ClinVar Miner

List of variants in gene APC reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 108
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HGVS dbSNP
NC_000005.10:g.112766534C>G
NC_000005.10:g.112780758T>C
NC_000005.10:g.112792712C>T
NC_000005.10:g.112801269A>G
NC_000005.10:g.112828010C>A
NC_000005.10:g.112834948T>C
NM_000038.6(APC):c.-19+45G>A
NM_000038.6(APC):c.-19+53T>C
NM_000038.6(APC):c.1240C>T (p.Arg414Cys) rs137854567
NM_000038.6(APC):c.135+6A>G
NM_000038.6(APC):c.1383G>A (p.Glu461=) rs1561546239
NM_000038.6(APC):c.1557A>G (p.Leu519=) rs765537673
NM_000038.6(APC):c.1604C>T (p.Ser535Phe) rs75870842
NM_000038.6(APC):c.1631T>C (p.Ile544Thr) rs144056494
NM_000038.6(APC):c.1686G>A (p.Thr562=) rs770256026
NM_000038.6(APC):c.1743+78A>G
NM_000038.6(APC):c.1825G>A (p.Val609Ile) rs147863331
NM_000038.6(APC):c.1965C>T (p.Ile655=) rs765309567
NM_000038.6(APC):c.220+249C>T
NM_000038.6(APC):c.2220C>T (p.Ala740=)
NM_000038.6(APC):c.2472A>T (p.Pro824=) rs746965994
NM_000038.6(APC):c.2593C>T (p.Pro865Ser) rs192620988
NM_000038.6(APC):c.2608C>T (p.Pro870Ser) rs33974176
NM_000038.6(APC):c.2640C>T (p.Ile880=) rs200184105
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.2805C>T (p.Tyr935=) rs137854575
NM_000038.6(APC):c.2820G>A (p.Ser940=) rs780366551
NM_000038.6(APC):c.2946G>A (p.Ser982=) rs377384463
NM_000038.6(APC):c.2985C>T (p.Cys995=)
NM_000038.6(APC):c.3173A>G (p.Asp1058Gly) rs148725540
NM_000038.6(APC):c.317G>A (p.Arg106His) rs201764637
NM_000038.6(APC):c.3249T>G (p.Asp1083Glu) rs201629780
NM_000038.6(APC):c.3374T>C (p.Val1125Ala) rs377278397
NM_000038.6(APC):c.3386T>C (p.Leu1129Ser) rs143638171
NM_000038.6(APC):c.3511C>T (p.Arg1171Cys) rs201830995
NM_000038.6(APC):c.3555A>G (p.Thr1185=) rs786201125
NM_000038.6(APC):c.3624C>T (p.Thr1208=) rs730882125
NM_000038.6(APC):c.3650A>C (p.Asn1217Thr) rs138933660
NM_000038.6(APC):c.3711G>A (p.Gln1237=) rs756939805
NM_000038.6(APC):c.3739G>A (p.Ala1247Thr) rs148223181
NM_000038.6(APC):c.3774A>G (p.Thr1258=) rs542928573
NM_000038.6(APC):c.3798T>C (p.Asp1266=) rs1488397941
NM_000038.6(APC):c.385G>C (p.Glu129Gln) rs376628500
NM_000038.6(APC):c.388A>G (p.Ser130Gly) rs150973053
NM_000038.6(APC):c.3920T>A (p.Ile1307Lys) rs1801155
NM_000038.6(APC):c.3949G>C (p.Glu1317Gln) rs1801166
NM_000038.6(APC):c.4005C>T (p.Ser1335=) rs751729992
NM_000038.6(APC):c.422+148T>C
NM_000038.6(APC):c.4326T>A (p.Pro1442=) rs67622085
NM_000038.6(APC):c.4336G>A (p.Ala1446Thr) rs146572883
NM_000038.6(APC):c.4360A>G (p.Lys1454Glu) rs111866410
NM_000038.6(APC):c.450A>G (p.Lys150=) rs116020626
NM_000038.6(APC):c.4524T>C (p.Ala1508=)
NM_000038.6(APC):c.4669A>G (p.Ile1557Val) rs763578917
NM_000038.6(APC):c.4761A>G (p.Ser1587=) rs863224280
NM_000038.6(APC):c.4833G>A (p.Gln1611=) rs762030106
NM_000038.6(APC):c.5009C>T (p.Ala1670Val) rs202228932
NM_000038.6(APC):c.5140G>A (p.Asp1714Asn) rs148275069
NM_000038.6(APC):c.5178A>G (p.Glu1726=) rs368494571
NM_000038.6(APC):c.5208A>G (p.Lys1736=)
NM_000038.6(APC):c.5265G>A (p.Ala1755=) rs34506289
NM_000038.6(APC):c.5274T>A (p.Ser1758=) rs199600387
NM_000038.6(APC):c.5298T>C (p.Asp1766=) rs781533317
NM_000038.6(APC):c.531+221A>G
NM_000038.6(APC):c.532-1064T>G
NM_000038.6(APC):c.532-1149T>G
NM_000038.6(APC):c.5478G>A (p.Lys1826=) rs768922376
NM_000038.6(APC):c.5571A>C (p.Ser1857=) rs376624613
NM_000038.6(APC):c.5690A>C (p.His1897Pro) rs112610898
NM_000038.6(APC):c.5790A>G (p.Gln1930=) rs141152252
NM_000038.6(APC):c.5805G>A (p.Gln1935=) rs377040690
NM_000038.6(APC):c.5839A>C (p.Thr1947Pro) rs746346292
NM_000038.6(APC):c.588C>T (p.Ile196=) rs147846364
NM_000038.6(APC):c.607C>G (p.Gln203Glu) rs141576417
NM_000038.6(APC):c.6135C>T (p.Ser2045=) rs187297940
NM_000038.6(APC):c.6162A>G (p.Ser2054=) rs776160547
NM_000038.6(APC):c.6474C>T (p.Pro2158=) rs772027192
NM_000038.6(APC):c.6510A>C (p.Pro2170=) rs138571760
NM_000038.6(APC):c.6526T>C (p.Leu2176=) rs183468041
NM_000038.6(APC):c.6609T>C (p.Val2203=) rs149328018
NM_000038.6(APC):c.6669A>G (p.Ser2223=) rs372680843
NM_000038.6(APC):c.6750C>T (p.Gly2250=) rs555799753
NM_000038.6(APC):c.6821C>T (p.Ala2274Val) rs34919187
NM_000038.6(APC):c.6857C>T (p.Ala2286Val) rs200587641
NM_000038.6(APC):c.6985A>G (p.Ile2329Val) rs146048493
NM_000038.6(APC):c.7026A>G (p.Leu2342=) rs766086022
NM_000038.6(APC):c.705A>G (p.Leu235=) rs147036141
NM_000038.6(APC):c.7137C>G (p.Thr2379=) rs141454910
NM_000038.6(APC):c.7194C>T (p.Ser2398=) rs565688379
NM_000038.6(APC):c.7395T>C (p.Leu2465=) rs369906346
NM_000038.6(APC):c.7443T>A (p.Thr2481=) rs147757080
NM_000038.6(APC):c.747G>A (p.Lys249=) rs878853470
NM_000038.6(APC):c.7514G>A (p.Arg2505Gln) rs147549623
NM_000038.6(APC):c.7731A>G (p.Ser2577=) rs537187449
NM_000038.6(APC):c.7862C>G (p.Ser2621Cys) rs72541816
NM_000038.6(APC):c.7878T>G (p.Thr2626=) rs757020188
NM_000038.6(APC):c.789T>A (p.Gly263=) rs767053295
NM_000038.6(APC):c.8043G>C (p.Pro2681=) rs149347068
NM_000038.6(APC):c.8061A>G (p.Ser2687=) rs746180965
NM_000038.6(APC):c.8148G>C (p.Val2716=) rs1158207177
NM_000038.6(APC):c.822T>C (p.Ser274=) rs776589022
NM_000038.6(APC):c.8266A>G (p.Ile2756Val) rs146115809
NM_000038.6(APC):c.8499C>G (p.Arg2833=) rs757921527
NM_000038.6(APC):c.8511T>C (p.Ser2837=) rs1010623341
NM_000038.6(APC):c.933+15C>T
NM_000038.6(APC):c.934-17del rs762333924
NM_001127511.3(APC):c.-3C>A

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