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.2512C>T (p.Gln838Ter)PALB2Pathogenic/Likely pathogenic162364096323640963GAcriteria provided, multiple submitters, no conflictsClinGen:CA395123923
DuplicationNM_024675.4(PALB2):c.2255_2267dup (p.Cys756fs)PALB2Pathogenic162364120723641208GGCAGCAAGTTCGTCcriteria provided, multiple submitters, no conflictsClinGen:CA658658405
DeletionNM_024675.4(PALB2):c.2219_2220del (p.Gln740fs)PALB2Pathogenic162364125523641256CTTCcriteria provided, multiple submitters, no conflictsClinGen:CA658658406
InsertionNM_024675.4(PALB2):c.2160_2161insG (p.Thr721fs)PALB2Pathogenic162364131423641315TTCcriteria provided, single submitterClinGen:CA658658409
DeletionNM_024675.4(PALB2):c.2002del (p.Met668fs)PALB2Pathogenic162364147323641473ATAcriteria provided, single submitterClinGen:CA658658410
DeletionNM_024675.4(PALB2):c.1653del (p.Gln552fs)PALB2Pathogenic162364621423646214GAGcriteria provided, single submitterClinGen:CA658658420
single nucleotide variantNM_024675.4(PALB2):c.1648A>T (p.Lys550Ter)PALB2Pathogenic162364621923646219TAcriteria provided, multiple submitters, no conflictsClinGen:CA395130127
DeletionNM_024675.4(PALB2):c.905del (p.Asn302fs)PALB2Pathogenic162364696223646962GTGcriteria provided, single submitterClinGen:CA658658437
DeletionNM_024675.4(PALB2):c.810_828del (p.Ser270fs)PALB2Pathogenic162364703923647057CGTGAGTAGTAAGTTCACTGCcriteria provided, single submitterClinGen:CA658658439
single nucleotide variantNM_024675.4(PALB2):c.814G>T (p.Glu272Ter)PALB2Pathogenic162364705323647053CAcriteria provided, single submitterClinGen:CA395135986