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)
single nucleotide variantNM_138694.4(PKHD1):c.7486+1G>TPKHD1Likely pathogenic65173530151735301CAcriteria provided, multiple submitters, no conflicts-
DeletionNM_138694.4(PKHD1):c.468del (p.Val155_Tyr156insTer)PKHD1Likely pathogenic65193832051938320CACcriteria provided, single submitter-
DeletionNM_138694.4(PKHD1):c.390+1delPKHD1Pathogenic/Likely pathogenic65194469751944697ACAcriteria provided, multiple submitters, no conflicts-
DeletionNM_138694.4(PKHD1):c.10036_10045del (p.Cys3346fs)PKHD1Pathogenic/Likely pathogenic65160929451609303GGACTTGCACAGcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_138694.4(PKHD1):c.11G>A (p.Trp4Ter)PKHD1Pathogenic/Likely pathogenic65194972151949721CTcriteria provided, multiple submitters, no conflicts-
DeletionNM_138694.4(PKHD1):c.6866-16_6866delPKHD1Likely pathogenic65176852551768541GTCTAATGTTTCAACAAAGcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_138694.4(PKHD1):c.1A>G (p.Met1Val)PKHD1Pathogenic/Likely pathogenic65194973151949731TCcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_138694.4(PKHD1):c.6809-2A>GPKHD1Likely pathogenic65176884251768842TCcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_138694.4(PKHD1):c.6491-1G>APKHD1Likely pathogenic65177427351774273CTcriteria provided, single submitter-
single nucleotide variantNM_138694.4(PKHD1):c.5448T>A (p.Tyr1816Ter)PKHD1Pathogenic/Likely pathogenic65188236051882360ATcriteria provided, multiple submitters, no conflicts-