List of variants in gene APC reported as benign for colonic neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.5034G>A (p.Gly1678=)	rs42427	0.59504
NM_000038.6(APC):c.5880G>A (p.Pro1960=)	rs465899	0.59308
NM_000038.6(APC):c.5268T>G (p.Ser1756=)	rs866006	0.59230
NM_000038.6(APC):c.4479G>A (p.Thr1493=)	rs41115	0.59177
NM_000038.6(APC):c.1635G>A (p.Ala545=)	rs351771	0.59150
NM_000038.6(APC):c.1458T>C (p.Tyr486=)	rs2229992	0.46792
NM_000038.6(APC):c.7504G>A (p.Gly2502Ser)	rs2229995	0.01693
NM_000038.6(APC):c.7201C>T (p.Leu2401=)	rs2229994	0.01134
NM_000038.6(APC):c.2608C>T (p.Pro870Ser)	rs33974176	0.00917
NM_000038.6(APC):c.4326T>A (p.Pro1442=)	rs67622085	0.00705
NM_000038.6(APC):c.1959G>A (p.Arg653=)	rs72541809	0.00583
NM_000038.6(APC):c.3949G>C (p.Glu1317Gln)	rs1801166	0.00570
NM_000038.6(APC):c.1958+8T>C	rs62626346	0.00510
NM_000038.6(APC):c.7862C>G (p.Ser2621Cys)	rs72541816	0.00358
NM_000038.6(APC):c.3471G>A (p.Glu1157=)	rs143927847	0.00308
NM_000038.6(APC):c.3165A>T (p.Ile1055=)	rs61734287	0.00286
NM_000038.6(APC):c.3386T>C (p.Leu1129Ser)	rs143638171	0.00250
NM_000038.6(APC):c.705A>G (p.Leu235=)	rs147036141	0.00213
NM_000038.6(APC):c.2322C>T (p.Asp774=)	rs145792879	0.00041
NM_000038.6(APC):c.2805C>T (p.Tyr935=)	rs137854575	0.00040
NM_000038.6(APC):c.3511C>T (p.Arg1171Cys)	rs201830995	0.00028
NM_000038.6(APC):c.1488A>T (p.Thr496=)	rs9282599	0.00019
NM_000038.6(APC):c.1554G>A (p.Thr518=)	rs546568052	0.00002

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