Knowledge base for genomic medicine in Japanese
ポイツ・イェガース症候群
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DeletionNM_000455.5(STK11):c.199del (p.Leu67fs)STK11Pathogenic/Likely pathogenic1912071111207111GCGcriteria provided, multiple submitters, no conflictsClinGen:CA645509244
DeletionNM_000455.5(STK11):c.727del (p.Val243fs)STK11Pathogenic1912207061220706TGTcriteria provided, multiple submitters, no conflictsClinGen:CA658653695
DuplicationNM_000455.5(STK11):c.179_180dup (p.Gly61fs)STK11Pathogenic1912070901207091TTACcriteria provided, single submitterClinGen:CA658656742
DeletionNM_000455.5(STK11):c.884_888del (p.Ala295fs)STK11Pathogenic1912219681221972GGCCAAGcriteria provided, single submitterClinGen:CA658656766
DeletionNC_000019.9:g.(?_1219317)_(1221345_?)delSTK11Pathogenic1912193171221345nanacriteria provided, single submitter-
DuplicationNM_000455.5(STK11):c.525_532dup (p.Lys178fs)STK11Pathogenic1912204301220431AAAGGACATCcriteria provided, single submitterClinGen:CA658656745
DeletionNM_000455.5(STK11):c.290+1_290+7delSTK11Likely pathogenic1912072021207208AAGTAAGTAcriteria provided, single submitterClinGen:CA658656744
DeletionNM_000455.5(STK11):c.816del (p.Ser271_Tyr272insTer)STK11Pathogenic1912212931221293ACAcriteria provided, single submitterClinGen:CA658656758
DeletionNM_000455.5(STK11):c.357del (p.Asn119fs)STK11Pathogenic1912184821218482ACAcriteria provided, single submitterClinGen:CA658656740
DeletionNM_000455.5(STK11):c.67del (p.Asp23fs)STK11Pathogenic1912069781206978TGTcriteria provided, single submitterClinGen:CA658656738