>G (p.Ala320Gly) c.437C>G (p.Ala146Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265131G= | CA1967915098 | ALX4 | c.959C= (p.Ala320=) c.437C= (p.Ala146=) | |
| 11 | g.44265131G>T | CA380181712 | ALX4 | c.959C>A (p.Ala320Asp) c.437C>A (p.Ala146Asp) | |
| 11 | g.44265132C>A | CA221487802 | ALX4 | c.958G>T (p.Ala320Ser) c.436G>T (p.Ala146Ser) | dbSNP |
| 11 | g.44265132C= | CA1967915101 | ALX4 | c.958G= (p.Ala320=) c.436G= (p.Ala146=) | |
| 11 | g.44265132C>G | CA380181713 | ALX4 | c.958G>C (p.Ala320Pro) c.436G>C (p.Ala146Pro) | |
| 11 | g.44265132C>T | CA380181714 | ALX4 | c.958G>A (p.Ala320Thr) c.436G>A (p.Ala146Thr) | |
| 11 | g.44265133T>A | CA474035408 | ALX4 | c.957A>T (p.Pro319=) c.435A>T (p.Pro145=) | |
| 11 | g.44265133T>C | CA474035409 | ALX4 | c.957A>G (p.Pro319=) c.435A>G (p.Pro145=) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.44265133T>G | CA474035410 | ALX4 | c.957A>C (p.Pro319=) c.435A>C (p.Pro145=) | gnomAD v4 |
| 11 | g.44265133T= | CA1967915109 | ALX4 | c.957A= (p.Pro319=) c.435A= (p.Pro145=) | |
| 11 | g.44265133_44265134insCCTGA | CA599370272 | ALX4 | c.956_957insTCAGG (p.Ala320GlnfsTer?) c.434_435insTCAGG (p.Ala146GlnfsTer?) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265134G>A | CA380181715 | ALX4 | c.956C>T (p.Pro319Leu) c.434C>T (p.Pro145Leu) | |
| 11 | g.44265134G>C | CA380181716 | ALX4 | c.956C>G (p.Pro319Arg) c.434C>G (p.Pro145Arg) | |
| 11 | g.44265134G>T | CA380181717 | ALX4 | c.956C>A (p.Pro319Gln) c.434C>A (p.Pro145Gln) | |
| 11 | g.44265135G>A | CA380181719 | ALX4 | c.955C>T (p.Pro319Ser) c.433C>T (p.Pro145Ser) | |
| 11 | g.44265135G>C | CA380181720 | ALX4 | c.955C>G (p.Pro319Ala) c.433C>G (p.Pro145Ala) | |
| 11 | g.44265135G= | CA1967915116 | ALX4 | c.955C= (p.Pro319=) c.433C= (p.Pro145=) | |
| 11 | g.44265135G>T | CA380181718 | ALX4 | c.955C>A (p.Pro319Thr) c.433C>A (p.Pro145Thr) | COSMIC |
| 11 | g.44265135_44265136insGGGGTGAGGAGCCTGGTGGTGTGAGGTGGGGTGAGGAGGGGGTGAGGA | CA599370273 | ALX4 | c.954_955insTCCTCACCCCCTCCTCACCCCACCTCACACCACCAGGCTCCTCACCCC (p.Val318_Pro319insSerSerProProProHisProThrSerHisHisGlnAlaProHisPro) c.432_433insTCCTCACCCCCTCCTCACCCCACCTCACACCACCAGGCTCCTCACCCC (p.Val144_Pro145insSerSerProProProHisProThrSerHisHisGlnAlaProHisPro) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265136C>A | CA474035414 | ALX4 | c.954G>T (p.Val318=) c.432G>T (p.Val144=) | |
| 11 | g.44265136C>G | CA474035415 | ALX4 | c.954G>C (p.Val318=) c.432G>C (p.Val144=) | |
| 11 | g.44265136C>T | CA474035416 | ALX4 | c.954G>A (p.Val318=) c.432G>A (p.Val144=) | |
| 11 | g.44265137A= | CA1967915124 | ALX4 | c.953T= (p.Val318=) c.431T= (p.Val144=) | |
| 11 | g.44265137A>C | CA380181721 | ALX4 | c.953T>G (p.Val318Gly) c.431T>G (p.Val144Gly) | dbSNP |
| 11 | g.44265137A>G | CA380181722 | ALX4 | c.953T>C (p.Val318Ala) c.431T>C (p.Val144Ala) | gnomAD v4 |
| 11 | g.44265137A>T | CA380181723 | ALX4 | c.953T>A (p.Val318Glu) c.431T>A (p.Val144Glu) | |
| 11 | g.44265138C>A | CA380181724 | ALX4 | c.952G>T (p.Val318Leu) c.430G>T (p.Val144Leu) | |
| 11 | g.44265138C= | CA1967915127 | ALX4 | c.952G= (p.Val318=) c.430G= (p.Val144=) | |
| 11 | g.44265138C>G | CA380181725 | ALX4 | c.952G>C (p.Val318Leu) c.430G>C (p.Val144Leu) | |
| 11 | g.44265138C>T | CA380181726 | ALX4 | c.952G>A (p.Val318Met) c.430G>A (p.Val144Met) | |
| 11 | g.44265138_44265139insGCAGGG | CA599370274 | ALX4 | c.951_952insCCCTGC (p.Pro317_Val318insProCys) c.429_430insCCCTGC (p.Pro143_Val144insProCys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265139T>A | CA474035417 | ALX4 | c.951A>T (p.Pro317=) c.429A>T (p.Pro143=) | |
| 11 | g.44265139T>C | CA474035418 | ALX4 | c.951A>G (p.Pro317=) c.429A>G (p.Pro143=) | |
| 11 | g.44265139T>G | CA474035419 | ALX4 | c.951A>C (p.Pro317=) c.429A>C (p.Pro143=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265139T= | CA1967915136 | ALX4 | c.951A= (p.Pro317=) c.429A= (p.Pro143=) | |
| 11 | g.44265140G>A | CA380181727 | ALX4 | c.950C>T (p.Pro317Leu) c.428C>T (p.Pro143Leu) | |
| 11 | g.44265140G>C | CA380181728 | ALX4 | c.950C>G (p.Pro317Arg) c.428C>G (p.Pro143Arg) | |
| 11 | g.44265140G>T | CA380181729 | ALX4 | c.950C>A (p.Pro317Gln) c.428C>A (p.Pro143Gln) | COSMIC |
| 11 | g.44265141G>A | CA5955566 | ALX4 | c.949C>T (p.Pro317Ser) c.427C>T (p.Pro143Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44265141G>C | CA380181730 | ALX4 | c.949C>G (p.Pro317Ala) c.427C>G (p.Pro143Ala) | |
| 11 | g.44265141G= | CA1967915139 | ALX4 | c.949C= (p.Pro317=) c.427C= (p.Pro143=) | |
| 11 | g.44265141G>T | CA380181731 | ALX4 | c.949C>A (p.Pro317Thr) c.427C>A (p.Pro143Thr) | COSMIC |
| 11 | g.44265142T>A | CA474035420 | ALX4 | c.948A>T (p.Ser316=) c.426A>T (p.Ser142=) | |
| 11 | g.44265142T>C | CA474035421 | ALX4 | c.948A>G (p.Ser316=) c.426A>G (p.Ser142=) | |
| 11 | g.44265142T>G | CA474035422 | ALX4 | c.948A>C (p.Ser316=) c.426A>C (p.Ser142=) | |
| 11 | g.44265143G>A | CA5955567 | ALX4 | c.947C>T (p.Ser316Leu) c.425C>T (p.Ser142Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44265143G>C | CA380181733 | ALX4 | c.947C>G (p.Ser316Ter) c.425C>G (p.Ser142Ter) | |
| 11 | g.44265143G= | CA1967915143 | ALX4 | c.947C= (p.Ser316=) c.425C= (p.Ser142=) | |
| 11 | g.44265143G>T | CA380181732 | ALX4 | c.947C>A (p.Ser316Ter) c.425C>A (p.Ser142Ter) | gnomAD v4 |
| 11 | g.44265144del | CA2613210126 | ALX4 | c.946del (p.Ser316HisfsTer?) c.424del (p.Ser142HisfsTer?) | gnomAD v4 |
| 11 | g.44265144A>C | CA380181734 | ALX4 | c.946T>G (p.Ser316Ala) c.424T>G (p.Ser142Ala) | |
| 11 | g.44265144A>G | CA380181735 | ALX4 | c.946T>C (p.Ser316Pro) c.424T>C (p.Ser142Pro) | gnomAD v4 |
| 11 | g.44265144A>T | CA380181736 | ALX4 | c.946T>A (p.Ser316Thr) c.424T>A (p.Ser142Thr) | |
| 11 | g.44265145G>A | CA474035426 | ALX4 | c.945C>T (p.Ala315=) c.423C>T (p.Ala141=) | |
| 11 | g.44265145G>C | CA474035423 | ALX4 | c.945C>G (p.Ala315=) c.423C>G (p.Ala141=) | |
| 11 | g.44265145G>T | CA474035424 | ALX4 | c.945C>A (p.Ala315=) c.423C>A (p.Ala141=) | COSMIC |
| 11 | g.44265146G>A | CA380181737 | ALX4 | c.944C>T (p.Ala315Val) c.422C>T (p.Ala141Val) | |
| 11 | g.44265146G>C | CA380181738 | ALX4 | c.944C>G (p.Ala315Gly) c.422C>G (p.Ala141Gly) | |
| 11 | g.44265146G>T | CA380181739 | ALX4 | c.944C>A (p.Ala315Asp) c.422C>A (p.Ala141Asp) | gnomAD v4 |
| 11 | g.44265147C>A | CA380181740 | ALX4 | c.943G>T (p.Ala315Ser) c.421G>T (p.Ala141Ser) | |
| 11 | g.44265147C= | CA1967915148 | ALX4 | c.943G= (p.Ala315=) c.421G= (p.Ala141=) | |
| 11 | g.44265147C>G | CA221487835 | ALX4 | c.943G>C (p.Ala315Pro) c.421G>C (p.Ala141Pro) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.44265147C>T | CA380181741 | ALX4 | c.943G>A (p.Ala315Thr) c.421G>A (p.Ala141Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.44265148del | CA2613210128 | ALX4 | c.942del (p.Ala315ProfsTer?) c.420del (p.Ala141ProfsTer?) | gnomAD v4 |
| 11 | g.44265148A= | CA1967915152 | ALX4 | c.942T= (p.Ala314=) c.420T= (p.Ala140=) | |
| 11 | g.44265148A>C | CA474035428 | ALX4 | c.942T>G (p.Ala314=) c.420T>G (p.Ala140=) | |
| 11 | g.44265148A>G | CA5955568 | ALX4 | c.942T>C (p.Ala314=) c.420T>C (p.Ala140=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44265148A>T | CA474035429 | ALX4 | c.942T>A (p.Ala314=) c.420T>A (p.Ala140=) | |
| 11 | g.44265149G>A | CA380181742 | ALX4 | c.941C>T (p.Ala314Val) c.419C>T (p.Ala140Val) | |
| 11 | g.44265149G>C | CA380181743 | ALX4 | c.941C>G (p.Ala314Gly) c.419C>G (p.Ala140Gly) | |
| 11 | g.44265149G>T | CA380181744 | ALX4 | c.941C>A (p.Ala314Asp) c.419C>A (p.Ala140Asp) | gnomAD v4 |
| 11 | g.44265150C>A | CA221487846 | ALX4 | c.940G>T (p.Ala314Ser) c.418G>T (p.Ala140Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265150C= | CA1967915155 | ALX4 | c.940G= (p.Ala314=) c.418G= (p.Ala140=) | |
| 11 | g.44265150C>G | CA221487852 | ALX4 | c.940G>C (p.Ala314Pro) c.418G>C (p.Ala140Pro) | dbSNP gnomAD v4 |
| 11 | g.44265150C>T | CA380181745 | ALX4 | c.940G>A (p.Ala314Thr) c.418G>A (p.Ala140Thr) | |
| 11 | g.44265151C>A | CA5955570 | ALX4 | c.939G>T (p.Gly313=) c.417G>T (p.Gly139=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44265151C= | CA1967915159 | ALX4 | c.939G= (p.Gly313=) c.417G= (p.Gly139=) | |
| 11 | g.44265151C>G | CA474035430 | ALX4 | c.939G>C (p.Gly313=) c.417G>C (p.Gly139=) | |
| 11 | g.44265151C>T | CA5955569 | ALX4 | c.939G>A (p.Gly313=) c.417G>A (p.Gly139=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265152C>A | CA380181746 | ALX4 | c.938G>T (p.Gly313Val) c.416G>T (p.Gly139Val) | |
| 11 | g.44265152C>G | CA380181748 | ALX4 | c.938G>C (p.Gly313Ala) c.416G>C (p.Gly139Ala) | gnomAD v4 |
| 11 | g.44265152C>T | CA380181747 | ALX4 | c.938G>A (p.Gly313Glu) c.416G>A (p.Gly139Glu) | |
| 11 | g.44265153C>A | CA380181749 | ALX4 | c.937G>T (p.Gly313Trp) c.415G>T (p.Gly139Trp) | |
| 11 | g.44265153C>G | CA380181751 | ALX4 | c.937G>C (p.Gly313Arg) c.415G>C (p.Gly139Arg) | |
| 11 | g.44265153C>T | CA380181750 | ALX4 | c.937G>A (p.Gly313Arg) c.415G>A (p.Gly139Arg) | gnomAD v4 |
| 11 | g.44265154G>A | CA5955571 | ALX4 | c.936C>T (p.Asn312=) c.414C>T (p.Asn138=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265154G>C | CA380181752 | ALX4 | c.936C>G (p.Asn312Lys) c.414C>G (p.Asn138Lys) | |
| 11 | g.44265154G= | CA1967915160 | ALX4 | c.936C= (p.Asn312=) c.414C= (p.Asn138=) | |
| 11 | g.44265154G>T | CA380181753 | ALX4 | c.936C>A (p.Asn312Lys) c.414C>A (p.Asn138Lys) | |
| 11 | g.44265158_44265160del | CA2613210129 | ALX4 | c.934_936del (p.Asn312del) c.412_414del (p.Asn138del) | gnomAD v4 |
| 11 | g.44265155T>A | CA380181754 | ALX4 | c.935A>T (p.Asn312Ile) c.413A>T (p.Asn138Ile) | |
| 11 | g.44265155T>C | CA380181755 | ALX4 | c.935A>G (p.Asn312Ser) c.413A>G (p.Asn138Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265155T>G | CA380181756 | ALX4 | c.935A>C (p.Asn312Thr) c.413A>C (p.Asn138Thr) | dbSNP |
| 11 | g.44265155T= | CA1967915163 | ALX4 | c.935A= (p.Asn312=) c.413A= (p.Asn138=) | |
| 11 | g.44265156T>A | CA380181757 | ALX4 | c.934A>T (p.Asn312Tyr) c.412A>T (p.Asn138Tyr) | |
| 11 | g.44265156T>C | CA380181758 | ALX4 | c.934A>G (p.Asn312Asp) c.412A>G (p.Asn138Asp) | |
| 11 | g.44265156T>G | CA380181759 | ALX4 | c.934A>C (p.Asn312His) c.412A>C (p.Asn138His) | |
| 11 | g.44265157G>A | CA474035432 | ALX4 | c.933C>T (p.Asn311=) c.411C>T (p.Asn137=) | dbSNP |
| 11 | g.44265157G>C | CA380181760 | ALX4 | c.933C>G (p.Asn311Lys) c.411C>G (p.Asn137Lys) | |
| 11 | g.44265157G= | CA1967915168 | ALX4 | c.933C= (p.Asn311=) c.411C= (p.Asn137=) | |
| 11 | g.44265157G>T | CA380181761 | ALX4 | c.933C>A (p.Asn311Lys) c.411C>A (p.Asn137Lys) | |
| 11 | g.44265158T>A | CA380181764 | ALX4 | c.932A>T (p.Asn311Ile) c.410A>T (p.Asn137Ile) | |
| 11 | g.44265158T>C | CA380181762 | ALX4 | c.932A>G (p.Asn311Ser) c.410A>G (p.Asn137Ser) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.44265158T>G | CA380181763 | ALX4 | c.932A>C (p.Asn311Thr) c.410A>C (p.Asn137Thr) | |
| 11 | g.44265158T= | CA1967915170 | ALX4 | c.932A= (p.Asn311=) c.410A= (p.Asn137=) | |
| 11 | g.44265159T>A | CA380181765 | ALX4 | c.931A>T (p.Asn311Tyr) c.409A>T (p.Asn137Tyr) | |
| 11 | g.44265159T>C | CA221487868 | ALX4 | c.931A>G (p.Asn311Asp) c.409A>G (p.Asn137Asp) | dbSNP |
| 11 | g.44265159T>G | CA380181766 | ALX4 | c.931A>C (p.Asn311His) c.409A>C (p.Asn137His) | |
| 11 | g.44265159T= | CA1967915174 | ALX4 | c.931A= (p.Asn311=) c.409A= (p.Asn137=) | |
| 11 | g.44265160G>A | CA474035433 | ALX4 | c.930C>T (p.Gly310=) c.408C>T (p.Gly136=) | gnomAD v4 |
| 11 | g.44265160G>C | CA474035434 | ALX4 | c.930C>G (p.Gly310=) c.408C>G (p.Gly136=) | |
| 11 | g.44265160G>T | CA474035435 | ALX4 | c.930C>A (p.Gly310=) c.408C>A (p.Gly136=) | |
| 11 | g.44265161C>A | CA380181767 | ALX4 | c.929G>T (p.Gly310Val) c.407G>T (p.Gly136Val) | |
| 11 | g.44265161C>G | CA380181768 | ALX4 | c.929G>C (p.Gly310Ala) c.407G>C (p.Gly136Ala) | |
| 11 | g.44265161C>T | CA380181769 | ALX4 | c.929G>A (p.Gly310Asp) c.407G>A (p.Gly136Asp) | gnomAD v4 |
| 11 | g.44265162C>A | CA380181770 | ALX4 | c.928G>T (p.Gly310Cys) c.406G>T (p.Gly136Cys) | |
| 11 | g.44265162C= | CA1967915177 | ALX4 | c.928G= (p.Gly310=) c.406G= (p.Gly136=) | |
| 11 | g.44265162C>G | CA380181771 | ALX4 | c.928G>C (p.Gly310Arg) c.406G>C (p.Gly136Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265162C>T | CA5955572 | ALX4 | c.928G>A (p.Gly310Ser) c.406G>A (p.Gly136Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265163G>A | CA5955573 | ALX4 | c.927C>T (p.Leu309=) c.405C>T (p.Leu135=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265163G>C | CA474035436 | ALX4 | c.927C>G (p.Leu309=) c.405C>G (p.Leu135=) | dbSNP |
| 11 | g.44265163G= | CA1967915180 | ALX4 | c.927C= (p.Leu309=) c.405C= (p.Leu135=) | |
| 11 | g.44265163G>T | CA474035437 | ALX4 | c.927C>A (p.Leu309=) c.405C>A (p.Leu135=) | COSMIC |
| 11 | g.44265164A>C | CA380181773 | ALX4 | c.926T>G (p.Leu309Arg) c.404T>G (p.Leu135Arg) | |
| 11 | g.44265164A>G | CA380181774 | ALX4 | c.926T>C (p.Leu309Pro) c.404T>C (p.Leu135Pro) | |
| 11 | g.44265164A>T | CA380181772 | ALX4 | c.926T>A (p.Leu309His) c.404T>A (p.Leu135His) | |
| 11 | g.44265165G>A | CA380181775 | ALX4 | c.925C>T (p.Leu309Phe) c.403C>T (p.Leu135Phe) | |
| 11 | g.44265165G>C | CA380181776 | ALX4 | c.925C>G (p.Leu309Val) c.403C>G (p.Leu135Val) | |
| 11 | g.44265165G>T | CA380181777 | ALX4 | c.925C>A (p.Leu309Ile) c.403C>A (p.Leu135Ile) | |
| 11 | g.44265166C>A | CA380181778 | ALX4 | c.924G>T (p.Trp308Cys) c.402G>T (p.Trp134Cys) | |
| 11 | g.44265166C>G | CA380181779 | ALX4 | c.924G>C (p.Trp308Cys) c.402G>C (p.Trp134Cys) | |
| 11 | g.44265166C>T | CA380181780 | ALX4 | c.924G>A (p.Trp308Ter) c.402G>A (p.Trp134Ter) | gnomAD v4 |
| 11 | g.44265167C>A | CA380181781 | ALX4 | c.923G>T (p.Trp308Leu) c.401G>T (p.Trp134Leu) | dbSNP |
| 11 | g.44265167C= | CA1967915181 | ALX4 | c.923G= (p.Trp308=) c.401G= (p.Trp134=) | |
| 11 | g.44265167C>G | CA380181782 | ALX4 | c.923G>C (p.Trp308Ser) c.401G>C (p.Trp134Ser) | |
| 11 | g.44265167C>T | CA380181783 | ALX4 | c.923G>A (p.Trp308Ter) c.401G>A (p.Trp134Ter) | |
| 11 | g.44265168A>C | CA380181784 | ALX4 | c.922T>G (p.Trp308Gly) c.400T>G (p.Trp134Gly) | |
| 11 | g.44265168A>G | CA380181785 | ALX4 | c.922T>C (p.Trp308Arg) c.400T>C (p.Trp134Arg) | |
| 11 | g.44265168A>T | CA380181786 | ALX4 | c.922T>A (p.Trp308Arg) c.400T>A (p.Trp134Arg) | |
| 11 | g.44265169G>A | CA474035439 | ALX4 | c.921C>T (p.Ser307=) c.399C>T (p.Ser133=) | |
| 11 | g.44265169G>C | CA474035440 | ALX4 | c.921C>G (p.Ser307=) c.399C>G (p.Ser133=) | |
| 11 | g.44265169G>T | CA474035441 | ALX4 | c.921C>A (p.Ser307=) c.399C>A (p.Ser133=) | |
| 11 | g.44265170G>A | CA380181789 | ALX4 | c.920C>T (p.Ser307Phe) c.398C>T (p.Ser133Phe) | |
| 11 | g.44265170G>C | CA380181787 | ALX4 | c.920C>G (p.Ser307Cys) c.398C>G (p.Ser133Cys) | |
| 11 | g.44265170G>T | CA380181788 | ALX4 | c.920C>A (p.Ser307Tyr) c.398C>A (p.Ser133Tyr) | |
| 11 | g.44265171A>C | CA380181790 | ALX4 | c.919T>G (p.Ser307Ala) c.397T>G (p.Ser133Ala) | |
| 11 | g.44265171A>G | CA380181791 | ALX4 | c.919T>C (p.Ser307Pro) c.397T>C (p.Ser133Pro) | gnomAD v4 |
| 11 | g.44265171A>T | CA380181792 | ALX4 | c.919T>A (p.Ser307Thr) c.397T>A (p.Ser133Thr) | gnomAD v4 |
| 11 | g.44265172C>A | CA474035442 | ALX4 | c.918G>T (p.Pro306=) c.396G>T (p.Pro132=) | gnomAD v4 |
| 11 | g.44265172C= | CA1967915185 | ALX4 | c.918G= (p.Pro306=) c.396G= (p.Pro132=) | |
| 11 | g.44265172C>G | CA474035443 | ALX4 | c.918G>C (p.Pro306=) c.396G>C (p.Pro132=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265172C>T | CA5955574 | ALX4 | c.918G>A (p.Pro306=) c.396G>A (p.Pro132=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.44265173G>A | CA5955575 | ALX4 | c.917C>T (p.Pro306Leu) c.395C>T (p.Pro132Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.44265173G>C | CA380181793 | ALX4 | c.917C>G (p.Pro306Arg) c.395C>G (p.Pro132Arg) | |
| 11 | g.44265173G= | CA1967915193 | ALX4 | c.917C= (p.Pro306=) c.395C= (p.Pro132=) | |
| 11 | g.44265173G>T | CA380181794 | ALX4 | c.917C>A (p.Pro306Gln) c.395C>A (p.Pro132Gln) | |
| 11 | g.44265174G>A | CA380181795 | ALX4 | c.916C>T (p.Pro306Ser) c.394C>T (p.Pro132Ser) | |
| 11 | g.44265174G>C | CA380181796 | ALX4 | c.916C>G (p.Pro306Ala) c.394C>G (p.Pro132Ala) | |
| 11 | g.44265174G>T | CA380181797 | ALX4 | c.916C>A (p.Pro306Thr) c.394C>A (p.Pro132Thr) | |
| 11 | g.44265175G>A | CA474035446 | ALX4 | c.915C>T (p.Asn305=) c.393C>T (p.Asn131=) | |
| 11 | g.44265175G>C | CA380181798 | ALX4 | c.915C>G (p.Asn305Lys) c.393C>G (p.Asn131Lys) | |
| 11 | g.44265175G= | CA1967915197 | ALX4 | c.915C= (p.Asn305=) c.393C= (p.Asn131=) | |
| 11 | g.44265175G>T | CA5955576 | ALX4 | c.915C>A (p.Asn305Lys) c.393C>A (p.Asn131Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.44265176T>A | CA380181801 | ALX4 | c.914A>T (p.Asn305Ile) c.392A>T (p.Asn131Ile) | |
| 11 | g.44265176T>C | CA380181800 | ALX4 | c.914A>G (p.Asn305Ser) c.392A>G (p.Asn131Ser) | |
| 11 | g.44265176T>G | CA380181799 | ALX4 | c.914A>C (p.Asn305Thr) c.392A>C (p.Asn131Thr) | dbSNP |
| 11 | g.44265176T= | CA1967915201 | ALX4 | c.914A= (p.Asn305=) c.392A= (p.Asn131=) | |
| 11 | g.44265177T>A | CA380181802 | ALX4 | c.913A>T (p.Asn305Tyr) c.391A>T (p.Asn131Tyr) | |
| 11 | g.44265177T>C | CA380181804 | ALX4 | c.913A>G (p.Asn305Asp) c.391A>G (p.Asn131Asp) | |
| 11 | g.44265177T>G | CA380181803 | ALX4 | c.913A>C (p.Asn305His) c.391A>C (p.Asn131His) | |
| 11 | g.44265178C>A | CA380181805 | ALX4 | c.912G>T (p.Gln304His) c.390G>T (p.Gln130His) | |
| 11 | g.44265178C>G | CA380181806 | ALX4 | c.912G>C (p.Gln304His) c.390G>C (p.Gln130His) | |
| 11 | g.44265178C>T | CA474035448 | ALX4 | c.912G>A (p.Gln304=) c.390G>A (p.Gln130=) | |
| 11 | g.44265179T>A | CA380181807 | ALX4 | c.911A>T (p.Gln304Leu) c.389A>T (p.Gln130Leu) | |
| 11 | g.44265179T>C | CA380181808 | ALX4 | c.911A>G (p.Gln304Arg) c.389A>G (p.Gln130Arg) | |
| 11 | g.44265179T>G | CA380181809 | ALX4 | c.911A>C (p.Gln304Pro) c.389A>C (p.Gln130Pro) | |
| 11 | g.44265180G>A | CA380181810 | ALX4 | c.910C>T (p.Gln304Ter) c.388C>T (p.Gln130Ter) | gnomAD v4 |
| 11 | g.44265180G>C | CA380181811 | ALX4 | c.910C>G (p.Gln304Glu) c.388C>G (p.Gln130Glu) | |
| 11 | g.44265180G>T | CA380181812 | ALX4 | c.910C>A (p.Gln304Lys) c.388C>A (p.Gln130Lys) | |
| 11 | g.44265181A>C | CA380181813 | ALX4 | c.909T>G (p.Ile303Met) c.387T>G (p.Ile129Met) | |
| 11 | g.44265181A>G | CA474035449 | ALX4 | c.909T>C (p.Ile303=) c.387T>C (p.Ile129=) | |
| 11 | g.44265181A>T | CA474035450 | ALX4 | c.909T>A (p.Ile303=) c.387T>A (p.Ile129=) | |
| 11 | g.44265182A>C | CA380181814 | ALX4 | c.908T>G (p.Ile303Ser) c.386T>G (p.Ile129Ser) | |
| 11 | g.44265182A>G | CA380181815 | ALX4 | c.908T>C (p.Ile303Thr) c.386T>C (p.Ile129Thr) | |
| 11 | g.44265182A>T | CA380181816 | ALX4 | c.908T>A (p.Ile303Asn) c.386T>A (p.Ile129Asn) | |
| 11 | g.44265183T>A | CA380181819 | ALX4 | c.907A>T (p.Ile303Phe) c.385A>T (p.Ile129Phe) | |
| 11 | g.44265183T>C | CA380181817 | ALX4 | c.907A>G (p.Ile303Val) c.385A>G (p.Ile129Val) | |
| 11 | g.44265183T>G | CA380181818 | ALX4 | c.907A>C (p.Ile303Leu) c.385A>C (p.Ile129Leu) | |
| 11 | g.44265184C>A | CA380181820 | ALX4 | c.907-1G>T (n.907-1G>T) c.385-1G>T (n.385-1G>T) | gnomAD v4 |
| 11 | g.44265184C= | CA1967915205 | ALX4 | c.907-1G= (n.907-1G=) c.385-1G= (n.385-1G=) | |
| 11 | g.44265184C>G | CA380181821 | ALX4 | c.907-1G>C (n.907-1G>C) c.385-1G>C (n.385-1G>C) | |
| 11 | g.44265184C>T | CA380181822 | ALX4 | c.907-1G>A (n.907-1G>A) c.385-1G>A (n.385-1G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.44265185T>A | CA380181823 | ALX4 | c.907-2A>T (n.907-2A>T) c.385-2A>T (n.385-2A>T) | gnomAD v4 |
| 11 | g.44265185T>C | CA380181824 | ALX4 | c.907-2A>G (n.907-2A>G) c.385-2A>G (n.385-2A>G) | |
| 11 | g.44265185T>G | CA380181825 | ALX4 | c.907-2A>C (n.907-2A>C) c.385-2A>C (n.385-2A>C) | |
| 11 | g.44265186G>T | CA2613210161 | ALX4 | c.907-3C>A (n.907-3C>A) c.385-3C>A (n.385-3C>A) | gnomAD v4 |
| 11 | g.44265187G>A | CA5955577 | ALX4 | c.907-4C>T (n.907-4C>T) c.385-4C>T (n.385-4C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44265187G>C | CA1967915211 | ALX4 | c.907-4C>G (n.907-4C>G) c.385-4C>G (n.385-4C>G) | dbSNP gnomAD v4 |
| 11 | g.44265187G= | CA1967915209 | ALX4 | c.907-4C= (n.907-4C=) c.385-4C= (n.385-4C=) | |
| 11 | g.44265187G>T | CA2613210168 | ALX4 | c.907-4C>A (n.907-4C>A) c.385-4C>A (n.385-4C>A) | gnomAD v4 |
| 11 | g.44265190G>A | CA1967915218 | ALX4 | c.907-7C>T (n.907-7C>T) c.385-7C>T (n.385-7C>T) | dbSNP gnomAD v4 |
| 11 | g.44265190G>C | CA676743534 | ALX4 | c.907-7C>G (n.907-7C>G) c.385-7C>G (n.385-7C>G) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.44265190G= | CA1967915215 | ALX4 | c.907-7C= (n.907-7C=) c.385-7C= (n.385-7C=) | |
| 11 | g.44265190_44265193del | CA2613210171 | ALX4 | c.907-10_907-7del (n.907-10_907-7del) c.385-10_385-7del (n.385-10_385-7del) | gnomAD v4 |
| 11 | g.44265191A= | CA1967915222 | ALX4 | c.907-8T= (n.907-8T=) c.385-8T= (n.385-8T=) | |
| 11 | g.44265191A>G | CA1967915223 | ALX4 | c.907-8T>C (n.907-8T>C) c.385-8T>C (n.385-8T>C) | dbSNP gnomAD v4 |
| 11 | g.44265192G>A | CA2613210175 | ALX4 | c.907-9C>T (n.907-9C>T) c.385-9C>T (n.385-9C>T) | gnomAD v4 |
| 11 | g.44265192G>C | CA2613210177 | ALX4 | c.907-9C>G (n.907-9C>G) c.385-9C>G (n.385-9C>G) | gnomAD v4 |
| 11 | g.44265192G>T | CA2613210178 | ALX4 | c.907-9C>A (n.907-9C>A) c.385-9C>A (n.385-9C>A) | gnomAD v4 |
| 11 | g.44265193G>A | CA2613210179 | ALX4 | c.907-10C>T (n.907-10C>T) c.385-10C>T (n.385-10C>T) | gnomAD v4 |
| 11 | g.44265193G>T | CA645590269 | ALX4 | c.907-10C>A (n.907-10C>A) c.385-10C>A (n.385-10C>A) | gnomAD v4 COSMIC |
| 11 | g.44265194A>G | CA2613210180 | ALX4 | c.907-11T>C (n.907-11T>C) c.385-11T>C (n.385-11T>C) | gnomAD v4 |
| 11 | g.44265195del | CA2574804022 | ALX4 | c.907-11del (n.907-11del) c.385-11del (n.385-11del) | |
| 11 | g.44265195A= | CA1967915227 | ALX4 | c.907-12T= (n.907-12T=) c.385-12T= (n.385-12T=) | |
| 11 | g.44265195A>G | CA598983469 | ALX4 | c.907-12T>C (n.907-12T>C) c.385-12T>C (n.385-12T>C) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.44265195A>T | CA2613210181 | ALX4 | c.907-12T>A (n.907-12T>A) c.385-12T>A (n.385-12T>A) | gnomAD v4 |
| 11 | g.44265196G>A | CA2574804023 | ALX4 | c.907-13C>T (n.907-13C>T) c.385-13C>T (n.385-13C>T) | gnomAD v4 |
| 11 | g.44265196G>T | CA2613210183 | ALX4 | c.907-13C>A (n.907-13C>A) c.385-13C>A (n.385-13C>A) | gnomAD v4 |
| 11 | g.44265197G>A | CA598983472 | ALX4 | c.907-14C>T (n.907-14C>T) c.385-14C>T (n.385-14C>T) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.44265197G= | CA1967915228 | ALX4 | c.907-14C= (n.907-14C=) c.385-14C= (n.385-14C=) | |
| 11 | g.44265198G>T | CA2613210185 | ALX4 | c.907-15C>A (n.907-15C>A) c.385-15C>A (n.385-15C>A) | gnomAD v4 |
| 11 | g.44265199A= | CA1967915229 | ALX4 | c.907-16T= (n.907-16T=) c.385-16T= (n.385-16T=) | |
| 11 | g.44265199A>G | CA1967915230 | ALX4 | c.907-16T>C (n.907-16T>C) c.385-16T>C (n.385-16T>C) | dbSNP gnomAD v4 |
| 11 | g.44265199A>T | CA2613210187 | ALX4 | c.907-16T>A (n.907-16T>A) c.385-16T>A (n.385-16T>A) | gnomAD v4 |
| 11 | g.44265200G>A | CA2613210188 | ALX4 | c.907-17C>T (n.907-17C>T) c.385-17C>T (n.385-17C>T) | gnomAD v4 |
| 11 | g.44265201A= | CA1967915231 | ALX4 | c.907-18T= (n.907-18T=) c.385-18T= (n.385-18T=) | |
| 11 | g.44265201A>G | CA5955578 | ALX4 | c.907-18T>C (n.907-18T>C) c.385-18T>C (n.385-18T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265203A>G | CA2613210190 | ALX4 | c.907-20T>C (n.907-20T>C) c.385-20T>C (n.385-20T>C) | gnomAD v4 |
| 11 | g.44265204T>C | CA2613210191 | ALX4 | c.907-21A>G (n.907-21A>G) c.385-21A>G (n.385-21A>G) | gnomAD v4 |
| 11 | g.44265204T>G | CA5955579 | ALX4 | c.907-21A>C (n.907-21A>C) c.385-21A>C (n.385-21A>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.44265204T= | CA1967915235 | ALX4 | c.907-21A= (n.907-21A=) c.385-21A= (n.385-21A=) | |
| 11 | g.44265206T>C | CA2613210194 | ALX4 | c.907-23A>G (n.907-23A>G) c.385-23A>G (n.385-23A>G) | gnomAD v4 |
| 11 | g.44265207C>A | CA2613210196 | ALX4 | c.907-24G>T (n.907-24G>T) c.385-24G>T (n.385-24G>T) | gnomAD v4 |
| 11 | g.44265208A= | CA1967915238 | ALX4 | c.907-25T= (n.907-25T=) c.385-25T= (n.385-25T=) | |
| 11 | g.44265208A>C | CA2791248880 | ALX4 | c.907-25T>G (n.907-25T>G) c.385-25T>G (n.385-25T>G) | |
| 11 | g.44265208A>T | CA598983475 | ALX4 | c.907-25T>A (n.907-25T>A) c.385-25T>A (n.385-25T>A) | dbSNP gnomAD v2 |
| 11 | g.44265209C>A | CA2613210197 | ALX4 | c.907-26G>T (n.907-26G>T) c.385-26G>T (n.385-26G>T) | gnomAD v4 |
| 11 | g.44265209C= | CA1967915241 | ALX4 | c.907-26G= (n.907-26G=) c.385-26G= (n.385-26G=) | |
| 11 | g.44265209C>G | CA676743544 | ALX4 | c.907-26G>C (n.907-26G>C) c.385-26G>C (n.385-26G>C) | dbSNP |
| 11 | g.44265209C>T | CA1967915245 | ALX4 | c.907-26G>A (n.907-26G>A) c.385-26G>A (n.385-26G>A) | dbSNP gnomAD v4 |
| 11 | g.44265210C>A | CA598983478 | ALX4 | c.907-27G>T (n.907-27G>T) c.385-27G>T (n.385-27G>T) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.44265210C= | CA1967915249 | ALX4 | c.907-27G= (n.907-27G=) c.385-27G= (n.385-27G=) | |
| 11 | g.44265210C>G | CA598983480 | ALX4 | c.907-27G>C (n.907-27G>C) c.385-27G>C (n.385-27G>C) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.44265210C>T | CA5955580 | ALX4 | c.907-27G>A (n.907-27G>A) c.385-27G>A (n.385-27G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.44265211G>A | CA5955581 | ALX4 | c.907-28C>T (n.907-28C>T) c.385-28C>T (n.385-28C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.44265211G>C | CA2791248881 | ALX4 | c.907-28C>G (n.907-28C>G) c.385-28C>G (n.385-28C>G) | |
| 11 | g.44265211G= | CA1967915254 | ALX4 | c.907-28C= (n.907-28C=) c.385-28C= (n.385-28C=) | |
| 11 | g.44265211G>T | CA598983486 | ALX4 | c.907-28C>A (n.907-28C>A) c.385-28C>A (n.385-28C>A) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.44265211_44265212insACA | CA5955582 | ALX4 | c.907-29_907-28insTGT (n.907-29_907-28insTGT) c.385-29_385-28insTGT (n.385-29_385-28insTGT) | dbSNP ExAC gnomAD v2 |
| 11 | g.44265212G>A | CA2613210207 | ALX4 | c.907-29C>T (n.907-29C>T) c.385-29C>T (n.385-29C>T) | gnomAD v4 |
| 11 | g.44265212G= | CA1967915263 | ALX4 | c.907-29C= (n.907-29C=) c.385-29C= (n.385-29C=) | |
| 11 | g.44265212G>T | CA5955583 | ALX4 | c.907-29C>A (n.907-29C>A) c.385-29C>A (n.385-29C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |