List of variants in gene APC reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
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.2334_2337del (p.Asn778fs)	rs1580620655
NM_000038.6(APC):c.5709_5717delinsT (p.Gln1904fs)
NM_000038.6(APC):c.6676C>T (p.Arg2226Ter)	rs1064794626
NM_000038.6(APC):c.7513C>T (p.Arg2505Ter)	rs79630786
NM_000038.6(APC):c.7619_7623del (p.Pro2540fs)	rs1580684796

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