List of variants in gene APC reported as likely pathogenic for adenocarcinoma

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.1312+3A>G	rs863225311
NM_000038.6(APC):c.2206A>T (p.Lys736Ter)
NM_000038.6(APC):c.3340C>T (p.Arg1114Ter)	rs121913331
NM_000038.6(APC):c.406G>T (p.Glu136Ter)
NM_000038.6(APC):c.4638_4639del (p.Asn1546fs)	rs1561594148

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