ClinVar Miner

List of variants in gene APC reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP
NM_000038.6(APC):c.*1132C>A rs886059811
NM_000038.6(APC):c.*1233_*1235TAT[1] rs886059812
NM_000038.6(APC):c.*1294A>G rs886059813
NM_000038.6(APC):c.*1320T>A rs373883680
NM_000038.6(APC):c.*1497C>T rs138754620
NM_000038.6(APC):c.*1555C>T rs886059814
NM_000038.6(APC):c.*1609T>C rs767384752
NM_000038.6(APC):c.*1834T>G rs886059815
NM_000038.6(APC):c.*1840A>G rs886059816
NM_000038.6(APC):c.*1937G>T rs886059817
NM_000038.6(APC):c.*1960C>G rs886059818
NM_000038.6(APC):c.*1970T>G rs886059819
NM_000038.6(APC):c.*2087C>A rs886059820
NM_000038.6(APC):c.*210_*213del rs763673039
NM_000038.6(APC):c.*404_*405insA rs1554089340
NM_000038.6(APC):c.*505C>A rs886059803
NM_000038.6(APC):c.*551T>C rs886059804
NM_000038.6(APC):c.*574T>C rs886059805
NM_000038.6(APC):c.*624A>C rs886059806
NM_000038.6(APC):c.*645A>G rs886059807
NM_000038.6(APC):c.*714G>T rs886059808
NM_000038.6(APC):c.*913T>C rs886059809
NM_000038.6(APC):c.1398G>A (p.Met466Ile) rs878853417
NM_000038.6(APC):c.1722A>G (p.Glu574=) rs786201277
NM_000038.6(APC):c.3210T>C (p.Asn1070=) rs886059794
NM_000038.6(APC):c.3341G>A (p.Arg1114Gln) rs753209586
NM_000038.6(APC):c.336T>A (p.Pro112=) rs886059793
NM_000038.6(APC):c.4594G>A (p.Asp1532Asn) rs730881251
NM_000038.6(APC):c.4833G>A (p.Gln1611=) rs762030106
NM_000038.6(APC):c.5050T>C (p.Phe1684Leu) rs886059795
NM_000038.6(APC):c.5194A>G (p.Met1732Val) rs752065261
NM_000038.6(APC):c.5363G>A (p.Arg1788His) rs201472075
NM_000038.6(APC):c.5399A>G (p.Asn1800Ser) rs865782682
NM_000038.6(APC):c.5524T>A (p.Ser1842Thr) rs754648125
NM_000038.6(APC):c.5840C>G (p.Thr1947Ser) rs575724078
NM_000038.6(APC):c.5894A>C (p.His1965Pro) rs773776516
NM_000038.6(APC):c.6316G>C (p.Glu2106Gln) rs886059796
NM_000038.6(APC):c.6492C>T (p.Gly2164=) rs765332758
NM_000038.6(APC):c.6525A>G (p.Thr2175=) rs200151646
NM_000038.6(APC):c.6556A>C (p.Lys2186Gln) rs886059797
NM_000038.6(APC):c.6609T>C (p.Val2203=) rs149328018
NM_000038.6(APC):c.6624A>G (p.Glu2208=) rs886059798
NM_000038.6(APC):c.7209G>A (p.Gln2403=) rs769603145
NM_000038.6(APC):c.7903A>G (p.Thr2635Ala) rs886059799
NM_000038.6(APC):c.8033A>G (p.Asn2678Ser) rs886059800
NM_000038.6(APC):c.8100T>C (p.Asn2700=) rs761326128
NM_000038.6(APC):c.8107A>G (p.Lys2703Glu) rs730881270
NM_000038.6(APC):c.8212A>G (p.Ile2738Val) rs876658839
NM_000038.6(APC):c.8389A>G (p.Ser2797Gly) rs147287751
NM_000038.6(APC):c.8425G>A (p.Val2809Met) rs886059801

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