ClinVar Miner

List of variants in gene ABCC9 reported as uncertain significance for Dilated cardiomyopathy 1O

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Total variants: 85
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HGVS dbSNP
NM_005691.3(ABCC9):c.1012-1G>C rs878854781
NM_005691.3(ABCC9):c.1022C>T (p.Thr341Ile) rs1565475592
NM_005691.3(ABCC9):c.1127C>T (p.Thr376Ile) rs372244832
NM_005691.3(ABCC9):c.1165-2A>G rs878854782
NM_005691.3(ABCC9):c.1262C>T (p.Thr421Ile)
NM_005691.3(ABCC9):c.136T>C (p.Phe46Leu) rs1555125391
NM_005691.3(ABCC9):c.1375G>A (p.Gly459Ser) rs1060503051
NM_005691.3(ABCC9):c.1381G>C (p.Ala461Pro) rs374535641
NM_005691.3(ABCC9):c.1577T>G (p.Leu526Arg) rs1555112333
NM_005691.3(ABCC9):c.1603T>C (p.Tyr535His) rs397517184
NM_005691.3(ABCC9):c.1618+6T>C
NM_005691.3(ABCC9):c.1817A>C (p.Asn606Thr) rs149229372
NM_005691.3(ABCC9):c.1849G>A (p.Asp617Asn) rs757681761
NM_005691.3(ABCC9):c.1874C>T (p.Ser625Leu)
NM_005691.3(ABCC9):c.1879C>G (p.Pro627Ala) rs367770980
NM_005691.3(ABCC9):c.1887G>T (p.Glu629Asp) rs150036969
NM_005691.3(ABCC9):c.1899_1901dup (p.His634_Thr635insGln)
NM_005691.3(ABCC9):c.1933A>G (p.Lys645Glu) rs876657734
NM_005691.3(ABCC9):c.1942G>C (p.Gly648Arg) rs368279608
NM_005691.3(ABCC9):c.1975A>G (p.Thr659Ala) rs878854783
NM_005691.3(ABCC9):c.1979G>A (p.Arg660Gln) rs150255709
NM_005691.3(ABCC9):c.1993G>A (p.Ala665Thr) rs200891785
NM_005691.3(ABCC9):c.2011G>A (p.Ala671Thr) rs1220942080
NM_005691.3(ABCC9):c.2045G>A (p.Gly682Asp) rs752106985
NM_005691.3(ABCC9):c.2072T>C (p.Ile691Thr) rs766197122
NM_005691.3(ABCC9):c.215G>A (p.Arg72Lys) rs369409311
NM_005691.3(ABCC9):c.2198+1G>A
NM_005691.3(ABCC9):c.2198+3A>G rs1555194960
NM_005691.3(ABCC9):c.2222T>C (p.Phe741Ser)
NM_005691.3(ABCC9):c.23A>G (p.Asn8Ser)
NM_005691.3(ABCC9):c.2408C>T (p.Thr803Ile) rs997660720
NM_005691.3(ABCC9):c.2424+3G>A
NM_005691.3(ABCC9):c.2495T>C (p.Ile832Thr)
NM_005691.3(ABCC9):c.2500T>C (p.Phe834Leu) rs367776754
NM_005691.3(ABCC9):c.2522C>T (p.Ala841Val) rs1555189354
NM_005691.3(ABCC9):c.2554C>T (p.Gln852Ter) rs193922683
NM_005691.3(ABCC9):c.2591G>A (p.Arg864Lys)
NM_005691.3(ABCC9):c.2599G>A (p.Val867Ile) rs376754153
NM_005691.3(ABCC9):c.2630C>T (p.Thr877Met) rs140872303
NM_005691.3(ABCC9):c.2643+6A>G rs1565740203
NM_005691.3(ABCC9):c.2784C>G (p.Asp928Glu) rs139472403
NM_005691.3(ABCC9):c.2857G>A (p.Glu953Lys) rs143685061
NM_005691.3(ABCC9):c.2865A>T (p.Glu955Asp) rs922212635
NM_005691.3(ABCC9):c.287G>A (p.Arg96Gln) rs202103893
NM_005691.3(ABCC9):c.2889_2891del (p.Glu963del) rs1555187363
NM_005691.3(ABCC9):c.293A>G (p.Glu98Gly)
NM_005691.3(ABCC9):c.2965G>A (p.Gly989Arg)
NM_005691.3(ABCC9):c.305T>C (p.Leu102Pro) rs374659816
NM_005691.3(ABCC9):c.3095A>G (p.Gln1032Arg) rs757471451
NM_005691.3(ABCC9):c.3245+3A>C
NM_005691.3(ABCC9):c.3315+6T>C rs201117578
NM_005691.3(ABCC9):c.3440A>G (p.Tyr1147Cys) rs1060503052
NM_005691.3(ABCC9):c.3574A>G (p.Thr1192Ala) rs1437273344
NM_005691.3(ABCC9):c.3589C>T (p.Arg1197Cys) rs778849288
NM_005691.3(ABCC9):c.3590G>A (p.Arg1197His) rs755156050
NM_005691.3(ABCC9):c.3594G>A (p.Met1198Ile) rs199900459
NM_005691.3(ABCC9):c.3669+1G>C
NM_005691.3(ABCC9):c.3669G>A (p.Thr1223=) rs146942382
NM_005691.3(ABCC9):c.3772-4A>C rs1555179333
NM_005691.3(ABCC9):c.377A>G (p.Glu126Gly) rs1060503054
NM_005691.3(ABCC9):c.3893-3C>T rs762931725
NM_005691.3(ABCC9):c.3982G>A (p.Val1328Ile) rs1060503053
NM_005691.3(ABCC9):c.3994G>A (p.Val1332Ile) rs200350065
NM_005691.3(ABCC9):c.4103-3C>T
NM_005691.3(ABCC9):c.4129A>G (p.Ile1377Val) rs1565687632
NM_005691.3(ABCC9):c.4202del (p.Gly1401fs)
NM_005691.3(ABCC9):c.4205C>G (p.Ser1402Cys)
NM_005691.3(ABCC9):c.4512+7A>G rs371646433
NM_005691.3(ABCC9):c.4512T>A (p.Ala1504=) rs777591544
NM_005691.3(ABCC9):c.4519G>A (p.Val1507Ile) rs876657737
NM_005691.3(ABCC9):c.4570_4572delinsAAAT (p.Leu1524fs) rs869025349
NM_005691.3(ABCC9):c.457G>A (p.Val153Ile)
NM_005691.3(ABCC9):c.4591C>T (p.Pro1531Ser) rs142875103
NM_005691.3(ABCC9):c.4631T>C (p.Leu1544Ser)
NM_005691.3(ABCC9):c.47A>G (p.Asn16Ser) rs727502877
NM_005691.3(ABCC9):c.483C>G (p.Asp161Glu)
NM_005691.3(ABCC9):c.497G>A (p.Arg166His)
NM_005691.3(ABCC9):c.4A>G (p.Ser2Gly) rs1485712335
NM_005691.3(ABCC9):c.52G>A (p.Gly18Ser) rs1322335430
NM_005691.3(ABCC9):c.5G>A (p.Ser2Asn) rs1359649036
NM_005691.3(ABCC9):c.816G>T (p.Lys272Asn)
NM_005691.3(ABCC9):c.884G>A (p.Arg295Gln)
NM_005691.3(ABCC9):c.918G>A (p.Leu306=) rs142115849
NM_005691.3(ABCC9):c.959G>T (p.Gly320Val) rs200272254
NM_005691.3(ABCC9):c.970C>T (p.Arg324Cys) rs779720018

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