ClinVar Miner

List of variants in gene combination ACTC1, LOC101928174 reported as likely benign

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Total variants: 70
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HGVS dbSNP
NM_005159.4(ACTC1):c.*1039G>A rs589759
NM_005159.4(ACTC1):c.*1445C>G rs8037241
NM_005159.4(ACTC1):c.*1674C>T rs112660730
NM_005159.4(ACTC1):c.*1682A>G rs533021
NM_005159.4(ACTC1):c.*2090A>G rs604689
NM_005159.4(ACTC1):c.*269C>T rs74009720
NM_005159.4(ACTC1):c.*388G>A rs1370154
NM_005159.4(ACTC1):c.*472T>C rs1370155
NM_005159.4(ACTC1):c.*868T>G rs80139141
NM_005159.4(ACTC1):c.*875G>C rs73387693
NM_005159.4(ACTC1):c.*918delA rs34323254
NM_005159.4(ACTC1):c.129+23dupC rs148433308
NM_005159.4(ACTC1):c.809-16_809-13delTGTG rs59431308
NM_005159.5(ACTC1):c.*5C>G rs756594449
NM_005159.5(ACTC1):c.-17C>G rs1411090601
NM_005159.5(ACTC1):c.-22-15C>G rs368171271
NM_005159.5(ACTC1):c.-36C>G rs886051091
NM_005159.5(ACTC1):c.-36_-32CCGCC[3] rs1064795891
NM_005159.5(ACTC1):c.-44G>A rs909469426
NM_005159.5(ACTC1):c.-57T>C rs113178069
NM_005159.5(ACTC1):c.1053G>A (p.Leu351=) rs151321743
NM_005159.5(ACTC1):c.1053G>C (p.Leu351=) rs151321743
NM_005159.5(ACTC1):c.1083G>A (p.Lys361=) rs754736799
NM_005159.5(ACTC1):c.1092C>T (p.Tyr364=) rs140261885
NM_005159.5(ACTC1):c.1098G>A (p.Glu366=) rs758173419
NM_005159.5(ACTC1):c.129+12_129+13delinsCT rs1555418997
NM_005159.5(ACTC1):c.129+18C>A rs368977747
NM_005159.5(ACTC1):c.129+219_129+224del
NM_005159.5(ACTC1):c.129+6C>G rs564151494
NM_005159.5(ACTC1):c.130-15T>G rs376417852
NM_005159.5(ACTC1):c.130-17A>C rs1057523026
NM_005159.5(ACTC1):c.130-9T>C rs147406641
NM_005159.5(ACTC1):c.165C>T (p.Tyr55=) rs149432225
NM_005159.5(ACTC1):c.219C>T (p.Ile73=) rs376566924
NM_005159.5(ACTC1):c.240C>T (p.Asn80=) rs1178754602
NM_005159.5(ACTC1):c.246C>T (p.Asp82=) rs373261583
NM_005159.5(ACTC1):c.272C>A (p.Thr91Asn) rs730880037
NM_005159.5(ACTC1):c.294G>A (p.Val98=) rs397517058
NM_005159.5(ACTC1):c.309C>T (p.His103=) rs769303249
NM_005159.5(ACTC1):c.318G>A (p.Leu106=) rs1335305223
NM_005159.5(ACTC1):c.333G>A (p.Pro111=) rs774767260
NM_005159.5(ACTC1):c.342C>T (p.Pro114=) rs878854754
NM_005159.5(ACTC1):c.399C>T (p.Ala133=) rs764630691
NM_005159.5(ACTC1):c.405C>T (p.Tyr135=) rs181479041
NM_005159.5(ACTC1):c.423G>A (p.Val141=) rs922191208
NM_005159.5(ACTC1):c.454+9G>A rs148695567
NM_005159.5(ACTC1):c.455-7C>T rs768363857
NM_005159.5(ACTC1):c.456C>T (p.Gly152=) rs771310484
NM_005159.5(ACTC1):c.465G>A (p.Leu155=) rs397517062
NM_005159.5(ACTC1):c.513C>T (p.Tyr171=) rs145023222
NM_005159.5(ACTC1):c.516T>C (p.Ala172=) rs397517064
NM_005159.5(ACTC1):c.537T>A (p.Arg179=) rs750131288
NM_005159.5(ACTC1):c.616+8T>C rs397517066
NM_005159.5(ACTC1):c.617-7T>C rs750536667
NM_005159.5(ACTC1):c.633C>A (p.Val211=) rs199947846
NM_005159.5(ACTC1):c.663C>T (p.Val221=) rs766868624
NM_005159.5(ACTC1):c.66C>T (p.Gly22=) rs1060504729
NM_005159.5(ACTC1):c.717G>A (p.Glu239=) rs369019849
NM_005159.5(ACTC1):c.798C>T (p.Pro266=) rs397517068
NM_005159.5(ACTC1):c.809-8G>A
NM_005159.5(ACTC1):c.840T>C (p.Thr280=) rs1057522193
NM_005159.5(ACTC1):c.846T>C (p.Asn282=) rs1566967111
NM_005159.5(ACTC1):c.903A>G (p.Leu301=) rs138347995
NM_005159.5(ACTC1):c.90C>T (p.Arg30=) rs1555419004
NM_005159.5(ACTC1):c.918T>A (p.Thr306=) rs397517074
NM_005159.5(ACTC1):c.927T>C (p.Pro309=) rs2307493
NM_005159.5(ACTC1):c.930T>C (p.Gly310=) rs561081869
NM_005159.5(ACTC1):c.990+64C>T
NM_005159.5(ACTC1):c.991-10C>T rs1298992263
NM_005159.5(ACTC1):c.991-262C>T

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