ClinVar Miner

List of variants in gene APC reported as uncertain significance by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 127
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001127511.3(APC):c.16G>A (p.Gly6Ser) rs1043505718 0.00034
NM_000038.6(APC):c.5009C>T (p.Ala1670Val) rs202228932 0.00018
NM_000038.6(APC):c.6637A>G (p.Met2213Val) rs186926737 0.00018
NM_000038.6(APC):c.3479C>A (p.Thr1160Lys) rs201004111 0.00017
NM_000038.6(APC):c.7109G>T (p.Gly2370Val) rs140079759 0.00014
NM_000038.6(APC):c.5801C>T (p.Pro1934Leu) rs587780600 0.00012
NM_000038.6(APC):c.7621A>G (p.Ile2541Val) rs587778033 0.00011
NM_000038.6(APC):c.6724A>G (p.Ser2242Gly) rs201375478 0.00008
NM_000038.6(APC):c.6473C>G (p.Pro2158Arg) rs587779804 0.00007
NM_000038.6(APC):c.7717A>G (p.Ile2573Val) rs145444830 0.00007
NM_000038.6(APC):c.8389A>G (p.Ser2797Gly) rs147287751 0.00007
NM_000038.6(APC):c.5026A>G (p.Arg1676Gly) rs370560998 0.00006
NM_000038.6(APC):c.5140G>A (p.Asp1714Asn) rs148275069 0.00006
NM_000038.6(APC):c.7399C>A (p.Pro2467Thr) rs372305287 0.00006
NM_000038.6(APC):c.7468G>A (p.Asp2490Asn) rs538230198 0.00006
NM_000038.6(APC):c.2438A>G (p.Asn813Ser) rs201522866 0.00005
NM_000038.6(APC):c.1762G>A (p.Val588Ile) rs372416031 0.00004
NM_000038.6(APC):c.2297C>T (p.Ala766Val) rs200339830 0.00004
NM_000038.6(APC):c.2356C>T (p.Arg786Cys) rs1165139414 0.00004
NM_000038.6(APC):c.317G>A (p.Arg106His) rs201764637 0.00004
NM_000038.6(APC):c.3368A>C (p.Gln1123Pro) rs587779789 0.00004
NM_000038.6(APC):c.449A>G (p.Lys150Arg) rs371085910 0.00004
NM_000038.6(APC):c.4901C>T (p.Pro1634Leu) rs370433763 0.00004
NM_000038.6(APC):c.5500G>A (p.Val1834Ile) rs555944438 0.00004
NM_000038.6(APC):c.5528C>T (p.Pro1843Leu) rs368080169 0.00004
NM_000038.6(APC):c.6019T>C (p.Tyr2007His) rs745811356 0.00004
NM_000038.6(APC):c.6020A>G (p.Tyr2007Cys) rs752604668 0.00004
NM_000038.6(APC):c.7099A>G (p.Thr2367Ala) rs772778630 0.00004
NM_000038.6(APC):c.7402T>C (p.Ser2468Pro) rs375586273 0.00004
NM_000038.6(APC):c.7540A>G (p.Thr2514Ala) rs545125246 0.00004
NM_000038.6(APC):c.1241G>A (p.Arg414His) rs730881233 0.00003
NM_000038.6(APC):c.2485A>G (p.Thr829Ala) rs768810807 0.00003
NM_000038.6(APC):c.7375T>C (p.Ser2459Pro) rs1554088287 0.00003
NM_001127511.3(APC):c.71C>T (p.Ser24Phe) rs770241997 0.00003
NM_001127511.3(APC):c.83G>A (p.Gly28Asp) rs1057517606 0.00003
NM_000038.6(APC):c.2026A>G (p.Ile676Val) rs745529713 0.00002
NM_000038.6(APC):c.2222A>G (p.Asn741Ser) rs150209825 0.00002
NM_000038.6(APC):c.2444A>C (p.Asn815Thr) rs762990578 0.00002
NM_000038.6(APC):c.3437G>A (p.Arg1146His) rs763486328 0.00002
NM_000038.6(APC):c.4709A>G (p.Asp1570Gly) rs373419559 0.00002
NM_000038.6(APC):c.5060G>A (p.Arg1687Gln) rs779068685 0.00002
NM_000038.6(APC):c.5147A>G (p.Asn1716Ser) rs141298709 0.00002
NM_000038.6(APC):c.5524T>A (p.Ser1842Thr) rs754648125 0.00002
NM_000038.6(APC):c.5752A>G (p.Ile1918Val) rs776966222 0.00002
NM_000038.6(APC):c.1342C>G (p.Pro448Ala) rs374195067 0.00001
NM_000038.6(APC):c.2308T>C (p.Ser770Pro) rs587781419 0.00001
NM_000038.6(APC):c.2414G>A (p.Arg805Gln) rs200593940 0.00001
NM_000038.6(APC):c.251G>T (p.Gly84Val) rs143145868 0.00001
NM_000038.6(APC):c.3323A>G (p.Asn1108Ser) rs151286353 0.00001
NM_000038.6(APC):c.3760A>G (p.Ile1254Val) rs769504783 0.00001
NM_000038.6(APC):c.3824G>C (p.Ser1275Thr) rs587781637 0.00001
NM_000038.6(APC):c.4100A>G (p.Gln1367Arg) rs1399790840 0.00001
NM_000038.6(APC):c.4906G>T (p.Asp1636Tyr) rs730882128 0.00001
NM_000038.6(APC):c.4963A>G (p.Thr1655Ala) rs759441332 0.00001
NM_000038.6(APC):c.5017G>A (p.Glu1673Lys) rs587779796 0.00001
NM_000038.6(APC):c.5282A>C (p.Asn1761Thr) rs752038930 0.00001
NM_000038.6(APC):c.5687G>A (p.Ser1896Asn) rs751088165 0.00001
NM_000038.6(APC):c.5794A>T (p.Thr1932Ser) rs777604445 0.00001
NM_000038.6(APC):c.6245A>G (p.Asp2082Gly) rs554370603 0.00001
NM_000038.6(APC):c.6446A>C (p.His2149Pro) rs749230730 0.00001
NM_000038.6(APC):c.6547T>A (p.Ser2183Thr) rs764180204 0.00001
NM_000038.6(APC):c.6554G>A (p.Ser2185Asn) rs764255983 0.00001
NM_000038.6(APC):c.67C>G (p.Leu23Val) rs372367350 0.00001
NM_000038.6(APC):c.7205A>G (p.Asn2402Ser) rs745843442 0.00001
NM_000038.6(APC):c.7284A>G (p.Glu2428=) rs876658194 0.00001
NM_000038.6(APC):c.7441A>T (p.Thr2481Ser) rs1321275331 0.00001
NM_000038.6(APC):c.7595A>G (p.His2532Arg) rs752702756 0.00001
NM_000038.6(APC):c.764A>G (p.His255Arg) rs530670052 0.00001
NM_000038.6(APC):c.76G>C (p.Glu26Gln) rs1554067127 0.00001
NM_000038.6(APC):c.8161C>T (p.Arg2721Cys) rs587782312 0.00001
NM_000038.6(APC):c.8182G>A (p.Val2728Met) rs587778045 0.00001
NM_000038.6(APC):c.8276G>A (p.Arg2759His) rs538289470 0.00001
NM_000038.6(APC):c.8291C>G (p.Ser2764Cys) rs1057520223 0.00001
NM_000038.6(APC):c.8310C>G (p.His2770Gln) rs200160084 0.00001
NM_000038.6(APC):c.8378G>A (p.Ser2793Asn) rs374853436 0.00001
NM_000038.6(APC):c.8524T>G (p.Ser2842Ala) rs587780610 0.00001
NM_000038.6(APC):c.-19+480C>T
NM_000038.6(APC):c.1171A>C (p.Ile391Leu)
NM_000038.6(APC):c.1295A>G (p.Asp432Gly) rs786202283
NM_000038.6(APC):c.1318G>A (p.Ala440Thr) rs1064793023
NM_000038.6(APC):c.1343C>T (p.Pro448Leu)
NM_000038.6(APC):c.1408+1316G>A
NM_000038.6(APC):c.1613A>T (p.Glu538Val) rs1561555761
NM_000038.6(APC):c.1640T>G (p.Val547Gly) rs1580574053
NM_000038.6(APC):c.170_175del (p.Asp57_Glu58del) rs1167769425
NM_000038.6(APC):c.2221A>G (p.Asn741Asp) rs1554084021
NM_000038.6(APC):c.2245T>A (p.Leu749Met) rs976000214
NM_000038.6(APC):c.2500T>G (p.Ser834Ala)
NM_000038.6(APC):c.2503T>C (p.Ser835Pro) rs748302469
NM_000038.6(APC):c.2552G>A (p.Ser851Asn) rs1554084260
NM_000038.6(APC):c.2588A>T (p.Tyr863Phe)
NM_000038.6(APC):c.2800A>G (p.Thr934Ala) rs1561579733
NM_000038.6(APC):c.3049_3051del (p.Asn1017del) rs730881229
NM_000038.6(APC):c.358A>G (p.Arg120Gly) rs876659470
NM_000038.6(APC):c.4088A>T (p.Lys1363Ile) rs373607243
NM_000038.6(APC):c.4376C>T (p.Thr1459Ile)
NM_000038.6(APC):c.437C>T (p.Ala146Val) rs1305794169
NM_000038.6(APC):c.4702G>C (p.Asp1568His) rs1554086115
NM_000038.6(APC):c.4765C>G (p.Arg1589Gly) rs72541813
NM_000038.6(APC):c.4828A>G (p.Ser1610Gly) rs587781512
NM_000038.6(APC):c.496A>G (p.Thr166Ala) rs889134189
NM_000038.6(APC):c.5113A>G (p.Thr1705Ala) rs1554086453
NM_000038.6(APC):c.5390A>G (p.Asn1797Ser) rs1278802463
NM_000038.6(APC):c.5421CAA[1] (p.Asn1808del) rs587782002
NM_000038.6(APC):c.5894A>G (p.His1965Arg) rs773776516
NM_000038.6(APC):c.5908A>C (p.Ser1970Arg) rs1561603616
NM_000038.6(APC):c.608A>G (p.Gln203Arg) rs1554072626
NM_000038.6(APC):c.6123A>C (p.Glu2041Asp) rs1554087227
NM_000038.6(APC):c.626A>T (p.Asp209Val) rs1554072636
NM_000038.6(APC):c.6349C>A (p.Gln2117Lys) rs587780546
NM_000038.6(APC):c.6426C>G (p.Ile2142Met) rs1554087419
NM_000038.6(APC):c.646-20_646-7del
NM_000038.6(APC):c.6677G>A (p.Arg2226Gln) rs1246580689
NM_000038.6(APC):c.707A>G (p.Gln236Arg) rs1433658799
NM_000038.6(APC):c.7117A>G (p.Met2373Val) rs879254221
NM_000038.6(APC):c.7411C>T (p.Pro2471Ser) rs1324082067
NM_000038.6(APC):c.7652A>T (p.His2551Leu) rs1060503314
NM_000038.6(APC):c.7853A>T (p.Asn2618Ile) rs1580687270
NM_000038.6(APC):c.790C>G (p.Gln264Glu) rs1434813233
NM_000038.6(APC):c.7910G>T (p.Gly2637Val) rs752753706
NM_000038.6(APC):c.8006C>G (p.Pro2669Arg) rs1335624903
NM_000038.6(APC):c.8104G>A (p.Ala2702Thr) rs587779808
NM_000038.6(APC):c.8206A>G (p.Thr2736Ala) rs1766677689
NM_000038.6(APC):c.8419A>G (p.Thr2807Ala) rs894164638
NM_000038.6(APC):c.841A>G (p.Thr281Ala) rs769727966
NM_000038.6(APC):c.8486A>G (p.Gln2829Arg) rs1561623710
NM_001127511.3(APC):c.157G>C (p.Val53Leu) rs888841371

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.