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)
DeletionNM_024675.4(PALB2):c.2092del (p.Leu698fs)PALB2Pathogenic162364138323641383AGAcriteria provided, multiple submitters, no conflictsClinGen:CA16609596
DeletionNM_024675.4(PALB2):c.1817_1818del (p.Phe606fs)PALB2Pathogenic162364165723641658GAAGcriteria provided, multiple submitters, no conflictsClinGen:CA16609597
DeletionNM_024675.4(PALB2):c.1591_1592del (p.Leu531fs)PALB2Pathogenic162364627523646276CAACcriteria provided, single submitterClinGen:CA16609598
DuplicationNM_024675.4(PALB2):c.1186dup (p.Cys396fs)PALB2Pathogenic162364668023646681CCAcriteria provided, multiple submitters, no conflictsClinGen:CA16609599
DuplicationNM_024675.4(PALB2):c.1114dup (p.Ser372fs)PALB2Pathogenic162364675223646753CCTcriteria provided, multiple submitters, no conflictsClinGen:CA16609600
DeletionNM_024675.4(PALB2):c.1047_1050del (p.Asn349fs)PALB2Pathogenic162364681723646820TTTGATcriteria provided, single submitterClinGen:CA16609601
single nucleotide variantNM_024675.4(PALB2):c.1039G>T (p.Glu347Ter)PALB2Pathogenic162364682823646828CAcriteria provided, multiple submitters, no conflictsClinGen:CA16609602
DuplicationNM_024675.4(PALB2):c.976dup (p.Ser326fs)PALB2Pathogenic162364689023646891GGAcriteria provided, multiple submitters, no conflictsClinGen:CA16609603
single nucleotide variantNM_024675.4(PALB2):c.931A>T (p.Lys311Ter)PALB2Pathogenic162364693623646936TAcriteria provided, single submitterClinGen:CA16609604
DeletionNM_024675.4(PALB2):c.759del (p.Ser254fs)PALB2Pathogenic/Likely pathogenic162364710823647108ATAcriteria provided, multiple submitters, no conflictsClinGen:CA16609605