ClinVar Miner

List of variants in gene ABCC9 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 101
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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.1062A>G (p.Leu354=) rs1555114097
NM_005691.3(ABCC9):c.1071T>A (p.Leu357=)
NM_005691.3(ABCC9):c.1165-54T>C
NM_005691.3(ABCC9):c.1200G>A (p.Thr400=) rs150096625
NM_005691.3(ABCC9):c.133T>C (p.Leu45=) rs1555125400
NM_005691.3(ABCC9):c.142+10C>A rs138917284
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.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.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.2092+5G>A rs763488230
NM_005691.3(ABCC9):c.2093-7T>G rs185235724
NM_005691.3(ABCC9):c.2154C>T (p.Ile718=) rs74067815
NM_005691.3(ABCC9):c.2199-13G>A rs201226082
NM_005691.3(ABCC9):c.2199-6T>C rs535477725
NM_005691.3(ABCC9):c.2238-1G>A rs141281214
NM_005691.3(ABCC9):c.231C>T (p.Phe77=) rs767694387
NM_005691.3(ABCC9):c.2339+17A>T rs1057523935
NM_005691.3(ABCC9):c.2424+78G>A
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.2607G>A (p.Val869=) rs762524104
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.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.3030T>C (p.Ala1010=) rs76102634
NM_005691.3(ABCC9):c.3060G>A (p.Ser1020=) rs769003781
NM_005691.3(ABCC9):c.3096+100A>T
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.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.3474-93A>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.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.4023+327A>G
NM_005691.3(ABCC9):c.4062G>A (p.Ser1354=) rs145005748
NM_005691.3(ABCC9):c.407-13T>C rs199717786
NM_005691.3(ABCC9):c.4102+17A>T rs761888147
NM_005691.3(ABCC9):c.4188A>G (p.Pro1396=) rs1057523571
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.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.4512+7A>G rs371646433
NM_005691.3(ABCC9):c.4512T>A (p.Ala1504=) rs777591544
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.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.837A>G (p.Pro279=) rs1264086698
NM_020297.3(ABCC9):c.4512+1094A>C
NM_020297.3(ABCC9):c.4638C>T (p.Arg1546=)
NM_020297.3(ABCC9):c.816+13_816+14delCT rs1555116429

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