List of variants in gene APC reported as pathogenic for not specified

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.70C>T (p.Arg24Ter)	rs145945630	0.00003
NM_000038.6(APC):c.1370C>G (p.Ser457Ter)	rs1060503333
NM_000038.6(APC):c.2547_2550del (p.Asp849fs)	rs398123118
NM_000038.6(APC):c.2626C>T (p.Arg876Ter)	rs121913333
NM_000038.6(APC):c.311C>G (p.Ser104Ter)	rs74953290
NM_000038.6(APC):c.3146G>A (p.Trp1049Ter)	rs876658667
NM_000038.6(APC):c.3523C>T (p.Gln1175Ter)	rs1554085081
NM_000038.6(APC):c.3709C>T (p.Gln1237Ter)	rs1185643240
NM_000038.6(APC):c.426_427del (p.Leu143fs)	rs587782557
NM_000038.6(APC):c.532-1G>A	rs1554072547
NM_000038.6(APC):c.643C>T (p.Gln215Ter)	rs137854577
NM_000038.6(APC):c.834+1G>A	rs1554076225

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