ClinVar Miner

List of variants in gene ABCC9 reported by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP
NM_001377273.1(ABCC9):c.1247T>C (p.Leu416Ser)
NM_005691.3(ABCC9):c.-11T>C rs72559432
NM_005691.3(ABCC9):c.1008T>C (p.Thr336=)
NM_005691.3(ABCC9):c.1164+11= rs4762720
NM_005691.3(ABCC9):c.1165-19dup rs35857705
NM_005691.3(ABCC9):c.1165-4del rs886049172
NM_005691.3(ABCC9):c.1165-6del rs35857705
NM_005691.3(ABCC9):c.1165-7_1165-6del rs35857705
NM_005691.3(ABCC9):c.1296= (p.Pro432=) rs10770865
NM_005691.3(ABCC9):c.1320+1G>A rs139620148
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.1374C>T (p.Val458=) rs200819464
NM_005691.3(ABCC9):c.1455+4A>C rs376587222
NM_005691.3(ABCC9):c.146G>C (p.Trp49Ser) rs886049175
NM_005691.3(ABCC9):c.1659+10T>C rs201753781
NM_005691.3(ABCC9):c.1670C>G (p.Thr557Ser) rs886049171
NM_005691.3(ABCC9):c.1875G>A (p.Ser625=) rs727502873
NM_005691.3(ABCC9):c.1877T>C (p.Leu626Pro)
NM_005691.3(ABCC9):c.1981C>T (p.Arg661Cys) rs199499109
NM_005691.3(ABCC9):c.1992C>T (p.Pro664=) rs780071007
NM_005691.3(ABCC9):c.2093-7T>C rs185235724
NM_005691.3(ABCC9):c.2158G>A (p.Gly720Ser)
NM_005691.3(ABCC9):c.2199-11= rs697250
NM_005691.3(ABCC9):c.2199-6T>C rs535477725
NM_005691.3(ABCC9):c.2238-16del rs886049170
NM_005691.3(ABCC9):c.2238-17del rs4148670
NM_005691.3(ABCC9):c.2238-1G>A rs141281214
NM_005691.3(ABCC9):c.2424+9T>C rs11835804
NM_005691.3(ABCC9):c.2481T>C (p.Tyr827=)
NM_005691.3(ABCC9):c.2644-11G>A rs61926078
NM_005691.3(ABCC9):c.2769+12T>C rs564071879
NM_005691.3(ABCC9):c.2770-13A>G rs184123387
NM_005691.3(ABCC9):c.2826T>C (p.Tyr942=) rs141025897
NM_005691.3(ABCC9):c.2863G>A (p.Glu955Lys)
NM_005691.3(ABCC9):c.3141T>C (p.Ile1047=)
NM_005691.3(ABCC9):c.3316-4A>C rs201147809
NM_005691.3(ABCC9):c.3357G>A (p.Leu1119=) rs2287626
NM_005691.3(ABCC9):c.3556C>T (p.Arg1186Trp) rs886049169
NM_005691.3(ABCC9):c.3589C>T (p.Arg1197Cys) rs778849288
NM_005691.3(ABCC9):c.3669+10T>C rs199640712
NM_005691.3(ABCC9):c.366T>C (p.Tyr122=) rs886049174
NM_005691.3(ABCC9):c.407-14C>A rs201279882
NM_005691.3(ABCC9):c.4103-14T>C
NM_005691.3(ABCC9):c.4316-14T>G rs886049168
NM_005691.3(ABCC9):c.4519G>T (p.Val1507Phe)
NM_005691.3(ABCC9):c.466T>C (p.Cys156Arg) rs886049173
NM_005691.3(ABCC9):c.574-5C>A rs3759236
NM_005691.3(ABCC9):c.669G>T (p.Leu223=) rs17846788
NM_005691.3(ABCC9):c.6C>T (p.Ser2=) rs765382139
NM_005691.3(ABCC9):c.75T>C (p.Phe25=) rs201972673
NM_005691.3(ABCC9):c.842G>A (p.Arg281Gln) rs753456211
NM_005691.3(ABCC9):c.882G>A (p.Gly294=)
NM_020297.3(ABCC9):c.1557G>A (p.Glu519=) rs143346402
NM_020297.3(ABCC9):c.1677G>A (p.Ala559=) rs76458291
NM_020297.3(ABCC9):c.1848C>T (p.Asp616=) rs61001398
NM_020297.3(ABCC9):c.1887G>T (p.Glu629Asp) rs150036969
NM_020297.3(ABCC9):c.2050G>A (p.Gly684Ser) rs148174226
NM_020297.3(ABCC9):c.2200G>A (p.Val734Ile) rs61688134
NM_020297.3(ABCC9):c.2262T>C (p.Tyr754=) rs145561881
NM_020297.3(ABCC9):c.2523C>T (p.Ala841=) rs144537241
NM_020297.3(ABCC9):c.2631G>A (p.Thr877=) rs139408145
NM_020297.3(ABCC9):c.2862C>T (p.Asp954=) rs2291550
NM_020297.3(ABCC9):c.3321C>T (p.Ile1107=) rs35404804
NM_020297.3(ABCC9):c.3339T>G (p.Ser1113=) rs138280089
NM_020297.3(ABCC9):c.3409G>A (p.Val1137Ile) rs147895473
NM_020297.3(ABCC9):c.372T>C (p.Asn124=) rs377384557
NM_020297.3(ABCC9):c.3768T>C (p.Leu1256=) rs150303433
NM_020297.3(ABCC9):c.789C>T (p.Cys263=) rs58386780

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