List of variants in gene APC reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.4420G>A (p.Ala1474Thr)	rs139387758	0.00324
NM_000038.6(APC):c.-19+512G>A	rs550306841	0.00176
NM_000038.6(APC):c.120G>A (p.Glu40=)	rs142720069	0.00161
NM_000038.6(APC):c.7514G>A (p.Arg2505Gln)	rs147549623	0.00093
NM_000038.6(APC):c.6821C>T (p.Ala2274Val)	rs34919187	0.00088
NM_000038.6(APC):c.3173A>G (p.Asp1058Gly)	rs148725540	0.00056
NM_000038.6(APC):c.2232T>G (p.Ser744=)	rs145751759	0.00032
NM_000038.6(APC):c.4905G>A (p.Gly1635=)	rs137988845	0.00031
NM_000038.6(APC):c.7490C>T (p.Ser2497Leu)	rs141010008	0.00031
NM_000038.6(APC):c.2593C>T (p.Pro865Ser)	rs192620988	0.00028
NM_000038.6(APC):c.3511C>T (p.Arg1171Cys)	rs201830995	0.00028
NM_000038.6(APC):c.3006C>T (p.Ala1002=)	rs72541810	0.00020
NM_000038.6(APC):c.3374T>C (p.Val1125Ala)	rs377278397	0.00018
NM_000038.6(APC):c.6669A>G (p.Ser2223=)	rs372680843	0.00016
NM_000038.6(APC):c.1548+17T>C	rs367690523	0.00013
NM_000038.6(APC):c.3875C>T (p.Thr1292Met)	rs371113837	0.00011
NM_000038.6(APC):c.-19+509G>A	rs745770540	0.00008
NM_000038.6(APC):c.6724A>G (p.Ser2242Gly)	rs201375478	0.00008
NM_000038.6(APC):c.789T>A (p.Gly263=)	rs767053295	0.00006
NM_000038.6(APC):c.729+15T>C	rs746211944	0.00002
NM_000038.6(APC):c.5541G>A (p.Thr1847=)	rs777449060	0.00001
NM_000038.6(APC):c.7143A>C (p.Gln2381His)	rs756153152	0.00001
NM_000038.6(APC):c.2651C>T (p.Ala884Val)	rs750217875
NM_000038.6(APC):c.2739T>C (p.His913=)	rs553363502
NM_000038.6(APC):c.3117A>C (p.Gly1039=)	rs1580631098
NM_000038.6(APC):c.5839A>C (p.Thr1947Pro)	rs746346292
NM_000038.6(APC):c.6354TGC[5] (p.Ala2122dup)	rs587780602
NM_000038.6(APC):c.6900T>C (p.Ser2300=)	rs202012533
NM_000038.6(APC):c.7794C>G (p.Thr2598=)	rs1554088662
NM_001127511.3(APC):c.166-28523C>T

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