Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.151186410dup | CA2778433433 | ASB10 | c.570dup (p.Pro191AlafsTer5) c.525dup (p.Pro176AlafsTer5) c.705dup (p.Pro236AlafsTer5) | |
7 | g.151186410del | CA4573854 | ASB10 | c.570del (p.Pro191LeufsTer?) c.525del (p.Pro176LeufsTer?) c.705del (p.Pro236LeufsTer?) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186408C>A | CA370035680 | ASB10 | c.568G>T (p.Gly190Trp) c.523G>T (p.Gly175Trp) c.703G>T (p.Gly235Trp) | gnomAD v4 |
7 | g.151186408C= | CA1752544783 | ASB10 | c.568G= (p.Gly190=) c.523G= (p.Gly175=) c.703G= (p.Gly235=) | |
7 | g.151186408C>G | CA370035682 | ASB10 | c.568G>C (p.Gly190Arg) c.523G>C (p.Gly175Arg) c.703G>C (p.Gly235Arg) | |
7 | g.151186408C>T | CA4573855 | ASB10 | c.568G>A (p.Gly190Arg) c.523G>A (p.Gly175Arg) c.703G>A (p.Gly235Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
7 | g.151186409C>A | CA458881311 | ASB10 | c.567G>T (p.Arg189=) c.522G>T (p.Arg174=) c.702G>T (p.Arg234=) | gnomAD v4 |
7 | g.151186409C= | CA1752544786 | ASB10 | c.567G= (p.Arg189=) c.522G= (p.Arg174=) c.702G= (p.Arg234=) | |
7 | g.151186409C>G | CA458881312 | ASB10 | c.567G>C (p.Arg189=) c.522G>C (p.Arg174=) c.702G>C (p.Arg234=) | |
7 | g.151186409C>T | CA458881310 | ASB10 | c.567G>A (p.Arg189=) c.522G>A (p.Arg174=) c.702G>A (p.Arg234=) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186410C>A | CA370035685 | ASB10 | c.566G>T (p.Arg189Leu) c.521G>T (p.Arg174Leu) c.701G>T (p.Arg234Leu) | gnomAD v4 |
7 | g.151186410C= | CA1752544789 | ASB10 | c.566G= (p.Arg189=) c.521G= (p.Arg174=) c.701G= (p.Arg234=) | |
7 | g.151186410C>G | CA370035687 | ASB10 | c.566G>C (p.Arg189Pro) c.521G>C (p.Arg174Pro) c.701G>C (p.Arg234Pro) | gnomAD v4 |
7 | g.151186410C>T | CA169125146 | ASB10 | c.566G>A (p.Arg189Gln) c.521G>A (p.Arg174Gln) c.701G>A (p.Arg234Gln) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186411G>A | CA150496 | ASB10 | c.565C>T (p.Arg189Trp) c.520C>T (p.Arg174Trp) c.700C>T (p.Arg234Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
7 | g.151186411G>C | CA370035690 | ASB10 | c.565C>G (p.Arg189Gly) c.520C>G (p.Arg174Gly) c.700C>G (p.Arg234Gly) | gnomAD v4 |
7 | g.151186411G= | CA1752544796 | ASB10 | c.565C= (p.Arg189=) c.520C= (p.Arg174=) c.700C= (p.Arg234=) | |
7 | g.151186411G>T | CA458881319 | ASB10 | c.565C>A (p.Arg189=) c.520C>A (p.Arg174=) c.700C>A (p.Arg234=) | gnomAD v4 |
7 | g.151186412G>A | CA458881322 | ASB10 | c.564C>T (p.Cys188=) c.519C>T (p.Cys173=) c.699C>T (p.Cys233=) | gnomAD v4 |
7 | g.151186412G>C | CA370035692 | ASB10 | c.564C>G (p.Cys188Trp) c.519C>G (p.Cys173Trp) c.699C>G (p.Cys233Trp) | |
7 | g.151186412G= | CA1752544801 | ASB10 | c.564C= (p.Cys188=) c.519C= (p.Cys173=) c.699C= (p.Cys233=) | |
7 | g.151186412G>T | CA143897 | ASB10 | c.564C>A (p.Cys188Ter) c.519C>A (p.Cys173Ter) c.699C>A (p.Cys233Ter) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186413C>A | CA4573856 | ASB10 | c.563G>T (p.Cys188Phe) c.518G>T (p.Cys173Phe) c.698G>T (p.Cys233Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186413C= | CA1752544807 | ASB10 | c.563G= (p.Cys188=) c.518G= (p.Cys173=) c.698G= (p.Cys233=) | |
7 | g.151186413C>G | CA370035698 | ASB10 | c.563G>C (p.Cys188Ser) c.518G>C (p.Cys173Ser) c.698G>C (p.Cys233Ser) | gnomAD v4 |
7 | g.151186413C>T | CA370035696 | ASB10 | c.563G>A (p.Cys188Tyr) c.518G>A (p.Cys173Tyr) c.698G>A (p.Cys233Tyr) | gnomAD v4 |
7 | g.151186414A>C | CA370035699 | ASB10 | c.562T>G (p.Cys188Gly) c.517T>G (p.Cys173Gly) c.697T>G (p.Cys233Gly) | |
7 | g.151186414A>G | CA370035701 | ASB10 | c.562T>C (p.Cys188Arg) c.517T>C (p.Cys173Arg) c.697T>C (p.Cys233Arg) | |
7 | g.151186414A>T | CA370035703 | ASB10 | c.562T>A (p.Cys188Ser) c.517T>A (p.Cys173Ser) c.697T>A (p.Cys233Ser) | |
7 | g.151186415G>A | CA458881329 | ASB10 | c.561C>T (p.Leu187=) c.516C>T (p.Leu172=) c.696C>T (p.Leu232=) | dbSNP |
7 | g.151186415G>C | CA458881331 | ASB10 | c.561C>G (p.Leu187=) c.516C>G (p.Leu172=) c.696C>G (p.Leu232=) | |
7 | g.151186415G>T | CA458881330 | ASB10 | c.561C>A (p.Leu187=) c.516C>A (p.Leu172=) c.696C>A (p.Leu232=) | gnomAD v4 |
7 | g.151186416A= | CA1752544813 | ASB10 | c.560T= (p.Leu187=) c.515T= (p.Leu172=) c.695T= (p.Leu232=) | |
7 | g.151186416A>C | CA370035705 | ASB10 | c.560T>G (p.Leu187Arg) c.515T>G (p.Leu172Arg) c.695T>G (p.Leu232Arg) | |
7 | g.151186416A>G | CA370035706 | ASB10 | c.560T>C (p.Leu187Pro) c.515T>C (p.Leu172Pro) c.695T>C (p.Leu232Pro) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186416A>T | CA370035708 | ASB10 | c.560T>A (p.Leu187His) c.515T>A (p.Leu172His) c.695T>A (p.Leu232His) | |
7 | g.151186417G>A | CA370035710 | ASB10 | c.559C>T (p.Leu187Phe) c.514C>T (p.Leu172Phe) c.694C>T (p.Leu232Phe) | gnomAD v4 |
7 | g.151186417G>C | CA370035712 | ASB10 | c.559C>G (p.Leu187Val) c.514C>G (p.Leu172Val) c.694C>G (p.Leu232Val) | |
7 | g.151186417G>T | CA370035713 | ASB10 | c.559C>A (p.Leu187Ile) c.514C>A (p.Leu172Ile) c.694C>A (p.Leu232Ile) | gnomAD v4 |
7 | g.151186418A= | CA1752544816 | ASB10 | c.558T= (p.His186=) c.513T= (p.His171=) c.693T= (p.His231=) | |
7 | g.151186418A>C | CA370035715 | ASB10 | c.558T>G (p.His186Gln) c.513T>G (p.His171Gln) c.693T>G (p.His231Gln) | |
7 | g.151186418A>G | CA458881463 | ASB10 | c.558T>C (p.His186=) c.513T>C (p.His171=) c.693T>C (p.His231=) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186418A>T | CA370035717 | ASB10 | c.558T>A (p.His186Gln) c.513T>A (p.His171Gln) c.693T>A (p.His231Gln) | gnomAD v4 |
7 | g.151186419T>A | CA370035722 | ASB10 | c.557A>T (p.His186Leu) c.512A>T (p.His171Leu) c.692A>T (p.His231Leu) | |
7 | g.151186419T>C | CA4573857 | ASB10 | c.557A>G (p.His186Arg) c.512A>G (p.His171Arg) c.692A>G (p.His231Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.151186419T>G | CA370035719 | ASB10 | c.557A>C (p.His186Pro) c.512A>C (p.His171Pro) c.692A>C (p.His231Pro) | gnomAD v4 |
7 | g.151186419T= | CA1752544818 | ASB10 | c.557A= (p.His186=) c.512A= (p.His171=) c.692A= (p.His231=) | |
7 | g.151186420G>A | CA370035724 | ASB10 | c.556C>T (p.His186Tyr) c.511C>T (p.His171Tyr) c.691C>T (p.His231Tyr) | |
7 | g.151186420G>C | CA370035728 | ASB10 | c.556C>G (p.His186Asp) c.511C>G (p.His171Asp) c.691C>G (p.His231Asp) | |
7 | g.151186420G= | CA1752544820 | ASB10 | c.556C= (p.His186=) c.511C= (p.His171=) c.691C= (p.His231=) | |
7 | g.151186420G>T | CA370035726 | ASB10 | c.556C>A (p.His186Asn) c.511C>A (p.His171Asn) c.691C>A (p.His231Asn) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186421C>A | CA458881466 | ASB10 | c.555G>T (p.Leu185=) c.510G>T (p.Leu170=) c.690G>T (p.Leu230=) | gnomAD v4 |
7 | g.151186421C>G | CA458881467 | ASB10 | c.555G>C (p.Leu185=) c.510G>C (p.Leu170=) c.690G>C (p.Leu230=) | |
7 | g.151186421C>T | CA458881468 | ASB10 | c.555G>A (p.Leu185=) c.510G>A (p.Leu170=) c.690G>A (p.Leu230=) | gnomAD v4 |
7 | g.151186422A= | CA1752544823 | ASB10 | c.554T= (p.Leu185=) c.509T= (p.Leu170=) c.689T= (p.Leu230=) | |
7 | g.151186422A>C | CA370035730 | ASB10 | c.554T>G (p.Leu185Arg) c.509T>G (p.Leu170Arg) c.689T>G (p.Leu230Arg) | |
7 | g.151186422A>G | CA4573858 | ASB10 | c.554T>C (p.Leu185Pro) c.509T>C (p.Leu170Pro) c.689T>C (p.Leu230Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.151186422A>T | CA370035731 | ASB10 | c.554T>A (p.Leu185Gln) c.509T>A (p.Leu170Gln) c.689T>A (p.Leu230Gln) | gnomAD v4 |
7 | g.151186423G>A | CA458881469 | ASB10 | c.553C>T (p.Leu185=) c.508C>T (p.Leu170=) c.688C>T (p.Leu230=) | |
7 | g.151186423G>C | CA370035734 | ASB10 | c.553C>G (p.Leu185Val) c.508C>G (p.Leu170Val) c.688C>G (p.Leu230Val) | |
7 | g.151186423G>T | CA370035735 | ASB10 | c.553C>A (p.Leu185Met) c.508C>A (p.Leu170Met) c.688C>A (p.Leu230Met) | |
7 | g.151186427dup | CA2685657514 | ASB10 | c.553dup (p.Leu185ProfsTer11) c.508dup (p.Leu170ProfsTer11) c.688dup (p.Leu230ProfsTer11) | gnomAD v4 |
7 | g.151186427del | CA2685657515 | ASB10 | c.553del (p.Leu185CysfsTer?) c.508del (p.Leu170CysfsTer?) c.688del (p.Leu230CysfsTer?) | gnomAD v4 |
7 | g.151186424G>A | CA458881470 | ASB10 | c.552C>T (p.Pro184=) c.507C>T (p.Pro169=) c.687C>T (p.Pro229=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186424G>C | CA458881471 | ASB10 | c.552C>G (p.Pro184=) c.507C>G (p.Pro169=) c.687C>G (p.Pro229=) | |
7 | g.151186424G= | CA1752544826 | ASB10 | c.552C= (p.Pro184=) c.507C= (p.Pro169=) c.687C= (p.Pro229=) | |
7 | g.151186424G>T | CA458881472 | ASB10 | c.552C>A (p.Pro184=) c.507C>A (p.Pro169=) c.687C>A (p.Pro229=) | |
7 | g.151186425G>A | CA370035738 | ASB10 | c.551C>T (p.Pro184Leu) c.506C>T (p.Pro169Leu) c.686C>T (p.Pro229Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186425G>C | CA169125157 | ASB10 | c.551C>G (p.Pro184Arg) c.506C>G (p.Pro169Arg) c.686C>G (p.Pro229Arg) | dbSNP |
7 | g.151186425G= | CA1752544830 | ASB10 | c.551C= (p.Pro184=) c.506C= (p.Pro169=) c.686C= (p.Pro229=) | |
7 | g.151186425G>T | CA370035739 | ASB10 | c.551C>A (p.Pro184His) c.506C>A (p.Pro169His) c.686C>A (p.Pro229His) | gnomAD v4 |
7 | g.151186426G>A | CA370035741 | ASB10 | c.550C>T (p.Pro184Ser) c.505C>T (p.Pro169Ser) c.685C>T (p.Pro229Ser) | |
7 | g.151186426G>C | CA370035743 | ASB10 | c.550C>G (p.Pro184Ala) c.505C>G (p.Pro169Ala) c.685C>G (p.Pro229Ala) | |
7 | g.151186426G>T | CA370035744 | ASB10 | c.550C>A (p.Pro184Thr) c.505C>A (p.Pro169Thr) c.685C>A (p.Pro229Thr) | |
7 | g.151186427G>A | CA169125158 | ASB10 | c.549C>T (p.Arg183=) c.504C>T (p.Arg168=) c.684C>T (p.Arg228=) | dbSNP gnomAD v4 |
7 | g.151186427G>C | CA458881476 | ASB10 | c.549C>G (p.Arg183=) c.504C>G (p.Arg168=) c.684C>G (p.Arg228=) | |
7 | g.151186427G= | CA1752544832 | ASB10 | c.549C= (p.Arg183=) c.504C= (p.Arg168=) c.684C= (p.Arg228=) | |
7 | g.151186427G>T | CA458881477 | ASB10 | c.549C>A (p.Arg183=) c.504C>A (p.Arg168=) c.684C>A (p.Arg228=) | gnomAD v4 |
7 | g.151186428C>A | CA370035746 | ASB10 | c.548G>T (p.Arg183Leu) c.503G>T (p.Arg168Leu) c.683G>T (p.Arg228Leu) | gnomAD v4 |
7 | g.151186428C= | CA1752544834 | ASB10 | c.548G= (p.Arg183=) c.503G= (p.Arg168=) c.683G= (p.Arg228=) | |
7 | g.151186428C>G | CA370035748 | ASB10 | c.548G>C (p.Arg183Pro) c.503G>C (p.Arg168Pro) c.683G>C (p.Arg228Pro) | gnomAD v4 |
7 | g.151186428C>T | CA370035750 | ASB10 | c.548G>A (p.Arg183His) c.503G>A (p.Arg168His) c.683G>A (p.Arg228His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186429G>A | CA150543 | ASB10 | c.547C>T (p.Arg183Cys) c.502C>T (p.Arg168Cys) c.682C>T (p.Arg228Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186429G>C | CA370035753 | ASB10 | c.547C>G (p.Arg183Gly) c.502C>G (p.Arg168Gly) c.682C>G (p.Arg228Gly) | |
7 | g.151186429G= | CA1752544836 | ASB10 | c.547C= (p.Arg183=) c.502C= (p.Arg168=) c.682C= (p.Arg228=) | |
7 | g.151186429G>T | CA370035755 | ASB10 | c.547C>A (p.Arg183Ser) c.502C>A (p.Arg168Ser) c.682C>A (p.Arg228Ser) | gnomAD v4 |
7 | g.151186430T>A | CA370035757 | ASB10 | c.546A>T (p.Lys182Asn) c.501A>T (p.Lys167Asn) c.681A>T (p.Lys227Asn) | ClinVar |
7 | g.151186430T>C | CA458881481 | ASB10 | c.546A>G (p.Lys182=) c.501A>G (p.Lys167=) c.681A>G (p.Lys227=) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.151186430T>G | CA370035758 | ASB10 | c.546A>C (p.Lys182Asn) c.501A>C (p.Lys167Asn) c.681A>C (p.Lys227Asn) | |
7 | g.151186430T= | CA1752544842 | ASB10 | c.546A= (p.Lys182=) c.501A= (p.Lys167=) c.681A= (p.Lys227=) | |
7 | g.151186432del | CA2685657516 | ASB10 | c.546del (p.Lys182AsnfsTer?) c.501del (p.Lys167AsnfsTer?) c.681del (p.Lys227AsnfsTer?) | gnomAD v4 |
7 | g.151186431T>A | CA370035764 | ASB10 | c.545A>T (p.Lys182Ile) c.500A>T (p.Lys167Ile) c.680A>T (p.Lys227Ile) | |
7 | g.151186431T>C | CA370035762 | ASB10 | c.545A>G (p.Lys182Arg) c.500A>G (p.Lys167Arg) c.680A>G (p.Lys227Arg) | gnomAD v4 |
7 | g.151186431T>G | CA370035761 | ASB10 | c.545A>C (p.Lys182Thr) c.500A>C (p.Lys167Thr) c.680A>C (p.Lys227Thr) | |
7 | g.151186432T>A | CA370035766 | ASB10 | c.544A>T (p.Lys182Ter) c.499A>T (p.Lys167Ter) c.679A>T (p.Lys227Ter) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186432T>C | CA370035767 | ASB10 | c.544A>G (p.Lys182Glu) c.499A>G (p.Lys167Glu) c.679A>G (p.Lys227Glu) | gnomAD v4 |
7 | g.151186432T>G | CA370035769 | ASB10 | c.544A>C (p.Lys182Gln) c.499A>C (p.Lys167Gln) c.679A>C (p.Lys227Gln) | |
7 | g.151186432T= | CA1752544846 | ASB10 | c.544A= (p.Lys182=) c.499A= (p.Lys167=) c.679A= (p.Lys227=) | |
7 | g.151186433C>A | CA458881485 | ASB10 | c.543G>T (p.Gly181=) c.498G>T (p.Gly166=) c.678G>T (p.Gly226=) | gnomAD v4 |
7 | g.151186433C= | CA1752544847 | ASB10 | c.543G= (p.Gly181=) c.498G= (p.Gly166=) c.678G= (p.Gly226=) | |
7 | g.151186433C>G | CA458881486 | ASB10 | c.543G>C (p.Gly181=) c.498G>C (p.Gly166=) c.678G>C (p.Gly226=) | |
7 | g.151186433C>T | CA458881487 | ASB10 | c.543G>A (p.Gly181=) c.498G>A (p.Gly166=) c.678G>A (p.Gly226=) | dbSNP gnomAD v4 |
7 | g.151186434C>A | CA370035770 | ASB10 | c.542G>T (p.Gly181Val) c.497G>T (p.Gly166Val) c.677G>T (p.Gly226Val) | gnomAD v4 |
7 | g.151186434C= | CA1752544850 | ASB10 | c.542G= (p.Gly181=) c.497G= (p.Gly166=) c.677G= (p.Gly226=) | |
7 | g.151186434C>G | CA370035771 | ASB10 | c.542G>C (p.Gly181Ala) c.497G>C (p.Gly166Ala) c.677G>C (p.Gly226Ala) | dbSNP |
7 | g.151186434C>T | CA370035773 | ASB10 | c.542G>A (p.Gly181Glu) c.497G>A (p.Gly166Glu) c.677G>A (p.Gly226Glu) | |
7 | g.151186435C>A | CA370035775 | ASB10 | c.541G>T (p.Gly181Trp) c.496G>T (p.Gly166Trp) c.676G>T (p.Gly226Trp) | gnomAD v4 |
7 | g.151186435C= | CA1752544853 | ASB10 | c.541G= (p.Gly181=) c.496G= (p.Gly166=) c.676G= (p.Gly226=) | |
7 | g.151186435C>G | CA370035777 | ASB10 | c.541G>C (p.Gly181Arg) c.496G>C (p.Gly166Arg) c.676G>C (p.Gly226Arg) | |
7 | g.151186435C>T | CA169125160 | ASB10 | c.541G>A (p.Gly181Arg) c.496G>A (p.Gly166Arg) c.676G>A (p.Gly226Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186436A>C | CA370035779 | ASB10 | c.540T>G (p.Asp180Glu) c.495T>G (p.Asp165Glu) c.675T>G (p.Asp225Glu) | |
7 | g.151186436A>G | CA458881492 | ASB10 | c.540T>C (p.Asp180=) c.495T>C (p.Asp165=) c.675T>C (p.Asp225=) | |
7 | g.151186436A>T | CA370035781 | ASB10 | c.540T>A (p.Asp180Glu) c.495T>A (p.Asp165Glu) c.675T>A (p.Asp225Glu) | gnomAD v4 |
7 | g.151186437T>A | CA370035787 | ASB10 | c.539A>T (p.Asp180Val) c.494A>T (p.Asp165Val) c.674A>T (p.Asp225Val) | |
7 | g.151186437T>C | CA370035785 | ASB10 | c.539A>G (p.Asp180Gly) c.494A>G (p.Asp165Gly) c.674A>G (p.Asp225Gly) | |
7 | g.151186437T>G | CA370035783 | ASB10 | c.539A>C (p.Asp180Ala) c.494A>C (p.Asp165Ala) c.674A>C (p.Asp225Ala) | |
7 | g.151186438C>A | CA370035789 | ASB10 | c.538G>T (p.Asp180Tyr) c.493G>T (p.Asp165Tyr) c.673G>T (p.Asp225Tyr) | gnomAD v4 |
7 | g.151186438C>G | CA370035791 | ASB10 | c.538G>C (p.Asp180His) c.493G>C (p.Asp165His) c.673G>C (p.Asp225His) | |
7 | g.151186438C>T | CA370035792 | ASB10 | c.538G>A (p.Asp180Asn) c.493G>A (p.Asp165Asn) c.673G>A (p.Asp225Asn) | gnomAD v4 |
7 | g.151186439C>A | CA370035794 | ASB10 | c.537G>T (p.Gln179His) c.492G>T (p.Gln164His) c.672G>T (p.Gln224His) | gnomAD v4 |
7 | g.151186439C= | CA1752544854 | ASB10 | c.537G= (p.Gln179=) c.492G= (p.Gln164=) c.672G= (p.Gln224=) | |
7 | g.151186439C>G | CA370035796 | ASB10 | c.537G>C (p.Gln179His) c.492G>C (p.Gln164His) c.672G>C (p.Gln224His) | |
7 | g.151186439C>T | CA458881496 | ASB10 | c.537G>A (p.Gln179=) c.492G>A (p.Gln164=) c.672G>A (p.Gln224=) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186440T>A | CA370035798 | ASB10 | c.536A>T (p.Gln179Leu) c.491A>T (p.Gln164Leu) c.671A>T (p.Gln224Leu) | |
7 | g.151186440T>C | CA370035800 | ASB10 | c.536A>G (p.Gln179Arg) c.491A>G (p.Gln164Arg) c.671A>G (p.Gln224Arg) | gnomAD v4 |
7 | g.151186440T>G | CA370035801 | ASB10 | c.536A>C (p.Gln179Pro) c.491A>C (p.Gln164Pro) c.671A>C (p.Gln224Pro) | |
7 | g.151186441G>A | CA370035803 | ASB10 | c.535C>T (p.Gln179Ter) c.490C>T (p.Gln164Ter) c.670C>T (p.Gln224Ter) | gnomAD v4 |
7 | g.151186441G>C | CA370035804 | ASB10 | c.535C>G (p.Gln179Glu) c.490C>G (p.Gln164Glu) c.670C>G (p.Gln224Glu) | |
7 | g.151186441G>T | CA370035806 | ASB10 | c.535C>A (p.Gln179Lys) c.490C>A (p.Gln164Lys) c.670C>A (p.Gln224Lys) | gnomAD v4 |
7 | g.151186442G>A | CA458881497 | ASB10 | c.534C>T (p.Asp178=) c.489C>T (p.Asp163=) c.669C>T (p.Asp223=) | dbSNP gnomAD v4 |
7 | g.151186442G>C | CA370035808 | ASB10 | c.534C>G (p.Asp178Glu) c.489C>G (p.Asp163Glu) c.669C>G (p.Asp223Glu) | |
7 | g.151186442G= | CA1752544856 | ASB10 | c.534C= (p.Asp178=) c.489C= (p.Asp163=) c.669C= (p.Asp223=) | |
7 | g.151186442G>T | CA370035810 | ASB10 | c.534C>A (p.Asp178Glu) c.489C>A (p.Asp163Glu) c.669C>A (p.Asp223Glu) | |
7 | g.151186443T>A | CA370035816 | ASB10 | c.533A>T (p.Asp178Val) c.488A>T (p.Asp163Val) c.668A>T (p.Asp223Val) | |
7 | g.151186443T>C | CA370035812 | ASB10 | c.533A>G (p.Asp178Gly) c.488A>G (p.Asp163Gly) c.668A>G (p.Asp223Gly) | |
7 | g.151186443T>G | CA370035814 | ASB10 | c.533A>C (p.Asp178Ala) c.488A>C (p.Asp163Ala) c.668A>C (p.Asp223Ala) | |
7 | g.151186444C>A | CA370035817 | ASB10 | c.532G>T (p.Asp178Tyr) c.487G>T (p.Asp163Tyr) c.667G>T (p.Asp223Tyr) | gnomAD v4 |
7 | g.151186444C= | CA1752544859 | ASB10 | c.532G= (p.Asp178=) c.487G= (p.Asp163=) c.667G= (p.Asp223=) | |
7 | g.151186444C>G | CA370035819 | ASB10 | c.532G>C (p.Asp178His) c.487G>C (p.Asp163His) c.667G>C (p.Asp223His) | |
7 | g.151186444C>T | CA370035820 | ASB10 | c.532G>A (p.Asp178Asn) c.487G>A (p.Asp163Asn) c.667G>A (p.Asp223Asn) | dbSNP |
7 | g.151186445A= | CA1752544861 | ASB10 | c.531T= (p.Ala177=) c.486T= (p.Ala162=) c.666T= (p.Ala222=) | |
7 | g.151186445A>C | CA458881500 | ASB10 | c.531T>G (p.Ala177=) c.486T>G (p.Ala162=) c.666T>G (p.Ala222=) | |
7 | g.151186445A>G | CA458881501 | ASB10 | c.531T>C (p.Ala177=) c.486T>C (p.Ala162=) c.666T>C (p.Ala222=) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186445A>T | CA458881503 | ASB10 | c.531T>A (p.Ala177=) c.486T>A (p.Ala162=) c.666T>A (p.Ala222=) | |
7 | g.151186446G>A | CA370035822 | ASB10 | c.530C>T (p.Ala177Val) c.485C>T (p.Ala162Val) c.665C>T (p.Ala222Val) | gnomAD v4 |
7 | g.151186446G>C | CA370035823 | ASB10 | c.530C>G (p.Ala177Gly) c.485C>G (p.Ala162Gly) c.665C>G (p.Ala222Gly) | |
7 | g.151186446G>T | CA370035825 | ASB10 | c.530C>A (p.Ala177Asp) c.485C>A (p.Ala162Asp) c.665C>A (p.Ala222Asp) | |
7 | g.151186447C>A | CA370035827 | ASB10 | c.529G>T (p.Ala177Ser) c.484G>T (p.Ala162Ser) c.664G>T (p.Ala222Ser) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186447C= | CA1752544866 | ASB10 | c.529G= (p.Ala177=) c.484G= (p.Ala162=) c.664G= (p.Ala222=) | |
7 | g.151186447C>G | CA370035829 | ASB10 | c.529G>C (p.Ala177Pro) c.484G>C (p.Ala162Pro) c.664G>C (p.Ala222Pro) | |
7 | g.151186447C>T | CA4573859 | ASB10 | c.529G>A (p.Ala177Thr) c.484G>A (p.Ala162Thr) c.664G>A (p.Ala222Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186448G>A | CA4573860 | ASB10 | c.528C>T (p.Ile176=) c.483C>T (p.Ile161=) c.663C>T (p.Ile221=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186448G>C | CA370035833 | ASB10 | c.528C>G (p.Ile176Met) c.483C>G (p.Ile161Met) c.663C>G (p.Ile221Met) | |
7 | g.151186448G= | CA1752544868 | ASB10 | c.528C= (p.Ile176=) c.483C= (p.Ile161=) c.663C= (p.Ile221=) | |
7 | g.151186448G>T | CA458881505 | ASB10 | c.528C>A (p.Ile176=) c.483C>A (p.Ile161=) c.663C>A (p.Ile221=) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.151186449A>C | CA370035839 | ASB10 | c.527T>G (p.Ile176Ser) c.482T>G (p.Ile161Ser) c.662T>G (p.Ile221Ser) | |
7 | g.151186449A>G | CA370035837 | ASB10 | c.527T>C (p.Ile176Thr) c.482T>C (p.Ile161Thr) c.662T>C (p.Ile221Thr) | |
7 | g.151186449A>T | CA370035835 | ASB10 | c.527T>A (p.Ile176Asn) c.482T>A (p.Ile161Asn) c.662T>A (p.Ile221Asn) | |
7 | g.151186450T>A | CA370035840 | ASB10 | c.526A>T (p.Ile176Phe) c.481A>T (p.Ile161Phe) c.661A>T (p.Ile221Phe) | |
7 | g.151186450T>C | CA370035843 | ASB10 | c.526A>G (p.Ile176Val) c.481A>G (p.Ile161Val) c.661A>G (p.Ile221Val) | |
7 | g.151186450T>G | CA370035842 | ASB10 | c.526A>C (p.Ile176Leu) c.481A>C (p.Ile161Leu) c.661A>C (p.Ile221Leu) | |
7 | g.151186451G>A | CA458881508 | ASB10 | c.525C>T (p.Asn175=) c.480C>T (p.Asn160=) c.660C>T (p.Asn220=) | gnomAD v4 |
7 | g.151186451G>C | CA370035845 | ASB10 | c.525C>G (p.Asn175Lys) c.480C>G (p.Asn160Lys) c.660C>G (p.Asn220Lys) | |
7 | g.151186451G>T | CA370035847 | ASB10 | c.525C>A (p.Asn175Lys) c.480C>A (p.Asn160Lys) c.660C>A (p.Asn220Lys) | gnomAD v4 |
7 | g.151186452T>A | CA370035849 | ASB10 | c.524A>T (p.Asn175Ile) c.479A>T (p.Asn160Ile) c.659A>T (p.Asn220Ile) | |
7 | g.151186452T>C | CA370035850 | ASB10 | c.524A>G (p.Asn175Ser) c.479A>G (p.Asn160Ser) c.659A>G (p.Asn220Ser) | |
7 | g.151186452T>G | CA150494 | ASB10 | c.524A>C (p.Asn175Thr) c.479A>C (p.Asn160Thr) c.659A>C (p.Asn220Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186452T= | CA1752544874 | ASB10 | c.524A= (p.Asn175=) c.479A= (p.Asn160=) c.659A= (p.Asn220=) | |
7 | g.151186453T>A | CA370035852 | ASB10 | c.523A>T (p.Asn175Tyr) c.478A>T (p.Asn160Tyr) c.658A>T (p.Asn220Tyr) | |
7 | g.151186453T>C | CA370035854 | ASB10 | c.523A>G (p.Asn175Asp) c.478A>G (p.Asn160Asp) c.658A>G (p.Asn220Asp) | gnomAD v4 |
7 | g.151186453T>G | CA370035856 | ASB10 | c.523A>C (p.Asn175His) c.478A>C (p.Asn160His) c.658A>C (p.Asn220His) | dbSNP |
7 | g.151186453T= | CA1752544877 | ASB10 | c.523A= (p.Asn175=) c.478A= (p.Asn160=) c.658A= (p.Asn220=) | |
7 | g.151186454G>A | CA4573861 | ASB10 | c.522C>T (p.Pro174=) c.477C>T (p.Pro159=) c.657C>T (p.Pro219=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186454G>C | CA458881511 | ASB10 | c.522C>G (p.Pro174=) c.477C>G (p.Pro159=) c.657C>G (p.Pro219=) | |
7 | g.151186454G= | CA1752544881 | ASB10 | c.522C= (p.Pro174=) c.477C= (p.Pro159=) c.657C= (p.Pro219=) | |
7 | g.151186454G>T | CA458881512 | ASB10 | c.522C>A (p.Pro174=) c.477C>A (p.Pro159=) c.657C>A (p.Pro219=) | gnomAD v4 |
7 | g.151186455G>A | CA370035859 | ASB10 | c.521C>T (p.Pro174Leu) c.476C>T (p.Pro159Leu) c.656C>T (p.Pro219Leu) | |
7 | g.151186455G>C | CA370035861 | ASB10 | c.521C>G (p.Pro174Arg) c.476C>G (p.Pro159Arg) c.656C>G (p.Pro219Arg) | |
7 | g.151186455G>T | CA370035863 | ASB10 | c.521C>A (p.Pro174His) c.476C>A (p.Pro159His) c.656C>A (p.Pro219His) | gnomAD v4 |
7 | g.151186456G>A | CA370035867 | ASB10 | c.520C>T (p.Pro174Ser) c.475C>T (p.Pro159Ser) c.655C>T (p.Pro219Ser) | COSMIC COSMIC COSMIC COSMIC |
7 | g.151186456G>C | CA370035865 | ASB10 | c.520C>G (p.Pro174Ala) c.475C>G (p.Pro159Ala) c.655C>G (p.Pro219Ala) | gnomAD v4 |
7 | g.151186456G>T | CA370035866 | ASB10 | c.520C>A (p.Pro174Thr) c.475C>A (p.Pro159Thr) c.655C>A (p.Pro219Thr) | gnomAD v4 |
7 | g.151186457G>A | CA458881515 | ASB10 | c.519C>T (p.Asp173=) c.474C>T (p.Asp158=) c.654C>T (p.Asp218=) | gnomAD v4 |
7 | g.151186457G>C | CA370035869 | ASB10 | c.519C>G (p.Asp173Glu) c.474C>G (p.Asp158Glu) c.654C>G (p.Asp218Glu) | |
7 | g.151186457G= | CA1752544886 | ASB10 | c.519C= (p.Asp173=) c.474C= (p.Asp158=) c.654C= (p.Asp218=) | |
7 | g.151186457G>T | CA4573862 | ASB10 | c.519C>A (p.Asp173Glu) c.474C>A (p.Asp158Glu) c.654C>A (p.Asp218Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186458T>A | CA370035872 | ASB10 | c.518A>T (p.Asp173Val) c.473A>T (p.Asp158Val) c.653A>T (p.Asp218Val) | |
7 | g.151186458T>C | CA370035873 | ASB10 | c.518A>G (p.Asp173Gly) c.473A>G (p.Asp158Gly) c.653A>G (p.Asp218Gly) | |
7 | g.151186458T>G | CA370035875 | ASB10 | c.518A>C (p.Asp173Ala) c.473A>C (p.Asp158Ala) c.653A>C (p.Asp218Ala) | |
7 | g.151186459C>A | CA370035878 | ASB10 | c.517G>T (p.Asp173Tyr) c.472G>T (p.Asp158Tyr) c.652G>T (p.Asp218Tyr) | gnomAD v4 |
7 | g.151186459C= | CA1752544889 | ASB10 | c.517G= (p.Asp173=) c.472G= (p.Asp158=) c.652G= (p.Asp218=) | |
7 | g.151186459C>G | CA370035879 | ASB10 | c.517G>C (p.Asp173His) c.472G>C (p.Asp158His) c.652G>C (p.Asp218His) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186459C>T | CA4573863 | ASB10 | c.517G>A (p.Asp173Asn) c.472G>A (p.Asp158Asn) c.652G>A (p.Asp218Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
7 | g.151186460G>A | CA150492 | ASB10 | c.516C>T (p.Ala172=) c.471C>T (p.Ala157=) c.651C>T (p.Ala217=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186460G>C | CA4573864 | ASB10 | c.516C>G (p.Ala172=) c.471C>G (p.Ala157=) c.651C>G (p.Ala217=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.151186460G= | CA1752544897 | ASB10 | c.516C= (p.Ala172=) c.471C= (p.Ala157=) c.651C= (p.Ala217=) | |
7 | g.151186460G>T | CA458881518 | ASB10 | c.516C>A (p.Ala172=) c.471C>A (p.Ala157=) c.651C>A (p.Ala217=) | gnomAD v4 |
7 | g.151186461G>A | CA150541 | ASB10 | c.515C>T (p.Ala172Val) c.470C>T (p.Ala157Val) c.650C>T (p.Ala217Val) | ClinVar dbSNP gnomAD v4 |
7 | g.151186461G>C | CA4573865 | ASB10 | c.515C>G (p.Ala172Gly) c.470C>G (p.Ala157Gly) c.650C>G (p.Ala217Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
7 | g.151186461G= | CA1752544904 | ASB10 | c.515C= (p.Ala172=) c.470C= (p.Ala157=) c.650C= (p.Ala217=) | |
7 | g.151186461G>T | CA370035882 | ASB10 | c.515C>A (p.Ala172Asp) c.470C>A (p.Ala157Asp) c.650C>A (p.Ala217Asp) | gnomAD v4 |
7 | g.151186462C>A | CA370035885 | ASB10 | c.514G>T (p.Ala172Ser) c.469G>T (p.Ala157Ser) c.649G>T (p.Ala217Ser) | gnomAD v4 |
7 | g.151186462C= | CA1752544909 | ASB10 | c.514G= (p.Ala172=) c.469G= (p.Ala157=) c.649G= (p.Ala217=) | |
7 | g.151186462C>G | CA370035887 | ASB10 | c.514G>C (p.Ala172Pro) c.469G>C (p.Ala157Pro) c.649G>C (p.Ala217Pro) | |
7 | g.151186462C>T | CA370035888 | ASB10 | c.514G>A (p.Ala172Thr) c.469G>A (p.Ala157Thr) c.649G>A (p.Ala217Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186463T>A | CA458881522 | ASB10 | c.513A>T (p.Gly171=) c.468A>T (p.Gly156=) c.648A>T (p.Gly216=) | |
7 | g.151186463T>C | CA458881523 | ASB10 | c.513A>G (p.Gly171=) c.468A>G (p.Gly156=) c.648A>G (p.Gly216=) | dbSNP gnomAD v4 |
7 | g.151186463T>G | CA458881524 | ASB10 | c.513A>C (p.Gly171=) c.468A>C (p.Gly156=) c.648A>C (p.Gly216=) | |
7 | g.151186463T= | CA1752544913 | ASB10 | c.513A= (p.Gly171=) c.468A= (p.Gly156=) c.648A= (p.Gly216=) | |
7 | g.151186464C>A | CA370035889 | ASB10 | c.512G>T (p.Gly171Val) c.467G>T (p.Gly156Val) c.647G>T (p.Gly216Val) | gnomAD v4 |
7 | g.151186464C= | CA1752544917 | ASB10 | c.512G= (p.Gly171=) c.467G= (p.Gly156=) c.647G= (p.Gly216=) | |
7 | g.151186464C>G | CA370035891 | ASB10 | c.512G>C (p.Gly171Ala) c.467G>C (p.Gly156Ala) c.647G>C (p.Gly216Ala) | |
7 | g.151186464C>T | CA169125197 | ASB10 | c.512G>A (p.Gly171Glu) c.467G>A (p.Gly156Glu) c.647G>A (p.Gly216Glu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.151186465C>A | CA370035894 | ASB10 | c.511G>T (p.Gly171Ter) c.466G>T (p.Gly156Ter) c.646G>T (p.Gly216Ter) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186465C= | CA1752544919 | ASB10 | c.511G= (p.Gly171=) c.466G= (p.Gly156=) c.646G= (p.Gly216=) | |
7 | g.151186465C>G | CA370035896 | ASB10 | c.511G>C (p.Gly171Arg) c.466G>C (p.Gly156Arg) c.646G>C (p.Gly216Arg) | |
7 | g.151186465C>T | CA4573866 | ASB10 | c.511G>A (p.Gly171Arg) c.466G>A (p.Gly156Arg) c.646G>A (p.Gly216Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.151186466T>A | CA458881527 | ASB10 | c.510A>T (p.Ala170=) c.465A>T (p.Ala155=) c.645A>T (p.Ala215=) | |
7 | g.151186466T>C | CA458881529 | ASB10 | c.510A>G (p.Ala170=) c.465A>G (p.Ala155=) c.645A>G (p.Ala215=) | gnomAD v4 |
7 | g.151186466T>G | CA458881530 | ASB10 | c.510A>C (p.Ala170=) c.465A>C (p.Ala155=) c.645A>C (p.Ala215=) | |
7 | g.151186467G>A | CA370035899 | ASB10 | c.509C>T (p.Ala170Val) c.464C>T (p.Ala155Val) c.644C>T (p.Ala215Val) | gnomAD v4 |
7 | g.151186467G>C | CA370035901 | ASB10 | c.509C>G (p.Ala170Gly) c.464C>G (p.Ala155Gly) c.644C>G (p.Ala215Gly) | |
7 | g.151186467G>T | CA370035903 | ASB10 | c.509C>A (p.Ala170Glu) c.464C>A (p.Ala155Glu) c.644C>A (p.Ala215Glu) | |
7 | g.151186468C>A | CA370035909 | ASB10 | c.508G>T (p.Ala170Ser) c.463G>T (p.Ala155Ser) c.643G>T (p.Ala215Ser) | gnomAD v4 |
7 | g.151186468C>G | CA370035907 | ASB10 | c.508G>C (p.Ala170Pro) c.463G>C (p.Ala155Pro) c.643G>C (p.Ala215Pro) | |
7 | g.151186468C>T | CA370035905 | ASB10 | c.508G>A (p.Ala170Thr) c.463G>A (p.Ala155Thr) c.643G>A (p.Ala215Thr) | |
7 | g.151186469C>A | CA458881532 | ASB10 | c.507G>T (p.Val169=) c.462G>T (p.Val154=) c.642G>T (p.Val214=) | gnomAD v4 |
7 | g.151186469C>G | CA458881533 | ASB10 | c.507G>C (p.Val169=) c.462G>C (p.Val154=) c.642G>C (p.Val214=) | |
7 | g.151186469C>T | CA458881534 | ASB10 | c.507G>A (p.Val169=) c.462G>A (p.Val154=) c.642G>A (p.Val214=) | |
7 | g.151186470A>C | CA370035910 | ASB10 | c.506T>G (p.Val169Gly) c.461T>G (p.Val154Gly) c.641T>G (p.Val214Gly) | |
7 | g.151186470A>G | CA370035912 | ASB10 | c.506T>C (p.Val169Ala) c.461T>C (p.Val154Ala) c.641T>C (p.Val214Ala) | |
7 | g.151186470A>T | CA370035914 | ASB10 | c.506T>A (p.Val169Glu) c.461T>A (p.Val154Glu) c.641T>A (p.Val214Glu) | |
7 | g.151186471C>A | CA370035916 | ASB10 | c.505G>T (p.Val169Leu) c.460G>T (p.Val154Leu) c.640G>T (p.Val214Leu) | gnomAD v4 |
7 | g.151186471C= | CA1752544921 | ASB10 | c.505G= (p.Val169=) c.460G= (p.Val154=) c.640G= (p.Val214=) | |
7 | g.151186471C>G | CA370035917 | ASB10 | c.505G>C (p.Val169Leu) c.460G>C (p.Val154Leu) c.640G>C (p.Val214Leu) | gnomAD v4 |
7 | g.151186471C>T | CA169125236 | ASB10 | c.505G>A (p.Val169Met) c.460G>A (p.Val154Met) c.640G>A (p.Val214Met) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186472C>A | CA458881537 | ASB10 | c.504G>T (p.Leu168=) c.459G>T (p.Leu153=) c.639G>T (p.Leu213=) | gnomAD v4 |
7 | g.151186472C>G | CA458881539 | ASB10 | c.504G>C (p.Leu168=) c.459G>C (p.Leu153=) c.639G>C (p.Leu213=) | |
7 | g.151186472C>T | CA458881538 | ASB10 | c.504G>A (p.Leu168=) c.459G>A (p.Leu153=) c.639G>A (p.Leu213=) | |
7 | g.151186473A>C | CA370035920 | ASB10 | c.503T>G (p.Leu168Arg) c.458T>G (p.Leu153Arg) c.638T>G (p.Leu213Arg) | |
7 | g.151186473A>G | CA370035922 | ASB10 | c.503T>C (p.Leu168Pro) c.458T>C (p.Leu153Pro) c.638T>C (p.Leu213Pro) | |
7 | g.151186473A>T | CA370035924 | ASB10 | c.503T>A (p.Leu168Gln) c.458T>A (p.Leu153Gln) c.638T>A (p.Leu213Gln) | |
7 | g.151186474G>A | CA458881540 | ASB10 | c.502C>T (p.Leu168=) c.457C>T (p.Leu153=) c.637C>T (p.Leu213=) | gnomAD v4 |
7 | g.151186474G>C | CA370035926 | ASB10 | c.502C>G (p.Leu168Val) c.457C>G (p.Leu153Val) c.637C>G (p.Leu213Val) | |
7 | g.151186474G>T | CA370035927 | ASB10 | c.502C>A (p.Leu168Met) c.457C>A (p.Leu153Met) c.637C>A (p.Leu213Met) | gnomAD v4 |
7 | g.151186475C>A | CA458881541 | ASB10 | c.501G>T (p.Leu167=) c.456G>T (p.Leu152=) c.636G>T (p.Leu212=) | gnomAD v4 |
7 | g.151186475C= | CA1752544925 | ASB10 | c.501G= (p.Leu167=) c.456G= (p.Leu152=) c.636G= (p.Leu212=) | |
7 | g.151186475C>G | CA458881542 | ASB10 | c.501G>C (p.Leu167=) c.456G>C (p.Leu152=) c.636G>C (p.Leu212=) | dbSNP |
7 | g.151186475C>T | CA4573867 | ASB10 | c.501G>A (p.Leu167=) c.456G>A (p.Leu152=) c.636G>A (p.Leu212=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186476A>C | CA370035934 | ASB10 | c.500T>G (p.Leu167Arg) c.455T>G (p.Leu152Arg) c.635T>G (p.Leu212Arg) | |
7 | g.151186476A>G | CA370035932 | ASB10 | c.500T>C (p.Leu167Pro) c.455T>C (p.Leu152Pro) c.635T>C (p.Leu212Pro) | gnomAD v4 |
7 | g.151186476A>T | CA370035930 | ASB10 | c.500T>A (p.Leu167Gln) c.455T>A (p.Leu152Gln) c.635T>A (p.Leu212Gln) | |
7 | g.151186477G>A | CA4573868 | ASB10 | c.499C>T (p.Leu167=) c.454C>T (p.Leu152=) c.634C>T (p.Leu212=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.151186477G>C | CA370035938 | ASB10 | c.499C>G (p.Leu167Val) c.454C>G (p.Leu152Val) c.634C>G (p.Leu212Val) | |
7 | g.151186477G= | CA1752544930 | ASB10 | c.499C= (p.Leu167=) c.454C= (p.Leu152=) c.634C= (p.Leu212=) | |
7 | g.151186477G>T | CA370035936 | ASB10 | c.499C>A (p.Leu167Met) c.454C>A (p.Leu152Met) c.634C>A (p.Leu212Met) | gnomAD v4 |
7 | g.151186478C>A | CA458881545 | ASB10 | c.498G>T (p.Val166=) c.453G>T (p.Val151=) c.633G>T (p.Val211=) | gnomAD v4 |
7 | g.151186478C>G | CA458881544 | ASB10 | c.498G>C (p.Val166=) c.453G>C (p.Val151=) c.633G>C (p.Val211=) | |
7 | g.151186478C>T | CA458881543 | ASB10 | c.498G>A (p.Val166=) c.453G>A (p.Val151=) c.633G>A (p.Val211=) | |
7 | g.151186479A= | CA1752544933 | ASB10 | c.497T= (p.Val166=) c.452T= (p.Val151=) c.632T= (p.Val211=) | |
7 | g.151186479A>C | CA370035940 | ASB10 | c.497T>G (p.Val166Gly) c.452T>G (p.Val151Gly) c.632T>G (p.Val211Gly) | |
7 | g.151186479A>G | CA370035942 | ASB10 | c.497T>C (p.Val166Ala) c.452T>C (p.Val151Ala) c.632T>C (p.Val211Ala) | |
7 | g.151186479A>T | CA370035944 | ASB10 | c.497T>A (p.Val166Glu) c.452T>A (p.Val151Glu) c.632T>A (p.Val211Glu) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186480C>A | CA370035946 | ASB10 | c.496G>T (p.Val166Leu) c.451G>T (p.Val151Leu) c.631G>T (p.Val211Leu) | |
7 | g.151186480C>G | CA370035947 | ASB10 | c.496G>C (p.Val166Leu) c.451G>C (p.Val151Leu) c.631G>C (p.Val211Leu) | |
7 | g.151186480C>T | CA370035949 | ASB10 | c.496G>A (p.Val166Met) c.451G>A (p.Val151Met) c.631G>A (p.Val211Met) | gnomAD v4 |
7 | g.151186481A= | CA1752544935 | ASB10 | c.495T= (p.His165=) c.450T= (p.His150=) c.630T= (p.His210=) | |
7 | g.151186481A>C | CA370035953 | ASB10 | c.495T>G (p.His165Gln) c.450T>G (p.His150Gln) c.630T>G (p.His210Gln) | |
7 | g.151186481A>G | CA458881546 | ASB10 | c.495T>C (p.His165=) c.450T>C (p.His150=) c.630T>C (p.His210=) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.151186481A>T | CA370035951 | ASB10 | c.495T>A (p.His165Gln) c.450T>A (p.His150Gln) c.630T>A (p.His210Gln) | |
7 | g.151186482T>A | CA370035955 | ASB10 | c.494A>T (p.His165Leu) c.449A>T (p.His150Leu) c.629A>T (p.His210Leu) | gnomAD v4 |
7 | g.151186482T>C | CA370035957 | ASB10 | c.494A>G (p.His165Arg) c.449A>G (p.His150Arg) c.629A>G (p.His210Arg) | gnomAD v4 |
7 | g.151186482T>G | CA370035958 | ASB10 | c.494A>C (p.His165Pro) c.449A>C (p.His150Pro) c.629A>C (p.His210Pro) | |
7 | g.151186483G>A | CA370035960 | ASB10 | c.493C>T (p.His165Tyr) c.448C>T (p.His150Tyr) c.628C>T (p.His210Tyr) | dbSNP gnomAD v4 |
7 | g.151186483G>C | CA370035961 | ASB10 | c.493C>G (p.His165Asp) c.448C>G (p.His150Asp) c.628C>G (p.His210Asp) | dbSNP |
7 | g.151186483G= | CA1752544938 | ASB10 | c.493C= (p.His165=) c.448C= (p.His150=) c.628C= (p.His210=) | |
7 | g.151186483G>T | CA370035963 | ASB10 | c.493C>A (p.His165Asn) c.448C>A (p.His150Asn) c.628C>A (p.His210Asn) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186484A>C | CA458881547 | ASB10 | c.492T>G (p.Val164=) c.447T>G (p.Val149=) c.627T>G (p.Val209=) | |
7 | g.151186484A>G | CA458881548 | ASB10 | c.492T>C (p.Val164=) c.447T>C (p.Val149=) c.627T>C (p.Val209=) | |
7 | g.151186484A>T | CA458881549 | ASB10 | c.492T>A (p.Val164=) c.447T>A (p.Val149=) c.627T>A (p.Val209=) | |
7 | g.151186485A= | CA1752544943 | ASB10 | c.491T= (p.Val164=) c.446T= (p.Val149=) c.626T= (p.Val209=) | |
7 | g.151186485A>C | CA370035965 | ASB10 | c.491T>G (p.Val164Gly) c.446T>G (p.Val149Gly) c.626T>G (p.Val209Gly) | |
7 | g.151186485A>G | CA370035969 | ASB10 | c.491T>C (p.Val164Ala) c.446T>C (p.Val149Ala) c.626T>C (p.Val209Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186485A>T | CA370035967 | ASB10 | c.491T>A (p.Val164Asp) c.446T>A (p.Val149Asp) c.626T>A (p.Val209Asp) | |
7 | g.151186485_151186506delinsACACAGGCAGTGTGGCCTGCAG | CA1752544946 | ASB10 | c.470_491delinsCTGCAGGCCACACTGCCTGTGT (p.Ala157=) c.425_446delinsCTGCAGGCCACACTGCCTGTGT (p.Ala142=) c.605_626delinsCTGCAGGCCACACTGCCTGTGT (p.Ala202=) | |
7 | g.151186486C>A | CA370035971 | ASB10 | c.490G>T (p.Val164Phe) c.445G>T (p.Val149Phe) c.625G>T (p.Val209Phe) | gnomAD v4 |
7 | g.151186486C= | CA1752544951 | ASB10 | c.490G= (p.Val164=) c.445G= (p.Val149=) c.625G= (p.Val209=) | |
7 | g.151186486C>G | CA370035973 | ASB10 | c.490G>C (p.Val164Leu) c.445G>C (p.Val149Leu) c.625G>C (p.Val209Leu) | |
7 | g.151186486C>T | CA4573869 | ASB10 | c.490G>A (p.Val164Ile) c.445G>A (p.Val149Ile) c.625G>A (p.Val209Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.151186493_151186513del | CA579077210 | ASB10 | c.470_490del (p.Ala157_Cys163del) c.425_445del (p.Ala142_Cys148del) c.605_625del (p.Ala202_Cys208del) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186487A= | CA1752544954 | ASB10 | c.489T= (p.Cys163=) c.444T= (p.Cys148=) c.624T= (p.Cys208=) | |
7 | g.151186487A>C | CA169125254 | ASB10 | c.489T>G (p.Cys163Trp) c.444T>G (p.Cys148Trp) c.624T>G (p.Cys208Trp) | dbSNP |
7 | g.151186487A>G | CA458881550 | ASB10 | c.489T>C (p.Cys163=) c.444T>C (p.Cys148=) c.624T>C (p.Cys208=) | COSMIC COSMIC COSMIC COSMIC |
7 | g.151186487A>T | CA370035976 | ASB10 | c.489T>A (p.Cys163Ter) c.444T>A (p.Cys148Ter) c.624T>A (p.Cys208Ter) | |
7 | g.151186488C>A | CA370035978 | ASB10 | c.488G>T (p.Cys163Phe) c.443G>T (p.Cys148Phe) c.623G>T (p.Cys208Phe) | |
7 | g.151186488C>G | CA370035980 | ASB10 | c.488G>C (p.Cys163Ser) c.443G>C (p.Cys148Ser) c.623G>C (p.Cys208Ser) | |
7 | g.151186488C>T | CA370035982 | ASB10 | c.488G>A (p.Cys163Tyr) c.443G>A (p.Cys148Tyr) c.623G>A (p.Cys208Tyr) | |
7 | g.151186489A= | CA1752544959 | ASB10 | c.487T= (p.Cys163=) c.442T= (p.Cys148=) c.622T= (p.Cys208=) | |
7 | g.151186489A>C | CA370035984 | ASB10 | c.487T>G (p.Cys163Gly) c.442T>G (p.Cys148Gly) c.622T>G (p.Cys208Gly) | |
7 | g.151186489A>G | CA370035986 | ASB10 | c.487T>C (p.Cys163Arg) c.442T>C (p.Cys148Arg) c.622T>C (p.Cys208Arg) | gnomAD v4 |
7 | g.151186489A>T | CA150490 | ASB10 | c.487T>A (p.Cys163Ser) c.442T>A (p.Cys148Ser) c.622T>A (p.Cys208Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186490G>A | CA4573870 | ASB10 | c.486C>T (p.Ala162=) c.441C>T (p.Ala147=) c.621C>T (p.Ala207=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186490G>C | CA458881551 | ASB10 | c.486C>G (p.Ala162=) c.441C>G (p.Ala147=) c.621C>G (p.Ala207=) | |
7 | g.151186490G= | CA1752544963 | ASB10 | c.486C= (p.Ala162=) c.441C= (p.Ala147=) c.621C= (p.Ala207=) | |
7 | g.151186490G>T | CA458881552 | ASB10 | c.486C>A (p.Ala162=) c.441C>A (p.Ala147=) c.621C>A (p.Ala207=) | gnomAD v4 |
7 | g.151186491G>A | CA370035993 | ASB10 | c.485C>T (p.Ala162Val) c.440C>T (p.Ala147Val) c.620C>T (p.Ala207Val) | gnomAD v4 |
7 | g.151186491G>C | CA370035990 | ASB10 | c.485C>G (p.Ala162Gly) c.440C>G (p.Ala147Gly) c.620C>G (p.Ala207Gly) | |
7 | g.151186491G>T | CA370035992 | ASB10 | c.485C>A (p.Ala162Asp) c.440C>A (p.Ala147Asp) c.620C>A (p.Ala207Asp) | gnomAD v4 |
7 | g.151186492C>A | CA370035995 | ASB10 | c.484G>T (p.Ala162Ser) c.439G>T (p.Ala147Ser) c.619G>T (p.Ala207Ser) | |
7 | g.151186492C= | CA1752544965 | ASB10 | c.484G= (p.Ala162=) c.439G= (p.Ala147=) c.619G= (p.Ala207=) | |
7 | g.151186492C>G | CA370035997 | ASB10 | c.484G>C (p.Ala162Pro) c.439G>C (p.Ala147Pro) c.619G>C (p.Ala207Pro) | |
7 | g.151186492C>T | CA4573871 | ASB10 | c.484G>A (p.Ala162Thr) c.439G>A (p.Ala147Thr) c.619G>A (p.Ala207Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186493A= | CA1752544969 | ASB10 | c.483T= (p.Thr161=) c.438T= (p.Thr146=) c.618T= (p.Thr206=) | |
7 | g.151186493A>C | CA458881553 | ASB10 | c.483T>G (p.Thr161=) c.438T>G (p.Thr146=) c.618T>G (p.Thr206=) | |
7 | g.151186493A>G | CA458881554 | ASB10 | c.483T>C (p.Thr161=) c.438T>C (p.Thr146=) c.618T>C (p.Thr206=) | dbSNP |
7 | g.151186493A>T | CA458881555 | ASB10 | c.483T>A (p.Thr161=) c.438T>A (p.Thr146=) c.618T>A (p.Thr206=) | |
7 | g.151186494G>A | CA370035999 | ASB10 | c.482C>T (p.Thr161Ile) c.437C>T (p.Thr146Ile) c.617C>T (p.Thr206Ile) | dbSNP |
7 | g.151186494G>C | CA370036000 | ASB10 | c.482C>G (p.Thr161Ser) c.437C>G (p.Thr146Ser) c.617C>G (p.Thr206Ser) | |
7 | g.151186494G= | CA1752544970 | ASB10 | c.482C= (p.Thr161=) c.437C= (p.Thr146=) c.617C= (p.Thr206=) | |
7 | g.151186494G>T | CA370036002 | ASB10 | c.482C>A (p.Thr161Asn) c.437C>A (p.Thr146Asn) c.617C>A (p.Thr206Asn) | gnomAD v4 |
7 | g.151186495T>A | CA370036004 | ASB10 | c.481A>T (p.Thr161Ser) c.436A>T (p.Thr146Ser) c.616A>T (p.Thr206Ser) | |
7 | g.151186495T>C | CA4573872 | ASB10 | c.481A>G (p.Thr161Ala) c.436A>G (p.Thr146Ala) c.616A>G (p.Thr206Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186495T>G | CA370036005 | ASB10 | c.481A>C (p.Thr161Pro) c.436A>C (p.Thr146Pro) c.616A>C (p.Thr206Pro) | |
7 | g.151186495T= | CA1752544975 | ASB10 | c.481A= (p.Thr161=) c.436A= (p.Thr146=) c.616A= (p.Thr206=) | |
7 | g.151186496G>A | CA458881556 | ASB10 | c.480C>T (p.His160=) c.435C>T (p.His145=) c.615C>T (p.His205=) | gnomAD v4 |
7 | g.151186496G>C | CA370036007 | ASB10 | c.480C>G (p.His160Gln) c.435C>G (p.His145Gln) c.615C>G (p.His205Gln) | |
7 | g.151186496G>T | CA370036009 | ASB10 | c.480C>A (p.His160Gln) c.435C>A (p.His145Gln) c.615C>A (p.His205Gln) | |
7 | g.151186497T>A | CA370036014 | ASB10 | c.479A>T (p.His160Leu) c.434A>T (p.His145Leu) c.614A>T (p.His205Leu) | |
7 | g.151186497T>C | CA370036011 | ASB10 | c.479A>G (p.His160Arg) c.434A>G (p.His145Arg) c.614A>G (p.His205Arg) | |
7 | g.151186497T>G | CA370036013 | ASB10 | c.479A>C (p.His160Pro) c.434A>C (p.His145Pro) c.614A>C (p.His205Pro) | |
7 | g.151186498G>A | CA370036017 | ASB10 | c.478C>T (p.His160Tyr) c.433C>T (p.His145Tyr) c.613C>T (p.His205Tyr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.151186498G>C | CA370036018 | ASB10 | c.478C>G (p.His160Asp) c.433C>G (p.His145Asp) c.613C>G (p.His205Asp) | |
7 | g.151186498G= | CA1752544978 | ASB10 | c.478C= (p.His160=) c.433C= (p.His145=) c.613C= (p.His205=) | |
7 | g.151186498G>T | CA370036020 | ASB10 | c.478C>A (p.His160Asn) c.433C>A (p.His145Asn) c.613C>A (p.His205Asn) | |
7 | g.151186499G>A | CA458881557 | ASB10 | c.477C>T (p.Gly159=) c.432C>T (p.Gly144=) c.612C>T (p.Gly204=) | |
7 | g.151186499G>C | CA458881558 | ASB10 | c.477C>G (p.Gly159=) c.432C>G (p.Gly144=) c.612C>G (p.Gly204=) | |
7 | g.151186499G>T | CA458881559 | ASB10 | c.477C>A (p.Gly159=) c.432C>A (p.Gly144=) c.612C>A (p.Gly204=) | gnomAD v4 |
7 | g.151186500C>A | CA370036022 | ASB10 | c.476G>T (p.Gly159Val) c.431G>T (p.Gly144Val) c.611G>T (p.Gly204Val) | gnomAD v4 |
7 | g.151186500C>G | CA370036024 | ASB10 | c.476G>C (p.Gly159Ala) c.431G>C (p.Gly144Ala) c.611G>C (p.Gly204Ala) | |
7 | g.151186500C>T | CA370036026 | ASB10 | c.476G>A (p.Gly159Asp) c.431G>A (p.Gly144Asp) c.611G>A (p.Gly204Asp) | gnomAD v4 |
7 | g.151186501C>A | CA370036028 | ASB10 | c.475G>T (p.Gly159Cys) c.430G>T (p.Gly144Cys) c.610G>T (p.Gly204Cys) | |
7 | g.151186501C>G | CA370036029 | ASB10 | c.475G>C (p.Gly159Arg) c.430G>C (p.Gly144Arg) c.610G>C (p.Gly204Arg) | |
7 | g.151186501C>T | CA370036031 | ASB10 | c.475G>A (p.Gly159Ser) c.430G>A (p.Gly144Ser) c.610G>A (p.Gly204Ser) | |
7 | g.151186502T>A | CA458881560 | ASB10 | c.474A>T (p.Ala158=) c.429A>T (p.Ala143=) c.609A>T (p.Ala203=) | |
7 | g.151186502T>C | CA458881562 | ASB10 | c.474A>G (p.Ala158=) c.429A>G (p.Ala143=) c.609A>G (p.Ala203=) | |
7 | g.151186502T>G | CA458881561 | ASB10 | c.474A>C (p.Ala158=) c.429A>C (p.Ala143=) c.609A>C (p.Ala203=) | |
7 | g.151186502_151186515del | CA2685657517 | ASB10 | c.461_474del (p.Glu154GlyfsTer20) c.416_429del (p.Glu139GlyfsTer20) c.596_609del (p.Glu199GlyfsTer20) | gnomAD v4 |
7 | g.151186503G>A | CA370036033 | ASB10 | c.473C>T (p.Ala158Val) c.428C>T (p.Ala143Val) c.608C>T (p.Ala203Val) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186503G>C | CA370036035 | ASB10 | c.473C>G (p.Ala158Gly) c.428C>G (p.Ala143Gly) c.608C>G (p.Ala203Gly) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.151186503G= | CA1752544980 | ASB10 | c.473C= (p.Ala158=) c.428C= (p.Ala143=) c.608C= (p.Ala203=) | |
7 | g.151186503G>T | CA370036037 | ASB10 | c.473C>A (p.Ala158Glu) c.428C>A (p.Ala143Glu) c.608C>A (p.Ala203Glu) | |
7 | g.151186504C>A | CA370036039 | ASB10 | c.472G>T (p.Ala158Ser) c.427G>T (p.Ala143Ser) c.607G>T (p.Ala203Ser) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.151186504C= | CA1752544982 | ASB10 | c.472G= (p.Ala158=) c.427G= (p.Ala143=) c.607G= (p.Ala203=) | |
7 | g.151186504C>G | CA370036041 | ASB10 | c.472G>C (p.Ala158Pro) c.427G>C (p.Ala143Pro) c.607G>C (p.Ala203Pro) | |
7 | g.151186504C>T | CA4573873 | ASB10 | c.472G>A (p.Ala158Thr) c.427G>A (p.Ala143Thr) c.607G>A (p.Ala203Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186505A>C | CA458881563 | ASB10 | c.471T>G (p.Ala157=) c.426T>G (p.Ala142=) c.606T>G (p.Ala202=) | |
7 | g.151186505A>G | CA458881564 | ASB10 | c.471T>C (p.Ala157=) c.426T>C (p.Ala142=) c.606T>C (p.Ala202=) | |
7 | g.151186505A>T | CA458881565 | ASB10 | c.471T>A (p.Ala157=) c.426T>A (p.Ala142=) c.606T>A (p.Ala202=) | |
7 | g.151186506G>A | CA150488 | ASB10 | c.470C>T (p.Ala157Val) c.425C>T (p.Ala142Val) c.605C>T (p.Ala202Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.151186506G>C | CA370036046 | ASB10 | c.470C>G (p.Ala157Gly) c.425C>G (p.Ala142Gly) c.605C>G (p.Ala202Gly) | |
7 | g.151186506G= | CA1752544989 | ASB10 | c.470C= (p.Ala157=) c.425C= (p.Ala142=) c.605C= (p.Ala202=) | |
7 | g.151186506G>T | CA370036044 | ASB10 | c.470C>A (p.Ala157Asp) c.425C>A (p.Ala142Asp) c.605C>A (p.Ala202Asp) | gnomAD v4 |
7 | g.151186507C>A | CA370036048 | ASB10 | c.469G>T (p.Ala157Ser) c.424G>T (p.Ala142Ser) c.604G>T (p.Ala202Ser) | gnomAD v4 |
7 | g.151186507C>G | CA370036050 | ASB10 | c.469G>C (p.Ala157Pro) c.424G>C (p.Ala142Pro) c.604G>C (p.Ala202Pro) | |
7 | g.151186507C>T | CA370036051 | ASB10 | c.469G>A (p.Ala157Thr) c.424G>A (p.Ala142Thr) c.604G>A (p.Ala202Thr) | gnomAD v4 |
7 | g.151186508A= | CA1752545000 | ASB10 | c.468T= (p.Cys156=) c.423T= (p.Cys141=) c.603T= (p.Cys201=) | |
7 | g.151186508A>C | CA370036053 | ASB10 | c.468T>G (p.Cys156Trp) c.423T>G (p.Cys141Trp) c.603T>G (p.Cys201Trp) | dbSNP |
7 | g.151186508A>G | CA458881566 | ASB10 | c.468T>C (p.Cys156=) c.423T>C (p.Cys141=) c.603T>C (p.Cys201=) | |
7 | g.151186508A>T | CA370036055 | ASB10 | c.468T>A (p.Cys156Ter) c.423T>A (p.Cys141Ter) c.603T>A (p.Cys201Ter) |