ClinVar Miner

List of variants in gene CETP studied for hyperlipoproteinemia

Included ClinVar conditions (22):
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Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_000078.2(CETP):c.*184C>G rs289742 0.80081
NM_000078.3(CETP):c.1264G>A (p.Val422Ile) rs5882 0.58912
NM_000078.3(CETP):c.1215-14C>T rs1800774 0.32028
NM_000078.3(CETP):c.*84G>A rs1801706 0.16507
NM_000078.3(CETP):c.861C>T (p.Phe287=) rs5883 0.06709
NM_000078.3(CETP):c.1168G>C (p.Ala390Pro) rs5880 0.03659
NM_000078.3(CETP):c.1403G>A (p.Arg468Gln) rs1800777 0.02796
NM_000078.3(CETP):c.-65G>A rs17231520 0.02173
NM_000078.3(CETP):c.1299G>A (p.Val433=) rs5886 0.02118
NM_000078.3(CETP):c.44C>G (p.Ala15Gly) rs34065661 0.01971
NM_000078.3(CETP):c.66C>A (p.Thr22=) rs5884 0.01514
NM_000078.3(CETP):c.460C>T (p.Arg154Trp) rs34716057 0.00764
NM_000078.3(CETP):c.534G>A (p.Gly178=) rs34611098 0.00148
NM_000078.3(CETP):c.1146+7C>T rs182237338 0.00146
NM_000078.3(CETP):c.1153G>A (p.Val385Met) rs34855278 0.00108
NM_000078.3(CETP):c.921C>T (p.Asp307=) rs28381708 0.00079
NM_000078.3(CETP):c.1376A>G (p.Asp459Gly) rs2303790 0.00066
NM_000078.3(CETP):c.940G>A (p.Glu314Lys) rs140547417 0.00046
NM_000078.3(CETP):c.466G>A (p.Asp156Asn) rs201778606 0.00023
NM_000078.3(CETP):c.1377C>T (p.Asp459=) rs144375086 0.00022
NM_000078.3(CETP):c.991G>A (p.Gly331Ser) rs5881 0.00020
NM_000078.3(CETP):c.1018G>A (p.Val340Ile) rs141310739 0.00019
NM_000078.3(CETP):c.316G>A (p.Val106Met) rs371258270 0.00019
NM_000078.3(CETP):c.663C>A (p.Ser221Arg) rs201438792 0.00019
NM_000078.3(CETP):c.1017C>T (p.Thr339=) rs138298866 0.00014
NM_000078.3(CETP):c.182C>T (p.Thr61Met) rs142464301 0.00014
NM_000078.3(CETP):c.1046C>A (p.Ser349Tyr) rs752298084 0.00013
NM_000078.3(CETP):c.312G>A (p.Gln104=) rs147740993 0.00013
NM_000078.3(CETP):c.752G>T (p.Gly251Val) rs144460063 0.00009
NM_000078.3(CETP):c.668T>G (p.Leu223Arg) rs747056056 0.00004
NM_000078.3(CETP):c.92G>A (p.Arg31His) rs147758502 0.00004
NM_000078.3(CETP):c.1302C>A (p.Gly434=) rs767606464 0.00003
NM_000078.3(CETP):c.1402C>T (p.Arg468Ter) rs577301331 0.00003
NM_000078.3(CETP):c.84C>T (p.Ile28=) rs142117489 0.00003
NM_000078.3(CETP):c.1253G>C (p.Ser418Thr) rs145141976 0.00002
NM_000078.3(CETP):c.1321+1G>A rs5742907 0.00002
NM_000078.3(CETP):c.1327G>A (p.Glu443Lys) rs536221680 0.00002
NM_000078.3(CETP):c.239A>G (p.Gln80Arg) rs371180917 0.00002
NM_000078.3(CETP):c.439+11A>C rs200855412 0.00002
NM_000078.3(CETP):c.1113C>A (p.Asp371Glu) rs138725242 0.00001
NM_000078.3(CETP):c.1470G>A (p.Gln490=) rs148336647 0.00001
NM_000078.3(CETP):c.818G>A (p.Gly273Glu) rs201503514 0.00001
NM_000078.3(CETP):c.1101T>C (p.Phe367=) rs2056163890
NM_000078.3(CETP):c.1161C>G (p.Thr387=) rs7192120
NM_000078.3(CETP):c.1161C>T (p.Thr387=) rs7192120
NM_000078.3(CETP):c.1215-15G>T rs7196174
NM_000078.3(CETP):c.1321+2dup rs1567476573
NM_000078.3(CETP):c.1345C>A (p.Leu449Ile) rs1164754201
NM_000078.3(CETP):c.1373del (p.Phe458fs) rs1567477038
NM_000078.3(CETP):c.1375G>C (p.Asp459His) rs1326253991
NM_000078.3(CETP):c.1408-7C>T rs1401491244
NM_000078.3(CETP):c.160C>T (p.Arg54Ter) rs780627434
NM_000078.3(CETP):c.214G>C (p.Val72Leu) rs767785661
NM_000078.3(CETP):c.23C>T (p.Thr8Ile)
NM_000078.3(CETP):c.266del (p.Ser89fs)
NM_000078.3(CETP):c.268C>T (p.Gln90Ter) rs2056091646
NM_000078.3(CETP):c.311A>G (p.Gln104Arg) rs765716703
NM_000078.3(CETP):c.443G>A (p.Cys148Tyr) rs778814831
NM_000078.3(CETP):c.544C>T (p.Gln182Ter)
NM_000078.3(CETP):c.667del (p.Leu223fs) rs759929211
NM_000078.3(CETP):c.804G>A (p.Ser268=) rs28381707
NM_000078.3(CETP):c.804G>T (p.Ser268=) rs28381707
NM_000078.3(CETP):c.895C>T (p.Arg299Cys)
NM_000078.3(CETP):c.964C>T (p.Gln322Ter)
NM_000078.3(CETP):c.981+2T>C rs2142001776

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