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.2818del (p.Glu940fs)PALB2Pathogenic162363534623635346TCTcriteria provided, single submitterClinGen:CA658658402
DeletionNM_024675.4(PALB2):c.1704_1707del (p.Lys569fs)PALB2Pathogenic162364176823641771CTTTTCcriteria provided, multiple submitters, no conflictsClinGen:CA658658418
DeletionNM_024675.4(PALB2):c.1565del (p.Pro522fs)PALB2Pathogenic/Likely pathogenic162364630223646302TGTcriteria provided, multiple submitters, no conflictsClinGen:CA645583278
DeletionNM_024675.4(PALB2):c.1490del (p.Asn497fs)PALB2Pathogenic/Likely pathogenic162364637723646377ATAcriteria provided, multiple submitters, no conflictsClinGen:CA658658421
DuplicationNM_024675.4(PALB2):c.442_457dup (p.Arg153fs)PALB2Pathogenic162364740923647410CCTCTTCTGCTGCTTCTTcriteria provided, multiple submitters, no conflictsClinGen:CA658658445
DeletionNM_024675.4(PALB2):c.2915del (p.Leu972fs)PALB2Pathogenic162363437123634371CACcriteria provided, multiple submitters, no conflictsClinGen:CA658658397
single nucleotide variantNM_024675.4(PALB2):c.1702C>T (p.Gln568Ter)PALB2Pathogenic162364177323641773GAcriteria provided, multiple submitters, no conflictsClinGen:CA395128442
DuplicationNM_024675.4(PALB2):c.801_802dup (p.Lys268fs)PALB2Pathogenic/Likely pathogenic162364706423647065TTTAcriteria provided, multiple submitters, no conflictsClinGen:CA658658440
DeletionNM_024675.4(PALB2):c.514_517del (p.Ser172fs)PALB2Pathogenic162364735023647353CCAGACreviewed by expert panelClinGen:CA658658444
single nucleotide variantNM_024675.4(PALB2):c.3165C>G (p.Tyr1055Ter)PALB2Pathogenic162362536123625361GCcriteria provided, multiple submitters, no conflictsClinGen:CA395141266