ClinVar Miner

List of variants in gene APC reported as likely pathogenic by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP
NC_000005.9:g.(?_112072721)_(112090728_?)dup
NC_000005.9:g.(?_112072721)_(112111440_?)dup
NC_000005.9:g.(?_112090570)_(112157688_?)dup
NC_000005.9:g.(?_112090578)_(112111444_?)dup
NC_000005.9:g.(?_112090582)_(112111440_?)dup
NM_000038.5(APC):c.-18-?_834+?dup
NM_000038.6(APC):c.-30418_-30417delinsTAGCAAGGG
NM_000038.6(APC):c.1313-2A>G rs1561545780
NM_000038.6(APC):c.135+1G>T rs750508765
NM_000038.6(APC):c.136-1G>A rs1554069481
NM_000038.6(APC):c.1530_1548+10del rs1554081752
NM_000038.6(APC):c.1626+1G>A rs1554081934
NM_000038.6(APC):c.1626+2T>C rs876658858
NM_000038.6(APC):c.1627-2A>G
NM_000038.6(APC):c.1743+1G>A rs761458613
NM_000038.6(APC):c.1743+1G>T rs761458613
NM_000038.6(APC):c.1744-11_1744-1del rs1064792977
NM_000038.6(APC):c.1956C>T (p.His652=) rs1064793716
NM_000038.6(APC):c.1957A>G (p.Arg653Gly) rs1114167580
NM_000038.6(APC):c.1958G>T (p.Arg653Met) rs1060503318
NM_000038.6(APC):c.1959-1G>A rs863225321
NM_000038.6(APC):c.220+2T>A rs587781809
NM_000038.6(APC):c.220G>T (p.Glu74Ter) rs876658941
NM_000038.6(APC):c.221-1G>C rs863225327
NM_000038.6(APC):c.221-2A>G rs786201291
NM_000038.6(APC):c.422+2T>G rs879254169
NM_000038.6(APC):c.423-9A>G rs1554071494
NM_000038.6(APC):c.424_531+69dup rs1561477658
NM_000038.6(APC):c.524_531+4del rs863225364
NM_000038.6(APC):c.531+5G>C rs587779798
NM_000038.6(APC):c.531+5_531+8del rs1554071617
NM_000038.6(APC):c.532-2A>G rs752152148
NM_000038.6(APC):c.532-8G>A rs1060503323
NM_000038.6(APC):c.5952_5955del (p.Glu1985fs) rs1057517544
NM_000038.6(APC):c.834G>A (p.Gln278=) rs1060503261
NM_000038.6(APC):c.933+1G>A rs876660765
NM_000038.6(APC):c.933+2T>C rs1057517559
NM_000038.6(APC):c.934-2A>G rs1554079938
NM_001127511.3(APC):c.-190G>A rs879253785
Single allele

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