List of variants in gene APC reported as likely benign by Illumina Laboratory Services, Illumina

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: 39

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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.*1304G>A	rs112588804	0.00487
NM_001127511.3(APC):c.166-28452G>C	rs115242894	0.00443
NM_000038.6(APC):c.*142C>T	rs6875894	0.00363
NM_000038.6(APC):c.4420G>A (p.Ala1474Thr)	rs139387758	0.00324
NM_000038.6(APC):c.4360A>G (p.Lys1454Glu)	rs111866410	0.00271
NM_000038.6(APC):c.4893T>C (p.Ser1631=)	rs35634377	0.00268
NM_000038.6(APC):c.3386T>C (p.Leu1129Ser)	rs143638171	0.00250
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.1240C>T (p.Arg414Cys)	rs137854567	0.00053
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.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.8266A>G (p.Ile2756Val)	rs146115809	0.00026
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.1488A>T (p.Thr496=)	rs9282599	0.00019
NM_000038.6(APC):c.3249T>G (p.Asp1083Glu)	rs201629780	0.00019
NM_000038.6(APC):c.3374T>C (p.Val1125Ala)	rs377278397	0.00018
NM_000038.6(APC):c.6609T>C (p.Val2203=)	rs149328018	0.00014
NM_000038.6(APC):c.*1497C>T	rs138754620	0.00013
NM_000038.6(APC):c.1631T>C (p.Ile544Thr)	rs144056494	0.00012
NM_000038.6(APC):c.1958+10G>T	rs375175370	0.00009
NM_000038.6(APC):c.573T>C (p.Tyr191=)	rs185154886	0.00008
NM_000038.6(APC):c.6724A>G (p.Ser2242Gly)	rs201375478	0.00008
NM_000038.6(APC):c.4833G>A (p.Gln1611=)	rs762030106	0.00006
NM_000038.6(APC):c.6387G>A (p.Ser2129=)	rs374310157	0.00004
NM_000038.6(APC):c.647G>A (p.Arg216Gln)	rs76685252	0.00003
NM_000038.6(APC):c.7209G>A (p.Gln2403=)	rs769603145	0.00003
NM_000038.6(APC):c.7415C>T (p.Ala2472Val)	rs200399245	0.00003
NM_000038.6(APC):c.2481T>C (p.Asn827=)	rs749477816	0.00002
NM_000038.6(APC):c.5225G>A (p.Arg1742His)	rs199775075	0.00002
NM_000038.6(APC):c.3378C>G (p.Ser1126Arg)	rs149353082	0.00001
NM_000038.6(APC):c.928_929del	rs555618339
NM_000038.6(APC):c.3462AGA[2] (p.Glu1157del)	rs386833391
NM_000038.6(APC):c.5840C>G (p.Thr1947Ser)	rs575724078

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