ClinVar Miner

List of variants in gene APC reported by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000038.6(APC):c.3173A>G (p.Asp1058Gly) rs148725540 0.00056
NM_000038.6(APC):c.2476T>G (p.Leu826Val) rs145245264 0.00054
NM_000038.6(APC):c.1240C>T (p.Arg414Cys) rs137854567 0.00053
NM_000038.6(APC):c.2593C>T (p.Pro865Ser) rs192620988 0.00028
NM_000038.6(APC):c.7109G>T (p.Gly2370Val) rs140079759 0.00014
NM_000038.6(APC):c.277C>G (p.Leu93Val) rs201567345 0.00011
NM_000038.6(APC):c.4918C>T (p.Arg1640Trp) rs373440614 0.00010
NM_000038.6(APC):c.6679G>T (p.Gly2227Cys) rs367905430 0.00008
NM_000038.6(APC):c.1408+3A>G rs534358523 0.00007
NM_000038.6(APC):c.6473C>G (p.Pro2158Arg) rs587779804 0.00007
NM_000038.6(APC):c.4072G>A (p.Ala1358Thr) rs139618756 0.00006
NM_000038.6(APC):c.8107A>G (p.Lys2703Glu) rs730881270 0.00006
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.449A>G (p.Lys150Arg) rs371085910 0.00004
NM_000038.6(APC):c.4714A>T (p.Ile1572Phe) rs750107668 0.00004
NM_000038.6(APC):c.669A>C (p.Gln223His) rs769482880 0.00004
NM_000038.6(APC):c.6977G>A (p.Arg2326Gln) rs531178000 0.00004
NM_000038.6(APC):c.7402T>C (p.Ser2468Pro) rs375586273 0.00004
NM_000038.6(APC):c.2090C>T (p.Ala697Val) rs761733547 0.00003
NM_000038.6(APC):c.296G>A (p.Arg99Gln) rs199842850 0.00003
NM_000038.6(APC):c.3299C>T (p.Ser1100Phe) rs863224541 0.00003
NM_000038.6(APC):c.70C>T (p.Arg24Ter) rs145945630 0.00003
NM_000038.6(APC):c.7150T>A (p.Leu2384Ile) rs755345693 0.00003
NM_000038.6(APC):c.8234C>T (p.Pro2745Leu) rs759421641 0.00003
NM_000038.6(APC):c.8383G>A (p.Ala2795Thr) rs369264968 0.00003
NM_000038.6(APC):c.2240C>T (p.Ser747Leu) rs773020689 0.00002
NM_000038.6(APC):c.2764C>T (p.Leu922Phe) rs150543576 0.00002
NM_000038.6(APC):c.7105C>T (p.Pro2369Ser) rs377308875 0.00002
NM_000038.6(APC):c.7646G>A (p.Arg2549His) rs199558585 0.00002
NM_000038.6(APC):c.1182G>T (p.Gln394His) rs776197565 0.00001
NM_000038.6(APC):c.1610G>A (p.Ser537Asn) rs1001526630 0.00001
NM_000038.6(APC):c.1829A>G (p.Asp610Gly) rs756090401 0.00001
NM_000038.6(APC):c.2993G>T (p.Gly998Val) rs759579036 0.00001
NM_000038.6(APC):c.319T>G (p.Ser107Ala) rs1485866385 0.00001
NM_000038.6(APC):c.4213G>A (p.Val1405Ile) rs761966904 0.00001
NM_000038.6(APC):c.4898C>T (p.Thr1633Ile) rs765215625 0.00001
NM_000038.6(APC):c.5105G>A (p.Gly1702Glu) rs769273526 0.00001
NM_000038.6(APC):c.5779C>A (p.Leu1927Ile) rs730881253 0.00001
NM_000038.6(APC):c.6700C>T (p.Pro2234Ser) rs749507584 0.00001
NM_000038.6(APC):c.1141G>T (p.Ala381Ser) rs1363425080
NM_000038.6(APC):c.1601A>G (p.Lys534Arg) rs2149813808
NM_000038.6(APC):c.2503T>C (p.Ser835Pro) rs748302469
NM_000038.6(APC):c.2575G>C (p.Gly859Arg) rs919202692
NM_000038.6(APC):c.2651C>T (p.Ala884Val) rs750217875
NM_000038.6(APC):c.2658G>T (p.Gln886His) rs587780593
NM_000038.6(APC):c.2834_2835delinsTT (p.Arg945Ile) rs786204162
NM_000038.6(APC):c.3183_3187del (p.Lys1061_Gln1062insTer) rs587779352
NM_000038.6(APC):c.3462AGA[2] (p.Glu1157del) rs386833391
NM_000038.6(APC):c.3485A>G (p.Tyr1162Cys) rs1289027772
NM_000038.6(APC):c.386A>G (p.Glu129Gly) rs759662717
NM_000038.6(APC):c.4473dup (p.Ala1492fs) rs398123122
NM_000038.6(APC):c.5421CAA[1] (p.Asn1808del) rs587782002
NM_000038.6(APC):c.6627_6629del (p.Ser2210del) rs2149969256
NM_000038.6(APC):c.682A>G (p.Ile228Val) rs1554074757
NM_000038.6(APC):c.7119G>A (p.Met2373Ile)
NM_000038.6(APC):c.7513C>G (p.Arg2505Gly) rs79630786
NM_000038.6(APC):c.7657A>C (p.Lys2553Gln) rs772318413
NM_000038.6(APC):c.7870A>G (p.Asn2624Asp) rs550242704
NM_000038.6(APC):c.7951G>C (p.Val2651Leu) rs1561619590

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.