List of variants in gene APC reported by Center for Human Genetics, Inc, Center for Human Genetics, Inc

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.2608C>T (p.Pro870Ser)	rs33974176	0.00917
NM_000038.6(APC):c.3920T>A (p.Ile1307Lys)	rs1801155	0.00116
NM_000038.6(APC):c.317G>A (p.Arg106His)	rs201764637	0.00004
NM_000038.6(APC):c.835-4T>G	rs756807560	0.00001
NM_000038.6(APC):c.1246dup (p.Tyr416fs)	rs1060503366
NM_000038.6(APC):c.1495C>T (p.Arg499Ter)	rs137854580
NM_000038.6(APC):c.1958+3A>G	rs879254032
NM_000038.6(APC):c.2434_2443delinsCC (p.Asp812fs)	rs1554084159
NM_000038.6(APC):c.3183_3187del (p.Lys1061_Gln1062insTer)	rs587779352
NM_000038.6(APC):c.4348C>T (p.Arg1450Ter)	rs121913332
NM_000038.6(APC):c.694C>T (p.Arg232Ter)	rs397515734
NM_000038.6(APC):c.8492C>T (p.Pro2831Leu)	rs773513581
NM_000038.6(APC):c.904C>T (p.Arg302Ter)	rs137854568
NM_000038.6(APC):c.937_938del (p.Glu313fs)	rs387906239

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