ClinVar Miner

List of variants in gene APC reported as uncertain significance by PreventionGenetics

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Gene type:
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Total variants: 52
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HGVS dbSNP
NM_000038.6(APC):c.1139G>A (p.Arg380Gln) rs587782886
NM_000038.6(APC):c.1241G>A (p.Arg414His) rs730881233
NM_000038.6(APC):c.2026A>G (p.Ile676Val) rs745529713
NM_000038.6(APC):c.2222A>G (p.Asn741Ser) rs150209825
NM_000038.6(APC):c.2297C>T (p.Ala766Val) rs200339830
NM_000038.6(APC):c.2438A>G (p.Asn813Ser) rs201522866
NM_000038.6(APC):c.2444A>C (p.Asn815Thr) rs762990578
NM_000038.6(APC):c.2503T>C (p.Ser835Pro) rs748302469
NM_000038.6(APC):c.2552G>A (p.Ser851Asn) rs1554084260
NM_000038.6(APC):c.3049_3051del (p.Asn1017del) rs730881229
NM_000038.6(APC):c.317G>A (p.Arg106His) rs201764637
NM_000038.6(APC):c.3368A>C (p.Gln1123Pro) rs587779789
NM_000038.6(APC):c.358A>G (p.Arg120Gly) rs876659470
NM_000038.6(APC):c.3650A>C (p.Asn1217Thr) rs138933660
NM_000038.6(APC):c.3920T>A (p.Ile1307Lys) rs1801155
NM_000038.6(APC):c.449A>G (p.Lys150Arg) rs371085910
NM_000038.6(APC):c.4765C>G (p.Arg1589Gly) rs72541813
NM_000038.6(APC):c.4828A>G (p.Ser1610Gly) rs587781512
NM_000038.6(APC):c.4963A>G (p.Thr1655Ala) rs759441332
NM_000038.6(APC):c.5009C>T (p.Ala1670Val) rs202228932
NM_000038.6(APC):c.5026A>G (p.Arg1676Gly) rs370560998
NM_000038.6(APC):c.5113A>G (p.Thr1705Ala) rs1554086453
NM_000038.6(APC):c.5140G>A (p.Asp1714Asn) rs148275069
NM_000038.6(APC):c.5147A>G (p.Asn1716Ser) rs141298709
NM_000038.6(APC):c.5282A>C (p.Asn1761Thr) rs752038930
NM_000038.6(APC):c.5421_5423CAA[1] (p.Asn1808del) rs587782002
NM_000038.6(APC):c.5500G>A (p.Val1834Ile) rs555944438
NM_000038.6(APC):c.5506G>A (p.Gly1836Arg) rs766739164
NM_000038.6(APC):c.5528C>T (p.Pro1843Leu) rs368080169
NM_000038.6(APC):c.5687G>A (p.Ser1896Asn) rs751088165
NM_000038.6(APC):c.5794A>T (p.Thr1932Ser) rs777604445
NM_000038.6(APC):c.5908A>C (p.Ser1970Arg) rs1561603616
NM_000038.6(APC):c.608A>G (p.Gln203Arg) rs1554072626
NM_000038.6(APC):c.6245A>G (p.Asp2082Gly) rs554370603
NM_000038.6(APC):c.626A>T (p.Asp209Val) rs1554072636
NM_000038.6(APC):c.6349C>A (p.Gln2117Lys) rs587780546
NM_000038.6(APC):c.6354_6356TGC[5] (p.Ala2122dup) rs587780602
NM_000038.6(APC):c.6446A>C (p.His2149Pro) rs749230730
NM_000038.6(APC):c.7205A>G (p.Asn2402Ser) rs745843442
NM_000038.6(APC):c.7399C>A (p.Pro2467Thr) rs372305287
NM_000038.6(APC):c.7621A>G (p.Ile2541Val) rs587778033
NM_000038.6(APC):c.7652A>T (p.His2551Leu) rs1060503314
NM_000038.6(APC):c.7717A>G (p.Ile2573Val) rs145444830
NM_000038.6(APC):c.8042C>T (p.Pro2681Leu) rs182456139
NM_000038.6(APC):c.8104G>A (p.Ala2702Thr) rs587779808
NM_000038.6(APC):c.8161C>T (p.Arg2721Cys) rs587782312
NM_000038.6(APC):c.8182G>A (p.Val2728Met) rs587778045
NM_000038.6(APC):c.8378G>A (p.Ser2793Asn) rs374853436
NM_000038.6(APC):c.8389A>G (p.Ser2797Gly) rs147287751
NM_000038.6(APC):c.8419A>G (p.Thr2807Ala) rs894164638
NM_001127511.3(APC):c.125G>A (p.Gly42Asp) rs1057517570
NM_001127511.3(APC):c.16G>A (p.Gly6Ser) rs1043505718

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