Knowledge base for genomic medicine in Japanese
多発性嚢胞腎
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DuplicationNM_138694.4(PKHD1):c.10199dup (p.Met3400fs)PKHD1Likely pathogenic65152472451524725CCAcriteria provided, single submitterClinGen:CA16041028
DeletionNM_138694.4(PKHD1):c.10186_10190del (p.Tyr3396fs)PKHD1Likely pathogenic65152473451524738TTGGTATcriteria provided, single submitterClinGen:CA3851132
DuplicationNM_138694.4(PKHD1):c.10109dup (p.Phe3371fs)PKHD1Pathogenic/Likely pathogenic65160922951609230TTAcriteria provided, multiple submitters, no conflictsClinGen:CA16041029
single nucleotide variantNM_138694.4(PKHD1):c.9901G>T (p.Glu3301Ter)PKHD1Pathogenic/Likely pathogenic65161161651611616CAcriteria provided, multiple submitters, no conflictsClinGen:CA3851295
DuplicationNM_138694.4(PKHD1):c.9856_9859dup (p.Cys3287Ter)PKHD1Likely pathogenic65161165751611658CCAACTcriteria provided, single submitterClinGen:CA16041030
DeletionNM_138694.4(PKHD1):c.9743del (p.Phe3248fs)PKHD1Likely pathogenic65161267151612671GAGcriteria provided, single submitterClinGen:CA3851347
single nucleotide variantNM_138694.4(PKHD1):c.9718C>T (p.Arg3240Ter)PKHD1Pathogenic/Likely pathogenic65161269651612696GAcriteria provided, multiple submitters, no conflictsClinGen:CA16041031
single nucleotide variantNM_138694.4(PKHD1):c.9683C>A (p.Ser3228Ter)PKHD1Pathogenic/Likely pathogenic65161273151612731GTcriteria provided, multiple submitters, no conflictsClinGen:CA16041032
DuplicationNM_138694.4(PKHD1):c.9470_9473dup (p.Met3158fs)PKHD1Likely pathogenic65161294051612941CCATGGcriteria provided, single submitterClinGen:CA16041033
DeletionNM_138694.4(PKHD1):c.8958del (p.Gln2987fs)PKHD1Likely pathogenic65161345651613456GAGcriteria provided, single submitterClinGen:CA16041034