"Illumina Laboratory Services, Illumina"[submitter] AND "APC"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 350408	NM_001127511.3(APC):c.166-28452G>C	APC	Single nucleotide variant (intron variant)	APC-Associated Polyposis Disorders +3 more	GBenign/Likely benign
Select item 906242	NM_000038.6(APC):c.72A>T (p.Arg24=)	APC	Single nucleotide variant (synonymous variant +2 more)	APC-Associated Polyposis Disorders	GUncertain significance
Select item 135683	NM_000038.6(APC):c.120G>A (p.Glu40=)	APC	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +4 more	GBenign/Likely benign
Select item 350409	NM_000038.6(APC):c.336T>A (p.Pro112=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 41505	NM_000038.6(APC):c.388A>G (p.Ser130Gly)	APC (S130G +3 more)	Single nucleotide variant (missense variant +1 more)	APC-Associated Polyposis Disorders +5 more	GConflicting classifications of pathogenicity
Select item 824696	NM_000038.6(APC):c.422G>A (p.Arg141Lys)	APC (R82K +3 more)	Single nucleotide variant (missense variant +1 more)	APC-Associated Polyposis Disorders +2 more	GUncertain significance
Select item 181782	NM_000038.6(APC):c.450A>G (p.Lys150=)	APC	Single nucleotide variant (synonymous variant +1 more)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 215430	NM_000038.6(APC):c.573T>C (p.Tyr191=)	APC	Single nucleotide variant (synonymous variant +1 more)	Familial adenomatous polyposis 1 +10 more	GBenign/Likely benign
Select item 41509	NM_000038.6(APC):c.607C>G (p.Gln203Glu)	APC (Q203E +3 more)	Single nucleotide variant (missense variant +1 more)	APC-Associated Polyposis Disorders +5 more	GConflicting classifications of pathogenicity
Select item 188275	NM_000038.6(APC):c.647G>A (p.Arg216Gln)	APC (R216Q +3 more)	Single nucleotide variant (missense variant +2 more)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 751722	NM_000038.6(APC):c.672C>A (p.Ile224=)	APC	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 92349	NM_000038.6(APC):c.705A>G (p.Leu235=)	APC	Single nucleotide variant (synonymous variant +2 more)	Familial adenomatous polyposis 1	GBenign FDA Recognized database
Select item 236647	NM_000038.6(APC):c.757G>A (p.Gly253Ser)	APC (G235S +5 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 229684	NM_000038.6(APC):c.772G>C (p.Glu258Gln)	APC (E240Q +5 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 135720	NM_000038.6(APC):c.777G>T (p.Arg259=)	APC	Single nucleotide variant (synonymous variant +1 more)	Familial adenomatous polyposis 1 +5 more	GConflicting classifications of pathogenicity
Select item 372038	NM_000038.6(APC):c.934-14C>T	APC	Single nucleotide variant (intron variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 797	NM_000038.6(APC):c.1240C>T (p.Arg414Cys)	APC (R414C +10 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1	GBenign FDA Recognized database
Select item 381514	NM_000038.6(APC):c.1312+12A>G	APC	Single nucleotide variant (intron variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 236559	NM_000038.6(APC):c.1398G>A (p.Met466Ile)	APC (M448I +10 more)	Single nucleotide variant (missense variant)	Classic or attenuated familial adenomatous polyposis +3 more	GUncertain significance
Select item 42238	NM_000038.6(APC):c.1458T>C (p.Tyr486=)	APC	Single nucleotide variant (synonymous variant)	Familial adenomatous polyposis 1	GBenign FDA Recognized database
Select item 135684	NM_000038.6(APC):c.1488A>T (p.Thr496=)	APC	Single nucleotide variant (synonymous variant)	Familial adenomatous polyposis 1 +5 more	GBenign/Likely benign
Select item 490214	NM_000038.6(APC):c.1562C>G (p.Ser521Cys)	APC (S503C +12 more)	Single nucleotide variant (missense variant)	APC-Associated Polyposis Disorders +2 more	GUncertain significance
Select item 41520	NM_000038.6(APC):c.1631T>C (p.Ile544Thr)	APC (I544T +12 more)	Single nucleotide variant (missense variant)	APC-Associated Polyposis Disorders +5 more	GConflicting classifications of pathogenicity
Select item 42239	NM_000038.6(APC):c.1635G>A (p.Ala545=)	APC	Single nucleotide variant (synonymous variant)	Familial adenomatous polyposis 1	GBenign FDA Recognized database
Select item 183766	NM_000038.6(APC):c.1695A>G (p.Glu565=)	APC	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 184100	NM_000038.6(APC):c.1722A>G (p.Glu574=)	APC	Single nucleotide variant (synonymous variant)	Familial adenomatous polyposis 1 +4 more	GConflicting classifications of pathogenicity
Select item 82616	NM_000038.6(APC):c.1958+8T>C	APC	Single nucleotide variant (intron variant)	not provided +4 more	GBenign
Select item 350410	NM_000038.6(APC):c.1958+10G>T	APC	Single nucleotide variant (intron variant)	Familial adenomatous polyposis 1 +4 more	GBenign/Likely benign
Select item 133524	NM_000038.6(APC):c.1959G>A (p.Arg653=)	APC	Single nucleotide variant (synonymous variant)	not specified +5 more	GBenign/Likely benign
Select item 185391	NM_000038.6(APC):c.2110G>A (p.Val704Ile)	APC (V686I +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 183919	NM_000038.6(APC):c.2205G>A (p.Ala735=)	APC	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 490240	NM_000038.6(APC):c.2223T>C (p.Asn741=)	APC	Single nucleotide variant (synonymous variant)	APC-Associated Polyposis Disorders +2 more	GConflicting classifications of pathogenicity
Select item 820974	NM_000038.6(APC):c.2258A>G (p.His753Arg)	APC (H652R +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 136407	NM_000038.6(APC):c.2322C>T (p.Asp774=)	APC	Single nucleotide variant (synonymous variant)	Familial adenomatous polyposis 1 +4 more	GBenign/Likely benign
Select item 216156	NM_000038.6(APC):c.2444A>C (p.Asn815Thr)	APC (N797T +12 more)	Single nucleotide variant (missense variant)	Classic or attenuated familial adenomatous polyposis +5 more	GConflicting classifications of pathogenicity
Select item 469749	NM_000038.6(APC):c.2481T>C (p.Asn827=)	APC	Single nucleotide variant (synonymous variant)	Familial adenomatous polyposis 1 +2 more	GBenign/Likely benign
Select item 378945	NM_000038.6(APC):c.2547T>C (p.Asp849=)	APC	Single nucleotide variant (synonymous variant)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 660204	NM_000038.6(APC):c.2555T>G (p.Leu852Trp)	APC (L726W +12 more)	Single nucleotide variant (missense variant)	Classic or attenuated familial adenomatous polyposis +3 more	GUncertain significance
Select item 133517	NM_000038.6(APC):c.2586C>G (p.Asn862Lys)	APC (N844K +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GBenign/Likely benign
Select item 135690	NM_000038.6(APC):c.2593C>T (p.Pro865Ser)	APC (P865S +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1 +6 more	GConflicting classifications of pathogenicity
Select item 41500	NM_000038.6(APC):c.2608C>T (p.Pro870Ser)	APC (P870S +12 more)	Single nucleotide variant (missense variant)	APC-Associated Polyposis Disorders +5 more	GBenign/Likely benign
Select item 907305	NM_000038.6(APC):c.2654C>T (p.Ala885Val)	APC (A602V +12 more)	Single nucleotide variant (missense variant)	APC-Associated Polyposis Disorders +2 more	GUncertain significance
Select item 135694	NM_000038.6(APC):c.2658G>T (p.Gln886His)	APC (Q886H +12 more)	Single nucleotide variant (missense variant)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 136408	NM_000038.6(APC):c.2805C>T (p.Tyr935=)	APC	Single nucleotide variant (synonymous variant)	Familial adenomatous polyposis 1 +5 more	GBenign/Likely benign
Select item 416719	NM_000038.6(APC):c.2958T>C (p.Tyr986=)	APC	Single nucleotide variant (synonymous variant)	Classic or attenuated familial adenomatous polyposis +5 more	GConflicting classifications of pathogenicity
Select item 181778	NM_000038.6(APC):c.3006C>T (p.Ala1002=)	APC	Single nucleotide variant (synonymous variant)	Familial adenomatous polyposis 1 +5 more	GBenign/Likely benign
Select item 132763	NM_000038.6(APC):c.3165A>T (p.Ile1055=)	APC	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +5 more	GBenign/Likely benign
Select item 41523	NM_000038.6(APC):c.3173A>G (p.Asp1058Gly)	APC (D1058G +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer +5 more	GConflicting classifications of pathogenicity
Select item 350411	NM_000038.6(APC):c.3210T>C (p.Asn1070=)	APC	Single nucleotide variant (synonymous variant)	APC-Associated Polyposis Disorders +3 more	GConflicting classifications of pathogenicity
Select item 41525	NM_000038.6(APC):c.3249T>G (p.Asp1083Glu)	APC (D1083E +12 more)	Single nucleotide variant (missense variant)	APC-Associated Polyposis Disorders +3 more	GBenign/Likely benign
Select item 216160	NM_000038.6(APC):c.3341G>A (p.Arg1114Gln)	APC (R1096Q +12 more)	Single nucleotide variant (missense variant)	Classic or attenuated familial adenomatous polyposis +3 more	GUncertain significance
Select item 41526	NM_000038.6(APC):c.3352A>G (p.Asn1118Asp)	APC (N1118D +12 more)	Single nucleotide variant (missense variant)	APC-Associated Polyposis Disorders +5 more	GBenign/Likely benign
Select item 132749	NM_000038.6(APC):c.3374T>C (p.Val1125Ala)	APC (V1125A +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 127288	NM_000038.6(APC):c.3378C>G (p.Ser1126Arg)	APC (S1126R +12 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 41502	NM_000038.6(APC):c.3386T>C (p.Leu1129Ser)	APC (L1129S +12 more)	Single nucleotide variant (missense variant)	APC-Associated Polyposis Disorders +5 more	GBenign/Likely benign
Select item 41527	NM_000038.6(APC):c.3462AGA[2] (p.Glu1157del)	APC (E1157del +12 more)	Microsatellite (inframe_deletion)	APC-Associated Polyposis Disorders +6 more	GBenign/Likely benign
Select item 92345	NM_000038.6(APC):c.3471G>A (p.Glu1157=)	APC	Single nucleotide variant (synonymous variant)	Familial adenomatous polyposis 1 +4 more	GBenign/Likely benign
Select item 141688	NM_000038.6(APC):c.3625G>A (p.Glu1209Lys)	APC (E1191K +12 more)	Single nucleotide variant (missense variant)	not provided +6 more	GConflicting classifications of pathogenicity
Select item 187505	NM_000038.6(APC):c.3653C>T (p.Thr1218Met)	APC (T1200M +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1 +5 more	GConflicting classifications of pathogenicity
Select item 183767	NM_000038.6(APC):c.3732A>G (p.Gln1244=)	APC	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 905850	NM_000038.6(APC):c.3901A>T (p.Thr1301Ser)	APC (T1210S +12 more)	Single nucleotide variant (missense variant)	APC-Associated Polyposis Disorders	GUncertain significance
Select item 829	NM_000038.6(APC):c.3949G>C (p.Glu1317Gln)	APC (E1317Q +12 more)	Single nucleotide variant (missense variant)	not provided +4 more	GBenign/Likely benign
Select item 906361	NM_000038.6(APC):c.4049A>C (p.Lys1350Thr)	APC (K1190T +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1 +2 more	GUncertain significance
Select item 469953	NM_000038.6(APC):c.4201A>G (p.Ile1401Val)	APC (I1383V +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1 +2 more	GUncertain significance
Select item 132705	NM_000038.6(APC):c.4326T>A (p.Pro1442=)	APC	Single nucleotide variant (synonymous variant)	Desmoid disease, hereditary +9 more	GBenign
Select item 469962	NM_000038.6(APC):c.4343C>T (p.Thr1448Ile)	APC (T1430I +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1 +4 more	GConflicting classifications of pathogenicity
Select item 127295	NM_000038.6(APC):c.4360A>G (p.Lys1454Glu)	APC (K1454E +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 133530	NM_000038.6(APC):c.4420G>A (p.Ala1474Thr)	APC (A1456T +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1	GBenign FDA Recognized database
Select item 42242	NM_000038.6(APC):c.4479G>A (p.Thr1493=)	APC	Single nucleotide variant (synonymous variant)	APC-Associated Polyposis Disorders +9 more	GBenign
Select item 186645	NM_000038.6(APC):c.4534G>A (p.Asp1512Asn)	APC (D1494N +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 181807	NM_000038.6(APC):c.4594G>A (p.Asp1532Asn)	APC (D1514N +12 more)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance
Select item 142201	NM_000038.6(APC):c.4765C>G (p.Arg1589Gly)	APC (R1571G +12 more)	Single nucleotide variant (missense variant)	Diffuse midline glioma, H3 K27-altered +7 more	GConflicting classifications of pathogenicity
Select item 350412	NM_000038.6(APC):c.4833G>A (p.Gln1611=)	APC	Single nucleotide variant (synonymous variant)	Familial adenomatous polyposis 1 +5 more	GBenign/Likely benign
Select item 132688	NM_000038.6(APC):c.4893T>C (p.Ser1631=)	APC	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign/Likely benign
Select item 135704	NM_000038.6(APC):c.4905G>A (p.Gly1635=)	APC	Single nucleotide variant (synonymous variant)	Familial adenomatous polyposis 1 +4 more	GBenign/Likely benign
Select item 231898	NM_000038.6(APC):c.4913T>C (p.Met1638Thr)	APC (M1620T +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1 +3 more	GConflicting classifications of pathogenicity
Select item 42243	NM_000038.6(APC):c.5034G>A (p.Gly1678=)	APC	Single nucleotide variant (synonymous variant)	APC-Associated Polyposis Disorders +4 more	GBenign
Select item 350413	NM_000038.6(APC):c.5050T>C (p.Phe1684Leu)	APC (F1684L +12 more)	Single nucleotide variant (missense variant)	APC-Associated Polyposis Disorders +3 more	GUncertain significance
Select item 825419	NM_000038.6(APC):c.5078A>G (p.Glu1693Gly)	APC (E1592G +12 more)	Single nucleotide variant (missense variant)	APC-Associated Polyposis Disorders +2 more	GConflicting classifications of pathogenicity
Select item 135706	NM_000038.6(APC):c.5140G>A (p.Asp1714Asn)	APC (D1714N +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1 +5 more	GConflicting classifications of pathogenicity
Select item 350414	NM_000038.6(APC):c.5194A>G (p.Met1732Val)	APC (M1732V +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1 +5 more	GUncertain significance
Select item 230908	NM_000038.6(APC):c.5224C>T (p.Arg1742Cys)	APC (R1724C +12 more)	Single nucleotide variant (missense variant)	APC-Associated Polyposis Disorders +4 more	GUncertain significance
Select item 41508	NM_000038.6(APC):c.5225G>A (p.Arg1742His)	APC (R1742H +12 more)	Single nucleotide variant (missense variant)	APC-Associated Polyposis Disorders +4 more	GConflicting classifications of pathogenicity
Select item 136410	NM_000038.6(APC):c.5250C>G (p.Val1750=)	APC	Single nucleotide variant (synonymous variant)	Familial adenomatous polyposis 1 +4 more	GBenign
Select item 42244	NM_000038.6(APC):c.5265G>A (p.Ala1755=)	APC	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign/Likely benign
Select item 186718	NM_000038.6(APC):c.5268T>A (p.Ser1756=)	APC	Single nucleotide variant (synonymous variant)	APC-related condition +5 more	GBenign/Likely benign
Select item 42245	NM_000038.6(APC):c.5268T>G (p.Ser1756=)	APC	Single nucleotide variant (synonymous variant)	APC-Associated Polyposis Disorders +4 more	GBenign
Select item 92348	NM_000038.6(APC):c.5363G>A (p.Arg1788His)	APC (R1770H +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1 +8 more	GConflicting classifications of pathogenicity
Select item 233507	NM_000038.6(APC):c.5399A>G (p.Asn1800Ser)	APC (N1782S +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1 +4 more	GUncertain significance
Select item 231814	NM_000038.6(APC):c.5424C>T (p.Asn1808=)	APC	Single nucleotide variant (synonymous variant)	APC-Associated Polyposis Disorders +3 more	GConflicting classifications of pathogenicity
Select item 21030	NM_000038.6(APC):c.5465T>A (p.Val1822Asp)	APC (V1804D +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1	GBenign FDA Recognized database
Select item 232546	NM_000038.6(APC):c.5524T>A (p.Ser1842Thr)	APC (S1824T +12 more)	Single nucleotide variant (missense variant)	Classic or attenuated familial adenomatous polyposis +5 more	GConflicting classifications of pathogenicity
Select item 490312	NM_000038.6(APC):c.5658A>G (p.Glu1886=)	APC	Single nucleotide variant (synonymous variant)	APC-Associated Polyposis Disorders +2 more	GConflicting classifications of pathogenicity
Select item 219614	NM_000038.6(APC):c.5712A>G (p.Gln1904=)	APC	Single nucleotide variant (synonymous variant)	Familial adenomatous polyposis 1 +3 more	GConflicting classifications of pathogenicity
Select item 184255	NM_000038.6(APC):c.5790A>G (p.Gln1930=)	APC	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign/Likely benign
Select item 135709	NM_000038.6(APC):c.5801C>T (p.Pro1934Leu)	APC (P1934L +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +11 more	GConflicting classifications of pathogenicity
Select item 350415	NM_000038.6(APC):c.5840C>G (p.Thr1947Ser)	APC (T1947S +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1 +4 more	GConflicting classifications of pathogenicity
Select item 141168	NM_000038.6(APC):c.5879C>T (p.Pro1960Leu)	APC (P1942L +12 more)	Single nucleotide variant (missense variant)	APC-Associated Polyposis Disorders +4 more	GConflicting classifications of pathogenicity
Select item 42247	NM_000038.6(APC):c.5880G>A (p.Pro1960=)	APC	Single nucleotide variant (synonymous variant)	APC-Associated Polyposis Disorders +4 more	GBenign
Select item 470024	NM_000038.6(APC):c.5894A>G (p.His1965Arg)	APC (H1947R +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity

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