Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.32434808_32434821del | CA658658039 | WT1 | c.543_556del (p.Tyr182SerfsTer17) c.528_541del (p.Tyr177SerfsTer17) n.722_735del | ClinVar dbSNP |
11 | g.32434819C>A | CA379964721 | WT1 | c.542G>T (p.Arg181Leu) c.527G>T (p.Arg176Leu) n.721G>T | |
11 | g.32434819C= | CA1962327156 | WT1 | c.542G= (p.Arg181=) c.527G= (p.Arg176=) n.721G= | |
11 | g.32434819C>G | CA379964720 | WT1 | c.542G>C (p.Arg181Pro) c.527G>C (p.Arg176Pro) n.721G>C | ClinVar dbSNP gnomAD v4 |
11 | g.32434819C>T | CA379964723 | WT1 | c.542G>A (p.Arg181His) c.527G>A (p.Arg176His) n.721G>A | dbSNP gnomAD v4 |
11 | g.32434820del | CA473571444 | WT1 | c.541del (p.Arg181AlafsTer?) c.526del (p.Arg176AlafsTer?) n.720del | COSMIC |
11 | g.32434820G>A | CA379964724 | WT1 | c.541C>T (p.Arg181Cys) c.526C>T (p.Arg176Cys) n.720C>T | COSMIC COSMIC |
11 | g.32434820G>C | CA379964726 | WT1 | c.541C>G (p.Arg181Gly) c.526C>G (p.Arg176Gly) n.720C>G | ClinVar gnomAD v4 |
11 | g.32434820G= | CA1962327157 | WT1 | c.541C= (p.Arg181=) c.526C= (p.Arg176=) n.720C= | |
11 | g.32434820G>T | CA379964728 | WT1 | c.541C>A (p.Arg181Ser) c.526C>A (p.Arg176Ser) n.720C>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
11 | g.32434821A>C | CA379964729 | WT1 | c.540T>G (p.Cys180Trp) c.525T>G (p.Cys175Trp) n.719T>G | |
11 | g.32434821A>G | CA473571449 | WT1 | c.540T>C (p.Cys180=) c.525T>C (p.Cys175=) n.719T>C | |
11 | g.32434821A>T | CA379964730 | WT1 | c.540T>A (p.Cys180Ter) c.525T>A (p.Cys175Ter) n.719T>A | dbSNP |
11 | g.32434822C>A | CA379964732 | WT1 | c.539G>T (p.Cys180Phe) c.524G>T (p.Cys175Phe) n.718G>T | |
11 | g.32434822C>G | CA379964734 | WT1 | c.539G>C (p.Cys180Ser) c.524G>C (p.Cys175Ser) n.718G>C | dbSNP |
11 | g.32434822C>T | CA379964735 | WT1 | c.539G>A (p.Cys180Tyr) c.524G>A (p.Cys175Tyr) n.718G>A | ClinVar |
11 | g.32434823A>C | CA379964736 | WT1 | c.538T>G (p.Cys180Gly) c.523T>G (p.Cys175Gly) n.717T>G | |
11 | g.32434823A>G | CA379964738 | WT1 | c.538T>C (p.Cys180Arg) c.523T>C (p.Cys175Arg) n.717T>C | |
11 | g.32434823A>T | CA379964739 | WT1 | c.538T>A (p.Cys180Ser) c.523T>A (p.Cys175Ser) n.717T>A | COSMIC |
11 | g.32434824G>A | CA473571462 | WT1 | c.537C>T (p.Ala179=) c.522C>T (p.Ala174=) n.716C>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434824G>C | CA473571463 | WT1 | c.537C>G (p.Ala179=) c.522C>G (p.Ala174=) n.716C>G | ClinVar |
11 | g.32434824G= | CA1962327158 | WT1 | c.537C= (p.Ala179=) c.522C= (p.Ala174=) n.716C= | |
11 | g.32434824G>T | CA473571465 | WT1 | c.537C>A (p.Ala179=) c.522C>A (p.Ala174=) n.716C>A | gnomAD v4 |
11 | g.32434825G>A | CA379964743 | WT1 | c.536C>T (p.Ala179Val) c.521C>T (p.Ala174Val) n.715C>T | dbSNP |
11 | g.32434825G>C | CA379964742 | WT1 | c.536C>G (p.Ala179Gly) c.521C>G (p.Ala174Gly) n.715C>G | |
11 | g.32434825G>T | CA379964741 | WT1 | c.536C>A (p.Ala179Asp) c.521C>A (p.Ala174Asp) n.715C>A | |
11 | g.32434826C>A | CA379964745 | WT1 | c.535G>T (p.Ala179Ser) c.520G>T (p.Ala174Ser) n.714G>T | |
11 | g.32434826C>G | CA379964747 | WT1 | c.535G>C (p.Ala179Pro) c.520G>C (p.Ala174Pro) n.714G>C | gnomAD v4 |
11 | g.32434826C>T | CA379964748 | WT1 | c.535G>A (p.Ala179Thr) c.520G>A (p.Ala174Thr) n.714G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434827T>A | CA473571476 | WT1 | c.534A>T (p.Gly178=) c.519A>T (p.Gly173=) n.713A>T | dbSNP |
11 | g.32434827T>C | CA473571475 | WT1 | c.534A>G (p.Gly178=) c.519A>G (p.Gly173=) n.713A>G | ClinVar |
11 | g.32434827T>G | CA473571473 | WT1 | c.534A>C (p.Gly178=) c.519A>C (p.Gly173=) n.713A>C | |
11 | g.32434828C>A | CA379964750 | WT1 | c.533G>T (p.Gly178Val) c.518G>T (p.Gly173Val) n.712G>T | |
11 | g.32434828C>G | CA379964751 | WT1 | c.533G>C (p.Gly178Ala) c.518G>C (p.Gly173Ala) n.712G>C | |
11 | g.32434828C>T | CA379964753 | WT1 | c.533G>A (p.Gly178Glu) c.518G>A (p.Gly173Glu) n.712G>A | ClinVar gnomAD v4 |
11 | g.32434829C>A | CA379964755 | WT1 | c.532G>T (p.Gly178Ter) c.517G>T (p.Gly173Ter) n.711G>T | |
11 | g.32434829C>G | CA379964756 | WT1 | c.532G>C (p.Gly178Arg) c.517G>C (p.Gly173Arg) n.711G>C | dbSNP |
11 | g.32434829C>T | CA379964758 | WT1 | c.532G>A (p.Gly178Arg) c.517G>A (p.Gly173Arg) n.711G>A | ClinVar dbSNP COSMIC |
11 | g.32434830G>A | CA473571491 | WT1 | c.531C>T (p.Ala177=) c.516C>T (p.Ala172=) n.710C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434830G>C | CA473571486 | WT1 | c.531C>G (p.Ala177=) c.516C>G (p.Ala172=) n.710C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32434830G= | CA1962327159 | WT1 | c.531C= (p.Ala177=) c.516C= (p.Ala172=) n.710C= | |
11 | g.32434830G>T | CA473571484 | WT1 | c.531C>A (p.Ala177=) c.516C>A (p.Ala172=) n.710C>A | |
11 | g.32434831G>A | CA379964759 | WT1 | c.530C>T (p.Ala177Val) c.515C>T (p.Ala172Val) n.709C>T | dbSNP gnomAD v4 |
11 | g.32434831G>C | CA379964760 | WT1 | c.530C>G (p.Ala177Gly) c.515C>G (p.Ala172Gly) n.709C>G | |
11 | g.32434831G>T | CA379964762 | WT1 | c.530C>A (p.Ala177Asp) c.515C>A (p.Ala172Asp) n.709C>A | ClinVar |
11 | g.32434832C>A | CA379964765 | WT1 | c.529G>T (p.Ala177Ser) c.514G>T (p.Ala172Ser) n.708G>T | ClinVar dbSNP |
11 | g.32434832C= | CA1962327160 | WT1 | c.529G= (p.Ala177=) c.514G= (p.Ala172=) n.708G= | |
11 | g.32434832C>G | CA379964766 | WT1 | c.529G>C (p.Ala177Pro) c.514G>C (p.Ala172Pro) n.708G>C | |
11 | g.32434832C>T | CA379964764 | WT1 | c.529G>A (p.Ala177Thr) c.514G>A (p.Ala172Thr) n.708G>A | dbSNP |
11 | g.32434833del | CA473571504 | WT1 | c.528del (p.Ala177ProfsTer?) c.513del (p.Ala172ProfsTer?) n.707del | COSMIC |
11 | g.32434833T>A | CA473571507 | WT1 | c.528A>T (p.Thr176=) c.513A>T (p.Thr171=) n.707A>T | |
11 | g.32434833T>C | CA473571501 | WT1 | c.528A>G (p.Thr176=) c.513A>G (p.Thr171=) n.707A>G | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434833T>G | CA473571506 | WT1 | c.528A>C (p.Thr176=) c.513A>C (p.Thr171=) n.707A>C | |
11 | g.32434833T= | CA1962327161 | WT1 | c.528A= (p.Thr176=) c.513A= (p.Thr171=) n.707A= | |
11 | g.32434834G>A | CA379964768 | WT1 | c.527C>T (p.Thr176Ile) c.512C>T (p.Thr171Ile) n.706C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434834G>C | CA379964769 | WT1 | c.527C>G (p.Thr176Arg) c.512C>G (p.Thr171Arg) n.706C>G | gnomAD v4 |
11 | g.32434834G= | CA1962327162 | WT1 | c.527C= (p.Thr176=) c.512C= (p.Thr171=) n.706C= | |
11 | g.32434834G>T | CA379964771 | WT1 | c.527C>A (p.Thr176Lys) c.512C>A (p.Thr171Lys) n.706C>A | |
11 | g.32434835T>A | CA379964773 | WT1 | c.526A>T (p.Thr176Ser) c.511A>T (p.Thr171Ser) n.705A>T | dbSNP |
11 | g.32434835T>C | CA379964774 | WT1 | c.526A>G (p.Thr176Ala) c.511A>G (p.Thr171Ala) n.705A>G | |
11 | g.32434835T>G | CA379964776 | WT1 | c.526A>C (p.Thr176Pro) c.511A>C (p.Thr171Pro) n.705A>C | dbSNP |
11 | g.32434836G>A | CA473571523 | WT1 | c.525C>T (p.Gly175=) c.510C>T (p.Gly170=) n.704C>T | gnomAD v4 COSMIC COSMIC |
11 | g.32434836G>C | CA473571524 | WT1 | c.525C>G (p.Gly175=) c.510C>G (p.Gly170=) n.704C>G | COSMIC COSMIC |
11 | g.32434836G>T | CA473571526 | WT1 | c.525C>A (p.Gly175=) c.510C>A (p.Gly170=) n.704C>A | gnomAD v4 |
11 | g.32434837C>A | CA379964777 | WT1 | c.524G>T (p.Gly175Val) c.509G>T (p.Gly170Val) n.703G>T | |
11 | g.32434837C= | CA1962327163 | WT1 | c.524G= (p.Gly175=) c.509G= (p.Gly170=) n.703G= | |
11 | g.32434837C>G | CA379964779 | WT1 | c.524G>C (p.Gly175Ala) c.509G>C (p.Gly170Ala) n.703G>C | |
11 | g.32434837C>T | CA379964781 | WT1 | c.524G>A (p.Gly175Asp) c.509G>A (p.Gly170Asp) n.703G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434838C>A | CA379964782 | WT1 | c.523G>T (p.Gly175Cys) c.508G>T (p.Gly170Cys) n.702G>T | ClinVar dbSNP |
11 | g.32434838C= | CA1962327164 | WT1 | c.523G= (p.Gly175=) c.508G= (p.Gly170=) n.702G= | |
11 | g.32434838C>G | CA379964783 | WT1 | c.523G>C (p.Gly175Arg) c.508G>C (p.Gly170Arg) n.702G>C | |
11 | g.32434838C>T | CA379964784 | WT1 | c.523G>A (p.Gly175Ser) c.508G>A (p.Gly170Ser) n.702G>A | |
11 | g.32434839A= | CA1962327165 | WT1 | c.522T= (p.Thr174=) c.507T= (p.Thr169=) n.701T= | |
11 | g.32434839A>C | CA473571533 | WT1 | c.522T>G (p.Thr174=) c.507T>G (p.Thr169=) n.701T>G | ClinVar |
11 | g.32434839A>G | CA065022 | WT1 | c.522T>C (p.Thr174=) c.507T>C (p.Thr169=) n.701T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32434839A>T | CA473571538 | WT1 | c.522T>A (p.Thr174=) c.507T>A (p.Thr169=) n.701T>A | |
11 | g.32434840G>A | CA379964789 | WT1 | c.521C>T (p.Thr174Ile) c.506C>T (p.Thr169Ile) n.700C>T | |
11 | g.32434840G>C | CA379964788 | WT1 | c.521C>G (p.Thr174Ser) c.506C>G (p.Thr169Ser) n.700C>G | |
11 | g.32434840G>T | CA379964787 | WT1 | c.521C>A (p.Thr174Asn) c.506C>A (p.Thr169Asn) n.700C>A | |
11 | g.32434841T>A | CA379964791 | WT1 | c.520A>T (p.Thr174Ser) c.505A>T (p.Thr169Ser) n.699A>T | |
11 | g.32434841T>C | CA379964793 | WT1 | c.520A>G (p.Thr174Ala) c.505A>G (p.Thr169Ala) n.699A>G | ClinVar dbSNP gnomAD v4 |
11 | g.32434841T>G | CA219510924 | WT1 | c.520A>C (p.Thr174Pro) c.505A>C (p.Thr169Pro) n.699A>C | dbSNP |
11 | g.32434841T= | CA1962327166 | WT1 | c.520A= (p.Thr174=) c.505A= (p.Thr169=) n.699A= | |
11 | g.32434841_32434842insAGC | CA2612989398 | WT1 | c.519_520insGCT (p.Phe173_Thr174insAla) c.504_505insGCT (p.Phe168_Thr169insAla) n.698_699insGCT | gnomAD v4 |
11 | g.32434842G>A | CA473571543 | WT1 | c.519C>T (p.Phe173=) c.504C>T (p.Phe168=) n.698C>T | |
11 | g.32434842G>C | CA379964795 | WT1 | c.519C>G (p.Phe173Leu) c.504C>G (p.Phe168Leu) n.698C>G | |
11 | g.32434842G>T | CA379964796 | WT1 | c.519C>A (p.Phe173Leu) c.504C>A (p.Phe168Leu) n.698C>A | ClinVar |
11 | g.32434843A>C | CA379964798 | WT1 | c.518T>G (p.Phe173Cys) c.503T>G (p.Phe168Cys) n.697T>G | |
11 | g.32434843A>G | CA379964800 | WT1 | c.518T>C (p.Phe173Ser) c.503T>C (p.Phe168Ser) n.697T>C | |
11 | g.32434843A>T | CA379964802 | WT1 | c.518T>A (p.Phe173Tyr) c.503T>A (p.Phe168Tyr) n.697T>A | |
11 | g.32434843_32434844insC | CA2612989399 | WT1 | c.517_518insG (p.Phe173CysfsTer?) c.502_503insG (p.Phe168CysfsTer?) n.696_697insG | gnomAD v4 |
11 | g.32434844A>C | CA379964803 | WT1 | c.517T>G (p.Phe173Val) c.502T>G (p.Phe168Val) n.696T>G | |
11 | g.32434844A>G | CA379964804 | WT1 | c.517T>C (p.Phe173Leu) c.502T>C (p.Phe168Leu) n.696T>C | |
11 | g.32434844A>T | CA379964805 | WT1 | c.517T>A (p.Phe173Ile) c.502T>A (p.Phe168Ile) n.696T>A | |
11 | g.32434844_32434845insGG | CA2612989400 | WT1 | c.516_517insCC (p.Phe173ProfsTer?) c.501_502insCC (p.Phe168ProfsTer?) n.695_696insCC | gnomAD v4 |
11 | g.32434845C>A | CA379964806 | WT1 | c.516G>T (p.Gln172His) c.501G>T (p.Gln167His) n.695G>T | |
11 | g.32434845C>G | CA379964807 | WT1 | c.516G>C (p.Gln172His) c.501G>C (p.Gln167His) n.695G>C | gnomAD v4 |
11 | g.32434845C>T | CA473571559 | WT1 | c.516G>A (p.Gln172=) c.501G>A (p.Gln167=) n.695G>A | |
11 | g.32434846T>A | CA379964809 | WT1 | c.515A>T (p.Gln172Leu) c.500A>T (p.Gln167Leu) n.694A>T | |
11 | g.32434846T>C | CA379964812 | WT1 | c.515A>G (p.Gln172Arg) c.500A>G (p.Gln167Arg) n.694A>G | |
11 | g.32434846T>G | CA379964810 | WT1 | c.515A>C (p.Gln172Pro) c.500A>C (p.Gln167Pro) n.694A>C | |
11 | g.32434846_32434847insCC | CA2612989401 | WT1 | c.514_515insGG (p.Gln172ArgfsTer?) c.499_500insGG (p.Gln167ArgfsTer?) n.693_694insGG | gnomAD v4 |
11 | g.32434847G>A | CA379964814 | WT1 | c.514C>T (p.Gln172Ter) c.499C>T (p.Gln167Ter) n.693C>T | ClinVar |
11 | g.32434847G>C | CA379964815 | WT1 | c.514C>G (p.Gln172Glu) c.499C>G (p.Gln167Glu) n.693C>G | |
11 | g.32434847G>T | CA379964816 | WT1 | c.514C>A (p.Gln172Lys) c.499C>A (p.Gln167Lys) n.693C>A | |
11 | g.32434848del | CA2580084154 | WT1 | c.514del (p.Gln172SerfsTer?) c.499del (p.Gln167SerfsTer?) n.693del | ClinVar dbSNP |
11 | g.32434848G>A | CA473571566 | WT1 | c.513C>T (p.Gly171=) c.498C>T (p.Gly166=) n.692C>T | ClinVar dbSNP |
11 | g.32434848G>C | CA473571568 | WT1 | c.513C>G (p.Gly171=) c.498C>G (p.Gly166=) n.692C>G | |
11 | g.32434848G= | CA1962327167 | WT1 | c.513C= (p.Gly171=) c.498C= (p.Gly166=) n.692C= | |
11 | g.32434848G>T | CA065010 | WT1 | c.513C>A (p.Gly171=) c.498C>A (p.Gly166=) n.692C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434849C>A | CA379964820 | WT1 | c.512G>T (p.Gly171Val) c.497G>T (p.Gly166Val) n.691G>T | ClinVar dbSNP |
11 | g.32434849C= | CA1962327168 | WT1 | c.512G= (p.Gly171=) c.497G= (p.Gly166=) n.691G= | |
11 | g.32434849C>G | CA379964821 | WT1 | c.512G>C (p.Gly171Ala) c.497G>C (p.Gly166Ala) n.691G>C | |
11 | g.32434849C>T | CA379964822 | WT1 | c.512G>A (p.Gly171Asp) c.497G>A (p.Gly166Asp) n.691G>A | gnomAD v4 |
11 | g.32434850C>A | CA379964824 | WT1 | c.511G>T (p.Gly171Cys) c.496G>T (p.Gly166Cys) n.690G>T | |
11 | g.32434850C>G | CA379964828 | WT1 | c.511G>C (p.Gly171Arg) c.496G>C (p.Gly166Arg) n.690G>C | ClinVar dbSNP |
11 | g.32434850C>T | CA379964826 | WT1 | c.511G>A (p.Gly171Ser) c.496G>A (p.Gly166Ser) n.690G>A | dbSNP |
11 | g.32434850_32434854delinsACAGTG | CA2580084156 | WT1 | c.507_511delinsCACTGT (p.Ser170ThrfsTer?) c.492_496delinsCACTGT (p.Ser165ThrfsTer?) n.686_690delinsCACTGT | ClinVar |
11 | g.32434851G>A | CA065003 | WT1 | c.510C>T (p.Ser170=) c.495C>T (p.Ser165=) n.689C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
11 | g.32434851G>C | CA473571577 | WT1 | c.510C>G (p.Ser170=) c.495C>G (p.Ser165=) n.689C>G | ClinVar dbSNP |
11 | g.32434851G= | CA1962327169 | WT1 | c.510C= (p.Ser170=) c.495C= (p.Ser165=) n.689C= | |
11 | g.32434851G>T | CA473571578 | WT1 | c.510C>A (p.Ser170=) c.495C>A (p.Ser165=) n.689C>A | gnomAD v4 |
11 | g.32434852G>A | CA379964830 | WT1 | c.509C>T (p.Ser170Phe) c.494C>T (p.Ser165Phe) n.688C>T | COSMIC COSMIC |
11 | g.32434852G>C | CA379964831 | WT1 | c.509C>G (p.Ser170Cys) c.494C>G (p.Ser165Cys) n.688C>G | |
11 | g.32434852G>T | CA379964832 | WT1 | c.509C>A (p.Ser170Tyr) c.494C>A (p.Ser165Tyr) n.688C>A | |
11 | g.32434853A>C | CA379964837 | WT1 | c.508T>G (p.Ser170Ala) c.493T>G (p.Ser165Ala) n.687T>G | |
11 | g.32434853A>G | CA379964834 | WT1 | c.508T>C (p.Ser170Pro) c.493T>C (p.Ser165Pro) n.687T>C | |
11 | g.32434853A>T | CA379964835 | WT1 | c.508T>A (p.Ser170Thr) c.493T>A (p.Ser165Thr) n.687T>A | |
11 | g.32434854A>C | CA379964839 | WT1 | c.507T>G (p.Phe169Leu) c.492T>G (p.Phe164Leu) n.686T>G | |
11 | g.32434854A>G | CA473571585 | WT1 | c.507T>C (p.Phe169=) c.492T>C (p.Phe164=) n.686T>C | |
11 | g.32434854A>T | CA379964841 | WT1 | c.507T>A (p.Phe169Leu) c.492T>A (p.Phe164Leu) n.686T>A | |
11 | g.32434855A>C | CA379964842 | WT1 | c.506T>G (p.Phe169Cys) c.491T>G (p.Phe164Cys) n.685T>G | |
11 | g.32434855A>G | CA379964844 | WT1 | c.506T>C (p.Phe169Ser) c.491T>C (p.Phe164Ser) n.685T>C | ClinVar |
11 | g.32434855A>T | CA379964845 | WT1 | c.506T>A (p.Phe169Tyr) c.491T>A (p.Phe164Tyr) n.685T>A | |
11 | g.32434856A>C | CA379964847 | WT1 | c.505T>G (p.Phe169Val) c.490T>G (p.Phe164Val) n.684T>G | |
11 | g.32434856A>G | CA379964848 | WT1 | c.505T>C (p.Phe169Leu) c.490T>C (p.Phe164Leu) n.684T>C | ClinVar dbSNP |
11 | g.32434856A>T | CA379964850 | WT1 | c.505T>A (p.Phe169Ile) c.490T>A (p.Phe164Ile) n.684T>A | |
11 | g.32434857G>A | CA473571593 | WT1 | c.504C>T (p.His168=) c.489C>T (p.His163=) n.683C>T | |
11 | g.32434857G>C | CA379964851 | WT1 | c.504C>G (p.His168Gln) c.489C>G (p.His163Gln) n.683C>G | |
11 | g.32434857G>T | CA379964853 | WT1 | c.504C>A (p.His168Gln) c.489C>A (p.His163Gln) n.683C>A | |
11 | g.32434858T>A | CA379964855 | WT1 | c.503A>T (p.His168Leu) c.488A>T (p.His163Leu) n.682A>T | dbSNP |
11 | g.32434858T>C | CA064994 | WT1 | c.503A>G (p.His168Arg) c.488A>G (p.His163Arg) n.682A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32434858T>G | CA379964857 | WT1 | c.503A>C (p.His168Pro) c.488A>C (p.His163Pro) n.682A>C | |
11 | g.32434858T= | CA1962327170 | WT1 | c.503A= (p.His168=) c.488A= (p.His163=) n.682A= | |
11 | g.32434859G>A | CA379964862 | WT1 | c.502C>T (p.His168Tyr) c.487C>T (p.His163Tyr) n.681C>T | gnomAD v4 |
11 | g.32434859G>C | CA379964859 | WT1 | c.502C>G (p.His168Asp) c.487C>G (p.His163Asp) n.681C>G | |
11 | g.32434859G>T | CA379964860 | WT1 | c.502C>A (p.His168Asn) c.487C>A (p.His163Asn) n.681C>A | |
11 | g.32434860G>A | CA473571604 | WT1 | c.501C>T (p.Val167=) c.486C>T (p.Val162=) n.680C>T | |
11 | g.32434860G>C | CA473571607 | WT1 | c.501C>G (p.Val167=) c.486C>G (p.Val162=) n.680C>G | dbSNP |
11 | g.32434860G>T | CA473571605 | WT1 | c.501C>A (p.Val167=) c.486C>A (p.Val162=) n.680C>A | |
11 | g.32434861A= | CA1962327171 | WT1 | c.500T= (p.Val167=) c.485T= (p.Val162=) n.679T= | |
11 | g.32434861A>C | CA379964864 | WT1 | c.500T>G (p.Val167Gly) c.485T>G (p.Val162Gly) n.679T>G | |
11 | g.32434861A>G | CA379964865 | WT1 | c.500T>C (p.Val167Ala) c.485T>C (p.Val162Ala) n.679T>C | ClinVar |
11 | g.32434861A>T | CA379964866 | WT1 | c.500T>A (p.Val167Asp) c.485T>A (p.Val162Asp) n.679T>A | ClinVar dbSNP |
11 | g.32434862_32434863del | CA2695213674 | WT1 | c.499_500del (p.Val167ProfsTer?) c.484_485del (p.Val162ProfsTer?) n.678_679del | |
11 | g.32434862C>A | CA379964868 | WT1 | c.499G>T (p.Val167Phe) c.484G>T (p.Val162Phe) n.678G>T | |
11 | g.32434862C= | CA1962327172 | WT1 | c.499G= (p.Val167=) c.484G= (p.Val162=) n.678G= | |
11 | g.32434862C>G | CA379964870 | WT1 | c.499G>C (p.Val167Leu) c.484G>C (p.Val162Leu) n.678G>C | dbSNP |
11 | g.32434862C>T | CA379964871 | WT1 | c.499G>A (p.Val167Ile) c.484G>A (p.Val162Ile) n.678G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434863A= | CA1962327173 | WT1 | c.498T= (p.Thr166=) c.483T= (p.Thr161=) n.677T= | |
11 | g.32434863A>C | CA473571616 | WT1 | c.498T>G (p.Thr166=) c.483T>G (p.Thr161=) n.677T>G | |
11 | g.32434863A>G | CA473571619 | WT1 | c.498T>C (p.Thr166=) c.483T>C (p.Thr161=) n.677T>C | ClinVar dbSNP |
11 | g.32434863A>T | CA473571623 | WT1 | c.498T>A (p.Thr166=) c.483T>A (p.Thr161=) n.677T>A | |
11 | g.32434864G>A | CA379964875 | WT1 | c.497C>T (p.Thr166Ile) c.482C>T (p.Thr161Ile) n.676C>T | dbSNP |
11 | g.32434864G>C | CA379964872 | WT1 | c.497C>G (p.Thr166Ser) c.482C>G (p.Thr161Ser) n.676C>G | ClinVar |
11 | g.32434864G>T | CA379964873 | WT1 | c.497C>A (p.Thr166Asn) c.482C>A (p.Thr161Asn) n.676C>A | |
11 | g.32434865T>A | CA379964878 | WT1 | c.496A>T (p.Thr166Ser) c.481A>T (p.Thr161Ser) n.675A>T | |
11 | g.32434865T>C | CA379964879 | WT1 | c.496A>G (p.Thr166Ala) c.481A>G (p.Thr161Ala) n.675A>G | ClinVar dbSNP |
11 | g.32434865T>G | CA379964880 | WT1 | c.496A>C (p.Thr166Pro) c.481A>C (p.Thr161Pro) n.675A>C | |
11 | g.32434865T= | CA1962327174 | WT1 | c.496A= (p.Thr166=) c.481A= (p.Thr161=) n.675A= | |
11 | g.32434866G>A | CA473571631 | WT1 | c.495C>T (p.Phe165=) c.480C>T (p.Phe160=) n.674C>T | |
11 | g.32434866G>C | CA379964882 | WT1 | c.495C>G (p.Phe165Leu) c.480C>G (p.Phe160Leu) n.674C>G | |
11 | g.32434866G>T | CA379964883 | WT1 | c.495C>A (p.Phe165Leu) c.480C>A (p.Phe160Leu) n.674C>A | |
11 | g.32434867A>C | CA379964885 | WT1 | c.494T>G (p.Phe165Cys) c.479T>G (p.Phe160Cys) n.673T>G | |
11 | g.32434867A>G | CA379964888 | WT1 | c.494T>C (p.Phe165Ser) c.479T>C (p.Phe160Ser) n.673T>C | dbSNP |
11 | g.32434867A>T | CA379964886 | WT1 | c.494T>A (p.Phe165Tyr) c.479T>A (p.Phe160Tyr) n.673T>A | |
11 | g.32434868A>C | CA379964890 | WT1 | c.493T>G (p.Phe165Val) c.478T>G (p.Phe160Val) n.672T>G | |
11 | g.32434868A>G | CA379964892 | WT1 | c.493T>C (p.Phe165Leu) c.478T>C (p.Phe160Leu) n.672T>C | gnomAD v4 |
11 | g.32434868A>T | CA379964893 | WT1 | c.493T>A (p.Phe165Ile) c.478T>A (p.Phe160Ile) n.672T>A | |
11 | g.32434869G>A | CA473571639 | WT1 | c.492C>T (p.Ala164=) c.477C>T (p.Ala159=) n.671C>T | |
11 | g.32434869G>C | CA473571645 | WT1 | c.492C>G (p.Ala164=) c.477C>G (p.Ala159=) n.671C>G | dbSNP |
11 | g.32434869G>T | CA473571647 | WT1 | c.492C>A (p.Ala164=) c.477C>A (p.Ala159=) n.671C>A | |
11 | g.32434870G>A | CA379964895 | WT1 | c.491C>T (p.Ala164Val) c.476C>T (p.Ala159Val) n.670C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434870G>C | CA379964896 | WT1 | c.491C>G (p.Ala164Gly) c.476C>G (p.Ala159Gly) n.670C>G | |
11 | g.32434870G= | CA1962327175 | WT1 | c.491C= (p.Ala164=) c.476C= (p.Ala159=) n.670C= | |
11 | g.32434870G>T | CA379964898 | WT1 | c.491C>A (p.Ala164Asp) c.476C>A (p.Ala159Asp) n.670C>A | |
11 | g.32434871C>A | CA219510930 | WT1 | c.490G>T (p.Ala164Ser) c.475G>T (p.Ala159Ser) n.669G>T | dbSNP gnomAD v4 |
11 | g.32434871C= | CA1962327176 | WT1 | c.490G= (p.Ala164=) c.475G= (p.Ala159=) n.669G= | |
11 | g.32434871C>G | CA379964899 | WT1 | c.490G>C (p.Ala164Pro) c.475G>C (p.Ala159Pro) n.669G>C | ClinVar dbSNP |
11 | g.32434871C>T | CA379964900 | WT1 | c.490G>A (p.Ala164Thr) c.475G>A (p.Ala159Thr) n.669G>A | dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434872G>A | CA219510935 | WT1 | c.489C>T (p.Ser163=) c.474C>T (p.Ser158=) n.668C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434872G>C | CA379964901 | WT1 | c.489C>G (p.Ser163Arg) c.474C>G (p.Ser158Arg) n.668C>G | ClinVar |
11 | g.32434872G= | CA1962327177 | WT1 | c.489C= (p.Ser163=) c.474C= (p.Ser158=) n.668C= | |
11 | g.32434872G>T | CA379964903 | WT1 | c.489C>A (p.Ser163Arg) c.474C>A (p.Ser158Arg) n.668C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434873C>A | CA379964905 | WT1 | c.488G>T (p.Ser163Ile) c.473G>T (p.Ser158Ile) n.667G>T | |
11 | g.32434873C= | CA1962327178 | WT1 | c.488G= (p.Ser163=) c.473G= (p.Ser158=) n.667G= | |
11 | g.32434873C>G | CA379964907 | WT1 | c.488G>C (p.Ser163Thr) c.473G>C (p.Ser158Thr) n.667G>C | dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434873C>T | CA379964906 | WT1 | c.488G>A (p.Ser163Asn) c.473G>A (p.Ser158Asn) n.667G>A | ClinVar dbSNP |
11 | g.32434874T>A | CA379964909 | WT1 | c.487A>T (p.Ser163Cys) c.472A>T (p.Ser158Cys) n.666A>T | |
11 | g.32434874T>C | CA379964911 | WT1 | c.487A>G (p.Ser163Gly) c.472A>G (p.Ser158Gly) n.666A>G | dbSNP |
11 | g.32434874T>G | CA379964913 | WT1 | c.487A>C (p.Ser163Arg) c.472A>C (p.Ser158Arg) n.666A>C | |
11 | g.32434875C>A | CA473571666 | WT1 | c.486G>T (p.Leu162=) c.471G>T (p.Leu157=) n.665G>T | dbSNP |
11 | g.32434875C= | CA1962327179 | WT1 | c.486G= (p.Leu162=) c.471G= (p.Leu157=) n.665G= | |
11 | g.32434875C>G | CA473571667 | WT1 | c.486G>C (p.Leu162=) c.471G>C (p.Leu157=) n.665G>C | |
11 | g.32434875C>T | CA473571668 | WT1 | c.486G>A (p.Leu162=) c.471G>A (p.Leu157=) n.665G>A | |
11 | g.32434878_32434911del | CA645584483 | WT1 | c.453_486del (p.Trp151Ter) c.438_471del (p.Trp146Ter) n.632_665del | COSMIC |
11 | g.32434876A>C | CA379964914 | WT1 | c.485T>G (p.Leu162Arg) c.470T>G (p.Leu157Arg) n.664T>G | gnomAD v4 |
11 | g.32434876A>G | CA379964915 | WT1 | c.485T>C (p.Leu162Pro) c.470T>C (p.Leu157Pro) n.664T>C | gnomAD v4 |
11 | g.32434876A>T | CA379964917 | WT1 | c.485T>A (p.Leu162Gln) c.470T>A (p.Leu157Gln) n.664T>A | |
11 | g.32434877G>A | CA064984 | WT1 | c.484C>T (p.Leu162=) c.469C>T (p.Leu157=) n.663C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32434877G>C | CA379964920 | WT1 | c.484C>G (p.Leu162Val) c.469C>G (p.Leu157Val) n.663C>G | dbSNP gnomAD v4 |
11 | g.32434877G= | CA1962327180 | WT1 | c.484C= (p.Leu162=) c.469C= (p.Leu157=) n.663C= | |
11 | g.32434877G>T | CA379964919 | WT1 | c.484C>A (p.Leu162Met) c.469C>A (p.Leu157Met) n.663C>A | |
11 | g.32434878G>A | CA064979 | WT1 | c.483C>T (p.Cys161=) c.468C>T (p.Cys156=) n.662C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32434878G>C | CA379964922 | WT1 | c.483C>G (p.Cys161Trp) c.468C>G (p.Cys156Trp) n.662C>G | |
11 | g.32434878G= | CA1962327181 | WT1 | c.483C= (p.Cys161=) c.468C= (p.Cys156=) n.662C= | |
11 | g.32434878G>T | CA379964924 | WT1 | c.483C>A (p.Cys161Ter) c.468C>A (p.Cys156Ter) n.662C>A | |
11 | g.32434879C>A | CA379964926 | WT1 | c.482G>T (p.Cys161Phe) c.467G>T (p.Cys156Phe) n.661G>T | ClinVar dbSNP |
11 | g.32434879C= | CA1962327182 | WT1 | c.482G= (p.Cys161=) c.467G= (p.Cys156=) n.661G= | |
11 | g.32434879C>G | CA379964928 | WT1 | c.482G>C (p.Cys161Ser) c.467G>C (p.Cys156Ser) n.661G>C | |
11 | g.32434879C>T | CA379964929 | WT1 | c.482G>A (p.Cys161Tyr) c.467G>A (p.Cys156Tyr) n.661G>A | dbSNP gnomAD v4 |
11 | g.32434880A>C | CA379964931 | WT1 | c.481T>G (p.Cys161Gly) c.466T>G (p.Cys156Gly) n.660T>G | ClinVar |
11 | g.32434880A>G | CA379964934 | WT1 | c.481T>C (p.Cys161Arg) c.466T>C (p.Cys156Arg) n.660T>C | |
11 | g.32434880A>T | CA379964932 | WT1 | c.481T>A (p.Cys161Ser) c.466T>A (p.Cys156Ser) n.660T>A | dbSNP |
11 | g.32434881C>A | CA379964936 | WT1 | c.480G>T (p.Gln160His) c.465G>T (p.Gln155His) n.659G>T | |
11 | g.32434881C= | CA1962327183 | WT1 | c.480G= (p.Gln160=) c.465G= (p.Gln155=) n.659G= | |
11 | g.32434881C>G | CA379964937 | WT1 | c.480G>C (p.Gln160His) c.465G>C (p.Gln155His) n.659G>C | ClinVar dbSNP gnomAD v4 |
11 | g.32434881C>T | CA064974 | WT1 | c.480G>A (p.Gln160=) c.465G>A (p.Gln155=) n.659G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434882T>A | CA379964940 | WT1 | c.479A>T (p.Gln160Leu) c.464A>T (p.Gln155Leu) n.658A>T | |
11 | g.32434882T>C | CA379964941 | WT1 | c.479A>G (p.Gln160Arg) c.464A>G (p.Gln155Arg) n.658A>G | |
11 | g.32434882T>G | CA379964943 | WT1 | c.479A>C (p.Gln160Pro) c.464A>C (p.Gln155Pro) n.658A>C | |
11 | g.32434883del | CA473571694 | WT1 | c.478del (p.Gln160SerfsTer3) c.463del (p.Gln155SerfsTer3) n.657del | COSMIC |
11 | g.32434883G>A | CA379964944 | WT1 | c.478C>T (p.Gln160Ter) c.463C>T (p.Gln155Ter) n.657C>T | ClinVar dbSNP |
11 | g.32434883G>C | CA379964946 | WT1 | c.478C>G (p.Gln160Glu) c.463C>G (p.Gln155Glu) n.657C>G | ClinVar dbSNP |
11 | g.32434883G= | CA1962327184 | WT1 | c.478C= (p.Gln160=) c.463C= (p.Gln155=) n.657C= | |
11 | g.32434883G>T | CA379964948 | WT1 | c.478C>A (p.Gln160Lys) c.463C>A (p.Gln155Lys) n.657C>A | |
11 | g.32434884C>A | CA379964949 | WT1 | c.477G>T (p.Glu159Asp) c.462G>T (p.Glu154Asp) n.656G>T | |
11 | g.32434884C>G | CA379964951 | WT1 | c.477G>C (p.Glu159Asp) c.462G>C (p.Glu154Asp) n.656G>C | ClinVar dbSNP |
11 | g.32434884C>T | CA473571698 | WT1 | c.477G>A (p.Glu159=) c.462G>A (p.Glu154=) n.656G>A | ClinVar dbSNP |
11 | g.32434885T>A | CA379964952 | WT1 | c.476A>T (p.Glu159Val) c.461A>T (p.Glu154Val) n.655A>T | |
11 | g.32434885T>C | CA379964956 | WT1 | c.476A>G (p.Glu159Gly) c.461A>G (p.Glu154Gly) n.655A>G | ClinVar dbSNP |
11 | g.32434885T>G | CA379964954 | WT1 | c.476A>C (p.Glu159Ala) c.461A>C (p.Glu154Ala) n.655A>C | |
11 | g.32434885T= | CA1962327185 | WT1 | c.476A= (p.Glu159=) c.461A= (p.Glu154=) n.655A= | |
11 | g.32434886C>A | CA379964958 | WT1 | c.475G>T (p.Glu159Ter) c.460G>T (p.Glu154Ter) n.654G>T | |
11 | g.32434886C= | CA1962327186 | WT1 | c.475G= (p.Glu159=) c.460G= (p.Glu154=) n.654G= | |
11 | g.32434886C>G | CA379964959 | WT1 | c.475G>C (p.Glu159Gln) c.460G>C (p.Glu154Gln) n.654G>C | |
11 | g.32434886C>T | CA064967 | WT1 | c.475G>A (p.Glu159Lys) c.460G>A (p.Glu154Lys) n.654G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434887del | CA2695213675 | WT1 | c.475del (p.Glu159SerfsTer4) c.460del (p.Glu154SerfsTer4) n.654del | |
11 | g.32434888_32434909del | CA645584484 | WT1 | c.454_475del (p.Gly152SerfsTer4) c.439_460del (p.Gly147SerfsTer4) n.633_654del | COSMIC COSMIC |
11 | g.32434887C>A | CA379964962 | WT1 | c.474G>T (p.Glu158Asp) c.459G>T (p.Glu153Asp) n.653G>T | |
11 | g.32434887C= | CA1962327187 | WT1 | c.474G= (p.Glu158=) c.459G= (p.Glu153=) n.653G= | |
11 | g.32434887C>G | CA379964963 | WT1 | c.474G>C (p.Glu158Asp) c.459G>C (p.Glu153Asp) n.653G>C | dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434887C>T | CA219510972 | WT1 | c.474G>A (p.Glu158=) c.459G>A (p.Glu153=) n.653G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434888T>A | CA379964965 | WT1 | c.473A>T (p.Glu158Val) c.458A>T (p.Glu153Val) n.652A>T | |
11 | g.32434888T>C | CA379964966 | WT1 | c.473A>G (p.Glu158Gly) c.458A>G (p.Glu153Gly) n.652A>G | |
11 | g.32434888T>G | CA379964968 | WT1 | c.473A>C (p.Glu158Ala) c.458A>C (p.Glu153Ala) n.652A>C | |
11 | g.32434889C>A | CA379964969 | WT1 | c.472G>T (p.Glu158Ter) c.457G>T (p.Glu153Ter) n.651G>T | ClinVar dbSNP |
11 | g.32434889C= | CA1962327188 | WT1 | c.472G= (p.Glu158=) c.457G= (p.Glu153=) n.651G= | |
11 | g.32434889C>G | CA379964971 | WT1 | c.472G>C (p.Glu158Gln) c.457G>C (p.Glu153Gln) n.651G>C | ClinVar dbSNP |
11 | g.32434889C>T | CA379964973 | WT1 | c.472G>A (p.Glu158Lys) c.457G>A (p.Glu153Lys) n.651G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
11 | g.32434890G>A | CA064961 | WT1 | c.471C>T (p.His157=) c.456C>T (p.His152=) n.650C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
11 | g.32434890G>C | CA379964975 | WT1 | c.471C>G (p.His157Gln) c.456C>G (p.His152Gln) n.650C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32434890G= | CA1962327189 | WT1 | c.471C= (p.His157=) c.456C= (p.His152=) n.650C= | |
11 | g.32434890G>T | CA379964974 | WT1 | c.471C>A (p.His157Gln) c.456C>A (p.His152Gln) n.650C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434891T>A | CA379964976 | WT1 | c.470A>T (p.His157Leu) c.455A>T (p.His152Leu) n.649A>T | dbSNP |
11 | g.32434891T>C | CA379964977 | WT1 | c.470A>G (p.His157Arg) c.455A>G (p.His152Arg) n.649A>G | dbSNP |
11 | g.32434891T>G | CA379964979 | WT1 | c.470A>C (p.His157Pro) c.455A>C (p.His152Pro) n.649A>C | dbSNP |
11 | g.32434892G>A | CA379964981 | WT1 | c.469C>T (p.His157Tyr) c.454C>T (p.His152Tyr) n.648C>T | |
11 | g.32434892G>C | CA379964983 | WT1 | c.469C>G (p.His157Asp) c.454C>G (p.His152Asp) n.648C>G | |
11 | g.32434892G>T | CA379964986 | WT1 | c.469C>A (p.His157Asn) c.454C>A (p.His152Asn) n.648C>A | gnomAD v4 |
11 | g.32434893C>A | CA16613331 | WT1 | c.468G>T (p.Pro156=) c.453G>T (p.Pro151=) n.647G>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434893C= | CA1962327190 | WT1 | c.468G= (p.Pro156=) c.453G= (p.Pro151=) n.647G= | |
11 | g.32434893C>G | CA473571721 | WT1 | c.468G>C (p.Pro156=) c.453G>C (p.Pro151=) n.647G>C | gnomAD v4 |
11 | g.32434893C>T | CA473571723 | WT1 | c.468G>A (p.Pro156=) c.453G>A (p.Pro151=) n.647G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434894G>A | CA379964988 | WT1 | c.467C>T (p.Pro156Leu) c.452C>T (p.Pro151Leu) n.646C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434894G>C | CA379964989 | WT1 | c.467C>G (p.Pro156Arg) c.452C>G (p.Pro151Arg) n.646C>G | |
11 | g.32434894G= | CA1962327191 | WT1 | c.467C= (p.Pro156=) c.452C= (p.Pro151=) n.646C= | |
11 | g.32434894G>T | CA379964991 | WT1 | c.467C>A (p.Pro156Gln) c.452C>A (p.Pro151Gln) n.646C>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434895G>A | CA379964993 | WT1 | c.466C>T (p.Pro156Ser) c.451C>T (p.Pro151Ser) n.645C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434895G>C | CA379964995 | WT1 | c.466C>G (p.Pro156Ala) c.451C>G (p.Pro151Ala) n.645C>G | |
11 | g.32434895G= | CA1962327192 | WT1 | c.466C= (p.Pro156=) c.451C= (p.Pro151=) n.645C= | |
11 | g.32434895G>T | CA379964996 | WT1 | c.466C>A (p.Pro156Thr) c.451C>A (p.Pro151Thr) n.645C>A | gnomAD v4 |
11 | g.32434896C>A | CA379965000 | WT1 | c.465G>T (p.Glu155Asp) c.450G>T (p.Glu150Asp) n.644G>T | |
11 | g.32434896C= | CA1962327193 | WT1 | c.465G= (p.Glu155=) c.450G= (p.Glu150=) n.644G= | |
11 | g.32434896C>G | CA379964998 | WT1 | c.465G>C (p.Glu155Asp) c.450G>C (p.Glu150Asp) n.644G>C | |
11 | g.32434896C>T | CA473571731 | WT1 | c.465G>A (p.Glu155=) c.450G>A (p.Glu150=) n.644G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434897T>A | CA379965001 | WT1 | c.464A>T (p.Glu155Val) c.449A>T (p.Glu150Val) n.643A>T | |
11 | g.32434897T>C | CA379965004 | WT1 | c.464A>G (p.Glu155Gly) c.449A>G (p.Glu150Gly) n.643A>G | dbSNP |
11 | g.32434897T>G | CA379965003 | WT1 | c.464A>C (p.Glu155Ala) c.449A>C (p.Glu150Ala) n.643A>C | |
11 | g.32434898C>A | CA379965006 | WT1 | c.463G>T (p.Glu155Ter) c.448G>T (p.Glu150Ter) n.642G>T | |
11 | g.32434898C= | CA1962327194 | WT1 | c.463G= (p.Glu155=) c.448G= (p.Glu150=) n.642G= | |
11 | g.32434898C>G | CA379965011 | WT1 | c.463G>C (p.Glu155Gln) c.448G>C (p.Glu150Gln) n.642G>C | |
11 | g.32434898C>T | CA379965008 | WT1 | c.463G>A (p.Glu155Lys) c.448G>A (p.Glu150Lys) n.642G>A | ClinVar dbSNP |
11 | g.32434899C>A | CA473571737 | WT1 | c.462G>T (p.Ala154=) c.447G>T (p.Ala149=) n.641G>T | |
11 | g.32434899C>G | CA473571738 | WT1 | c.462G>C (p.Ala154=) c.447G>C (p.Ala149=) n.641G>C | |
11 | g.32434899C>T | CA473571739 | WT1 | c.462G>A (p.Ala154=) c.447G>A (p.Ala149=) n.641G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434902_32434903del | CA2723464976 | WT1 | c.461_462del (p.Ala154GlyfsTer?) c.446_447del (p.Ala149GlyfsTer?) n.640_641del | dbSNP |
11 | g.32434900G>A | CA379965013 | WT1 | c.461C>T (p.Ala154Val) c.446C>T (p.Ala149Val) n.640C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434900G>C | CA379965015 | WT1 | c.461C>G (p.Ala154Gly) c.446C>G (p.Ala149Gly) n.640C>G | dbSNP |
11 | g.32434900G>T | CA379965014 | WT1 | c.461C>A (p.Ala154Glu) c.446C>A (p.Ala149Glu) n.640C>A | |
11 | g.32434901C>A | CA379965018 | WT1 | c.460G>T (p.Ala154Ser) c.445G>T (p.Ala149Ser) n.639G>T | gnomAD v4 |
11 | g.32434901C>G | CA379965019 | WT1 | c.460G>C (p.Ala154Pro) c.445G>C (p.Ala149Pro) n.639G>C | |
11 | g.32434901C>T | CA379965021 | WT1 | c.460G>A (p.Ala154Thr) c.445G>A (p.Ala149Thr) n.639G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
11 | g.32434902G>A | CA473571744 | WT1 | c.459C>T (p.Gly153=) c.444C>T (p.Gly148=) n.638C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434902G>C | CA473571747 | WT1 | c.459C>G (p.Gly153=) c.444C>G (p.Gly148=) n.638C>G | |
11 | g.32434902G= | CA1962327195 | WT1 | c.459C= (p.Gly153=) c.444C= (p.Gly148=) n.638C= | |
11 | g.32434902G>T | CA473571745 | WT1 | c.459C>A (p.Gly153=) c.444C>A (p.Gly148=) n.638C>A | |
11 | g.32434903C>A | CA379965022 | WT1 | c.458G>T (p.Gly153Val) c.443G>T (p.Gly148Val) n.637G>T | |
11 | g.32434903C>G | CA379965024 | WT1 | c.458G>C (p.Gly153Ala) c.443G>C (p.Gly148Ala) n.637G>C | |
11 | g.32434903C>T | CA379965025 | WT1 | c.458G>A (p.Gly153Asp) c.443G>A (p.Gly148Asp) n.637G>A | |
11 | g.32434904C>A | CA379965027 | WT1 | c.457G>T (p.Gly153Cys) c.442G>T (p.Gly148Cys) n.636G>T | gnomAD v4 |
11 | g.32434904C>G | CA379965029 | WT1 | c.457G>C (p.Gly153Arg) c.442G>C (p.Gly148Arg) n.636G>C | |
11 | g.32434904C>T | CA379965030 | WT1 | c.457G>A (p.Gly153Ser) c.442G>A (p.Gly148Ser) n.636G>A | gnomAD v4 |
11 | g.32434905G>A | CA473571755 | WT1 | c.456C>T (p.Gly152=) c.441C>T (p.Gly147=) n.635C>T | ClinVar dbSNP COSMIC COSMIC |
11 | g.32434905G>C | CA473571756 | WT1 | c.456C>G (p.Gly152=) c.441C>G (p.Gly147=) n.635C>G | |
11 | g.32434905G>T | CA473571758 | WT1 | c.456C>A (p.Gly152=) c.441C>A (p.Gly147=) n.635C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434906C>A | CA379965032 | WT1 | c.455G>T (p.Gly152Val) c.440G>T (p.Gly147Val) n.634G>T | |
11 | g.32434906C= | CA1962327196 | WT1 | c.455G= (p.Gly152=) c.440G= (p.Gly147=) n.634G= | |
11 | g.32434906C>G | CA379965034 | WT1 | c.455G>C (p.Gly152Ala) c.440G>C (p.Gly147Ala) n.634G>C | |
11 | g.32434906C>T | CA379965035 | WT1 | c.455G>A (p.Gly152Asp) c.440G>A (p.Gly147Asp) n.634G>A | ClinVar dbSNP |
11 | g.32434909del | CA2499220922 | WT1 | c.455del (p.Gly152AlafsTer11) c.440del (p.Gly147AlafsTer11) n.634del | ClinVar dbSNP |
11 | g.32434907C>A | CA379965037 | WT1 | c.454G>T (p.Gly152Cys) c.439G>T (p.Gly147Cys) n.633G>T | dbSNP |
11 | g.32434907C= | CA1962327197 | WT1 | c.454G= (p.Gly152=) c.439G= (p.Gly147=) n.633G= | |
11 | g.32434907C>G | CA379965040 | WT1 | c.454G>C (p.Gly152Arg) c.439G>C (p.Gly147Arg) n.633G>C | |
11 | g.32434907C>T | CA379965038 | WT1 | c.454G>A (p.Gly152Ser) c.439G>A (p.Gly147Ser) n.633G>A | gnomAD v4 |
11 | g.32434908C>A | CA379965042 | WT1 | c.453G>T (p.Trp151Cys) c.438G>T (p.Trp146Cys) n.632G>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434908C= | CA1962327198 | WT1 | c.453G= (p.Trp151=) c.438G= (p.Trp146=) n.632G= | |
11 | g.32434908C>G | CA379965044 | WT1 | c.453G>C (p.Trp151Cys) c.438G>C (p.Trp146Cys) n.632G>C | |
11 | g.32434908C>T | CA379965045 | WT1 | c.453G>A (p.Trp151Ter) c.438G>A (p.Trp146Ter) n.632G>A | ClinVar |
11 | g.32434909C>A | CA379965047 | WT1 | c.452G>T (p.Trp151Leu) c.437G>T (p.Trp146Leu) n.631G>T | gnomAD v4 |
11 | g.32434909C>G | CA379965048 | WT1 | c.452G>C (p.Trp151Ser) c.437G>C (p.Trp146Ser) n.631G>C | |
11 | g.32434909C>T | CA379965050 | WT1 | c.452G>A (p.Trp151Ter) c.437G>A (p.Trp146Ter) n.631G>A | |
11 | g.32434909_32434913delinsCAGCT | CA1962327199 | WT1 | c.448_452delinsAGCTG (p.Ser150=) c.433_437delinsAGCTG (p.Ser145=) n.627_631delinsAGCTG | |
11 | g.32434910A= | CA1962327200 | WT1 | c.451T= (p.Trp151=) c.436T= (p.Trp146=) n.630T= | |
11 | g.32434910A>C | CA379965052 | WT1 | c.451T>G (p.Trp151Gly) c.436T>G (p.Trp146Gly) n.630T>G | ClinVar |
11 | g.32434910A>G | CA379965053 | WT1 | c.451T>C (p.Trp151Arg) c.436T>C (p.Trp146Arg) n.630T>C | |
11 | g.32434910A>T | CA379965055 | WT1 | c.451T>A (p.Trp151Arg) c.436T>A (p.Trp146Arg) n.630T>A | ClinVar dbSNP |
11 | g.32434910_32434913del | CA598513625 | WT1 | c.448_451del (p.Ser150GlyfsTer12) c.433_436del (p.Ser145GlyfsTer12) n.627_630del | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434911G>A | CA473571771 | WT1 | c.450C>T (p.Ser150=) c.435C>T (p.Ser145=) n.629C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434911G>C | CA379965057 | WT1 | c.450C>G (p.Ser150Arg) c.435C>G (p.Ser145Arg) n.629C>G | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434911G= | CA1962327201 | WT1 | c.450C= (p.Ser150=) c.435C= (p.Ser145=) n.629C= | |
11 | g.32434911G>T | CA379965058 | WT1 | c.450C>A (p.Ser150Arg) c.435C>A (p.Ser145Arg) n.629C>A | ClinVar dbSNP |
11 | g.32434912C>A | CA379965060 | WT1 | c.449G>T (p.Ser150Ile) c.434G>T (p.Ser145Ile) n.628G>T | ClinVar |
11 | g.32434912C= | CA1962327202 | WT1 | c.449G= (p.Ser150=) c.434G= (p.Ser145=) n.628G= | |
11 | g.32434912C>G | CA379965061 | WT1 | c.449G>C (p.Ser150Thr) c.434G>C (p.Ser145Thr) n.628G>C | |
11 | g.32434912C>T | CA379965063 | WT1 | c.449G>A (p.Ser150Asn) c.434G>A (p.Ser145Asn) n.628G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434913T>A | CA379965065 | WT1 | c.448A>T (p.Ser150Cys) c.433A>T (p.Ser145Cys) n.627A>T | dbSNP |
11 | g.32434913T>C | CA379965066 | WT1 | c.448A>G (p.Ser150Gly) c.433A>G (p.Ser145Gly) n.627A>G | ClinVar dbSNP gnomAD v4 |
11 | g.32434913T>G | CA379965068 | WT1 | c.448A>C (p.Ser150Arg) c.433A>C (p.Ser145Arg) n.627A>C | |
11 | g.32434913T= | CA1962327203 | WT1 | c.448A= (p.Ser150=) c.433A= (p.Ser145=) n.627A= | |
11 | g.32434914C>A | CA219510988 | WT1 | c.447G>T (p.Pro149=) c.432G>T (p.Pro144=) n.626G>T | dbSNP gnomAD v4 |
11 | g.32434914C= | CA1962327204 | WT1 | c.447G= (p.Pro149=) c.432G= (p.Pro144=) n.626G= | |
11 | g.32434914C>G | CA473571783 | WT1 | c.447G>C (p.Pro149=) c.432G>C (p.Pro144=) n.626G>C | |
11 | g.32434914C>T | CA473571785 | WT1 | c.447G>A (p.Pro149=) c.432G>A (p.Pro144=) n.626G>A | ClinVar |
11 | g.32434915G>A | CA379965070 | WT1 | c.446C>T (p.Pro149Leu) c.431C>T (p.Pro144Leu) n.625C>T | |
11 | g.32434915G>C | CA379965071 | WT1 | c.446C>G (p.Pro149Arg) c.431C>G (p.Pro144Arg) n.625C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32434915G= | CA1962327205 | WT1 | c.446C= (p.Pro149=) c.431C= (p.Pro144=) n.625C= | |
11 | g.32434915G>T | CA379965073 | WT1 | c.446C>A (p.Pro149Gln) c.431C>A (p.Pro144Gln) n.625C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434916G>A | CA379965074 | WT1 | c.445C>T (p.Pro149Ser) c.430C>T (p.Pro144Ser) n.624C>T | ClinVar dbSNP |
11 | g.32434916G>C | CA379965076 | WT1 | c.445C>G (p.Pro149Ala) c.430C>G (p.Pro144Ala) n.624C>G | |
11 | g.32434916G= | CA1962327206 | WT1 | c.445C= (p.Pro149=) c.430C= (p.Pro144=) n.624C= | |
11 | g.32434916G>T | CA379965078 | WT1 | c.445C>A (p.Pro149Thr) c.430C>A (p.Pro144Thr) n.624C>A | gnomAD v4 |
11 | g.32434917C>A | CA379965082 | WT1 | c.444G>T (p.Glu148Asp) c.429G>T (p.Glu143Asp) n.623G>T | gnomAD v4 |
11 | g.32434917C= | CA1962327207 | WT1 | c.444G= (p.Glu148=) c.429G= (p.Glu143=) n.623G= | |
11 | g.32434917C>G | CA379965080 | WT1 | c.444G>C (p.Glu148Asp) c.429G>C (p.Glu143Asp) n.623G>C | |
11 | g.32434917C>T | CA064949 | WT1 | c.444G>A (p.Glu148=) c.429G>A (p.Glu143=) n.623G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434918T>A | CA379965084 | WT1 | c.443A>T (p.Glu148Val) c.428A>T (p.Glu143Val) n.622A>T | |
11 | g.32434918T>C | CA379965086 | WT1 | c.443A>G (p.Glu148Gly) c.428A>G (p.Glu143Gly) n.622A>G | |
11 | g.32434918T>G | CA379965087 | WT1 | c.443A>C (p.Glu148Ala) c.428A>C (p.Glu143Ala) n.622A>C | |
11 | g.32434919C>A | CA379965088 | WT1 | c.442G>T (p.Glu148Ter) c.427G>T (p.Glu143Ter) n.621G>T | COSMIC COSMIC |
11 | g.32434919C>G | CA379965090 | WT1 | c.442G>C (p.Glu148Gln) c.427G>C (p.Glu143Gln) n.621G>C | |
11 | g.32434919C>T | CA379965092 | WT1 | c.442G>A (p.Glu148Lys) c.427G>A (p.Glu143Lys) n.621G>A |