Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.33301780_33301952del | CA2584317398 | CEBPA | c.471_643del (p.Leu158AspfsTer?) c.114_286del (p.Leu39AspfsTer?) c.576_748del (p.Leu193AspfsTer?) c.429_601del (p.Leu144AspfsTer?) | gnomAD v4 |
19 | g.33301855_33301947del | CA2584317459 | CEBPA | c.473_565del (p.Leu158_Pro188del) c.116_208del (p.Leu39_Pro69del) c.578_670del (p.Leu193_Pro223del) c.431_523del (p.Leu144_Pro174del) | gnomAD v4 |
19 | g.33301865_33301960del | CA2584317466 | CEBPA | c.460_555del (p.Ala154_Pro185del) c.103_198del (p.Ala35_Pro66del) c.565_660del (p.Ala189_Pro220del) c.418_513del (p.Ala140_Pro171del) | gnomAD v4 |
19 | g.33301868_33301960del | CA2584317467 | CEBPA | c.460_552del (p.Ala154_Pro184del) c.103_195del (p.Ala35_Pro65del) c.565_657del (p.Ala189_Pro219del) c.418_510del (p.Ala140_Pro170del) | gnomAD v4 |
19 | g.33301870_33301959del | CA2584317468 | CEBPA | c.460_549del (p.Ala154_Pro183del) c.103_192del (p.Ala35_Pro64del) c.565_654del (p.Ala189_Pro218del) c.418_507del (p.Ala140_Pro169del) | gnomAD v4 |
19 | g.33301893_33302183del | CA645612682 | CEBPA | c.239_529del (p.Asp80_Ala176del) c.-119_172del c.344_634del (p.Asp115_Ala211del) c.197_487del (p.Asp66_Ala162del) | COSMIC |
19 | g.33301897_33301956del | CA2584317474 | CEBPA | c.466_525del (p.Arg156_Leu175del) c.109_168del (p.Arg37_Leu56del) c.571_630del (p.Arg191_Leu210del) c.424_483del (p.Arg142_Leu161del) | gnomAD v4 |
19 | g.33301897_33301962del | CA2695198167 | CEBPA | c.458_523del (p.Pro153_Ala174del) c.101_166del (p.Pro34_Ala55del) c.563_628del (p.Pro188_Ala209del) c.416_481del (p.Pro139_Ala160del) | ClinVar |
19 | g.33301910C>A | CA405274807 | CEBPA | c.505G>T (p.Glu169Ter) c.148G>T (p.Glu50Ter) c.610G>T (p.Glu204Ter) c.463G>T (p.Glu155Ter) | gnomAD v4 |
19 | g.33301910C>G | CA405274809 | CEBPA | c.505G>C (p.Glu169Gln) c.148G>C (p.Glu50Gln) c.610G>C (p.Glu204Gln) c.463G>C (p.Glu155Gln) | gnomAD v4 |
19 | g.33301910C>T | CA405274808 | CEBPA | c.505G>A (p.Glu169Lys) c.148G>A (p.Glu50Lys) c.610G>A (p.Glu204Lys) c.463G>A (p.Glu155Lys) | gnomAD v4 |
19 | g.33301911A= | CA2332660229 | CEBPA | c.504T= (p.Asp168=) c.147T= (p.Asp49=) c.609T= (p.Asp203=) c.462T= (p.Asp154=) | |
19 | g.33301911A>C | CA405274810 | CEBPA | c.504T>G (p.Asp168Glu) c.147T>G (p.Asp49Glu) c.609T>G (p.Asp203Glu) c.462T>G (p.Asp154Glu) | |
19 | g.33301911A>G | CA507007737 | CEBPA | c.504T>C (p.Asp168=) c.147T>C (p.Asp49=) c.609T>C (p.Asp203=) c.462T>C (p.Asp154=) | ClinVar dbSNP gnomAD v4 |
19 | g.33301911A>T | CA405274811 | CEBPA | c.504T>A (p.Asp168Glu) c.147T>A (p.Asp49Glu) c.609T>A (p.Asp203Glu) c.462T>A (p.Asp154Glu) | |
19 | g.33301912T>A | CA405274812 | CEBPA | c.503A>T (p.Asp168Val) c.146A>T (p.Asp49Val) c.608A>T (p.Asp203Val) c.461A>T (p.Asp154Val) | ClinVar dbSNP gnomAD v4 |
19 | g.33301912T>C | CA405274813 | CEBPA | c.503A>G (p.Asp168Gly) c.146A>G (p.Asp49Gly) c.608A>G (p.Asp203Gly) c.461A>G (p.Asp154Gly) | gnomAD v4 |
19 | g.33301912T>G | CA405274814 | CEBPA | c.503A>C (p.Asp168Ala) c.146A>C (p.Asp49Ala) c.608A>C (p.Asp203Ala) c.461A>C (p.Asp154Ala) | gnomAD v4 |
19 | g.33301912dup | CA2332660230 | CEBPA | c.503dup (p.Asp168GlufsTer2) c.146dup (p.Asp49GlufsTer2) c.608dup (p.Asp203GlufsTer2) c.461dup (p.Asp154GlufsTer2) | dbSNP |
19 | g.33301917_33301919del | CA645612685 | CEBPA | c.501_503del (p.Glu167del) c.144_146del (p.Glu48del) c.606_608del (p.Glu202del) c.459_461del (p.Glu153del) | gnomAD v4 COSMIC |
19 | g.33301913C>A | CA405274815 | CEBPA | c.502G>T (p.Asp168Tyr) c.145G>T (p.Asp49Tyr) c.607G>T (p.Asp203Tyr) c.460G>T (p.Asp154Tyr) | gnomAD v4 |
19 | g.33301913C>G | CA405274816 | CEBPA | c.502G>C (p.Asp168His) c.145G>C (p.Asp49His) c.607G>C (p.Asp203His) c.460G>C (p.Asp154His) | |
19 | g.33301913C>T | CA405274817 | CEBPA | c.502G>A (p.Asp168Asn) c.145G>A (p.Asp49Asn) c.607G>A (p.Asp203Asn) c.460G>A (p.Asp154Asn) | ClinVar gnomAD v4 |
19 | g.33301914C>A | CA405274818 | CEBPA | c.501G>T (p.Glu167Asp) c.144G>T (p.Glu48Asp) c.606G>T (p.Glu202Asp) c.459G>T (p.Glu153Asp) | dbSNP gnomAD v4 |
19 | g.33301914C= | CA2332660231 | CEBPA | c.501G= (p.Glu167=) c.144G= (p.Glu48=) c.606G= (p.Glu202=) c.459G= (p.Glu153=) | |
19 | g.33301914C>G | CA405274819 | CEBPA | c.501G>C (p.Glu167Asp) c.144G>C (p.Glu48Asp) c.606G>C (p.Glu202Asp) c.459G>C (p.Glu153Asp) | gnomAD v4 |
19 | g.33301914C>T | CA507007742 | CEBPA | c.501G>A (p.Glu167=) c.144G>A (p.Glu48=) c.606G>A (p.Glu202=) c.459G>A (p.Glu153=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
19 | g.33301915_33301916dup | CA645612686 | CEBPA | c.500_501dup (p.Asp168ArgfsTer?) c.143_144dup (p.Asp49ArgfsTer?) c.605_606dup (p.Asp203ArgfsTer?) c.458_459dup (p.Asp154ArgfsTer?) | COSMIC |
19 | g.33301915del | CA2584317476 | CEBPA | c.500del (p.Glu167GlyfsTer?) c.143del (p.Glu48GlyfsTer?) c.605del (p.Glu202GlyfsTer?) c.458del (p.Glu153GlyfsTer?) | gnomAD v4 |
19 | g.33301915T>A | CA405274820 | CEBPA | c.500A>T (p.Glu167Val) c.143A>T (p.Glu48Val) c.605A>T (p.Glu202Val) c.458A>T (p.Glu153Val) | gnomAD v4 |
19 | g.33301915T>C | CA405274822 | CEBPA | c.500A>G (p.Glu167Gly) c.143A>G (p.Glu48Gly) c.605A>G (p.Glu202Gly) c.458A>G (p.Glu153Gly) | dbSNP gnomAD v4 |
19 | g.33301915T>G | CA405274821 | CEBPA | c.500A>C (p.Glu167Ala) c.143A>C (p.Glu48Ala) c.605A>C (p.Glu202Ala) c.458A>C (p.Glu153Ala) | gnomAD v4 |
19 | g.33301916C>A | CA405274823 | CEBPA | c.499G>T (p.Glu167Ter) c.142G>T (p.Glu48Ter) c.604G>T (p.Glu202Ter) c.457G>T (p.Glu153Ter) | gnomAD v4 |
19 | g.33301916C= | CA2332660232 | CEBPA | c.499G= (p.Glu167=) c.142G= (p.Glu48=) c.604G= (p.Glu202=) c.457G= (p.Glu153=) | |
19 | g.33301916C>G | CA405274825 | CEBPA | c.499G>C (p.Glu167Gln) c.142G>C (p.Glu48Gln) c.604G>C (p.Glu202Gln) c.457G>C (p.Glu153Gln) | |
19 | g.33301916C>T | CA405274824 | CEBPA | c.499G>A (p.Glu167Lys) c.142G>A (p.Glu48Lys) c.604G>A (p.Glu202Lys) c.457G>A (p.Glu153Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.33301917dup | CA645612687 | CEBPA | c.499dup (p.Glu167GlyfsTer3) c.142dup (p.Glu48GlyfsTer3) c.604dup (p.Glu202GlyfsTer3) c.457dup (p.Glu153GlyfsTer3) | COSMIC COSMIC |
19 | g.33301917C>A | CA405274826 | CEBPA | c.498G>T (p.Glu166Asp) c.141G>T (p.Glu47Asp) c.603G>T (p.Glu201Asp) c.456G>T (p.Glu152Asp) | gnomAD v4 |
19 | g.33301917C>G | CA405274827 | CEBPA | c.498G>C (p.Glu166Asp) c.141G>C (p.Glu47Asp) c.603G>C (p.Glu201Asp) c.456G>C (p.Glu152Asp) | gnomAD v4 |
19 | g.33301917C>T | CA507007747 | CEBPA | c.498G>A (p.Glu166=) c.141G>A (p.Glu47=) c.603G>A (p.Glu201=) c.456G>A (p.Glu152=) | gnomAD v4 |
19 | g.33301917_33301918insG | CA507007748 | CEBPA | c.497_498insC (p.Glu166AspfsTer4) c.140_141insC (p.Glu47AspfsTer4) c.602_603insC (p.Glu201AspfsTer4) c.455_456insC (p.Glu152AspfsTer4) | |
19 | g.33301918T>A | CA405274828 | CEBPA | c.497A>T (p.Glu166Val) c.140A>T (p.Glu47Val) c.602A>T (p.Glu201Val) c.455A>T (p.Glu152Val) | |
19 | g.33301918T>C | CA405274830 | CEBPA | c.497A>G (p.Glu166Gly) c.140A>G (p.Glu47Gly) c.602A>G (p.Glu201Gly) c.455A>G (p.Glu152Gly) | dbSNP gnomAD v4 |
19 | g.33301918T>G | CA405274829 | CEBPA | c.497A>C (p.Glu166Ala) c.140A>C (p.Glu47Ala) c.602A>C (p.Glu201Ala) c.455A>C (p.Glu152Ala) | gnomAD v4 |
19 | g.33301919C>A | CA405274831 | CEBPA | c.496G>T (p.Glu166Ter) c.139G>T (p.Glu47Ter) c.601G>T (p.Glu201Ter) c.454G>T (p.Glu152Ter) | gnomAD v4 COSMIC |
19 | g.33301919C= | CA2332660233 | CEBPA | c.496G= (p.Glu166=) c.139G= (p.Glu47=) c.601G= (p.Glu201=) c.454G= (p.Glu152=) | |
19 | g.33301919C>G | CA405274832 | CEBPA | c.496G>C (p.Glu166Gln) c.139G>C (p.Glu47Gln) c.601G>C (p.Glu201Gln) c.454G>C (p.Glu152Gln) | gnomAD v4 |
19 | g.33301919C>T | CA9363711 | CEBPA | c.496G>A (p.Glu166Lys) c.139G>A (p.Glu47Lys) c.601G>A (p.Glu201Lys) c.454G>A (p.Glu152Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.33301920G>A | CA507007751 | CEBPA | c.495C>T (p.Arg165=) c.138C>T (p.Arg46=) c.600C>T (p.Arg200=) c.453C>T (p.Arg151=) | gnomAD v4 |
19 | g.33301920G>C | CA507007750 | CEBPA | c.495C>G (p.Arg165=) c.138C>G (p.Arg46=) c.600C>G (p.Arg200=) c.453C>G (p.Arg151=) | dbSNP gnomAD v4 |