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.1776dup (p.His593fs)PALB2Pathogenic162364169823641699GGAcriteria provided, single submitter-
DeletionNM_024675.4(PALB2):c.1765_1771del (p.Thr589fs)PALB2Pathogenic162364170423641710GGAGCCGTGcriteria provided, single submitter-
DuplicationNM_024675.4(PALB2):c.1156dup (p.Thr386fs)PALB2Pathogenic162364671023646711GGTcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_024675.4(PALB2):c.1129C>T (p.Gln377Ter)PALB2Pathogenic162364673823646738GAcriteria provided, multiple submitters, no conflicts-
DeletionNM_024675.4(PALB2):c.1042del (p.Gln348fs)PALB2Pathogenic162364682523646825TGTcriteria provided, multiple submitters, no conflicts-
DeletionNM_024675.4(PALB2):c.1037_1038del (p.Lys346fs)PALB2Pathogenic162364682923646830CTTCcriteria provided, single submitter-
single nucleotide variantNM_024675.4(PALB2):c.1010T>A (p.Leu337Ter)PALB2Pathogenic162364685723646857ATcriteria provided, single submitter-
DeletionNM_024675.4(PALB2):c.832del (p.Asp277_Leu278insTer)PALB2Pathogenic162364703523647035AGAcriteria provided, single submitter-
InsertionNM_024675.4(PALB2):c.521_522insCA (p.Lys174fs)PALB2Pathogenic162364734523647346TTTGcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_024675.4(PALB2):c.512T>A (p.Leu171Ter)PALB2Pathogenic162364735523647355ATcriteria provided, single submitter-