Knowledge base for genomic medicine in Japanese
家族性膵がん
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DeletionNM_024675.4(PALB2):c.2936del (p.Ser979fs)PALB2Pathogenic162363435023634350ACAcriteria provided, multiple submitters, no conflictsClinGen:CA16614818
DeletionNM_024675.4(PALB2):c.2056del (p.Arg686fs)PALB2Pathogenic162364141923641419CTCcriteria provided, single submitterClinGen:CA16614833
DeletionNM_024675.4(PALB2):c.1742del (p.Leu581fs)PALB2Pathogenic162364173323641733TATcriteria provided, single submitterClinGen:CA16614842
single nucleotide variantNM_024675.4(PALB2):c.1553C>G (p.Ser518Ter)PALB2Pathogenic162364631423646314GCcriteria provided, multiple submitters, no conflictsClinGen:CA16614852
single nucleotide variantNM_024675.4(PALB2):c.2749-1G>CPALB2Likely pathogenic162363541623635416CGcriteria provided, multiple submitters, no conflictsClinGen:CA16614853
single nucleotide variantNM_024675.4(PALB2):c.2730T>A (p.Tyr910Ter)PALB2Pathogenic/Likely pathogenic162363757523637575ATcriteria provided, multiple submitters, no conflictsClinGen:CA16614856
DeletionNC_000016.10:g.(?_23603162)_(23641357_?)delPALB2Pathogenic162361448323652678nanacriteria provided, single submitter-
DeletionNM_024675.4(PALB2):c.953_954del (p.Ser318fs)PALB2Pathogenic162364691323646914AACAcriteria provided, multiple submitters, no conflictsClinGen:CA16614862
DeletionNC_000016.10:g.(?_23624009)_(23624094_?)delPALB2Pathogenic162363533023635415nanacriteria provided, single submitter-
DuplicationNM_024675.4(PALB2):c.886dup (p.Met296fs)PALB2Pathogenic162364698023646981AATcriteria provided, multiple submitters, no conflictsClinGen:CA16614863