ClinVar Miner

List of variants in gene APC reported as uncertain significance by 3DMed Clinical Laboratory Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
Download table as spreadsheet
HGVS dbSNP
NM_000038.6(APC):c.10G>C (p.Ala4Pro) rs774219012
NM_000038.6(APC):c.1396A>G (p.Met466Val) rs781364007
NM_000038.6(APC):c.1463T>C (p.Leu488Pro) rs368434773
NM_000038.6(APC):c.1576A>G (p.Met526Val) rs777219286
NM_000038.6(APC):c.1803G>C (p.Glu601Asp) rs1447250546
NM_000038.6(APC):c.1984C>A (p.Leu662Ile) rs756859993
NM_000038.6(APC):c.2190G>A (p.Met730Ile) rs1281171015
NM_000038.6(APC):c.2204C>T (p.Ala735Val) rs147655929
NM_000038.6(APC):c.2414G>A (p.Arg805Gln) rs200593940
NM_000038.6(APC):c.2527A>G (p.Ser843Gly) rs536223189
NM_000038.6(APC):c.2558A>G (p.Glu853Gly) rs1554084263
NM_000038.6(APC):c.2804A>G (p.Tyr935Cys) rs1554084481
NM_000038.6(APC):c.2986A>G (p.Ser996Gly) rs1554084628
NM_000038.6(APC):c.3160C>T (p.His1054Tyr) rs1195583636
NM_000038.6(APC):c.3374T>C (p.Val1125Ala) rs377278397
NM_000038.6(APC):c.3378C>G (p.Ser1126Arg) rs149353082
NM_000038.6(APC):c.3381G>C (p.Gln1127His) rs1554084977
NM_000038.6(APC):c.3511C>T (p.Arg1171Cys) rs201830995
NM_000038.6(APC):c.3716G>A (p.Arg1239Lys) rs754067085
NM_000038.6(APC):c.4297C>T (p.Pro1433Ser) rs1554085738
NM_000038.6(APC):c.4440G>C (p.Gln1480His) rs876659881
NM_000038.6(APC):c.4591A>C (p.Asn1531His) rs771096141
NM_000038.6(APC):c.4658C>T (p.Ala1553Val) rs1554086050
NM_000038.6(APC):c.4687C>G (p.Leu1563Val) rs1554086098
NM_000038.6(APC):c.5026_5028del (p.Arg1676del) rs768369050
NM_000038.6(APC):c.5267C>T (p.Ser1756Phe) rs773178712
NM_000038.6(APC):c.5290C>G (p.Gln1764Glu) rs529543591
NM_000038.6(APC):c.5473G>T (p.Asp1825Tyr) rs1203079846
NM_000038.6(APC):c.5478G>C (p.Lys1826Asn) rs768922376
NM_000038.6(APC):c.5912C>G (p.Ser1971Cys) rs754691867
NM_000038.6(APC):c.6152A>G (p.Lys2051Arg) rs1554087256
NM_000038.6(APC):c.6553A>G (p.Ser2185Gly) rs1060503292
NM_000038.6(APC):c.6893C>T (p.Ala2298Val) rs1554087829
NM_000038.6(APC):c.6994G>A (p.Gly2332Ser) rs1389311736
NM_000038.6(APC):c.7026A>T (p.Leu2342Phe) rs766086022
NM_000038.6(APC):c.7172T>G (p.Ile2391Ser) rs747797803
NM_000038.6(APC):c.7447G>A (p.Val2483Ile) rs1554088371
NM_000038.6(APC):c.757G>A (p.Gly253Ser) rs772806807
NM_000038.6(APC):c.7832C>T (p.Thr2611Ile) rs587778037
NM_000038.6(APC):c.811A>G (p.Met271Val) rs587781464
NM_000038.6(APC):c.8332G>T (p.Ala2778Ser) rs587778046
NM_000038.6(APC):c.8396C>T (p.Ser2799Leu) rs1554089094
NM_000038.6(APC):c.8461G>A (p.Asp2821Asn) rs1554089164
NM_000038.6(APC):c.876G>C (p.Leu292Phe) rs760059672
NM_000038.6(APC):c.95A>G (p.Asn32Ser) rs539108537

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.