ClinVar for Gene (Select 324) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3412752	NM_000038.6(APC):c.4447C>A (p.Pro1483Thr)	APC (P1354T +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412743	NM_000038.6(APC):c.4195C>G (p.Arg1399Gly)	APC (R1116G +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412716	NM_000038.6(APC):c.7789G>C (p.Gly2597Arg)	APC (G2213R +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412696	NM_000038.6(APC):c.6243A>G (p.Lys2081=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3412671	NM_000038.6(APC):c.5242G>A (p.Asp1748Asn)	APC (D1364N +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412666	NM_000038.6(APC):c.3497A>G (p.Tyr1166Cys)	APC (Y1006C +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412661	NM_000038.6(APC):c.2091A>C (p.Ala697=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3412625	NM_000038.6(APC):c.518C>G (p.Pro173Arg)	APC (P148R +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412608	NM_000038.6(APC):c.6953G>C (p.Ser2318Thr)	APC (S2158T +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412588	NM_000038.6(APC):c.3305A>C (p.Tyr1102Ser)	APC (Y1011S +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412551	NM_000038.6(APC):c.6912T>A (p.Ser2304=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3412540	NM_000038.6(APC):c.4976A>G (p.Asp1659Gly)	APC (D1499G +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412530	NM_000038.6(APC):c.7886C>A (p.Thr2629Asn)	APC (T2500N +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412472	NM_000038.6(APC):c.4851T>A (p.Leu1617=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3412450	NM_000038.6(APC):c.5327T>A (p.Val1776Glu)	APC (V1493E +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412440	NM_000038.6(APC):c.3035A>T (p.Asn1012Ile)	APC (N1002I +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412429	NM_000038.6(APC):c.2482A>T (p.Thr828Ser)	APC (T668S +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412418	NM_000038.6(APC):c.5656_5660del (p.Lys1885_Glu1886insTer)	APC	Deletion (nonsense +1 more)	Hereditary cancer-predisposing syndrome	GLikely pathogenic
Select item 3412399	NM_000038.6(APC):c.32A>T (p.Lys11Met)	APC (K11M)	Single nucleotide variant (missense variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412382	NM_000038.6(APC):c.5605G>C (p.Asp1869His)	APC (D1778H +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412367	NM_000038.6(APC):c.7565C>A (p.Pro2522Gln)	APC (P2532Q +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412353	NM_000038.6(APC):c.2522T>C (p.Leu841Ser)	APC (L813S +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412342	NM_000038.6(APC):c.5092G>C (p.Asp1698His)	APC (D1569H +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412315	NM_000038.6(APC):c.6194C>T (p.Pro2065Leu)	APC (P1936L +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412299	NM_000038.6(APC):c.7627A>T (p.Arg2543Trp)	APC (R2442W +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412289	NM_000038.6(APC):c.7510T>G (p.Trp2504Gly)	APC (W2403G +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412270	NM_000038.6(APC):c.1326T>C (p.Val442=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3412185	NM_000038.6(APC):c.109C>G (p.Leu37Val)	APC (L37V)	Single nucleotide variant (missense variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412176	NM_000038.6(APC):c.7729T>G (p.Ser2577Ala)	APC (S2570A +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412167	NM_000038.6(APC):c.6149A>G (p.Lys2050Arg)	APC (K1666R +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412147	NM_000038.6(APC):c.1151G>C (p.Ser384Thr)	APC (S101T +6 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412138	NM_000038.6(APC):c.4800A>G (p.Lys1600=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3412040	NM_000038.6(APC):c.3583T>G (p.Phe1195Val)	APC (F1195V +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412030	NM_000038.6(APC):c.164_165dup (p.Glu56fs)	APC (E56fs +2 more)	Duplication (frameshift variant +2 more)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3412019	NM_000038.6(APC):c.6202_6225del (p.Met2068_Asp2075del)	APC	Deletion (non-coding transcript variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3412009	NM_000038.6(APC):c.4857A>C (p.Pro1619=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3411999	NM_000038.6(APC):c.4878C>A (p.Pro1626=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3411987	NM_000038.6(APC):c.4876C>G (p.Pro1626Ala)	APC (P1242A +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3411977	NM_000038.6(APC):c.80T>C (p.Leu27Pro)	APC (L27P)	Single nucleotide variant (missense variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411967	NM_000038.6(APC):c.623A>T (p.Gln208Leu)	APC (Q208L +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411948	NM_000038.6(APC):c.3097G>A (p.Asp1033Asn)	APC (D1051N +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411931	NM_000038.6(APC):c.407A>C (p.Glu136Ala)	APC (E146A +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411920	NM_000038.6(APC):c.7529A>C (p.Asn2510Thr)	APC (N2381T +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411902	NM_000038.6(APC):c.5282A>T (p.Asn1761Ile)	APC (N1670I +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411854	NM_000038.6(APC):c.3442T>C (p.Ser1148Pro)	APC (S1047P +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411844	NM_000038.6(APC):c.1672A>G (p.Asn558Asp)	APC (N174D +18 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411825	NM_000038.6(APC):c.5798T>C (p.Phe1933Ser)	APC (F1549S +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411795	NM_000038.6(APC):c.1330C>G (p.His444Asp)	APC (H315D +12 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411766	NM_000038.6(APC):c.2537C>T (p.Ser846Phe)	APC (S462F +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411746	NM_000038.6(APC):c.6292A>G (p.Asn2098Asp)	APC (N2073D +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411725	NM_000038.6(APC):c.4374T>C (p.Pro1458=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3411714	NM_000038.6(APC):c.6230C>G (p.Thr2077Arg)	APC (T1986R +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411705	NM_000038.6(APC):c.2216A>T (p.Asp739Val)	APC (D613V +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411661	NM_000038.6(APC):c.599T>C (p.Met200Thr)	APC (M175T +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411650	NM_000038.6(APC):c.1336A>T (p.Ile446Phe)	APC (I317F +12 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411623	NM_000038.6(APC):c.1852G>A (p.Gly618Ser)	APC (G335S +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411603	NM_000038.6(APC):c.1020C>A (p.Ser340=)	APC	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3411583	NM_000038.6(APC):c.1412_1413delinsTT (p.Gly471Val)	APC (G370V +18 more)	Indel (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411572	NM_000038.6(APC):c.1041G>T (p.Met347Ile)	APC (M357I +6 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411562	NM_000038.6(APC):c.7511G>T (p.Trp2504Leu)	APC (W2403L +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411552	NM_000038.6(APC):c.718A>C (p.Thr240Pro)	APC (T240P +3 more)	Single nucleotide variant (missense variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411544	NM_000038.6(APC):c.4733G>A (p.Cys1578Tyr)	APC (C1537Y +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411517	NM_000038.6(APC):c.3843A>C (p.Ser1281=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3411506	NM_000038.6(APC):c.201T>A (p.Asp67Glu)	APC (D42E +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411496	NM_000038.6(APC):c.2030_2031delinsGT (p.Val677Gly)	APC (V293G +18 more)	Indel (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411475	NM_000038.6(APC):c.6530A>T (p.Glu2177Val)	APC (E1894V +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411465	NM_000038.6(APC):c.1413A>T (p.Gly471=)	APC	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3411448	NM_000038.6(APC):c.5387_5390del (p.Lys1796fs)	APC (K1713fs +18 more)	Deletion (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely pathogenic
Select item 3411437	NM_000038.6(APC):c.3374T>G (p.Val1125Gly)	APC (V1115G +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411389	NM_000038.6(APC):c.8284T>C (p.Phe2762Leu)	APC (F2378L +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411369	NM_000038.6(APC):c.6268C>G (p.His2090Asp)	APC (H1930D +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411358	NM_000038.6(APC):c.6261_6266del (p.Asp2087_Ser2088del)	APC	Deletion (non-coding transcript variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411348	NM_000038.6(APC):c.7994C>A (p.Pro2665His)	APC (P2281H +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411311	NM_000038.6(APC):c.408A>C (p.Glu136Asp)	APC (E146D +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411301	NM_000038.6(APC):c.221-10T>G	APC	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411292	NM_000038.6(APC):c.3648G>A (p.Glu1216=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3411274	NM_000038.6(APC):c.6150_6152del (p.Lys2052del)	APC (K1769del +18 more)	Deletion (non-coding transcript variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411254	NM_000038.6(APC):c.126_127del (p.Asn43fs)	APC (N43fs)	Deletion (frameshift variant +3 more)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3411233	NM_000038.6(APC):c.5945A>T (p.Lys1982Ile)	APC (K1853I +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411222	NM_000038.6(APC):c.3774A>T (p.Thr1258=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3411211	NM_000038.6(APC):c.389G>A (p.Ser130Asn)	APC (S130N +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3411193	NM_000038.6(APC):c.670A>T (p.Ile224Phe)	APC (I165F +3 more)	Single nucleotide variant (missense variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411184	NM_000038.6(APC):c.8123A>T (p.Asn2708Ile)	APC (N2617I +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411174	NM_000038.6(APC):c.7970T>C (p.Val2657Ala)	APC (V2497A +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411155	NM_000038.6(APC):c.7427G>T (p.Arg2476Met)	APC (R2092M +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411135	NM_000038.6(APC):c.5464G>A (p.Val1822Ile)	APC (V1662I +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411127	NM_000038.6(APC):c.4412C>T (p.Ala1471Val)	APC (A1370V +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411117	NM_000038.6(APC):c.1992T>A (p.Thr664=)	APC	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3411107	NM_000038.6(APC):c.352T>A (p.Phe118Ile)	APC (F118I +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411086	NM_000038.6(APC):c.8162G>C (p.Arg2721Pro)	APC (R2630P +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411066	NM_000038.6(APC):c.2525A>C (p.Asp842Ala)	APC (D559A +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411046	NM_000038.6(APC):c.1455_1457delinsTTT (p.Met485_Tyr486delinsIlePhe)	APC	Indel (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411036	NM_000038.6(APC):c.824G>T (p.Gly275Val)	APC (G250V +5 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411030	NM_000038.6(APC):c.3862G>A (p.Gly1288Arg)	APC (G1005R +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411011	NM_000038.6(APC):c.6386C>G (p.Ser2129Trp)	APC (S1969W +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3411003	NM_000038.6(APC):c.4005C>G (p.Ser1335Arg)	APC (S1206R +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3410977	NM_000038.6(APC):c.8222G>A (p.Gly2741Glu)	APC (G2357E +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3410957	NM_000038.6(APC):c.3597G>C (p.Lys1199Asn)	APC (K1192N +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3410900	NM_000038.6(APC):c.5473G>A (p.Asp1825Asn)	APC (D1724N +18 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3410870	NM_000038.6(APC):c.5091del (p.Asp1698fs)	APC (D1569fs +18 more)	Deletion (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely pathogenic

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