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)
DuplicationNM_024675.4(PALB2):c.734_735dup (p.Thr246fs)PALB2Pathogenic162364713123647132TTCGcriteria provided, single submitterClinGen:CA7963765
DeletionNM_024675.4(PALB2):c.232del (p.Val78fs)PALB2Pathogenic162364763523647635ACAcriteria provided, single submitterClinGen:CA658658448
single nucleotide variantNM_024675.4(PALB2):c.48+1G>APALB2Likely pathogenic162365243023652430CTcriteria provided, multiple submitters, no conflictsClinGen:CA395140998
DeletionNM_024675.4(PALB2):c.2456_2463del (p.Lys819fs)PALB2Pathogenic/Likely pathogenic162364101223641019GATTTTCTTGcriteria provided, multiple submitters, no conflictsClinGen:CA658658404
DeletionNM_024675.4(PALB2):c.1485del (p.Asp496fs)PALB2Pathogenic/Likely pathogenic162364638223646382CTCcriteria provided, multiple submitters, no conflictsClinGen:CA658658422
single nucleotide variantNM_024675.4(PALB2):c.866T>A (p.Leu289Ter)PALB2Pathogenic/Likely pathogenic162364700123647001ATcriteria provided, multiple submitters, no conflictsClinGen:CA395135804
DeletionNM_024675.4(PALB2):c.620del (p.Pro207fs)PALB2Pathogenic/Likely pathogenic162364724723647247TGTcriteria provided, multiple submitters, no conflictsClinGen:CA658658443
DeletionNM_024675.4(PALB2):c.444del (p.Lys149fs)PALB2Pathogenic/Likely pathogenic162364742323647423TCTcriteria provided, multiple submitters, no conflictsClinGen:CA658658447
single nucleotide variantNM_024675.4(PALB2):c.3067C>T (p.Gln1023Ter)PALB2Pathogenic/Likely pathogenic162363272923632729GAcriteria provided, multiple submitters, no conflictsClinGen:CA395142961
DuplicationNM_024675.4(PALB2):c.1546dup (p.Arg516fs)PALB2Pathogenic162364632023646321CCTcriteria provided, multiple submitters, no conflictsClinGen:CA658683909