ClinVar Miner

List of variants in gene combination ACTC1, LOC101928174 studied for Familial hypertrophic cardiomyopathy 11

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 85
Download table as spreadsheet
HGVS dbSNP
NC_000015.10:g.34788151T>C
NC_000015.10:g.34788224A>G
NC_000015.10:g.34788233A>G
NC_000015.10:g.34788359C>A
NC_000015.10:g.34788493C>T
NC_000015.10:g.34788602G>A
NC_000015.10:g.34788610G>A
NC_000015.10:g.34788612G>A
NC_000015.10:g.34788638C>T
NC_000015.10:g.34788663G>A
NC_000015.10:g.34788680C>G
NC_000015.10:g.34788788C>A
NC_000015.10:g.34789034G>A
NC_000015.10:g.34789109G>C
NC_000015.10:g.34789150C>G
NC_000015.10:g.34789182G>A
NC_000015.10:g.34789485C>T
NC_000015.10:g.34789556C>T
NC_000015.10:g.34789631C>T
NC_000015.10:g.34789656G>A
NC_000015.10:g.34789660G>T
NC_000015.10:g.34789724A>C
NC_000015.10:g.34789822T>C
NC_000015.10:g.34789828A>C
NC_000015.10:g.34789928G>A
NC_000015.10:g.34790024C>G
NC_000015.10:g.34790198C>T
NC_000015.10:g.34795675T>C
NM_005159.4(ACTC1):c.*1004A>G rs116034611
NM_005159.4(ACTC1):c.*1039G>A rs589759
NM_005159.4(ACTC1):c.*1133G>T rs750686235
NM_005159.4(ACTC1):c.*1219C>T rs139559367
NM_005159.4(ACTC1):c.*1221A>T rs886051068
NM_005159.4(ACTC1):c.*1445C>G rs8037241
NM_005159.4(ACTC1):c.*1471G>A rs886051067
NM_005159.4(ACTC1):c.*1513T>C rs113063427
NM_005159.4(ACTC1):c.*1674C>T rs112660730
NM_005159.4(ACTC1):c.*1682A>G rs533021
NM_005159.4(ACTC1):c.*1893C>T rs185151197
NM_005159.4(ACTC1):c.*1987G>A rs886051062
NM_005159.4(ACTC1):c.*2090A>G rs604689
NM_005159.4(ACTC1):c.*2206C>G rs886051060
NM_005159.4(ACTC1):c.*2275C>T rs140004011
NM_005159.4(ACTC1):c.*2292C>T rs886051059
NM_005159.4(ACTC1):c.*269C>T rs74009720
NM_005159.4(ACTC1):c.*388G>A rs1370154
NM_005159.4(ACTC1):c.*393G>T rs886051085
NM_005159.4(ACTC1):c.*472T>C rs1370155
NM_005159.4(ACTC1):c.*518A>G rs115295911
NM_005159.4(ACTC1):c.*619A>T rs886051082
NM_005159.4(ACTC1):c.*679C>G rs886051078
NM_005159.4(ACTC1):c.*737C>T rs868013105
NM_005159.4(ACTC1):c.*742C>G rs746732857
NM_005159.4(ACTC1):c.*757G>A rs78727649
NM_005159.4(ACTC1):c.*777C>T rs886051074
NM_005159.4(ACTC1):c.*846G>A rs78596978
NM_005159.4(ACTC1):c.*865T>C rs886051073
NM_005159.4(ACTC1):c.*868T>G rs80139141
NM_005159.4(ACTC1):c.*875G>C rs73387693
NM_005159.4(ACTC1):c.-228C>A rs370499568
NM_005159.4(ACTC1):c.-79G>A rs886051094
NM_005159.5(ACTC1):c.*137A>T
NM_005159.5(ACTC1):c.*20T>A
NM_005159.5(ACTC1):c.*22C>T
NM_005159.5(ACTC1):c.*35A>T rs748053539
NM_005159.5(ACTC1):c.*39C>T
NM_005159.5(ACTC1):c.*40G>A rs377546862
NM_005159.5(ACTC1):c.-23+15G>T rs566201991
NM_005159.5(ACTC1):c.-50G>A
NM_005159.5(ACTC1):c.-57T>C rs113178069
NM_005159.5(ACTC1):c.1053G>C (p.Leu351=) rs151321743
NM_005159.5(ACTC1):c.129+6C>G rs564151494
NM_005159.5(ACTC1):c.268C>T (p.His90Tyr) rs121912676
NM_005159.5(ACTC1):c.270C>T (p.His90=) rs138812333
NM_005159.5(ACTC1):c.281A>G (p.Asn94Ser) rs767734253
NM_005159.5(ACTC1):c.28C>A (p.Leu10Met) rs397517057
NM_005159.5(ACTC1):c.301G>A (p.Glu101Lys) rs193922680
NM_005159.5(ACTC1):c.496C>G (p.Pro166Ala) rs267606628
NM_005159.5(ACTC1):c.537T>A (p.Arg179=) rs750131288
NM_005159.5(ACTC1):c.809-12A>G rs587780846
NM_005159.5(ACTC1):c.889G>T (p.Ala297Ser) rs121912675
NM_005159.5(ACTC1):c.894C>G (p.Asn298Lys) rs863225303
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.997G>C (p.Ala333Pro) rs267606629

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.