ClinVar Miner

List of variants in gene ABCC9 reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 171
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HGVS dbSNP
NC_000012.12:g.21863322_21863324del
NC_000012.12:g.21872489del
NM_005691.3(ABCC9):c.-11T>C rs72559432
NM_005691.3(ABCC9):c.1011+7T>C rs1224367944
NM_005691.3(ABCC9):c.1012-14del rs727505105
NM_005691.3(ABCC9):c.1062A>G (p.Leu354=) rs1555114097
NM_005691.3(ABCC9):c.1071T>A (p.Leu357=)
NM_005691.3(ABCC9):c.1164+10G>A rs876657427
NM_005691.3(ABCC9):c.1164+11= rs4762720
NM_005691.3(ABCC9):c.1165-19dup rs35857705
NM_005691.3(ABCC9):c.1165-54T>C
NM_005691.3(ABCC9):c.1165-5G>T rs1411076886
NM_005691.3(ABCC9):c.1165-6del rs35857705
NM_005691.3(ABCC9):c.1194C>T (p.Leu398=) rs1430745818
NM_005691.3(ABCC9):c.1200G>A (p.Thr400=) rs150096625
NM_005691.3(ABCC9):c.1212C>T (p.Ser404=) rs376726505
NM_005691.3(ABCC9):c.1296= (p.Pro432=) rs10770865
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.133T>C (p.Leu45=) rs1555125400
NM_005691.3(ABCC9):c.1416T>C (p.Phe472=) rs777308898
NM_005691.3(ABCC9):c.142+10C>A rs138917284
NM_005691.3(ABCC9):c.142+15dup rs571187142
NM_005691.3(ABCC9):c.142+19T>A rs547603072
NM_005691.3(ABCC9):c.1425A>G (p.Thr475=) rs772284924
NM_005691.3(ABCC9):c.1455+10A>G rs1555113022
NM_005691.3(ABCC9):c.1455T>G (p.Leu485=) rs1057523907
NM_005691.3(ABCC9):c.1521G>A (p.Leu507=) rs1565470512
NM_005691.3(ABCC9):c.1524T>C (p.Tyr508=) rs1555112390
NM_005691.3(ABCC9):c.1557G>A (p.Glu519=) rs143346402
NM_005691.3(ABCC9):c.1603T>C (p.Tyr535His) rs397517184
NM_005691.3(ABCC9):c.1619-10C>A rs1169346732
NM_005691.3(ABCC9):c.1619-7T>C rs769816456
NM_005691.3(ABCC9):c.1638T>C (p.Ile546=) rs370463895
NM_005691.3(ABCC9):c.1659+10T>C rs201753781
NM_005691.3(ABCC9):c.1660-276C>A
NM_005691.3(ABCC9):c.1785A>G (p.Ala595=) rs1555106091
NM_005691.3(ABCC9):c.1848C>T (p.Asp616=) rs61001398
NM_005691.3(ABCC9):c.1875G>A (p.Ser625=) rs727502873
NM_005691.3(ABCC9):c.1887G>T (p.Glu629Asp) rs150036969
NM_005691.3(ABCC9):c.1909G>A (p.Val637Ile) rs113542001
NM_005691.3(ABCC9):c.1912-12T>C
NM_005691.3(ABCC9):c.2019+14C>T rs1057523719
NM_005691.3(ABCC9):c.2019+85T>A
NM_005691.3(ABCC9):c.2022C>T (p.Val674=) rs1555195612
NM_005691.3(ABCC9):c.2050G>A (p.Gly684Ser) rs148174226
NM_005691.3(ABCC9):c.2092+5G>A rs763488230
NM_005691.3(ABCC9):c.2093-7T>C rs185235724
NM_005691.3(ABCC9):c.2093-7T>G rs185235724
NM_005691.3(ABCC9):c.2154C>T (p.Ile718=) rs74067815
NM_005691.3(ABCC9):c.2157C>T (p.Leu719=) rs201848437
NM_005691.3(ABCC9):c.2199-11= rs697250
NM_005691.3(ABCC9):c.2199-13G>A rs201226082
NM_005691.3(ABCC9):c.2199-6T>C rs535477725
NM_005691.3(ABCC9):c.2200G>A (p.Val734Ile) rs61688134
NM_005691.3(ABCC9):c.2238-17del rs4148670
NM_005691.3(ABCC9):c.2238-1G>A rs141281214
NM_005691.3(ABCC9):c.2262T>C (p.Tyr754=) rs145561881
NM_005691.3(ABCC9):c.231C>T (p.Phe77=) rs767694387
NM_005691.3(ABCC9):c.2339+13A>G rs189255166
NM_005691.3(ABCC9):c.2339+17A>T rs1057523935
NM_005691.3(ABCC9):c.2355A>T (p.Thr785=) rs886038653
NM_005691.3(ABCC9):c.2424+78G>A
NM_005691.3(ABCC9):c.2424+9T>C rs11835804
NM_005691.3(ABCC9):c.2457A>G (p.Arg819=) rs1057523572
NM_005691.3(ABCC9):c.2506-301G>T
NM_005691.3(ABCC9):c.2524C>T (p.Leu842=) rs1555189349
NM_005691.3(ABCC9):c.2547T>C (p.His849=) rs876657428
NM_005691.3(ABCC9):c.2574C>T (p.Phe858=) rs1273498300
NM_005691.3(ABCC9):c.2607G>A (p.Val869=) rs762524104
NM_005691.3(ABCC9):c.2631G>A (p.Thr877=) rs139408145
NM_005691.3(ABCC9):c.2644-11G>C rs61926078
NM_005691.3(ABCC9):c.2703C>T (p.Thr901=) rs1000035870
NM_005691.3(ABCC9):c.2769+13A>G rs771938422
NM_005691.3(ABCC9):c.2799G>A (p.Glu933=) rs1565735141
NM_005691.3(ABCC9):c.2826T>C (p.Tyr942=) rs141025897
NM_005691.3(ABCC9):c.284+14G>C rs373386719
NM_005691.3(ABCC9):c.2856C>T (p.Asp952=) rs758697683
NM_005691.3(ABCC9):c.2862C>T (p.Asp954=) rs2291550
NM_005691.3(ABCC9):c.2866+171T>A
NM_005691.3(ABCC9):c.2867-5T>C rs369841241
NM_005691.3(ABCC9):c.287G>A (p.Arg96Gln) rs202103893
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.3030T>C (p.Ala1010=) rs76102634
NM_005691.3(ABCC9):c.3057A>G (p.Thr1019=) rs886038903
NM_005691.3(ABCC9):c.3060G>A (p.Ser1020=) rs769003781
NM_005691.3(ABCC9):c.3096+100A>T
NM_005691.3(ABCC9):c.3096+13C>T rs370712530
NM_005691.3(ABCC9):c.3096+9G>T rs765048337
NM_005691.3(ABCC9):c.3097-15T>A rs1057524442
NM_005691.3(ABCC9):c.3097-42T>C
NM_005691.3(ABCC9):c.3246-10T>C rs1057524220
NM_005691.3(ABCC9):c.324C>T (p.Ala108=) rs770552940
NM_005691.3(ABCC9):c.3288T>C (p.Phe1096=) rs377372612
NM_005691.3(ABCC9):c.3309T>A (p.Ile1103=) rs767919730
NM_005691.3(ABCC9):c.3316-4A>C rs201147809
NM_005691.3(ABCC9):c.3331T>C (p.Leu1111=) rs764155671
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.3462G>A (p.Arg1154=) rs1336342134
NM_005691.3(ABCC9):c.3473+112C>T
NM_005691.3(ABCC9):c.3474-14C>T rs876657429
NM_005691.3(ABCC9):c.3474-93A>G
NM_005691.3(ABCC9):c.3566+15T>C rs766079858
NM_005691.3(ABCC9):c.3567-180A>G
NM_005691.3(ABCC9):c.3567-197T>A
NM_005691.3(ABCC9):c.3567-19_3567-13del rs1177684407
NM_005691.3(ABCC9):c.3567-20C>T
NM_005691.3(ABCC9):c.3621T>C (p.Ile1207=) rs767458242
NM_005691.3(ABCC9):c.363T>C (p.Tyr121=)
NM_005691.3(ABCC9):c.3669+7T>A rs1183466743
NM_005691.3(ABCC9):c.3729G>A (p.Ser1243=) rs140182559
NM_005691.3(ABCC9):c.372T>C (p.Asn124=) rs377384557
NM_005691.3(ABCC9):c.3739T>C (p.Leu1247=) rs1057522334
NM_005691.3(ABCC9):c.3772-16T>C rs745509782
NM_005691.3(ABCC9):c.3772-250T>C
NM_005691.3(ABCC9):c.3772-65C>T
NM_005691.3(ABCC9):c.3831T>A (p.Gly1277=) rs760351484
NM_005691.3(ABCC9):c.3993C>T (p.His1331=) rs377704379
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.4023+327A>G
NM_005691.3(ABCC9):c.406+14C>G rs752547896
NM_005691.3(ABCC9):c.4062G>A (p.Ser1354=) rs145005748
NM_005691.3(ABCC9):c.407-13T>C rs199717786
NM_005691.3(ABCC9):c.407-14C>A rs201279882
NM_005691.3(ABCC9):c.4102+17A>T rs761888147
NM_005691.3(ABCC9):c.4188A>G (p.Pro1396=) rs1057523571
NM_005691.3(ABCC9):c.420T>C (p.Tyr140=) rs397517189
NM_005691.3(ABCC9):c.4211+10A>G rs776928239
NM_005691.3(ABCC9):c.4211+123A>T
NM_005691.3(ABCC9):c.4320G>A (p.Ala1440=) rs377289768
NM_005691.3(ABCC9):c.4332A>G (p.Glu1444=) rs1555176704
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.4365G>A (p.Gln1455=) rs727504785
NM_005691.3(ABCC9):c.4366C>T (p.Leu1456=) rs1370019085
NM_005691.3(ABCC9):c.4389T>C (p.Phe1463=)
NM_005691.3(ABCC9):c.4437T>C (p.Ile1479=) rs368079660
NM_005691.3(ABCC9):c.444A>G (p.Lys148=)
NM_005691.3(ABCC9):c.4450-5del rs4148680
NM_005691.3(ABCC9):c.4470A>G (p.Val1490=) rs727505001
NM_005691.3(ABCC9):c.4497C>T (p.Thr1499=) rs1060504811
NM_005691.3(ABCC9):c.4512+7A>G rs371646433
NM_005691.3(ABCC9):c.4512T>A (p.Ala1504=) rs777591544
NM_005691.3(ABCC9):c.4570T>A (p.Leu1524Ile) rs139703258
NM_005691.3(ABCC9):c.4571T>A (p.Leu1524Ter) rs150631550
NM_005691.3(ABCC9):c.4572_4573insT (p.Val1525fs) rs761784169
NM_005691.3(ABCC9):c.48C>T (p.Asn16=) rs199631710
NM_005691.3(ABCC9):c.558T>C (p.Asn186=) rs1555116969
NM_005691.3(ABCC9):c.573+12A>C
NM_005691.3(ABCC9):c.573+19T>C rs1555116939
NM_005691.3(ABCC9):c.574-18G>A rs376566343
NM_005691.3(ABCC9):c.574-5C>A rs3759236
NM_005691.3(ABCC9):c.639G>A (p.Val213=)
NM_005691.3(ABCC9):c.6C>T (p.Ser2=) rs765382139
NM_005691.3(ABCC9):c.798T>C (p.Asp266=) rs138356189
NM_005691.3(ABCC9):c.816+10C>T rs559193279
NM_005691.3(ABCC9):c.816+11G>A rs200986421
NM_005691.3(ABCC9):c.816+13_816+14del rs1555116429
NM_005691.3(ABCC9):c.817-14_817-4del rs774857795
NM_005691.3(ABCC9):c.837A>G (p.Pro279=) rs1264086698
NM_005691.3(ABCC9):c.852T>A (p.Ser284=) rs113562970
NM_005691.3(ABCC9):c.918G>A (p.Leu306=) rs142115849
NM_005691.3(ABCC9):c.928C>T (p.Leu310=) rs747640613
NM_005691.3(ABCC9):c.96C>T (p.Val32=) rs727505034
NM_020297.3(ABCC9):c.4512+1094A>C
NM_020297.3(ABCC9):c.4569T>C (p.Asn1523=) rs727504538
NM_020297.3(ABCC9):c.4638C>T (p.Arg1546=)
NM_020297.3(ABCC9):c.817-7del rs193922684

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