ClinVar Miner

List of variants in gene ABCC9 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 101
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HGVS dbSNP gnomAD frequency
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.1296C>T (p.Pro432=) rs10770865 0.00308
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.372T>C (p.Asn124=) rs377384557 0.00051
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.1887G>T (p.Glu629Asp) rs150036969 0.00032
NM_020297.4(ABCC9):c.2154C>T (p.Ile718=) rs74067815 0.00031
NM_020297.4(ABCC9):c.3339T>G (p.Ser1113=) rs138280089 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.3729G>A (p.Ser1243=) rs140182559 0.00023
NM_020297.4(ABCC9):c.3096+13C>T rs370712530 0.00017
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.1909G>A (p.Val637Ile) rs113542001 0.00016
NM_020297.4(ABCC9):c.4062G>A (p.Ser1354=) rs145005748 0.00016
NM_020297.4(ABCC9):c.2339+13A>G rs189255166 0.00012
NM_020297.4(ABCC9):c.3288T>C (p.Phe1096=) rs377372612 0.00011
NM_020297.4(ABCC9):c.96C>T (p.Val32=) rs727505034 0.00011
NM_020297.4(ABCC9):c.852T>A (p.Ser284=) rs113562970 0.00010
NM_020297.4(ABCC9):c.4344T>C (p.Asn1448=) rs146782703 0.00009
NM_020297.4(ABCC9):c.3993C>T (p.His1331=) rs377704379 0.00008
NM_020297.4(ABCC9):c.142+10C>A rs138917284 0.00007
NM_020297.4(ABCC9):c.2856C>T (p.Asp952=) rs758697683 0.00007
NM_020297.4(ABCC9):c.3566+15T>C rs766079858 0.00006
NM_020297.4(ABCC9):c.4211+10A>G rs776928239 0.00006
NM_020297.4(ABCC9):c.4437T>C (p.Ile1479=) rs368079660 0.00006
NM_020297.4(ABCC9):c.4512+7A>G rs371646433 0.00005
NM_020297.4(ABCC9):c.48C>T (p.Asn16=) rs199631710 0.00005
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.2157C>T (p.Leu719=) rs201848437 0.00004
NM_020297.4(ABCC9):c.284+14G>C rs373386719 0.00004
NM_020297.4(ABCC9):c.3567-19_3567-13del rs1177684407 0.00004
NM_020297.4(ABCC9):c.816+11G>A rs200986421 0.00004
NM_020297.4(ABCC9):c.1164+10G>A rs876657427 0.00003
NM_020297.4(ABCC9):c.1212C>T (p.Ser404=) rs376726505 0.00003
NM_020297.4(ABCC9):c.3096+9G>T rs765048337 0.00003
NM_020297.4(ABCC9):c.4569T>C (p.Asn1523=) rs727504538 0.00003
NM_020297.4(ABCC9):c.2004G>A (p.Glu668=) rs751485829 0.00002
NM_020297.4(ABCC9):c.2607G>A (p.Val869=) rs762524104 0.00002
NM_020297.4(ABCC9):c.2769+13A>G rs771938422 0.00002
NM_020297.4(ABCC9):c.3060G>A (p.Ser1020=) rs769003781 0.00002
NM_020297.4(ABCC9):c.4470A>G (p.Val1490=) rs727505001 0.00002
NM_020297.4(ABCC9):c.816+10C>T rs559193279 0.00002
NM_020297.4(ABCC9):c.918G>A (p.Leu306=) rs142115849 0.00002
NM_020297.4(ABCC9):c.1194C>T (p.Leu398=) rs1430745818 0.00001
NM_020297.4(ABCC9):c.1425A>G (p.Thr475=) rs772284924 0.00001
NM_020297.4(ABCC9):c.1603T>C (p.Tyr535His) rs397517184 0.00001
NM_020297.4(ABCC9):c.1619-10C>A rs1169346732 0.00001
NM_020297.4(ABCC9):c.1659+10T>C rs201753781 0.00001
NM_020297.4(ABCC9):c.1875G>A (p.Ser625=) rs727502873 0.00001
NM_020297.4(ABCC9):c.2199-6T>C rs535477725 0.00001
NM_020297.4(ABCC9):c.231C>T (p.Phe77=) rs767694387 0.00001
NM_020297.4(ABCC9):c.2547T>C (p.His849=) rs876657428 0.00001
NM_020297.4(ABCC9):c.2703C>T (p.Thr901=) rs1000035870 0.00001
NM_020297.4(ABCC9):c.324C>T (p.Ala108=) rs770552940 0.00001
NM_020297.4(ABCC9):c.3739T>C (p.Leu1247=) rs1057522334 0.00001
NM_020297.4(ABCC9):c.3772-16T>C rs745509782 0.00001
NM_020297.4(ABCC9):c.3831T>A (p.Gly1277=) rs760351484 0.00001
NM_020297.4(ABCC9):c.406+14C>G rs752547896 0.00001
NM_020297.4(ABCC9):c.4320G>A (p.Ala1440=) rs377289768 0.00001
NM_020297.4(ABCC9):c.4365G>A (p.Gln1455=) rs727504785 0.00001
NM_020297.4(ABCC9):c.573+19T>C rs1555116939 0.00001
NM_020297.4(ABCC9):c.957T>C (p.Ser319=) rs768245158 0.00001
NM_020297.4(ABCC9):c.1012-14del rs727505105
NM_020297.4(ABCC9):c.1062A>G (p.Leu354=) rs1555114097
NM_020297.4(ABCC9):c.1165-6dup rs35857705
NM_020297.4(ABCC9):c.133T>C (p.Leu45=) rs1555125400
NM_020297.4(ABCC9):c.142+19T>A rs547603072
NM_020297.4(ABCC9):c.1455+10A>G rs1555113022
NM_020297.4(ABCC9):c.1455T>G (p.Leu485=) rs1057523907
NM_020297.4(ABCC9):c.1619-20C>A rs1357942810
NM_020297.4(ABCC9):c.1629T>C (p.Asn543=)
NM_020297.4(ABCC9):c.1638T>C (p.Ile546=) rs370463895
NM_020297.4(ABCC9):c.2019+14C>T rs1057523719
NM_020297.4(ABCC9):c.2022C>T (p.Val674=) rs1555195612
NM_020297.4(ABCC9):c.2092+5G>A rs763488230
NM_020297.4(ABCC9):c.2339+17A>T rs1057523935
NM_020297.4(ABCC9):c.2355A>T (p.Thr785=) rs886038653
NM_020297.4(ABCC9):c.2457A>G (p.Arg819=) rs1057523572
NM_020297.4(ABCC9):c.2524C>T (p.Leu842=) rs1555189349
NM_020297.4(ABCC9):c.3063G>A (p.Glu1021=) rs1555187269
NM_020297.4(ABCC9):c.3097-15T>A rs1057524442
NM_020297.4(ABCC9):c.3246-10T>C rs1057524220
NM_020297.4(ABCC9):c.3309T>A (p.Ile1103=) rs767919730
NM_020297.4(ABCC9):c.3474-14C>T rs876657429
NM_020297.4(ABCC9):c.3669+7T>A rs1183466743
NM_020297.4(ABCC9):c.4102+17A>T rs761888147
NM_020297.4(ABCC9):c.420T>C (p.Tyr140=) rs397517189
NM_020297.4(ABCC9):c.4332A>G (p.Glu1444=) rs1555176704
NM_020297.4(ABCC9):c.4366C>T (p.Leu1456=) rs1370019085
NM_020297.4(ABCC9):c.6C>T (p.Ser2=) rs765382139
NM_020297.4(ABCC9):c.771A>C (p.Ala257=)
NM_020297.4(ABCC9):c.816+13_816+14del rs1555116429
NM_020297.4(ABCC9):c.817-7del rs193922684

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