ClinVar Miner

List of variants in gene ABCC9 reported by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP
NM_005691.3(ABCC9):c.-11T>C rs72559432
NM_005691.3(ABCC9):c.-14_-8del rs746420722
NM_005691.3(ABCC9):c.1012-14del rs727505105
NM_005691.3(ABCC9):c.1012-7G>A rs727502874
NM_005691.3(ABCC9):c.1056C>T (p.Tyr352=) rs149408382
NM_005691.3(ABCC9):c.1063G>T (p.Ala355Ser) rs145455570
NM_005691.3(ABCC9):c.1142T>A (p.Ile381Asn) rs397517181
NM_005691.3(ABCC9):c.1164+10G>A rs876657427
NM_005691.3(ABCC9):c.1165-19dup rs35857705
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.1358G>C (p.Gly453Ala) rs397517183
NM_005691.3(ABCC9):c.142+15dup rs571187142
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.1677G>A (p.Ala559=) rs76458291
NM_005691.3(ABCC9):c.169C>T (p.Gln57Ter) rs727502876
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.1933A>G (p.Lys645Glu) rs876657734
NM_005691.3(ABCC9):c.1982G>A (p.Arg661His) rs397517185
NM_005691.3(ABCC9):c.1987C>T (p.Arg663Cys) rs200349671
NM_005691.3(ABCC9):c.2000C>A (p.Thr667Lys) rs397517186
NM_005691.3(ABCC9):c.2050G>A (p.Gly684Ser) rs148174226
NM_005691.3(ABCC9):c.2081G>A (p.Arg694Gln) rs267603424
NM_005691.3(ABCC9):c.2093-7T>C rs185235724
NM_005691.3(ABCC9):c.2149G>A (p.Ala717Thr) rs397517187
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.2200G>A (p.Val734Ile) rs61688134
NM_005691.3(ABCC9):c.2238-1G>A rs141281214
NM_005691.3(ABCC9):c.2262T>C (p.Tyr754=) rs145561881
NM_005691.3(ABCC9):c.2339+13A>G rs189255166
NM_005691.3(ABCC9):c.2424+9T>C rs11835804
NM_005691.3(ABCC9):c.2425-13G>A rs397517188
NM_005691.3(ABCC9):c.2523C>T (p.Ala841=) rs144537241
NM_005691.3(ABCC9):c.2547T>C (p.His849=) rs876657428
NM_005691.3(ABCC9):c.2631G>A (p.Thr877=) rs139408145
NM_005691.3(ABCC9):c.2644-11G>A rs61926078
NM_005691.3(ABCC9):c.2644-11G>C rs61926078
NM_005691.3(ABCC9):c.2746C>T (p.Arg916Trp) rs533032970
NM_005691.3(ABCC9):c.2770-13A>G rs184123387
NM_005691.3(ABCC9):c.2862C>T (p.Asp954=) rs2291550
NM_005691.3(ABCC9):c.289C>T (p.Arg97Trp) rs727502875
NM_005691.3(ABCC9):c.2932C>A (p.Pro978Thr) rs376874273
NM_005691.3(ABCC9):c.3030T>C (p.Ala1010=) rs76102634
NM_005691.3(ABCC9):c.305T>C (p.Leu102Pro) rs374659816
NM_005691.3(ABCC9):c.3096+13C>T rs370712530
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.3315+4A>G rs727504847
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.3409G>A (p.Val1137Ile) rs147895473
NM_005691.3(ABCC9):c.3474-14C>T rs876657429
NM_005691.3(ABCC9):c.3668C>T (p.Thr1223Met) rs137907278
NM_005691.3(ABCC9):c.3669G>A (p.Thr1223=) rs146942382
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.3768T>C (p.Leu1256=) rs150303433
NM_005691.3(ABCC9):c.395A>G (p.Lys132Arg) rs727505161
NM_005691.3(ABCC9):c.3993C>T (p.His1331=) rs377704379
NM_005691.3(ABCC9):c.406+14C>G rs752547896
NM_005691.3(ABCC9):c.4062G>A (p.Ser1354=) rs145005748
NM_005691.3(ABCC9):c.407-14C>A rs201279882
NM_005691.3(ABCC9):c.4196dup (p.Ser1400fs) rs730880370
NM_005691.3(ABCC9):c.420T>C (p.Tyr140=) rs397517189
NM_005691.3(ABCC9):c.4352T>C (p.Val1451Ala) rs397517190
NM_005691.3(ABCC9):c.4365G>A (p.Gln1455=) rs727504785
NM_005691.3(ABCC9):c.4437T>C (p.Ile1479=) rs368079660
NM_005691.3(ABCC9):c.4450-16dup rs4148680
NM_005691.3(ABCC9):c.4470A>G (p.Val1490=) rs727505001
NM_005691.3(ABCC9):c.4516C>T (p.Arg1506Cys) rs397517191
NM_005691.3(ABCC9):c.4519G>A (p.Val1507Ile) rs876657737
NM_005691.3(ABCC9):c.4570_4572delinsAAAT (p.Leu1524fs) rs869025349
NM_005691.3(ABCC9):c.4591C>T (p.Pro1531Ser) rs142875103
NM_005691.3(ABCC9):c.4613A>G (p.Asn1538Ser) rs372859669
NM_005691.3(ABCC9):c.47A>G (p.Asn16Ser) rs727502877
NM_005691.3(ABCC9):c.48C>T (p.Asn16=) rs199631710
NM_005691.3(ABCC9):c.573+6T>C rs397517192
NM_005691.3(ABCC9):c.574-5= rs3759236
NM_005691.3(ABCC9):c.574-5C>A rs3759236
NM_005691.3(ABCC9):c.575G>A (p.Arg192Lys) rs727504612
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.816+11G>A rs200986421
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.924T>C (p.Asp308=) rs139127928
NM_005691.3(ABCC9):c.96C>T (p.Val32=) rs727505034
NM_020297.3(ABCC9):c.*5G>C rs876657736
NM_020297.3(ABCC9):c.1164+11A>G rs4762720
NM_020297.3(ABCC9):c.2199-11T>C rs697250
NM_020297.3(ABCC9):c.4569T>C (p.Asn1523=) rs727504538
NM_020297.3(ABCC9):c.817-7del rs193922684

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