ClinVar Miner

List of variants in gene ABCC9 reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Gene type:
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Total variants: 79
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HGVS dbSNP gnomAD frequency
NM_020297.4(ABCC9):c.3321C>T (p.Ile1107=) rs35404804 0.01226
NM_020297.4(ABCC9):c.789C>T (p.Cys263=) rs58386780 0.01183
NM_020297.4(ABCC9):c.2200G>A (p.Val734Ile) rs61688134 0.00769
NM_020297.4(ABCC9):c.2643+17G>C rs151310554 0.00584
NM_020297.4(ABCC9):c.2644-19G>A rs73254534 0.00507
NM_020297.4(ABCC9):c.285-16G>A rs144825585 0.00448
NM_020297.4(ABCC9):c.142+15dup rs571187142 0.00428
NM_020297.4(ABCC9):c.2631G>A (p.Thr877=) rs139408145 0.00386
NM_020297.4(ABCC9):c.2523C>T (p.Ala841=) rs144537241 0.00345
NM_020297.4(ABCC9):c.1056C>T (p.Tyr352=) rs149408382 0.00276
NM_020297.4(ABCC9):c.2093-7T>C rs185235724 0.00261
NM_020297.4(ABCC9):c.407-14C>A rs201279882 0.00248
NM_020297.4(ABCC9):c.3768T>C (p.Leu1256=) rs150303433 0.00209
NM_020297.4(ABCC9):c.1677G>A (p.Ala559=) rs76458291 0.00193
NM_020297.4(ABCC9):c.924T>C (p.Asp308=) rs139127928 0.00140
NM_020297.4(ABCC9):c.2826T>C (p.Tyr942=) rs141025897 0.00092
NM_020297.4(ABCC9):c.2238-1G>A rs141281214 0.00056
NM_020297.4(ABCC9):c.372T>C (p.Asn124=) rs377384557 0.00051
NM_020297.4(ABCC9):c.4512+16C>T rs376147813 0.00049
NM_020297.4(ABCC9):c.2862C>T (p.Asp954=) rs2291550 0.00041
NM_020297.4(ABCC9):c.2050G>A (p.Gly684Ser) rs148174226 0.00039
NM_020297.4(ABCC9):c.3030T>C (p.Ala1010=) rs76102634 0.00039
NM_020297.4(ABCC9):c.1200G>A (p.Thr400=) rs150096625 0.00038
NM_020297.4(ABCC9):c.407-13T>C rs199717786 0.00037
NM_020297.4(ABCC9):c.1165-20del rs768812471 0.00032
NM_020297.4(ABCC9):c.1887G>T (p.Glu629Asp) rs150036969 0.00032
NM_020297.4(ABCC9):c.2154C>T (p.Ile718=) rs74067815 0.00031
NM_020297.4(ABCC9):c.1557G>A (p.Glu519=) rs143346402 0.00029
NM_020297.4(ABCC9):c.2262T>C (p.Tyr754=) rs145561881 0.00029
NM_020297.4(ABCC9):c.305T>C (p.Leu102Pro) rs374659816 0.00029
NM_020297.4(ABCC9):c.4512+690C>T rs397517191 0.00017
NM_020297.4(ABCC9):c.574-18G>A rs376566343 0.00017
NM_020297.4(ABCC9):c.4344T>C (p.Asn1448=) rs146782703 0.00009
NM_020297.4(ABCC9):c.3070A>G (p.Ile1024Val) rs376701259 0.00006
NM_020297.4(ABCC9):c.4212-18A>C rs761501699 0.00006
NM_020297.4(ABCC9):c.-11T>C rs72559432 0.00004
NM_020297.4(ABCC9):c.1551T>C (p.Ser517=) rs996266050 0.00004
NM_020297.4(ABCC9):c.1063G>T (p.Ala355Ser) rs145455570 0.00003
NM_020297.4(ABCC9):c.3357G>A (p.Leu1119=) rs2287626 0.00003
NM_020297.4(ABCC9):c.2004G>A (p.Glu668=) rs751485829 0.00002
NM_020297.4(ABCC9):c.2554C>T (p.Gln852Ter) rs193922683 0.00002
NM_020297.4(ABCC9):c.3331T>C (p.Leu1111=) rs764155671 0.00002
NM_020297.4(ABCC9):c.928C>T (p.Leu310=) rs747640613 0.00002
NM_020297.4(ABCC9):c.1050C>T (p.Asn350=) rs143373045 0.00001
NM_020297.4(ABCC9):c.1194C>T (p.Leu398=) rs1430745818 0.00001
NM_020297.4(ABCC9):c.1770G>A (p.Thr590=) rs746239063 0.00001
NM_020297.4(ABCC9):c.1858C>T (p.Arg620Ter) rs1024095026 0.00001
NM_020297.4(ABCC9):c.3669+1G>C rs950805207 0.00001
NM_020297.4(ABCC9):c.3772-10C>T rs1315658031 0.00001
NM_020297.4(ABCC9):c.4094T>C (p.Ile1365Thr) rs1328493674 0.00001
NM_020297.4(ABCC9):c.4512T>A (p.Ala1504=) rs777591544 0.00001
NM_020297.4(ABCC9):c.957T>C (p.Ser319=) rs768245158 0.00001
NM_020297.4(ABCC9):c.1006A>G (p.Thr336Ala)
NM_020297.4(ABCC9):c.1165-6del rs35857705
NM_020297.4(ABCC9):c.143-1G>C
NM_020297.4(ABCC9):c.1456-10del rs763459861
NM_020297.4(ABCC9):c.1619-20C>A rs1357942810
NM_020297.4(ABCC9):c.1629T>C (p.Asn543=)
NM_020297.4(ABCC9):c.1680T>G (p.Tyr560Ter) rs1326389765
NM_020297.4(ABCC9):c.2238-17del rs4148670
NM_020297.4(ABCC9):c.233C>T (p.Ala78Val) rs1253372454
NM_020297.4(ABCC9):c.23ACA[1] (p.Asn9del) rs1949499149
NM_020297.4(ABCC9):c.2644-11G>A rs61926078
NM_020297.4(ABCC9):c.2914A>T (p.Arg972Trp) rs1565731883
NM_020297.4(ABCC9):c.3063G>A (p.Glu1021=) rs1555187269
NM_020297.4(ABCC9):c.3076A>G (p.Asn1026Asp) rs369389402
NM_020297.4(ABCC9):c.3669+4C>T rs189565793
NM_020297.4(ABCC9):c.3868T>C (p.Ser1290Pro)
NM_020297.4(ABCC9):c.4103-1G>A rs1189432427
NM_020297.4(ABCC9):c.4112T>G (p.Val1371Gly)
NM_020297.4(ABCC9):c.4450-5del rs4148680
NM_020297.4(ABCC9):c.4512+744_4512+746delinsAAAT rs869025349
NM_020297.4(ABCC9):c.4512+826C>T rs2137103904
NM_020297.4(ABCC9):c.771A>C (p.Ala257=)
NM_020297.4(ABCC9):c.817-14_817-4del rs774857795
NM_020297.4(ABCC9):c.817-18del rs199947733
NM_020297.4(ABCC9):c.817-18dup rs199947733
NM_020297.4(ABCC9):c.817-7del rs193922684
NM_020297.4(ABCC9):c.907T>C (p.Phe303Leu)

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