ClinVar Miner

List of variants in gene APC reported as likely pathogenic for Hereditary cancer-predisposing syndrome

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Total variants: 34
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HGVS dbSNP
NM_000038.6(APC):c.1312+3A>C rs863225311
NM_000038.6(APC):c.1312+3A>G rs863225311
NM_000038.6(APC):c.135+1G>T rs750508765
NM_000038.6(APC):c.135+2T>C rs1554067164
NM_000038.6(APC):c.136-1G>A rs1554069481
NM_000038.6(APC):c.1409-2A>T rs1064794163
NM_000038.6(APC):c.1409-3T>G rs1554081629
NM_000038.6(APC):c.1626+2T>G rs876658858
NM_000038.6(APC):c.1743+1G>T rs761458613
NM_000038.6(APC):c.1743G>C (p.Lys581Asn) rs1114167592
NM_000038.6(APC):c.1902T>G (p.Ser634Arg) rs876659460
NM_000038.6(APC):c.1958G>A (p.Arg653Lys) rs1060503318
NM_000038.6(APC):c.1959-2A>G rs876658214
NM_000038.6(APC):c.220+2T>A rs587781809
NM_000038.6(APC):c.221-1G>A rs863225327
NM_000038.6(APC):c.221-1G>C rs863225327
NM_000038.6(APC):c.221-2A>G rs786201291
NM_000038.6(APC):c.3077A>C (p.Asn1026Thr) rs1114167603
NM_000038.6(APC):c.3083G>A (p.Ser1028Asn) rs1114167617
NM_000038.6(APC):c.3084T>A (p.Ser1028Arg) rs876660265
NM_000038.6(APC):c.3920T>A (p.Ile1307Lys) rs1801155
NM_000038.6(APC):c.422+2T>G rs879254169
NM_000038.6(APC):c.423-3T>A rs587782293
NM_000038.6(APC):c.4732T>G (p.Cys1578Gly) rs138367627
NM_000038.6(APC):c.531+2T>A rs863225365
NM_000038.6(APC):c.531+3A>C rs1114167550
NM_000038.6(APC):c.531+5G>C rs587779798
NM_000038.6(APC):c.6281del (p.Pro2094fs) rs876660816
NM_000038.6(APC):c.645+2T>G rs786202351
NM_000038.6(APC):c.7692dup (p.Arg2565fs) rs1554088600
NM_000038.6(APC):c.834G>A (p.Gln278=) rs1060503261
NM_000038.6(APC):c.8514C>A (p.Tyr2838Ter) rs876660375
NM_000038.6(APC):c.8514C>G (p.Tyr2838Ter) rs876660375
NM_000038.6(APC):c.933+2T>C rs1057517559

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