ClinVar Miner

List of variants in gene APC reported as uncertain significance by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
Download table as spreadsheet
HGVS dbSNP
NM_000038.5(APC):c.1240C>T (p.Arg414Cys) rs137854567
NM_000038.5(APC):c.1462C>T (p.Leu488Phe) rs587779782
NM_000038.5(APC):c.1498T>C (p.Tyr500His) rs762019672
NM_000038.5(APC):c.1589T>C (p.Val530Ala) rs202199891
NM_000038.5(APC):c.1604C>T (p.Ser535Phe) rs75870842
NM_000038.5(APC):c.1631T>C (p.Ile544Thr) rs144056494
NM_000038.5(APC):c.1685C>T (p.Thr562Met) rs587783034
NM_000038.5(APC):c.1829A>G (p.Asp610Gly) rs756090401
NM_000038.5(APC):c.1904G>C (p.Gly635Ala) rs730881239
NM_000038.5(APC):c.1984C>A (p.Leu662Ile) rs756859993
NM_000038.5(APC):c.2819C>G (p.Ser940Trp) rs544709767
NM_000038.5(APC):c.295C>T (p.Arg99Trp) rs139196838
NM_000038.5(APC):c.3161A>C (p.His1054Pro) rs777538550
NM_000038.5(APC):c.317G>A (p.Arg106His) rs201764637
NM_000038.5(APC):c.3365A>G (p.Asn1122Ser) rs372855304
NM_000038.5(APC):c.3479C>A (p.Thr1160Lys) rs201004111
NM_000038.5(APC):c.4100A>G (p.Gln1367Arg) rs1399790840
NM_000038.5(APC):c.4101G>C (p.Gln1367His) rs761886683
NM_000038.5(APC):c.4237A>G (p.Met1413Val) rs141519952
NM_000038.5(APC):c.4424C>T (p.Ala1475Val) rs375380414
NM_000038.5(APC):c.449A>G (p.Lys150Arg) rs371085910
NM_000038.5(APC):c.4540C>T (p.Pro1514Ser) rs1060503266
NM_000038.5(APC):c.4546A>G (p.Ile1516Val) rs1554085952
NM_000038.5(APC):c.4885C>G (p.His1629Asp) rs765849654
NM_000038.5(APC):c.5201A>C (p.Lys1734Thr) rs1204161988
NM_000038.5(APC):c.5392A>G (p.Asn1798Asp) rs200794097
NM_000038.5(APC):c.5528C>T (p.Pro1843Leu) rs368080169
NM_000038.5(APC):c.5585_5586insT (p.Leu1862Phefs) rs1554086823
NM_000038.5(APC):c.5645G>C (p.Arg1882Thr) rs34157245
NM_000038.5(APC):c.5801C>T (p.Pro1934Leu) rs587780600
NM_000038.5(APC):c.5866A>G (p.Ile1956Val) rs749597014
NM_000038.5(APC):c.5912C>G (p.Ser1971Cys) rs754691867
NM_000038.5(APC):c.592G>A (p.Val198Ile) rs1168791940
NM_000038.5(APC):c.6040G>A (p.Val2014Ile) rs143313902
NM_000038.5(APC):c.638G>A (p.Arg213Gln) rs1235428754
NM_000038.5(APC):c.6434G>T (p.Gly2145Val) rs1554087422
NM_000038.5(APC):c.6473C>G (p.Pro2158Arg) rs587779804
NM_000038.5(APC):c.6512G>A (p.Gly2171Glu) rs748745776
NM_000038.5(APC):c.6658A>G (p.Asn2220Asp) rs374464049
NM_000038.5(APC):c.6679G>T (p.Gly2227Cys) rs367905430
NM_000038.5(APC):c.6873A>T (p.Gln2291His) rs148878262
NM_000038.5(APC):c.7289A>C (p.Asp2430Ala) rs1554088226
NM_000038.5(APC):c.7399C>A (p.Pro2467Thr) rs372305287
NM_000038.5(APC):c.7498C>G (p.Gln2500Glu) rs372535376
NM_000038.5(APC):c.7717A>G (p.Ile2573Val) rs145444830
NM_000038.5(APC):c.811A>T (p.Met271Leu) rs587781464
NM_000038.5(APC):c.8181G>C (p.Gln2727His) rs756467505
NM_000038.5(APC):c.8383G>A (p.Ala2795Thr) rs369264968
NM_000038.5(APC):c.933+5C>A rs573528468
NM_000038.5(APC):c.942G>T (p.Met314Ile) rs1350080370
NM_001127511.2(APC):c.137C>T (p.Thr46Ile) rs1016971418

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.