ClinVar Miner

List of variants in gene ANKRD1 studied for cardiovascular disorder

Included ClinVar conditions (1435):
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Gene type:
ClinVar version:
Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_014391.2(ANKRD1):c.-145T>C rs10881855 0.67382
NM_014391.3(ANKRD1):c.*59A>G rs3939 0.38933
NM_014391.3(ANKRD1):c.346-15T>A rs11595794 0.01849
NM_014391.3(ANKRD1):c.*366G>A rs17102330 0.01092
NM_014391.3(ANKRD1):c.346-15_346-14insA rs60700562 0.01084
NM_014391.3(ANKRD1):c.*41T>G rs150520404 0.00788
NM_014391.3(ANKRD1):c.-17A>G rs79341122 0.00753
NM_014391.3(ANKRD1):c.348G>A (p.Thr116=) rs137914723 0.00748
NM_014391.3(ANKRD1):c.*319A>G rs142439928 0.00587
NM_014391.3(ANKRD1):c.-34C>T rs114144205 0.00522
NM_014391.3(ANKRD1):c.*588A>C rs137950655 0.00510
NM_014391.3(ANKRD1):c.148G>C (p.Ala50Pro) rs28730751 0.00387
NM_014391.3(ANKRD1):c.319G>T (p.Val107Leu) rs114435632 0.00269
NM_014391.3(ANKRD1):c.827C>T (p.Ala276Val) rs35550482 0.00244
NM_014391.3(ANKRD1):c.*343A>G rs41286920 0.00174
NM_014391.3(ANKRD1):c.208-16C>T rs79793575 0.00161
NM_014391.2(ANKRD1):c.-79C>T rs369861544 0.00095
NM_014391.3(ANKRD1):c.197G>A (p.Arg66Gln) rs150797476 0.00092
NM_014391.3(ANKRD1):c.369G>A (p.Thr123=) rs148979787 0.00069
NM_014391.3(ANKRD1):c.417C>A (p.Phe139Leu) rs201398260 0.00043
NM_014391.3(ANKRD1):c.313C>T (p.Pro105Ser) rs148189486 0.00037
NM_014391.3(ANKRD1):c.368C>T (p.Thr123Met) rs145387010 0.00030
NM_014391.3(ANKRD1):c.*642G>A rs184423047 0.00027
NM_014391.3(ANKRD1):c.652-10A>T rs397517252 0.00023
NM_014391.2(ANKRD1):c.-167C>T rs568634889 0.00021
NM_014391.3(ANKRD1):c.*489G>A rs192827821 0.00013
NM_014391.2(ANKRD1):c.-102C>T rs549813663 0.00010
NM_014391.2(ANKRD1):c.-131C>T rs538475043 0.00010
NM_014391.3(ANKRD1):c.108T>C (p.Ala36=) rs145211719 0.00009
NM_014391.3(ANKRD1):c.806G>A (p.Arg269Gln) rs367609929 0.00009
NM_014391.3(ANKRD1):c.133C>G (p.Leu45Val) rs372030578 0.00008
NM_014391.3(ANKRD1):c.820T>C (p.Tyr274His) rs377074932 0.00007
NM_014391.3(ANKRD1):c.150C>G (p.Ala50=) rs147484763 0.00006
NM_014391.3(ANKRD1):c.544C>T (p.Arg182Cys) rs754717867 0.00006
NM_014391.3(ANKRD1):c.821A>G (p.Tyr274Cys) rs374486076 0.00004
NM_014391.3(ANKRD1):c.838A>G (p.Ile280Val) rs144770680 0.00004
NM_014391.3(ANKRD1):c.881A>G (p.His294Arg) rs754657888 0.00004
NM_014391.3(ANKRD1):c.*627A>G rs886047475 0.00003
NM_014391.3(ANKRD1):c.154C>G (p.Pro52Ala) rs397517248 0.00003
NM_014391.3(ANKRD1):c.27+1G>T rs779910001 0.00003
NM_014391.3(ANKRD1):c.388G>T (p.Glu130Ter) rs1048316962 0.00003
NM_014391.3(ANKRD1):c.944G>C (p.Arg315Pro) rs746392266 0.00003
NM_014391.3(ANKRD1):c.909C>T (p.Phe303=) rs765093690 0.00002
NM_014391.3(ANKRD1):c.109G>A (p.Val37Ile) rs1401851050 0.00001
NM_014391.3(ANKRD1):c.3G>C (p.Met1Ile) rs188706671 0.00001
NM_014391.3(ANKRD1):c.523G>A (p.Ala175Thr) rs914206942 0.00001
NM_014391.3(ANKRD1):c.560C>T (p.Ser187Phe) rs397517251 0.00001
NM_014391.3(ANKRD1):c.651+6C>T rs762041559 0.00001
NM_014391.3(ANKRD1):c.710A>G (p.His237Arg) rs145326465 0.00001
NM_014391.3(ANKRD1):c.805C>T (p.Arg269Ter) rs397517254 0.00001
NM_014391.3(ANKRD1):c.896C>A (p.Thr299Asn) rs751174664 0.00001
NM_014391.3(ANKRD1):c.943C>T (p.Arg315Cys) rs775584071 0.00001
NM_014391.2(ANKRD1):c.-131C>G rs538475043
NM_014391.3(ANKRD1):c.*286C>T rs886047479
NM_014391.3(ANKRD1):c.*371T>G rs531523887
NM_014391.3(ANKRD1):c.*607C>A rs146219881
NM_014391.3(ANKRD1):c.*634G>A rs1301081047
NM_014391.3(ANKRD1):c.196C>G (p.Arg66Gly) rs397517249
NM_014391.3(ANKRD1):c.222dup (p.Leu75fs) rs776659587
NM_014391.3(ANKRD1):c.229C>G (p.Gln77Glu) rs869025362
NM_014391.3(ANKRD1):c.346-14_346-9del rs773314113
NM_014391.3(ANKRD1):c.346-15_346-14del rs794728971
NM_014391.3(ANKRD1):c.346-16_346-15insATA rs60923931
NM_014391.3(ANKRD1):c.346-17_346-10del rs397517250
NM_014391.3(ANKRD1):c.346-19_346-14del rs58762441
NM_014391.3(ANKRD1):c.346-19_346-18del rs398014415
NM_014391.3(ANKRD1):c.346-21ATTT[2] rs397517250
NM_014391.3(ANKRD1):c.346-29_346-12del rs72003210
NM_014391.3(ANKRD1):c.346-35_346-12del rs751458325
NM_014391.3(ANKRD1):c.37_93dup (p.Lys13_Gly31dup) rs1564575040
NM_014391.3(ANKRD1):c.437C>T (p.Pro146Leu) rs1181799982
NM_014391.3(ANKRD1):c.55G>C (p.Glu19Gln) rs886047480
NM_014391.3(ANKRD1):c.612G>T (p.Leu204Phe) rs869025363
NM_014391.3(ANKRD1):c.646G>C (p.Asp216His) rs1416570961
NM_014391.3(ANKRD1):c.677C>T (p.Ala226Val) rs730880050
NM_014391.3(ANKRD1):c.796A>G (p.Lys266Glu) rs759544911
NM_014391.3(ANKRD1):c.798G>C (p.Lys266Asn) rs1847359872

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