ClinVar Miner

List of variants in gene ABCC9 reported as uncertain significance for not provided

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Gene type:
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Total variants: 67
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HGVS dbSNP
NM_005691.3(ABCC9):c.1012-2A>G rs1345994016
NM_005691.3(ABCC9):c.1063G>T (p.Ala355Ser) rs145455570
NM_005691.3(ABCC9):c.1130T>C (p.Ile377Thr) rs368908490
NM_005691.3(ABCC9):c.1165-19dup rs35857705
NM_005691.3(ABCC9):c.1252G>A (p.Ala418Thr) rs781206225
NM_005691.3(ABCC9):c.1305G>A (p.Trp435Ter) rs1555113677
NM_005691.3(ABCC9):c.1320+1G>A rs139620148
NM_005691.3(ABCC9):c.1501G>A (p.Gly501Ser) rs1057523010
NM_005691.3(ABCC9):c.158del (p.Ser53fs)
NM_005691.3(ABCC9):c.1603T>C (p.Tyr535His) rs397517184
NM_005691.3(ABCC9):c.1616C>G (p.Ser539Cys) rs1565470260
NM_005691.3(ABCC9):c.1618+2T>G rs1273224034
NM_005691.3(ABCC9):c.1805T>C (p.Val602Ala) rs1555103539
NM_005691.3(ABCC9):c.1849G>A (p.Asp617Asn) rs757681761
NM_005691.3(ABCC9):c.1901A>C (p.His634Pro) rs1555103438
NM_005691.3(ABCC9):c.1919A>G (p.Lys640Arg) rs1555100847
NM_005691.3(ABCC9):c.1981C>T (p.Arg661Cys) rs199499109
NM_005691.3(ABCC9):c.1987C>T (p.Arg663Cys) rs200349671
NM_005691.3(ABCC9):c.2000C>A (p.Thr667Lys) rs397517186
NM_005691.3(ABCC9):c.2019G>A (p.Lys673=) rs794728954
NM_005691.3(ABCC9):c.2066C>T (p.Ser689Phe) rs200288646
NM_005691.3(ABCC9):c.2080C>T (p.Arg694Ter) rs1194330942
NM_005691.3(ABCC9):c.2197A>G (p.Asn733Asp) rs369604693
NM_005691.3(ABCC9):c.2198+6T>C rs1057522523
NM_005691.3(ABCC9):c.2199-13G>A rs201226082
NM_005691.3(ABCC9):c.2215C>G (p.Pro739Ala) rs201223488
NM_005691.3(ABCC9):c.2312C>T (p.Thr771Ile) rs180739851
NM_005691.3(ABCC9):c.2470C>T (p.Arg824Ter) rs779866340
NM_005691.3(ABCC9):c.2557G>A (p.Glu853Lys) rs1207537871
NM_005691.3(ABCC9):c.2599G>A (p.Val867Ile) rs376754153
NM_005691.3(ABCC9):c.2608A>T (p.Thr870Ser) rs1057521460
NM_005691.3(ABCC9):c.2746C>T (p.Arg916Trp) rs533032970
NM_005691.3(ABCC9):c.2813G>A (p.Arg938Gln) rs201838439
NM_005691.3(ABCC9):c.2848A>T (p.Met950Leu) rs1448325219
NM_005691.3(ABCC9):c.287G>A (p.Arg96Gln) rs202103893
NM_005691.3(ABCC9):c.289C>T (p.Arg97Trp) rs727502875
NM_005691.3(ABCC9):c.2927A>T (p.Lys976Ile) rs149319186
NM_005691.3(ABCC9):c.2951G>A (p.Arg984His) rs148752791
NM_005691.3(ABCC9):c.305T>C (p.Leu102Pro) rs374659816
NM_005691.3(ABCC9):c.3063G>A (p.Glu1021=) rs1555187269
NM_005691.3(ABCC9):c.3070A>G (p.Ile1024Val) rs376701259
NM_005691.3(ABCC9):c.3201del (p.Leu1068fs) rs794728958
NM_005691.3(ABCC9):c.3221A>G (p.Asn1074Ser) rs765629988
NM_005691.3(ABCC9):c.3299C>T (p.Thr1100Ile) rs201358406
NM_005691.3(ABCC9):c.3473+4A>G rs794728956
NM_005691.3(ABCC9):c.3557G>A (p.Arg1186Gln) rs776973456
NM_005691.3(ABCC9):c.3572A>G (p.Glu1191Gly) rs758873590
NM_005691.3(ABCC9):c.3575C>A (p.Thr1192Asn) rs1475546623
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.3604A>G (p.Thr1202Ala) rs794728952
NM_005691.3(ABCC9):c.3669G>A (p.Thr1223=) rs146942382
NM_005691.3(ABCC9):c.3698C>T (p.Thr1233Ile) rs1555179638
NM_005691.3(ABCC9):c.3772-10C>T rs1315658031
NM_005691.3(ABCC9):c.3783T>A (p.Tyr1261Ter) rs794728953
NM_005691.3(ABCC9):c.3814C>G (p.Leu1272Val) rs1057523124
NM_005691.3(ABCC9):c.3896C>T (p.Pro1299Leu) rs794728957
NM_005691.3(ABCC9):c.3955G>A (p.Val1319Ile) rs200499616
NM_005691.3(ABCC9):c.406+2111C>G rs786205274
NM_005691.3(ABCC9):c.4196dup (p.Ser1400fs) rs730880370
NM_005691.3(ABCC9):c.4492C>T (p.Arg1498Trp) rs1020626669
NM_005691.3(ABCC9):c.4559C>G (p.Ser1520Cys) rs1416247885
NM_005691.3(ABCC9):c.4570_4572delinsAAAT (p.Leu1524fs) rs869025349
NM_005691.3(ABCC9):c.4603G>A (p.Ala1535Thr) rs542730918
NM_005691.3(ABCC9):c.4613A>G (p.Asn1538Ser) rs372859669
NM_005691.3(ABCC9):c.970C>T (p.Arg324Cys) rs779720018

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