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)
single nucleotide variantNM_024675.4(PALB2):c.2630G>A (p.Trp877Ter)PALB2Pathogenic162363767523637675CTcriteria provided, multiple submitters, no conflictsClinGen:CA10579959
IndelNM_024675.4(PALB2):c.2482_2504delinsAAGGTACAAT (p.Cys828fs)PALB2Pathogenic162364097123640993GAATGTTTATGCAGCTCCTGGCAATTGTACCTTcriteria provided, single submitterClinGen:CA10579965
DeletionNM_024675.4(PALB2):c.2488del (p.Glu830fs)PALB2Pathogenic162364098723640987TCTcriteria provided, multiple submitters, no conflictsClinGen:CA10579966
DeletionNM_024675.4(PALB2):c.2470del (p.Cys824fs)PALB2Pathogenic162364100523641005CACcriteria provided, multiple submitters, no conflictsClinGen:CA10579969
DuplicationNM_024675.4(PALB2):c.2325dup (p.Phe776fs)PALB2Pathogenic162364114923641150AATcriteria provided, multiple submitters, no conflictsClinGen:CA10579974
DeletionNM_024675.4(PALB2):c.2296_2297del (p.Val767fs)PALB2Pathogenic162364117823641179TGATcriteria provided, multiple submitters, no conflictsClinGen:CA10579975
DeletionNM_024675.4(PALB2):c.2288_2291del (p.His762_Leu763insTer)PALB2Pathogenic/Likely pathogenic162364118423641187TTTCATcriteria provided, multiple submitters, no conflictsClinGen:CA10579976
DeletionNM_024675.4(PALB2):c.2280del (p.Ala761fs)PALB2Pathogenic162364119523641195CACcriteria provided, single submitterClinGen:CA10579977
DeletionNM_024675.4(PALB2):c.2156del (p.Pro719fs)PALB2Pathogenic/Likely pathogenic162364131923641319AGAcriteria provided, multiple submitters, no conflictsClinGen:CA10579983
InsertionNM_024675.4(PALB2):c.2142_2143insTAA (p.Asp715Ter)PALB2Pathogenic162364133223641333CCTTAcriteria provided, single submitterClinGen:CA10579984