ClinVar Miner

List of variants in gene APC reported as uncertain significance by Department of Pathology and Laboratory Medicine,Sinai Health System

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Total variants: 33
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HGVS dbSNP
NM_000038.6(APC):c.1631T>C (p.Ile544Thr) rs144056494
NM_000038.6(APC):c.1744-2A>G rs587783035
NM_000038.6(APC):c.1744-4C>G rs772745309
NM_000038.6(APC):c.1904G>A (p.Gly635Glu) rs730881239
NM_000038.6(APC):c.1904G>C (p.Gly635Ala) rs730881239
NM_000038.6(APC):c.262C>T (p.Arg88Trp) rs746592911
NM_000038.6(APC):c.2819C>T (p.Ser940Leu) rs544709767
NM_000038.6(APC):c.3077A>C (p.Asn1026Thr) rs1114167603
NM_000038.6(APC):c.3205A>G (p.Arg1069Gly) rs375408871
NM_000038.6(APC):c.3378C>G (p.Ser1126Arg) rs149353082
NM_000038.6(APC):c.3415A>C (p.Lys1139Gln) rs201550951
NM_000038.6(APC):c.3632T>G (p.Met1211Arg) rs575268622
NM_000038.6(APC):c.3920T>A (p.Ile1307Lys) rs1801155
NM_000038.6(APC):c.3920_3924del (p.Ile1307fs) rs1064794229
NM_000038.6(APC):c.423-3T>A rs587782293
NM_000038.6(APC):c.4666dup (p.Thr1556fs) rs587783031
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.52A>G (p.Met18Val) rs587782402
NM_000038.6(APC):c.5302A>G (p.Lys1768Glu) rs199630012
NM_000038.6(APC):c.532-14_532-12del rs765893314
NM_000038.6(APC):c.6117G>T (p.Leu2039Phe) rs372418435
NM_000038.6(APC):c.620G>A (p.Cys207Tyr) rs1268298845
NM_000038.6(APC):c.6354_6356TGC[5] (p.Ala2122dup) rs587780602
NM_000038.6(APC):c.6724A>G (p.Ser2242Gly) rs201375478
NM_000038.6(APC):c.6830C>G (p.Ser2277Cys) rs1554087778
NM_000038.6(APC):c.7399C>A (p.Pro2467Thr) rs372305287
NM_000038.6(APC):c.7468G>A (p.Asp2490Asn) rs538230198
NM_000038.6(APC):c.7508G>A (p.Gly2503Glu) rs750111908
NM_000038.6(APC):c.7621A>G (p.Ile2541Val) rs587778033
NM_000038.6(APC):c.7838G>A (p.Arg2613Lys) rs1554088693
NM_000038.6(APC):c.7966G>T (p.Asp2656Tyr) rs1554088797
NM_000038.6(APC):c.937_938del (p.Glu313fs) rs387906239

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