List of variants in gene APC reported as likely benign by True Health Diagnostics

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.7704A>G (p.Gly2568=)	rs35043160	0.02992
NM_000038.6(APC):c.3732A>G (p.Gln1244=)	rs74380081	0.01174
NM_000038.6(APC):c.1695A>G (p.Glu565=)	rs77921116	0.01170
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.5265G>A (p.Ala1755=)	rs34506289	0.00675
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.8068G>A (p.Ala2690Thr)	rs140868933	0.00146
NM_000038.6(APC):c.6921G>A (p.Ser2307=)	rs2229993	0.00143
NM_000038.6(APC):c.7514G>A (p.Arg2505Gln)	rs147549623	0.00093
NM_000038.6(APC):c.3173A>G (p.Asp1058Gly)	rs148725540	0.00056
NM_000038.6(APC):c.1240C>T (p.Arg414Cys)	rs137854567	0.00053
NM_000038.6(APC):c.607C>G (p.Gln203Glu)	rs141576417	0.00034
NM_000038.6(APC):c.1419G>A (p.Gln473=)	rs141579422	0.00021
NM_000038.6(APC):c.3352A>G (p.Asn1118Asp)	rs140493115	0.00021
NM_000038.6(APC):c.3006C>T (p.Ala1002=)	rs72541810	0.00020
NM_000038.6(APC):c.6609T>C (p.Val2203=)	rs149328018	0.00014
NM_000038.6(APC):c.450A>G (p.Lys150=)	rs116020626	0.00012
NM_000038.6(APC):c.6873A>T (p.Gln2291His)	rs148878262	0.00012
NM_000038.6(APC):c.5026A>G (p.Arg1676Gly)	rs370560998	0.00006
NM_000038.6(APC):c.7786T>G (p.Ser2596Ala)	rs138137162	0.00004
NM_000038.6(APC):c.2547T>C (p.Asp849=)	rs766086010
NM_000038.6(APC):c.3462AGA[2] (p.Glu1157del)	rs386833391
NM_000038.6(APC):c.7536T>C (p.Ser2512=)	rs587780604

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