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.223A>T (p.Lys75Ter)PALB2Pathogenic162364764423647644TAcriteria provided, multiple submitters, no conflictsClinGen:CA395138968
DeletionNM_024675.4(PALB2):c.226del (p.Ile76fs)PALB2Pathogenic/Likely pathogenic162364764123647641ATAcriteria provided, multiple submitters, no conflictsClinGen:CA294388
DeletionNM_024675.4(PALB2):c.229del (p.Cys77fs)PALB2Pathogenic162364763823647638CACcriteria provided, multiple submitters, no conflictsClinGen:CA331794
DeletionNM_024675.4(PALB2):c.232del (p.Val78fs)PALB2Pathogenic162364763523647635ACAcriteria provided, single submitterClinGen:CA658658448
DuplicationNM_024675.4(PALB2):c.274dup (p.Thr92fs)PALB2Pathogenic162364759223647593GGTcriteria provided, single submitter-
DuplicationNM_024675.4(PALB2):c.284dup (p.Thr96fs)PALB2Pathogenic162364758223647583CCTcriteria provided, single submitterClinGen:CA16614875
DeletionNM_024675.4(PALB2):c.338del (p.Pro113fs)PALB2Pathogenic162364752923647529TGTcriteria provided, single submitterClinGen:CA658798564
single nucleotide variantNM_024675.4(PALB2):c.347T>A (p.Leu116Ter)PALB2Pathogenic162364752023647520ATcriteria provided, multiple submitters, no conflictsClinGen:CA10580044
DeletionNM_024675.4(PALB2):c.355del (p.Gln119fs)PALB2Pathogenic162364751223647512TGTcriteria provided, multiple submitters, no conflictsClinGen:CA16615125
DeletionNM_024675.4(PALB2):c.395del (p.Val132fs)PALB2Pathogenic162364747223647472GAGcriteria provided, multiple submitters, no conflictsClinGen:CA269628