ClinVar Miner

List of variants in gene APC reported as pathogenic by Quest Diagnostics Nichols Institute San Juan Capistrano

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP
NM_000038.6(APC):c.1213C>T (p.Arg405Ter) rs587779780
NM_000038.6(APC):c.1333C>T (p.Gln445Ter) rs876658802
NM_000038.6(APC):c.1626+1G>A rs1554081934
NM_000038.6(APC):c.1690C>T (p.Arg564Ter) rs137854574
NM_000038.6(APC):c.1958+3A>G rs879254032
NM_000038.6(APC):c.2008_2014delinsTAGTTTTGTA (p.Lys670_His672delinsTer) rs1554083888
NM_000038.6(APC):c.2031_2034del (p.Ser678fs) rs878853422
NM_000038.6(APC):c.2107del (p.Ala703fs) rs587783030
NM_000038.6(APC):c.2621C>G (p.Ser874Ter) rs1554084318
NM_000038.6(APC):c.2795C>A (p.Ser932Ter) rs878853432
NM_000038.6(APC):c.2802_2805del (p.Tyr935fs) rs1131691143
NM_000038.6(APC):c.2805C>A (p.Tyr935Ter) rs137854575
NM_000038.6(APC):c.288T>A (p.Tyr96Ter) rs376213437
NM_000038.6(APC):c.3149del (p.Ala1050fs) rs730882135
NM_000038.6(APC):c.3164_3168del (p.Ile1055fs) rs1554084772
NM_000038.6(APC):c.3183_3187del (p.Lys1061_Gln1062insTer) rs587779352
NM_000038.6(APC):c.3211C>T (p.Gln1071Ter) rs876659539
NM_000038.6(APC):c.3810T>A (p.Cys1270Ter) rs863225347
NM_000038.6(APC):c.3922_3926AAAGA[1] (p.Glu1309fs) rs121913224
NM_000038.6(APC):c.426_427del (p.Leu143fs) rs587782557
NM_000038.6(APC):c.5038C>T (p.Gln1680Ter) rs754122018
NM_000038.6(APC):c.5822_5825CAGA[1] (p.Asp1942fs) rs864622228
NM_000038.6(APC):c.583C>T (p.Gln195Ter) rs749479682
NM_000038.6(APC):c.636dup (p.Arg213fs) rs1561485947
NM_000038.6(APC):c.646C>T (p.Arg216Ter) rs62619935
NM_000038.6(APC):c.6496C>T (p.Arg2166Ter) rs764527706
NM_000038.6(APC):c.694C>T (p.Arg232Ter) rs397515734
NM_000038.6(APC):c.894_895CT[1] (p.Ser299fs) rs397515735
NM_000038.6(APC):c.904C>T (p.Arg302Ter) rs137854568
NM_000038.6(APC):c.994C>T (p.Arg332Ter) rs775126020

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