List of variants in gene APC reported as likely pathogenic for colorectal cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.3920T>A (p.Ile1307Lys)	rs1801155	0.00116
NM_000038.6(APC):c.1312+3A>G	rs863225311
NM_000038.6(APC):c.2206A>T (p.Lys736Ter)
NM_000038.6(APC):c.2928_2929del (p.Gly977fs)	rs2149880355
NM_000038.6(APC):c.3036T>A (p.Asn1012Lys)
NM_000038.6(APC):c.406G>T (p.Glu136Ter)
NM_000038.6(APC):c.4638_4639del (p.Asn1546fs)	rs1561594148
NM_000038.6(APC):c.532-8G>A	rs1060503323
NM_000038.6(APC):c.645+1G>T	rs863225370
NM_000038.6(APC):c.645+2T>C	rs786202351
NM_000038.6(APC):c.6634dup (p.Gln2212fs)
NM_000038.6(APC):c.834+1G>A	rs1554076225

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