"GeneDx"[submitter] AND "CETP"[gene] - ClinVar

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Items: 88

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 369115	NM_000078.3(CETP):c.-65G>A	CETP	Single nucleotide variant	Hyperalphalipoproteinemia 1 +1 more	GBenign
Select item 319970	NM_000078.3(CETP):c.44C>G (p.Ala15Gly)	CETP (A15G)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 319971	NM_000078.3(CETP):c.66C>A (p.Thr22=)	CETP	Single nucleotide variant (synonymous variant)	Hyperalphalipoproteinemia 1 +1 more	GBenign/Likely benign
Select item 1314022	NM_000078.3(CETP):c.89G>A (p.Cys30Tyr)	CETP (C30Y)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1204331	NM_000078.3(CETP):c.118+51C>A	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1282916	NM_000078.3(CETP):c.118+95C>A	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267499	NM_000078.3(CETP):c.118+149T>C	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1255212	NM_000078.3(CETP):c.118+202G>A	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1214705	NM_000078.3(CETP):c.118+270C>T	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1239762	NM_000078.3(CETP):c.118+279G>A	CETP	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1275353	NM_000078.3(CETP):c.119-274_119-273del	CETP	Deletion (intron variant)	not provided	GBenign
Select item 1257695	NM_000078.3(CETP):c.119-273C>A	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1205094	NM_000078.3(CETP):c.119-215G>T	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1266117	NM_000078.3(CETP):c.233+36A>G	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1181969	NM_000078.3(CETP):c.233+197G>A	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1213364	NM_000078.3(CETP):c.233+227G>T	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1202787	NM_000078.3(CETP):c.234-273G>T	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1274340	NM_000078.3(CETP):c.234-255C>T	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182498	NM_000078.3(CETP):c.234-152T>C	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 319976	NM_000078.3(CETP):c.316G>A (p.Val106Met)	CETP (V106M)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1186201	NM_000078.3(CETP):c.368+29T>C	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1229341	NM_000078.3(CETP):c.440-103G>T	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 885591	NM_000078.3(CETP):c.443G>A (p.Cys148Tyr)	CETP (C148Y)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 319978	NM_000078.3(CETP):c.460C>T (p.Arg154Trp)	CETP (R154W)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1281349	NM_000078.3(CETP):c.527+64T>C	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229319	NM_000078.3(CETP):c.527+67T>C	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272137	NM_000078.3(CETP):c.528-198A>G	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249684	NM_000078.3(CETP):c.528-56G>A	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 319980	NM_000078.3(CETP):c.534G>A (p.Gly178=)	CETP	Single nucleotide variant (synonymous variant)	Hyperalphalipoproteinemia 1 +1 more	GBenign/Likely benign
Select item 319981	NM_000078.3(CETP):c.658+8C>T	CETP, LOC130059064	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1217149	NM_000078.3(CETP):c.658+132T>C	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 225955	NM_000078.3(CETP):c.658+186C>A	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225266	NM_000078.3(CETP):c.658+257C>T	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1196187	NM_000078.3(CETP):c.659-142C>T	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1275162	NM_000078.3(CETP):c.659-140C>G	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232007	NM_000078.3(CETP):c.659-22C>T	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 319982	NM_000078.3(CETP):c.663C>A (p.Ser221Arg)	CETP (S221R)	Single nucleotide variant (missense variant)	Hyperalphalipoproteinemia 1 +1 more	GBenign/Likely benign
Select item 1200716	NM_000078.3(CETP):c.750+77G>A	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1297243	NM_000078.3(CETP):c.751-51T>C	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 319984	NM_000078.3(CETP):c.861C>T (p.Phe287=)	CETP	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 1804584	NM_000078.3(CETP):c.869T>C (p.Leu290Pro)	CETP (L290P)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 721350	NM_000078.3(CETP):c.921C>T (p.Asp307=)	CETP	Single nucleotide variant (synonymous variant +1 more)	Hyperalphalipoproteinemia 1 +1 more	GBenign/Likely benign
Select item 1267902	NM_000078.3(CETP):c.930+24T>G	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1181918	NM_000078.3(CETP):c.930+29G>A	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1187154	NM_000078.3(CETP):c.930+90G>A	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1271769	NM_000078.3(CETP):c.930+188G>A	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1191702	NM_000078.3(CETP):c.930+230A>G	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 426658	NM_000078.3(CETP):c.953_962del (p.Phe318fs)	CETP (F318fs +1 more)	Deletion (frameshift variant)	not provided	GLikely pathogenic
Select item 1209013	NM_000078.3(CETP):c.981+102A>G	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1291729	NM_000078.3(CETP):c.981+132T>G	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272803	NM_000078.3(CETP):c.981+137C>T	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1198467	NM_000078.3(CETP):c.982-177C>T	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1197658	NM_000078.3(CETP):c.982-119C>T	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1228339	NM_000078.3(CETP):c.982-67C>T	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2577704	NM_000078.3(CETP):c.1022A>G (p.His341Arg)	CETP (H281R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1305453	NM_000078.3(CETP):c.1105C>T (p.Arg369Cys)	CETP (R309C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1214816	NM_000078.3(CETP):c.1146+187C>T	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1278306	NM_000078.3(CETP):c.1146+212T>G	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1278970	NM_000078.3(CETP):c.1147-195A>G	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 319990	NM_000078.3(CETP):c.1153G>A (p.Val385Met)	CETP (V385M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3369355	NM_000078.3(CETP):c.1159A>G (p.Thr387Ala)	CETP (T327A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 319992	NM_000078.3(CETP):c.1161C>T (p.Thr387=)	CETP	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 319991	NM_000078.3(CETP):c.1161C>G (p.Thr387=)	CETP	Single nucleotide variant (synonymous variant)	Hyperalphalipoproteinemia 1 +1 more	GBenign
Select item 319993	NM_000078.3(CETP):c.1168G>C (p.Ala390Pro)	CETP (A390P +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1264685	NM_000078.3(CETP):c.1214+108T>C	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1201051	NM_000078.3(CETP):c.1214+152A>C	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1236709	NM_000078.3(CETP):c.1214+199_1214+210del	CETP	Deletion (intron variant)	not provided	GBenign
Select item 1235149	NM_000078.3(CETP):c.1215-179A>G	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1206669	NM_000078.3(CETP):c.1215-140G>A	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1273149	NM_000078.3(CETP):c.1215-112C>G	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235072	NM_000078.3(CETP):c.1215-96G>A	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 319994	NM_000078.3(CETP):c.1215-15G>T	CETP	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 319995	NM_000078.3(CETP):c.1215-14C>T	CETP	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1225204	NM_000078.3(CETP):c.1248+133T>C	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 17525	NM_000078.3(CETP):c.1264G>A (p.Val422Ile)	CETP (V422I +1 more)	Single nucleotide variant (missense variant)	Coronary artery disorder +2 more	GBenign
Select item 1305650	NM_000078.3(CETP):c.1294G>A (p.Ala432Thr)	CETP (A372T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 319996	NM_000078.3(CETP):c.1299G>A (p.Val433=)	CETP	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1282960	NM_000078.3(CETP):c.1321+153T>C	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1189685	NM_000078.3(CETP):c.1321+165A>G	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1222632	NM_000078.3(CETP):c.1322-236T>G	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1192120	NM_000078.3(CETP):c.1322-72C>T	CETP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 17527	NM_000078.3(CETP):c.1376A>G (p.Asp459Gly)	CETP (D459G +1 more)	Single nucleotide variant (missense variant)	Hyperalphalipoproteinemia 1 +1 more	GConflicting classifications of pathogenicity
Select item 319999	NM_000078.3(CETP):c.1403G>A (p.Arg468Gln)	CETP (R468Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1285774	NM_000078.3(CETP):c.1408-30G>A	CETP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2078436	NM_000078.3(CETP):c.1456G>A (p.Val486Met)	CETP (V426M +1 more)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 320000	NM_000078.3(CETP):c.*84G>A	CETP	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 369116	NM_000078.2(CETP):c.*184C>G	CETP	Single nucleotide variant	Hyperalphalipoproteinemia 1 +1 more	GBenign
Select item 1282914	NC_000016.10:g.56983884G>A	CETP	Single nucleotide variant	not provided	GBenign

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Items: 88