Knowledge base for genomic medicine in Japanese
PALB2変異陽性乳がん・膵臓がん
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
InsertionNM_024675.4(PALB2):c.774_775insC (p.Ser259fs)PALB2Likely pathogenic162364709223647093TTGcriteria provided, single submitter-
DeletionNM_024675.4(PALB2):c.770del (p.Gly257fs)PALB2Likely pathogenic162364709723647097ACAcriteria provided, single submitter-
DuplicationNM_024675.4(PALB2):c.502dup (p.Ser168fs)PALB2Pathogenic162364736423647365GGAcriteria provided, multiple submitters, no conflicts-
DeletionNM_024675.4(PALB2):c.204del (p.Lys68fs)PALB2Pathogenic162364917823649178GTGcriteria provided, multiple submitters, no conflicts-
DuplicationNM_024675.4(PALB2):c.117_120dup (p.Ala41fs)PALB2Likely pathogenic162364926123649262CCTCTTcriteria provided, single submitter-
DeletionNM_024675.4(PALB2):c.1725del (p.Ser574_Trp575insTer)PALB2Likely pathogenic162364175023641750TCTcriteria provided, single submitter-
DeletionNM_024675.4(PALB2):c.1103del (p.Asn368fs)PALB2Pathogenic/Likely pathogenic162364676423646764ATAcriteria provided, multiple submitters, no conflicts-
DeletionNM_024675.4(PALB2):c.666_669del (p.Leu222fs)PALB2Likely pathogenic162364719823647201GAATTGcriteria provided, single submitter-
single nucleotide variantNM_024675.4(PALB2):c.475G>T (p.Glu159Ter)PALB2Pathogenic/Likely pathogenic162364739223647392CAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_024675.4(PALB2):c.212-2A>TPALB2Likely pathogenic162364765723647657TAcriteria provided, single submitter-