Knowledge base for genomic medicine in Japanese
PALB2変異陽性乳がん・膵臓がん
腫瘍性疾患
Excelでダウンロード
表のタイトル行が青色の項目は、クリックすることでソートすることができます。
TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DeletionNM_024675.4(PALB2):c.2727_2728del (p.Thr911fs)PALB2Pathogenic/Likely pathogenic162363757723637578TAATcriteria provided, multiple submitters, no conflictsClinGen:CA299664
DuplicationNM_024675.4(PALB2):c.2642_2645dup (p.Cys882fs)PALB2Pathogenic162363765923637660AACAACcriteria provided, multiple submitters, no conflictsClinGen:CA299663
single nucleotide variantNM_024675.4(PALB2):c.2229T>A (p.Tyr743Ter)PALB2Pathogenic/Likely pathogenic162364124623641246ATcriteria provided, multiple submitters, no conflictsClinGen:CA299725
DeletionNM_024675.4(PALB2):c.2154del (p.Arg718fs)PALB2Pathogenic162364132123641321GCGcriteria provided, single submitterClinGen:CA299662
DeletionNM_024675.4(PALB2):c.2032del (p.Leu678fs)PALB2Pathogenic162364144323641443AGAcriteria provided, multiple submitters, no conflictsClinGen:CA299661
DeletionNM_024675.4(PALB2):c.1924del (p.Met642fs)PALB2Pathogenic/Likely pathogenic162364155123641551ATAcriteria provided, multiple submitters, no conflictsClinGen:CA299660
single nucleotide variantNM_024675.4(PALB2):c.1724G>A (p.Trp575Ter)PALB2Pathogenic/Likely pathogenic162364175123641751CTcriteria provided, multiple submitters, no conflictsClinGen:CA299691
DeletionNM_024675.4(PALB2):c.1059del (p.Lys353fs)PALB2Pathogenic162364680823646808ATAcriteria provided, multiple submitters, no conflictsClinGen:CA299667
DeletionNM_024675.4(PALB2):c.948del (p.Thr317fs)PALB2Pathogenic162364691923646919TGTcriteria provided, multiple submitters, no conflictsClinGen:CA299666
DeletionNM_024675.4(PALB2):c.786del (p.Glu263fs)PALB2Pathogenic162364708123647081CACcriteria provided, multiple submitters, no conflictsClinGen:CA299665