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.695del (p.Gly232fs)PALB2Pathogenic162364717223647172ACAcriteria provided, multiple submitters, no conflictsClinGen:CA16615300
DeletionNM_024675.4(PALB2):c.2878del (p.Leu960fs)PALB2Pathogenic/Likely pathogenic162363440823634408AGAcriteria provided, multiple submitters, no conflictsClinGen:CA16620122
DeletionNM_024675.4(PALB2):c.2634_2635del (p.Arg879fs)PALB2Pathogenic/Likely pathogenic162363767023637671CTTCcriteria provided, multiple submitters, no conflictsClinGen:CA16620128
DeletionNM_024675.4(PALB2):c.2275del (p.Gln759fs)PALB2Pathogenic162364120023641200TGTcriteria provided, single submitterClinGen:CA16620136
DeletionNM_024675.4(PALB2):c.1465del (p.Ser489fs)PALB2Pathogenic162364640223646402GAGcriteria provided, single submitterClinGen:CA16620144
DuplicationNM_024675.4(PALB2):c.1163dup (p.Leu389fs)PALB2Pathogenic/Likely pathogenic162364670323646704AAGcriteria provided, multiple submitters, no conflictsClinGen:CA16620152
InsertionNM_024675.4(PALB2):c.1067_1068insTA (p.Lys356fs)PALB2Pathogenic162364679923646800TTTAcriteria provided, multiple submitters, no conflictsClinGen:CA16620153
DeletionNM_024675.4(PALB2):c.548del (p.Ser183fs)PALB2Pathogenic/Likely pathogenic162364731923647319ACAcriteria provided, multiple submitters, no conflictsClinGen:CA16620159
single nucleotide variantNM_024675.4(PALB2):c.163C>T (p.Gln55Ter)PALB2Pathogenic162364921923649219GAcriteria provided, multiple submitters, no conflictsClinGen:CA16620162
DuplicationNM_024675.3(PALB2):c.1724dup (p.Ser576Glufs)PALB2Pathogenic/Likely pathogenic162364174923641750TTCcriteria provided, multiple submitters, no conflictsClinGen:CA645509224