ClinVar Miner

List of variants in gene ANKRD1 reported as uncertain significance for Primary dilated cardiomyopathy

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_014391.3(ANKRD1):c.*319A>G rs142439928 0.00587
NM_014391.3(ANKRD1):c.*343A>G rs41286920 0.00174
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.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_014391.2(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.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.909C>T (p.Phe303=) rs765093690 0.00002
NM_014391.3(ANKRD1):c.3G>C (p.Met1Ile) rs188706671 0.00001
NM_014391.3(ANKRD1):c.560C>T (p.Ser187Phe) rs397517251 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.222dup (p.Leu75fs) rs776659587
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.677C>T (p.Ala226Val) rs730880050
NM_014391.3(ANKRD1):c.798G>C (p.Lys266Asn) rs1847359872

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