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.2066C>A (p.Ser689Ter)PALB2Pathogenic162364140923641409GTcriteria provided, multiple submitters, no conflictsClinGen:CA10584512
DeletionNM_024675.4(PALB2):c.1714del (p.Ser572fs)PALB2Likely pathogenic162364176123641761GAGcriteria provided, single submitterClinGen:CA10584515
DeletionNM_024675.4(PALB2):c.1538del (p.Thr513fs)PALB2Pathogenic/Likely pathogenic162364632923646329TGTcriteria provided, multiple submitters, no conflictsClinGen:CA10584518
single nucleotide variantNM_024675.4(PALB2):c.472C>T (p.Gln158Ter)PALB2Pathogenic/Likely pathogenic162364739523647395GAcriteria provided, multiple submitters, no conflictsClinGen:CA10584523
DuplicationNM_024675.4(PALB2):c.12dup (p.Pro5fs)PALB2Pathogenic162365246623652467GGAcriteria provided, multiple submitters, no conflictsClinGen:CA10584526
single nucleotide variantNM_024675.4(PALB2):c.1A>G (p.Met1Val)PALB2Likely pathogenic162365247823652478TCcriteria provided, multiple submitters, no conflictsClinGen:CA10584527
DeletionNM_024675.4(PALB2):c.3295_3301del (p.Thr1099fs)PALB2Likely pathogenic162361923423619240AGAGTCGTAcriteria provided, single submitterClinGen:CA10588599
single nucleotide variantNM_024675.4(PALB2):c.3234T>A (p.Cys1078Ter)PALB2Pathogenic/Likely pathogenic162361930123619301ATcriteria provided, multiple submitters, no conflictsClinGen:CA10588601
single nucleotide variantNM_024675.4(PALB2):c.3114-1G>APALB2Likely pathogenic162362541323625413CTcriteria provided, multiple submitters, no conflictsClinGen:CA10588602
DeletionNM_024675.4(PALB2):c.3041_3042del (p.Leu1014fs)PALB2Likely pathogenic162363275423632755TTATcriteria provided, single submitterClinGen:CA10588603