ClinVar Miner

List of variants in gene ABCC9 reported as benign

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Gene type:
ClinVar version:
Total variants: 91
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HGVS dbSNP
NC_000012.12:g.21845349_21845350del
NC_000012.12:g.21852069T>G
NM_005691.3(ABCC9):c.1012-276A>G
NM_005691.3(ABCC9):c.1056C>T (p.Tyr352=) rs149408382
NM_005691.3(ABCC9):c.1164+85T>A
NM_005691.3(ABCC9):c.1165-19dup rs35857705
NM_005691.3(ABCC9):c.1165-6del rs35857705
NM_005691.3(ABCC9):c.1296= (p.Pro432=) rs10770865
NM_005691.3(ABCC9):c.1321-287A>G
NM_005691.3(ABCC9):c.1374C>T (p.Val458=) rs200819464
NM_005691.3(ABCC9):c.142+15dup rs571187142
NM_005691.3(ABCC9):c.143-301A>G
NM_005691.3(ABCC9):c.1557G>A (p.Glu519=) rs143346402
NM_005691.3(ABCC9):c.1660-43C>A rs704216
NM_005691.3(ABCC9):c.1677G>A (p.Ala559=) rs76458291
NM_005691.3(ABCC9):c.1803-188_1803-177del
NM_005691.3(ABCC9):c.1848C>T (p.Asp616=) rs61001398
NM_005691.3(ABCC9):c.1912-234T>C
NM_005691.3(ABCC9):c.1912-66G>A
NM_005691.3(ABCC9):c.2019+275T>C
NM_005691.3(ABCC9):c.2093-7T>C rs185235724
NM_005691.3(ABCC9):c.2200G>A (p.Val734Ile) rs61688134
NM_005691.3(ABCC9):c.2237+216C>G
NM_005691.3(ABCC9):c.2238-17del rs4148670
NM_005691.3(ABCC9):c.2238-1G>A rs141281214
NM_005691.3(ABCC9):c.2238-274_2238-229del
NM_005691.3(ABCC9):c.2262T>C (p.Tyr754=) rs145561881
NM_005691.3(ABCC9):c.2339+119C>T
NM_005691.3(ABCC9):c.2340-233A>G
NM_005691.3(ABCC9):c.2424+9T>C rs11835804
NM_005691.3(ABCC9):c.2475G>A (p.Ala825=) rs587780845
NM_005691.3(ABCC9):c.2506-332T>C
NM_005691.3(ABCC9):c.2523C>T (p.Ala841=) rs144537241
NM_005691.3(ABCC9):c.2631G>A (p.Thr877=) rs139408145
NM_005691.3(ABCC9):c.2643+17G>C rs151310554
NM_005691.3(ABCC9):c.2643+44C>A
NM_005691.3(ABCC9):c.2644-11G>A rs61926078
NM_005691.3(ABCC9):c.2769+194del
NM_005691.3(ABCC9):c.2769+28A>C rs2307024
NM_005691.3(ABCC9):c.2770-13A>G rs184123387
NM_005691.3(ABCC9):c.2770-192C>T
NM_005691.3(ABCC9):c.2826T>C (p.Tyr942=) rs141025897
NM_005691.3(ABCC9):c.285-16G>A rs144825585
NM_005691.3(ABCC9):c.285-266A>G
NM_005691.3(ABCC9):c.285-321C>T
NM_005691.3(ABCC9):c.2862C>T (p.Asp954=) rs2291550
NM_005691.3(ABCC9):c.2867-342A>C
NM_005691.3(ABCC9):c.3030T>C (p.Ala1010=) rs76102634
NM_005691.3(ABCC9):c.3096+13C>T rs370712530
NM_005691.3(ABCC9):c.3267G>A (p.Leu1089=) rs780998911
NM_005691.3(ABCC9):c.3315+17C>T rs200692327
NM_005691.3(ABCC9):c.3315+296C>G
NM_005691.3(ABCC9):c.3321C>T (p.Ile1107=) rs35404804
NM_005691.3(ABCC9):c.3339T>G (p.Ser1113=) rs138280089
NM_005691.3(ABCC9):c.3357G>A (p.Leu1119=) rs2287626
NM_005691.3(ABCC9):c.3409G>A (p.Val1137Ile) rs147895473
NM_005691.3(ABCC9):c.3473+216T>C
NM_005691.3(ABCC9):c.3473+293C>G
NM_005691.3(ABCC9):c.3567-287T>C
NM_005691.3(ABCC9):c.3567-333T>C
NM_005691.3(ABCC9):c.3670-94G>T
NM_005691.3(ABCC9):c.372T>C (p.Asn124=) rs377384557
NM_005691.3(ABCC9):c.3768T>C (p.Leu1256=) rs150303433
NM_005691.3(ABCC9):c.3892+102G>A
NM_005691.3(ABCC9):c.3892+224C>T
NM_005691.3(ABCC9):c.406+305A>T
NM_005691.3(ABCC9):c.406+320A>G
NM_005691.3(ABCC9):c.406+38A>C rs2277405
NM_005691.3(ABCC9):c.407-14C>A rs201279882
NM_005691.3(ABCC9):c.407-194A>G
NM_005691.3(ABCC9):c.4103-79A>G
NM_005691.3(ABCC9):c.4212-129G>T
NM_005691.3(ABCC9):c.4315+11T>C rs781522912
NM_005691.3(ABCC9):c.4449+204C>T
NM_005691.3(ABCC9):c.4450-16dup rs4148680
NM_005691.3(ABCC9):c.4450-5del rs4148680
NM_005691.3(ABCC9):c.4512+16C>T rs376147813
NM_005691.3(ABCC9):c.4513-154C>G
NM_005691.3(ABCC9):c.574-270C>A
NM_005691.3(ABCC9):c.574-5= rs3759236
NM_005691.3(ABCC9):c.574-5C>A rs3759236
NM_005691.3(ABCC9):c.789C>T (p.Cys263=) rs58386780
NM_005691.3(ABCC9):c.798T>C (p.Asp266=) rs138356189
NM_005691.3(ABCC9):c.817-17C>T rs76350525
NM_005691.3(ABCC9):c.817-180G>A
NM_005691.3(ABCC9):c.924T>C (p.Asp308=) rs139127928
NM_020297.3(ABCC9):c.*19T>C rs114906131
NM_020297.3(ABCC9):c.1164+11A>G rs4762720
NM_020297.3(ABCC9):c.1164+23C>A rs4762719
NM_020297.3(ABCC9):c.2199-11T>C rs697250
NM_020297.3(ABCC9):c.817-7del rs193922684

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