List of variants in gene APC reported as 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.1213C>T (p.Arg405Ter)	rs587779780	0.00001
NM_000038.6(APC):c.1370C>G (p.Ser457Ter)	rs1060503333
NM_000038.6(APC):c.1987C>T (p.Gln663Ter)	rs730881240
NM_000038.6(APC):c.233_236del (p.Asp78fs)	rs1064793020
NM_000038.6(APC):c.2893_2896del (p.Asn965fs)	rs2149879574
NM_000038.6(APC):c.3183_3187del (p.Lys1061_Gln1062insTer)	rs587779352
NM_000038.6(APC):c.3581C>A (p.Ser1194Ter)	rs2149894857
NM_000038.6(APC):c.3595_3596del (p.Lys1199fs)	rs864622106
NM_000038.6(APC):c.4099C>T (p.Gln1367Ter)	rs121913328
NM_000038.6(APC):c.4796C>G (p.Ser1599Ter)	rs1554086212
NM_000038.6(APC):c.5957del (p.Pro1986fs)	rs2149953403
NM_000038.6(APC):c.994C>T (p.Arg332Ter)	rs775126020

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