ClinVar Miner

List of variants in gene EVC reported as benign for Curry-Hall syndrome

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Gene type:
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Total variants: 43
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HGVS dbSNP
NM_153717.3(EVC):c.*1060A>C rs71599848
NM_153717.3(EVC):c.*1083T>G rs71599850
NM_153717.3(EVC):c.*1218C>T rs12501119
NM_153717.3(EVC):c.*1318G>C rs67547790
NM_153717.3(EVC):c.*1375A>G rs114994758
NM_153717.3(EVC):c.*14G>A rs2291151
NM_153717.3(EVC):c.*1845del rs397690241
NM_153717.3(EVC):c.*1849C>G rs75438311
NM_153717.3(EVC):c.*2009T>C rs79152885
NM_153717.3(EVC):c.*210C>A rs16837692
NM_153717.3(EVC):c.*2268G>A rs4261923
NM_153717.3(EVC):c.*2417T>C rs6848370
NM_153717.3(EVC):c.*2617G>A rs3733186
NM_153717.3(EVC):c.*2680G>A rs3733187
NM_153717.3(EVC):c.*2713C>T rs3733188
NM_153717.3(EVC):c.*2871C>T rs3733189
NM_153717.3(EVC):c.*3165T>C rs3755847
NM_153717.3(EVC):c.*53T>C rs7676531
NM_153717.3(EVC):c.*748T>C rs62297707
NM_153717.3(EVC):c.*820C>T rs137860758
NM_153717.3(EVC):c.*908G>A rs13119698
NM_153717.3(EVC):c.*931T>C rs6840435
NM_153717.3(EVC):c.1026G>C (p.Leu342=) rs4688962
NM_153717.3(EVC):c.1068A>G (p.Leu356=) rs33929747
NM_153717.3(EVC):c.1096C>T (p.Leu366=) rs6854138
NM_153717.3(EVC):c.1115C>T (p.Thr372Met) rs28483498
NM_153717.3(EVC):c.1320T>A (p.Phe440Leu) rs60582583
NM_153717.3(EVC):c.1346C>A (p.Thr449Lys) rs2302075
NM_153717.3(EVC):c.1727G>A (p.Arg576Gln) rs1383180
NM_153717.3(EVC):c.1854C>T (p.Gly618=) rs11737221
NM_153717.3(EVC):c.221A>C (p.Gln74Pro) rs2291157
NM_153717.3(EVC):c.2305-8T>C rs1031919
NM_153717.3(EVC):c.2449+15del rs398092136
NM_153717.3(EVC):c.249A>G (p.Ser83=) rs35870680
NM_153717.3(EVC):c.2562-4C>G rs60082311
NM_153717.3(EVC):c.341C>T (p.Ala114Val) rs16837598
NM_153717.3(EVC):c.769C>T (p.Leu257=) rs6446393
NM_153717.3(EVC):c.772T>C (p.Tyr258His) rs6414624
NM_153717.3(EVC):c.802-15C>T rs4689313
NM_153717.3(EVC):c.939+10A>G rs2286342
NM_153717.3(EVC):c.939+11G>T rs55955937
NM_153717.3(EVC):c.939+4C>T rs2286343
NM_153717.3(EVC):c.969T>C (p.Asn323=) rs4688963

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