Knowledge base for genomic medicine in Japanese
家族性大腸腺腫症
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DeletionNM_000038.6(APC):c.8047del (p.Ile2683fs)APCPathogenic5112179338112179338GAGcriteria provided, single submitterClinGen:CA645369385
DeletionNM_000038.6(APC):c.7959_7962del (p.Thr2654fs)APCPathogenic/Likely pathogenic5112179249112179252AAAACAcriteria provided, multiple submitters, no conflicts-
DeletionNM_000038.6(APC):c.7960del (p.Thr2654fs)APCPathogenic5112179248112179248TATcriteria provided, single submitterClinGen:CA562217625
DeletionNM_000038.6(APC):c.7946_7955del (p.Pro2649fs)APCPathogenic5112179236112179245ACCTGCTGTTTAcriteria provided, single submitter-
DeletionNM_000038.6(APC):c.7932_7935del (p.Tyr2645fs)APCPathogenic5112179221112179224AATTTAcriteria provided, multiple submitters, no conflictsClinGen:CA658657465
DeletionNM_000038.6(APC):c.7931_7937del (p.Ile2644fs)APCPathogenic5112179221112179227AATTTATCAcriteria provided, multiple submitters, no conflictsClinGen:CA10588389
DeletionNM_000038.6(APC):c.7930_7934del (p.Ile2644fs)APCPathogenic5112179219112179223CTAATTCcriteria provided, multiple submitters, no conflicts-
DeletionNM_000038.6(APC):c.7891del (p.Ser2631fs)APCLikely pathogenic5112179180112179180GTGcriteria provided, single submitter-
DeletionNM_000038.6(APC):c.7803_7807del (p.Ser2601fs)APCPathogenic/Likely pathogenic5112179090112179094CAAAGTCcriteria provided, multiple submitters, no conflicts-
DeletionNM_000038.6(APC):c.7744del (p.Glu2582fs)APCPathogenic5112179035112179035TGTcriteria provided, single submitterClinGen:CA658657464