Knowledge base for genomic medicine in Japanese
家族性膵がん
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DuplicationNM_000059.4(BRCA2):c.403_410dup (p.Ser137_Cys138insTer)BRCA2Pathogenic/Likely pathogenic133289929832899299TTCTAAATTCcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000059.4(BRCA2):c.376C>T (p.Gln126Ter)BRCA2Pathogenic/Likely pathogenic133289927232899272CTcriteria provided, multiple submitters, no conflicts-
DeletionNM_000059.4(BRCA2):c.1846del (p.Cys616fs)BRCA2Pathogenic/Likely pathogenic133290746132907461CTCcriteria provided, multiple submitters, no conflicts-
DeletionNM_000059.4(BRCA2):c.3914_3915del (p.Phe1305fs)BRCA2Pathogenic/Likely pathogenic133291240432912405CTTCcriteria provided, multiple submitters, no conflicts-
DeletionNM_000059.4(BRCA2):c.3937del (p.Tyr1313fs)BRCA2Pathogenic/Likely pathogenic133291242832912428ATAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000059.4(BRCA2):c.4921G>T (p.Glu1641Ter)BRCA2Pathogenic/Likely pathogenic133291341332913413GTcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000059.4(BRCA2):c.7423G>T (p.Glu2475Ter)BRCA2Pathogenic/Likely pathogenic133292941332929413GTcriteria provided, multiple submitters, no conflicts-
DuplicationNM_000059.4(BRCA2):c.7568dup (p.Lys2524fs)BRCA2Pathogenic/Likely pathogenic133293069632930697CCTcriteria provided, multiple submitters, no conflicts-
DeletionNM_000059.4(BRCA2):c.9770_9771del (p.Lys3257fs)BRCA2Pathogenic/Likely pathogenic133297241932972420GAAGcriteria provided, multiple submitters, no conflicts-
InsertionNM_024675.4(PALB2):c.3297_3298insT (p.Thr1100fs)PALB2Pathogenic/Likely pathogenic162361923723619238TTAcriteria provided, multiple submitters, no conflicts-