Knowledge base for genomic medicine in Japanese
多発性嚢胞腎
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_138694.4(PKHD1):c.11330del (p.Leu3777fs)PKHD1Likely pathogenic65151289751512897CACcriteria provided, single submitter-
DeletionNM_138694.4(PKHD1):c.11276del (p.Pro3759fs)PKHD1Likely pathogenic65151391751513917TGTcriteria provided, single submitter-
DeletionNM_138694.4(PKHD1):c.10856del (p.Lys3619fs)PKHD1Pathogenic65152406851524068CTCcriteria provided, multiple submitters, no conflicts-
DeletionNM_138694.4(PKHD1):c.10852del (p.Arg3618fs)PKHD1Pathogenic/Likely pathogenic65152407251524072CTCcriteria provided, multiple submitters, no conflicts-
IndelNM_138694.4(PKHD1):c.10086_10087delinsC (p.Gly3363fs)PKHD1Likely pathogenic65160925251609253CCGcriteria provided, multiple submitters, no conflicts-
DuplicationNM_138694.4(PKHD1):c.8677dup (p.His2893fs)PKHD1Pathogenic/Likely pathogenic65161970151619702TTGcriteria provided, multiple submitters, no conflicts-
DeletionNM_138694.4(PKHD1):c.5909-2delPKHD1Pathogenic/Likely pathogenic65179912251799122CTCcriteria provided, multiple submitters, no conflicts-
DuplicationNM_138694.4(PKHD1):c.5688_5691dup (p.Asn1898fs)PKHD1Likely pathogenic65187516651875167TTGGGCcriteria provided, single submitter-
single nucleotide variantNM_138694.4(PKHD1):c.5323C>T (p.Arg1775Ter)PKHD1Pathogenic65188765651887656GAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_138694.4(PKHD1):c.5237-2A>CPKHD1Likely pathogenic65188774451887744TGcriteria provided, single submitter-