ClinVar Miner

List of variants in gene ABCC9 reported by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 39
Download table as spreadsheet
HGVS dbSNP
NM_005691.3(ABCC9):c.1043T>G (p.Leu348Arg) rs876661339
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.1296= (p.Pro432=) rs10770865
NM_005691.3(ABCC9):c.1320+1G>A rs139620148
NM_005691.3(ABCC9):c.1455+4A>C rs376587222
NM_005691.3(ABCC9):c.1557G>A (p.Glu519=) rs143346402
NM_005691.3(ABCC9):c.1677G>A (p.Ala559=) rs76458291
NM_005691.3(ABCC9):c.1848C>T (p.Asp616=) rs61001398
NM_005691.3(ABCC9):c.1887G>T (p.Glu629Asp) rs150036969
NM_005691.3(ABCC9):c.2050G>A (p.Gly684Ser) rs148174226
NM_005691.3(ABCC9):c.2190C>A (p.His730Gln) rs771887289
NM_005691.3(ABCC9):c.2200G>A (p.Val734Ile) rs61688134
NM_005691.3(ABCC9):c.2238-1G>A rs141281214
NM_005691.3(ABCC9):c.2238-4T>C rs770513703
NM_005691.3(ABCC9):c.2262T>C (p.Tyr754=) rs145561881
NM_005691.3(ABCC9):c.2285T>G (p.Leu762Ter) rs1555192419
NM_005691.3(ABCC9):c.2523C>T (p.Ala841=) rs144537241
NM_005691.3(ABCC9):c.256G>C (p.Glu86Gln) rs774026262
NM_005691.3(ABCC9):c.2631G>A (p.Thr877=) rs139408145
NM_005691.3(ABCC9):c.2826T>C (p.Tyr942=) rs141025897
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.3076A>G (p.Asn1026Asp) rs369389402
NM_005691.3(ABCC9):c.3321C>T (p.Ile1107=) rs35404804
NM_005691.3(ABCC9):c.3357G>A (p.Leu1119=) rs2287626
NM_005691.3(ABCC9):c.3590G>A (p.Arg1197His) rs755156050
NM_005691.3(ABCC9):c.372T>C (p.Asn124=) rs377384557
NM_005691.3(ABCC9):c.3796G>A (p.Val1266Met) rs1555179320
NM_005691.3(ABCC9):c.4450-5del rs4148680
NM_005691.3(ABCC9):c.4516C>T (p.Arg1506Cys) rs397517191
NM_005691.3(ABCC9):c.4517G>A (p.Arg1506His) rs777661095
NM_005691.3(ABCC9):c.558T>C (p.Asn186=) rs1555116969
NM_005691.3(ABCC9):c.574-5C>A rs3759236
NM_005691.3(ABCC9):c.826G>A (p.Ala276Thr) rs201783967
NM_005691.3(ABCC9):c.928C>T (p.Leu310=) rs747640613
NM_005691.3(ABCC9):c.971G>A (p.Arg324His) rs886039121
NM_020297.3(ABCC9):c.4512+744_4512+746delinsAAAT rs869025349

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.