ClinVar Miner

List of variants in gene APC reported as likely benign by Counsyl

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Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP
NM_000038.5(APC):c.-30105C>T rs1057517584
NM_000038.5(APC):c.-30179T>C rs980704771
NM_000038.6(APC):c.1240C>T (p.Arg414Cys) rs137854567
NM_000038.6(APC):c.1312+16T>A rs376965806
NM_000038.6(APC):c.1409-17T>G rs764042245
NM_000038.6(APC):c.1419G>A (p.Gln473=) rs141579422
NM_000038.6(APC):c.1548+17T>C rs367690523
NM_000038.6(APC):c.1686G>A (p.Thr562=) rs770256026
NM_000038.6(APC):c.1744-14C>A rs761403505
NM_000038.6(APC):c.1744-14_1744-13del rs1554083086
NM_000038.6(APC):c.1958+10G>T rs375175370
NM_000038.6(APC):c.1958+27del rs1402242990
NM_000038.6(APC):c.2196T>C (p.Asn732=) rs781693283
NM_000038.6(APC):c.2205G>A (p.Ala735=) rs141001261
NM_000038.6(APC):c.221-16T>C rs1046591128
NM_000038.6(APC):c.2232T>G (p.Ser744=) rs145751759
NM_000038.6(APC):c.2262T>G (p.Val754=) rs148987776
NM_000038.6(APC):c.228C>T (p.Asn76=) rs766325173
NM_000038.6(APC):c.2322C>T (p.Asp774=) rs145792879
NM_000038.6(APC):c.2385C>T (p.Leu795=) rs80188155
NM_000038.6(APC):c.2586C>G (p.Asn862Lys) rs147972247
NM_000038.6(APC):c.2838A>G (p.Thr946=) rs142835322
NM_000038.6(APC):c.3006C>T (p.Ala1002=) rs72541810
NM_000038.6(APC):c.3374T>C (p.Val1125Ala) rs377278397
NM_000038.6(APC):c.3552C>T (p.Ala1184=) rs759407858
NM_000038.6(APC):c.3555A>G (p.Thr1185=) rs786201125
NM_000038.6(APC):c.3612A>G (p.Gln1204=) rs864622196
NM_000038.6(APC):c.3909A>G (p.Gln1303=) rs746289994
NM_000038.6(APC):c.3949G>C (p.Glu1317Gln) rs1801166
NM_000038.6(APC):c.4005C>T (p.Ser1335=) rs751729992
NM_000038.6(APC):c.422+19G>C rs767046355
NM_000038.6(APC):c.423-28G>T rs570467572
NM_000038.6(APC):c.4311A>G (p.Lys1437=) rs371784771
NM_000038.6(APC):c.4416A>T (p.Val1472=) rs773352404
NM_000038.6(APC):c.450A>G (p.Lys150=) rs116020626
NM_000038.6(APC):c.477C>T (p.Tyr159=) rs863224281
NM_000038.6(APC):c.4905G>A (p.Gly1635=) rs137988845
NM_000038.6(APC):c.5250C>T (p.Val1750=) rs2229997
NM_000038.6(APC):c.5271T>C (p.Ser1757=) rs752875511
NM_000038.6(APC):c.5274T>A (p.Ser1758=) rs199600387
NM_000038.6(APC):c.531+16G>A rs770126046
NM_000038.6(APC):c.532-17A>T rs997606437
NM_000038.6(APC):c.532-939G>A rs551489857
NM_000038.6(APC):c.532-939G>T rs551489857
NM_000038.6(APC):c.5805G>A (p.Gln1935=) rs377040690
NM_000038.6(APC):c.597G>A (p.Ala199=) rs587780601
NM_000038.6(APC):c.646-20G>A rs1057517635
NM_000038.6(APC):c.6474C>A (p.Pro2158=) rs772027192
NM_000038.6(APC):c.6510A>C (p.Pro2170=) rs138571760
NM_000038.6(APC):c.6669A>G (p.Ser2223=) rs372680843
NM_000038.6(APC):c.6821C>T (p.Ala2274Val) rs34919187
NM_000038.6(APC):c.6945A>G (p.Gln2315=) rs786201348
NM_000038.6(APC):c.730-22G>C rs115634618
NM_000038.6(APC):c.7533C>T (p.Leu2511=) rs1057522957
NM_000038.6(APC):c.7821C>T (p.Ser2607=) rs532235331
NM_000038.6(APC):c.7878T>G (p.Thr2626=) rs757020188
NM_000038.6(APC):c.789T>A (p.Gly263=) rs767053295
NM_000038.6(APC):c.7929A>G (p.Leu2643=) rs138796072
NM_000038.6(APC):c.7986G>A (p.Glu2662=) rs571645304
NM_000038.6(APC):c.8100T>C (p.Asn2700=) rs761326128
NM_000038.6(APC):c.8325G>A (p.Gly2775=) rs770719841
NM_000038.6(APC):c.835-15G>A rs1057521022
NM_000038.6(APC):c.835-20A>G rs777546674
NM_000038.6(APC):c.933+16A>G rs1057517599
NM_000038.6(APC):c.933+19C>A rs778599778
NM_000038.6(APC):c.934-14C>T rs778707022
NM_000038.6(APC):c.934-21C>A rs754906600
NM_000038.6(APC):c.993G>A (p.Ser331=) rs148343173

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