ClinVar Miner

List of variants in gene ABCC9 reported as likely benign for Dilated cardiomyopathy 1O

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Gene type:
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Total variants: 63
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HGVS dbSNP
NM_005691.3(ABCC9):c.-11T>C rs72559432
NM_005691.3(ABCC9):c.1011+7T>C rs1224367944
NM_005691.3(ABCC9):c.1296C>T (p.Pro432=) rs10770865
NM_005691.3(ABCC9):c.1332C>T (p.Gly444=) rs369830406
NM_005691.3(ABCC9):c.1416T>C (p.Phe472=) rs777308898
NM_005691.3(ABCC9):c.142+10C>A rs138917284
NM_005691.3(ABCC9):c.1524T>C (p.Tyr508=) rs1555112390
NM_005691.3(ABCC9):c.1619-7T>C rs769816456
NM_005691.3(ABCC9):c.1660-9dup rs1592166889
NM_005691.3(ABCC9):c.1704T>A (p.Pro568=) rs1317064787
NM_005691.3(ABCC9):c.1785A>G (p.Ala595=) rs1555106091
NM_005691.3(ABCC9):c.192T>C (p.Leu64=) rs1592270142
NM_005691.3(ABCC9):c.1988G>A (p.Arg663His) rs141999048
NM_005691.3(ABCC9):c.2157C>T (p.Leu719=) rs201848437
NM_005691.3(ABCC9):c.2424+10A>G rs770053314
NM_005691.3(ABCC9):c.2424+9T>C rs11835804
NM_005691.3(ABCC9):c.2574C>T (p.Phe858=) rs1273498300
NM_005691.3(ABCC9):c.2613C>T (p.His871=) rs373909378
NM_005691.3(ABCC9):c.2644-11G>A rs61926078
NM_005691.3(ABCC9):c.2784C>G (p.Asp928Glu) rs139472403
NM_005691.3(ABCC9):c.2856C>T (p.Asp952=) rs758697683
NM_005691.3(ABCC9):c.2867-5T>C rs369841241
NM_005691.3(ABCC9):c.2927A>T (p.Lys976Ile) rs149319186
NM_005691.3(ABCC9):c.2961A>G (p.Thr987=) rs1555187333
NM_005691.3(ABCC9):c.3018G>A (p.Ser1006=) rs1030642418
NM_005691.3(ABCC9):c.3096+7T>C rs572074725
NM_005691.3(ABCC9):c.3237A>G (p.Gly1079=) rs554189538
NM_005691.3(ABCC9):c.3273G>C (p.Leu1091=) rs144325590
NM_005691.3(ABCC9):c.3316-4A>C rs201147809
NM_005691.3(ABCC9):c.3331T>C (p.Leu1111=) rs764155671
NM_005691.3(ABCC9):c.3589C>T (p.Arg1197Cys) rs778849288
NM_005691.3(ABCC9):c.3621T>C (p.Ile1207=) rs767458242
NM_005691.3(ABCC9):c.3948T>C (p.Asp1316=) rs368875701
NM_005691.3(ABCC9):c.3999G>A (p.Lys1333=) rs1555178738
NM_005691.3(ABCC9):c.4014T>C (p.Pro1338=) rs1555178731
NM_005691.3(ABCC9):c.4093A>G (p.Ile1365Val) rs778634668
NM_005691.3(ABCC9):c.4344T>C (p.Asn1448=) rs146782703
NM_005691.3(ABCC9):c.4353T>C (p.Val1451=) rs771226136
NM_005691.3(ABCC9):c.4497C>T (p.Thr1499=) rs1060504811
NM_005691.3(ABCC9):c.4513-8C>T rs1591928188
NM_005691.3(ABCC9):c.817-14_817-4del rs774857795
NM_005691.3(ABCC9):c.817-6C>T rs879206459
NM_005691.3(ABCC9):c.837A>G (p.Pro279=) rs1264086698
NM_005691.3(ABCC9):c.957T>C (p.Ser319=) rs768245158
NM_005691.3(ABCC9):c.99T>G (p.Pro33=) rs1591760857
NM_020297.3(ABCC9):c.1200G>A (p.Thr400=) rs150096625
NM_020297.3(ABCC9):c.1212C>T (p.Ser404=) rs376726505
NM_020297.3(ABCC9):c.1557G>A (p.Glu519=) rs143346402
NM_020297.3(ABCC9):c.1848C>T (p.Asp616=) rs61001398
NM_020297.3(ABCC9):c.2050G>A (p.Gly684Ser) rs148174226
NM_020297.3(ABCC9):c.2154C>T (p.Ile718=) rs74067815
NM_020297.3(ABCC9):c.2262T>C (p.Tyr754=) rs145561881
NM_020297.3(ABCC9):c.2631G>A (p.Thr877=) rs139408145
NM_020297.3(ABCC9):c.305T>C (p.Leu102Pro) rs374659816
NM_020297.3(ABCC9):c.3288T>C (p.Phe1096=) rs377372612
NM_020297.3(ABCC9):c.3321C>T (p.Ile1107=) rs35404804
NM_020297.3(ABCC9):c.3409G>A (p.Val1137Ile) rs147895473
NM_020297.3(ABCC9):c.3729G>A (p.Ser1243=) rs140182559
NM_020297.3(ABCC9):c.3993C>T (p.His1331=) rs377704379
NM_020297.3(ABCC9):c.4062G>A (p.Ser1354=) rs145005748
NM_020297.3(ABCC9):c.4437T>C (p.Ile1479=) rs368079660
NM_020297.3(ABCC9):c.48C>T (p.Asn16=) rs199631710
NM_020297.3(ABCC9):c.789C>T (p.Cys263=) rs58386780

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