ClinVar Miner

List of variants in gene combination ACTC1, LOC101928174 reported as uncertain significance for Hypertrophic cardiomyopathy

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 72
Download table as spreadsheet
HGVS dbSNP
NM_005159.4(ACTC1):c.*1004A>G rs116034611
NM_005159.4(ACTC1):c.*1062G>A rs886051072
NM_005159.4(ACTC1):c.*1070A>C rs886051071
NM_005159.4(ACTC1):c.*1090A>G rs886051070
NM_005159.4(ACTC1):c.*1115A>T rs886051069
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.*1318T>G rs759530643
NM_005159.4(ACTC1):c.*1471G>A rs886051067
NM_005159.4(ACTC1):c.*1482G>T rs886051066
NM_005159.4(ACTC1):c.*1502G>T rs886051065
NM_005159.4(ACTC1):c.*1513T>C rs113063427
NM_005159.4(ACTC1):c.*1753G>T rs886051064
NM_005159.4(ACTC1):c.*1781C>T rs560065427
NM_005159.4(ACTC1):c.*1797C>A rs886051063
NM_005159.4(ACTC1):c.*1893C>T rs185151197
NM_005159.4(ACTC1):c.*1987G>A rs886051062
NM_005159.4(ACTC1):c.*2168G>T rs886051061
NM_005159.4(ACTC1):c.*2206C>G rs886051060
NM_005159.4(ACTC1):c.*224G>C rs551820554
NM_005159.4(ACTC1):c.*2275C>T rs140004011
NM_005159.4(ACTC1):c.*2292C>T rs886051059
NM_005159.4(ACTC1):c.*247G>A rs886051088
NM_005159.4(ACTC1):c.*284G>A rs886051087
NM_005159.4(ACTC1):c.*307T>A rs886051086
NM_005159.4(ACTC1):c.*393G>T rs886051085
NM_005159.4(ACTC1):c.*422T>A rs886051084
NM_005159.4(ACTC1):c.*518A>G rs115295911
NM_005159.4(ACTC1):c.*561C>A rs886051083
NM_005159.4(ACTC1):c.*619A>T rs886051082
NM_005159.4(ACTC1):c.*643C>A rs886051081
NM_005159.4(ACTC1):c.*646C>A rs886051080
NM_005159.4(ACTC1):c.*674C>A rs886051079
NM_005159.4(ACTC1):c.*679C>G rs886051078
NM_005159.4(ACTC1):c.*708G>T rs886051077
NM_005159.4(ACTC1):c.*737C>T rs868013105
NM_005159.4(ACTC1):c.*739G>T rs886051076
NM_005159.4(ACTC1):c.*742C>G rs746732857
NM_005159.4(ACTC1):c.*757G>A rs78727649
NM_005159.4(ACTC1):c.*775C>A rs886051075
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.*935G>T rs766542832
NM_005159.4(ACTC1):c.*983C>T rs549986676
NM_005159.4(ACTC1):c.-101G>T rs886051095
NM_005159.4(ACTC1):c.-105C>A rs886051096
NM_005159.4(ACTC1):c.-109C>A rs886051097
NM_005159.4(ACTC1):c.-175C>A rs886051098
NM_005159.4(ACTC1):c.-194C>A rs886051099
NM_005159.4(ACTC1):c.-228C>A rs370499568
NM_005159.4(ACTC1):c.-79G>A rs886051094
NM_005159.5(ACTC1):c.*35A>T rs748053539
NM_005159.5(ACTC1):c.*40G>A rs377546862
NM_005159.5(ACTC1):c.-23+15G>T rs566201991
NM_005159.5(ACTC1):c.-36C>G rs886051091
NM_005159.5(ACTC1):c.-55C>A rs886051093
NM_005159.5(ACTC1):c.-55_-53CCG[3] rs886051092
NM_005159.5(ACTC1):c.1053G>C (p.Leu351=) rs151321743
NM_005159.5(ACTC1):c.28C>A (p.Leu10Met) rs397517057
NM_005159.5(ACTC1):c.537T>A (p.Arg179=) rs750131288
NM_005159.5(ACTC1):c.809-12_809-11insGT rs774238821
NM_005159.5(ACTC1):c.809-58TG[17] rs59431308
NM_005159.5(ACTC1):c.809-58TG[21] rs59431308
NM_005159.5(ACTC1):c.809-58TG[22] rs59431308
NM_005159.5(ACTC1):c.809-58TG[24] rs59431308
NM_005159.5(ACTC1):c.809-58TG[25] rs59431308
NM_005159.5(ACTC1):c.809-58TG[26] rs59431308
NM_005159.5(ACTC1):c.922T>A (p.Tyr308Asn) rs1566967093
NM_005159.5(ACTC1):c.968C>T (p.Ala323Val) rs730880404
NM_005159.5(ACTC1):c.978C>A (p.Thr326=) rs886051089

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.