| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.32417632_32417649delinsATGTCATTTGGTATAAAT | CA1962318455 | WT1 | c.893_910delinsATTTATACCAAATGACAT (p.Asn298=) c.242_259delinsATTTATACCAAATGACAT (p.Asn81=) c.269_286delinsATTTATACCAAATGACAT (p.Asn90=) c.878_895delinsATTTATACCAAATGACAT (p.Asn293=) c.131_148delinsATTTATACCAAATGACAT (p.Asn44=) n.1072_1089delinsATTTATACCAAATGACAT | |
| 11 | g.32417638_32417654del | CA016460 | WT1 | c.893_909del (p.Asn298IlefsTer4) c.242_258del (p.Asn81IlefsTer4) c.269_285del (p.Asn90IlefsTer4) c.878_894del (p.Asn293IlefsTer4) c.131_147del (p.Asn44IlefsTer4) n.1072_1088del | ClinVar dbSNP |
| 11 | g.32417638T>A | CA379962187 | WT1 | c.904A>T (p.Met302Leu) c.253A>T (p.Met85Leu) c.280A>T (p.Met94Leu) c.889A>T (p.Met297Leu) c.142A>T (p.Met48Leu) n.1083A>T | dbSNP |
| 11 | g.32417638T>C | CA379962188 | WT1 | c.904A>G (p.Met302Val) c.253A>G (p.Met85Val) c.280A>G (p.Met94Val) c.889A>G (p.Met297Val) c.142A>G (p.Met48Val) n.1083A>G | |
| 11 | g.32417638T>G | CA379962189 | WT1 | c.904A>C (p.Met302Leu) c.253A>C (p.Met85Leu) c.280A>C (p.Met94Leu) c.889A>C (p.Met297Leu) c.142A>C (p.Met48Leu) n.1083A>C | |
| 11 | g.32417640del | CA645577704 | WT1 | c.904del (p.Met302Ter) c.253del (p.Met85Ter) c.280del (p.Met94Ter) c.889del (p.Met297Ter) c.142del (p.Met48Ter) n.1083del | COSMIC |
| 11 | g.32417639T>A | CA379962190 | WT1 | c.903A>T (p.Gln301His) c.252A>T (p.Gln84His) c.279A>T (p.Gln93His) c.888A>T (p.Gln296His) c.141A>T (p.Gln47His) n.1082A>T | dbSNP |
| 11 | g.32417639T>C | CA473568335 | WT1 | c.903A>G (p.Gln301=) c.252A>G (p.Gln84=) c.279A>G (p.Gln93=) c.888A>G (p.Gln296=) c.141A>G (p.Gln47=) n.1082A>G | ClinVar |
| 11 | g.32417639T>G | CA379962191 | WT1 | c.903A>C (p.Gln301His) c.252A>C (p.Gln84His) c.279A>C (p.Gln93His) c.888A>C (p.Gln296His) c.141A>C (p.Gln47His) n.1082A>C | |
| 11 | g.32417640T>A | CA379962192 | WT1 | c.902A>T (p.Gln301Leu) c.251A>T (p.Gln84Leu) c.278A>T (p.Gln93Leu) c.887A>T (p.Gln296Leu) c.140A>T (p.Gln47Leu) n.1081A>T | |
| 11 | g.32417640T>C | CA379962193 | WT1 | c.902A>G (p.Gln301Arg) c.251A>G (p.Gln84Arg) c.278A>G (p.Gln93Arg) c.887A>G (p.Gln296Arg) c.140A>G (p.Gln47Arg) n.1081A>G | |
| 11 | g.32417640T>G | CA379962194 | WT1 | c.902A>C (p.Gln301Pro) c.251A>C (p.Gln84Pro) c.278A>C (p.Gln93Pro) c.887A>C (p.Gln296Pro) c.140A>C (p.Gln47Pro) n.1081A>C | |
| 11 | g.32417641G>A | CA065867 | WT1 | c.901C>T (p.Gln301Ter) c.250C>T (p.Gln84Ter) c.277C>T (p.Gln93Ter) c.886C>T (p.Gln296Ter) c.139C>T (p.Gln47Ter) n.1080C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.32417641G>C | CA379962195 | WT1 | c.901C>G (p.Gln301Glu) c.250C>G (p.Gln84Glu) c.277C>G (p.Gln93Glu) c.886C>G (p.Gln296Glu) c.139C>G (p.Gln47Glu) n.1080C>G | dbSNP |
| 11 | g.32417641G= | CA1962318460 | WT1 | c.901C= (p.Gln301=) c.250C= (p.Gln84=) c.277C= (p.Gln93=) c.886C= (p.Gln296=) c.139C= (p.Gln47=) n.1080C= | |
| 11 | g.32417641G>T | CA379962196 | WT1 | c.901C>A (p.Gln301Lys) c.250C>A (p.Gln84Lys) c.277C>A (p.Gln93Lys) c.886C>A (p.Gln296Lys) c.139C>A (p.Gln47Lys) n.1080C>A | dbSNP gnomAD v4 |
| 11 | g.32417642G>A | CA065860 | WT1 | c.900C>T (p.Tyr300=) c.249C>T (p.Tyr83=) c.276C>T (p.Tyr92=) c.885C>T (p.Tyr295=) c.138C>T (p.Tyr46=) n.1079C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.32417642G>C | CA379962198 | WT1 | c.900C>G (p.Tyr300Ter) c.249C>G (p.Tyr83Ter) c.276C>G (p.Tyr92Ter) c.885C>G (p.Tyr295Ter) c.138C>G (p.Tyr46Ter) n.1079C>G | ClinVar dbSNP |
| 11 | g.32417642G= | CA1962318461 | WT1 | c.900C= (p.Tyr300=) c.249C= (p.Tyr83=) c.276C= (p.Tyr92=) c.885C= (p.Tyr295=) c.138C= (p.Tyr46=) n.1079C= | |
| 11 | g.32417642G>T | CA379962197 | WT1 | c.900C>A (p.Tyr300Ter) c.249C>A (p.Tyr83Ter) c.276C>A (p.Tyr92Ter) c.885C>A (p.Tyr295Ter) c.138C>A (p.Tyr46Ter) n.1079C>A | dbSNP |
| 11 | g.32417643T>A | CA379962199 | WT1 | c.899A>T (p.Tyr300Phe) c.248A>T (p.Tyr83Phe) c.275A>T (p.Tyr92Phe) c.884A>T (p.Tyr295Phe) c.137A>T (p.Tyr46Phe) n.1078A>T | |
| 11 | g.32417643T>C | CA379962201 | WT1 | c.899A>G (p.Tyr300Cys) c.248A>G (p.Tyr83Cys) c.275A>G (p.Tyr92Cys) c.884A>G (p.Tyr295Cys) c.137A>G (p.Tyr46Cys) n.1078A>G | dbSNP gnomAD v4 |
| 11 | g.32417643T>G | CA379962200 | WT1 | c.899A>C (p.Tyr300Ser) c.248A>C (p.Tyr83Ser) c.275A>C (p.Tyr92Ser) c.884A>C (p.Tyr295Ser) c.137A>C (p.Tyr46Ser) n.1078A>C | dbSNP |
| 11 | g.32417644A= | CA1962318462 | WT1 | c.898T= (p.Tyr300=) c.247T= (p.Tyr83=) c.274T= (p.Tyr92=) c.883T= (p.Tyr295=) c.136T= (p.Tyr46=) n.1077T= | |
| 11 | g.32417644A>C | CA379962202 | WT1 | c.898T>G (p.Tyr300Asp) c.247T>G (p.Tyr83Asp) c.274T>G (p.Tyr92Asp) c.883T>G (p.Tyr295Asp) c.136T>G (p.Tyr46Asp) n.1077T>G | |
| 11 | g.32417644A>G | CA065855 | WT1 | c.898T>C (p.Tyr300His) c.247T>C (p.Tyr83His) c.274T>C (p.Tyr92His) c.883T>C (p.Tyr295His) c.136T>C (p.Tyr46His) n.1077T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.32417644A>T | CA379962203 | WT1 | c.898T>A (p.Tyr300Asn) c.247T>A (p.Tyr83Asn) c.274T>A (p.Tyr92Asn) c.883T>A (p.Tyr295Asn) c.136T>A (p.Tyr46Asn) n.1077T>A | dbSNP |
| 11 | g.32417644_32417645delinsAT | CA1962318463 | WT1 | c.897_898delinsAT (p.Leu299=) c.246_247delinsAT (p.Leu82=) c.273_274delinsAT (p.Leu91=) c.882_883delinsAT (p.Leu294=) c.135_136delinsAT (p.Leu45=) n.1076_1077delinsAT | |
| 11 | g.32417645del | CA1139661877 | WT1 | c.897del (p.Leu299PhefsTer4) c.246del (p.Leu82PhefsTer4) c.273del (p.Leu91PhefsTer4) c.882del (p.Leu294PhefsTer4) c.135del (p.Leu45PhefsTer4) n.1076del | ClinVar dbSNP |
| 11 | g.32417645T>A | CA379962204 | WT1 | c.897A>T (p.Leu299Phe) c.246A>T (p.Leu82Phe) c.273A>T (p.Leu91Phe) c.882A>T (p.Leu294Phe) c.135A>T (p.Leu45Phe) n.1076A>T | |
| 11 | g.32417645T>C | CA473568336 | WT1 | c.897A>G (p.Leu299=) c.246A>G (p.Leu82=) c.273A>G (p.Leu91=) c.882A>G (p.Leu294=) c.135A>G (p.Leu45=) n.1076A>G | |
| 11 | g.32417645T>G | CA379962205 | WT1 | c.897A>C (p.Leu299Phe) c.246A>C (p.Leu82Phe) c.273A>C (p.Leu91Phe) c.882A>C (p.Leu294Phe) c.135A>C (p.Leu45Phe) n.1076A>C | |
| 11 | g.32417646_32417647insTTA | CA645577705 | WT1 | c.897_898insATA (p.Leu299_Tyr300insIle) c.246_247insATA (p.Leu82_Tyr83insIle) c.273_274insATA (p.Leu91_Tyr92insIle) c.882_883insATA (p.Leu294_Tyr295insIle) c.135_136insATA (p.Leu45_Tyr46insIle) n.1076_1077insATA | COSMIC |
| 11 | g.32417646A>C | CA379962206 | WT1 | c.896T>G (p.Leu299Ter) c.245T>G (p.Leu82Ter) c.272T>G (p.Leu91Ter) c.881T>G (p.Leu294Ter) c.134T>G (p.Leu45Ter) n.1075T>G | |
| 11 | g.32417646A>G | CA379962207 | WT1 | c.896T>C (p.Leu299Ser) c.245T>C (p.Leu82Ser) c.272T>C (p.Leu91Ser) c.881T>C (p.Leu294Ser) c.134T>C (p.Leu45Ser) n.1075T>C | |
| 11 | g.32417646A>T | CA379962208 | WT1 | c.896T>A (p.Leu299Ter) c.245T>A (p.Leu82Ter) c.272T>A (p.Leu91Ter) c.881T>A (p.Leu294Ter) c.134T>A (p.Leu45Ter) n.1075T>A | COSMIC |
| 11 | g.32417648del | CA2723457797 | WT1 | c.896del (p.Leu299TyrfsTer4) c.245del (p.Leu82TyrfsTer4) c.272del (p.Leu91TyrfsTer4) c.881del (p.Leu294TyrfsTer4) c.134del (p.Leu45TyrfsTer4) n.1075del | dbSNP |
| 11 | g.32417647A= | CA1962318464 | WT1 | c.895T= (p.Leu299=) c.244T= (p.Leu82=) c.271T= (p.Leu91=) c.880T= (p.Leu294=) c.133T= (p.Leu45=) n.1074T= | |
| 11 | g.32417647A>C | CA379962209 | WT1 | c.895T>G (p.Leu299Val) c.244T>G (p.Leu82Val) c.271T>G (p.Leu91Val) c.880T>G (p.Leu294Val) c.133T>G (p.Leu45Val) n.1074T>G | |
| 11 | g.32417647A>G | CA473568337 | WT1 | c.895T>C (p.Leu299=) c.244T>C (p.Leu82=) c.271T>C (p.Leu91=) c.880T>C (p.Leu294=) c.133T>C (p.Leu45=) n.1074T>C | |
| 11 | g.32417647A>T | CA065845 | WT1 | c.895T>A (p.Leu299Ile) c.244T>A (p.Leu82Ile) c.271T>A (p.Leu91Ile) c.880T>A (p.Leu294Ile) c.133T>A (p.Leu45Ile) n.1074T>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.32417648A>C | CA379962210 | WT1 | c.894T>G (p.Asn298Lys) c.243T>G (p.Asn81Lys) c.270T>G (p.Asn90Lys) c.879T>G (p.Asn293Lys) c.132T>G (p.Asn44Lys) n.1073T>G | COSMIC COSMIC COSMIC |
| 11 | g.32417648A>G | CA473568338 | WT1 | c.894T>C (p.Asn298=) c.243T>C (p.Asn81=) c.270T>C (p.Asn90=) c.879T>C (p.Asn293=) c.132T>C (p.Asn44=) n.1073T>C | |
| 11 | g.32417648A>T | CA379962211 | WT1 | c.894T>A (p.Asn298Lys) c.243T>A (p.Asn81Lys) c.270T>A (p.Asn90Lys) c.879T>A (p.Asn293Lys) c.132T>A (p.Asn44Lys) n.1073T>A | dbSNP |
| 11 | g.32417649T>A | CA379962212 | WT1 | c.893A>T (p.Asn298Ile) c.242A>T (p.Asn81Ile) c.269A>T (p.Asn90Ile) c.878A>T (p.Asn293Ile) c.131A>T (p.Asn44Ile) n.1072A>T | |
| 11 | g.32417649T>C | CA219496227 | WT1 | c.893A>G (p.Asn298Ser) c.242A>G (p.Asn81Ser) c.269A>G (p.Asn90Ser) c.878A>G (p.Asn293Ser) c.131A>G (p.Asn44Ser) n.1072A>G | ClinVar dbSNP |
| 11 | g.32417649T>G | CA379962214 | WT1 | c.893A>C (p.Asn298Thr) c.242A>C (p.Asn81Thr) c.269A>C (p.Asn90Thr) c.878A>C (p.Asn293Thr) c.131A>C (p.Asn44Thr) n.1072A>C | |
| 11 | g.32417649T= | CA1962318465 | WT1 | c.893A= (p.Asn298=) c.242A= (p.Asn81=) c.269A= (p.Asn90=) c.878A= (p.Asn293=) c.131A= (p.Asn44=) n.1072A= | |
| 11 | g.32417650T>A | CA379962217 | WT1 | c.892A>T (p.Asn298Tyr) c.241A>T (p.Asn81Tyr) c.268A>T (p.Asn90Tyr) c.877A>T (p.Asn293Tyr) c.130A>T (p.Asn44Tyr) n.1071A>T | dbSNP |
| 11 | g.32417650T>C | CA379962216 | WT1 | c.892A>G (p.Asn298Asp) c.241A>G (p.Asn81Asp) c.268A>G (p.Asn90Asp) c.877A>G (p.Asn293Asp) c.130A>G (p.Asn44Asp) n.1071A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |