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: 74
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HGVS dbSNP gnomAD frequency
NC_000005.10:g.(?_112754891)_(112767400_?)dup
NC_000005.9:g.(?_112072721)_(112090728_?)dup
NC_000005.9:g.(?_112072721)_(112090732_?)dup
NC_000005.9:g.(?_112072721)_(112111440_?)dup
NC_000005.9:g.(?_112072721)_(112116610_?)dup
NC_000005.9:g.(?_112090570)_(112157688_?)dup
NC_000005.9:g.(?_112090582)_(112137086_?)dup
NC_000005.9:g.(?_112090582)_(112157694_?)dup
NC_000005.9:g.(?_112090588)_(112137090_?)dup
NC_000005.9:g.(?_112111314)_(112116610_?)dup
NC_000005.9:g.(?_112169968)_(112170785_?)del
NC_000005.9:g.(?_112170638)_(112170872_?)dup
NM_000038.5(APC):c.-18-?_834+?dup
NM_000038.6(APC):c.1312+5G>C rs886039507
NM_000038.6(APC):c.1313-2A>C rs1561545780
NM_000038.6(APC):c.1313-2A>G rs1561545780
NM_000038.6(APC):c.135+1G>T rs750508765
NM_000038.6(APC):c.135+2T>C rs1554067164
NM_000038.6(APC):c.136-2A>G rs886039625
NM_000038.6(APC):c.136-2A>T
NM_000038.6(APC):c.1409-3T>G rs1554081629
NM_000038.6(APC):c.1530_1548+10del rs1554081752
NM_000038.6(APC):c.1549-19T>G rs2149812994
NM_000038.6(APC):c.1549-1G>A rs863225316
NM_000038.6(APC):c.1549-1G>T rs863225316
NM_000038.6(APC):c.1549-2A>G
NM_000038.6(APC):c.1626+1G>A rs1554081934
NM_000038.6(APC):c.1626+1G>T rs1554081934
NM_000038.6(APC):c.1626+2T>C rs876658858
NM_000038.6(APC):c.1626G>C (p.Gln542His) rs1580569744
NM_000038.6(APC):c.1627-2A>G rs1580573837
NM_000038.6(APC):c.1740_1743+16del
NM_000038.6(APC):c.1743+1G>A rs761458613
NM_000038.6(APC):c.1743+1G>C
NM_000038.6(APC):c.1743+1G>T rs761458613
NM_000038.6(APC):c.1743+2T>A
NM_000038.6(APC):c.1743+2T>C
NM_000038.6(APC):c.1743G>C (p.Lys581Asn) rs1114167592
NM_000038.6(APC):c.1744-11_1744-1del rs1064792977
NM_000038.6(APC):c.1959-1G>A rs863225321
NM_000038.6(APC):c.1959-1G>C rs863225321
NM_000038.6(APC):c.1959-2A>G rs876658214
NM_000038.6(APC):c.1959-2A>T rs876658214
NM_000038.6(APC):c.1959-7_1964del rs2149857426
NM_000038.6(APC):c.219A>G (p.Lys73=) rs2149784873
NM_000038.6(APC):c.369_422+44delinsG rs2149789411
NM_000038.6(APC):c.4139C>T (p.Thr1380Ile) rs876660713
NM_000038.6(APC):c.422+1G>A
NM_000038.6(APC):c.422+1G>C rs1756480727
NM_000038.6(APC):c.422+2T>C rs879254169
NM_000038.6(APC):c.422+2T>G rs879254169
NM_000038.6(APC):c.422+2_422+3del
NM_000038.6(APC):c.424_531+69dup rs1561477658
NM_000038.6(APC):c.4732T>G (p.Cys1578Gly) rs138367627
NM_000038.6(APC):c.524_531+4del rs863225364
NM_000038.6(APC):c.531+3A>C rs1114167550
NM_000038.6(APC):c.531+5_531+8del rs1554071617
NM_000038.6(APC):c.532-8G>A rs1060503323
NM_000038.6(APC):c.646-1G>A rs78847145
NM_000038.6(APC):c.646-2A>C
NM_000038.6(APC):c.646-2A>G rs777848503
NM_000038.6(APC):c.7959_7962del (p.Thr2654fs) rs1554088793
NM_000038.6(APC):c.834G>A (p.Gln278=) rs1060503261
NM_000038.6(APC):c.835-2A>G
NM_000038.6(APC):c.835-7T>G rs1554079128
NM_000038.6(APC):c.835-8A>G rs1064793022
NM_000038.6(APC):c.931_933+2delinsCA
NM_000038.6(APC):c.933+1G>A rs876660765
NM_000038.6(APC):c.933+2T>A rs1057517559
NM_000038.6(APC):c.933+2T>C rs1057517559
NM_000038.6(APC):c.933+809T>G rs2149767732
NM_000038.6(APC):c.933G>C (p.Lys311Asn) rs1762431806
NM_000038.6(APC):c.934-2A>G rs1554079938
Single allele

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