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)
single nucleotide variantNM_001009944.3(PKD1):c.12354C>A (p.Tyr4118Ter)PKD1Pathogenic1621403762140376GTcriteria provided, single submitter-
DeletionNM_001009944.3(PKD1):c.11200_11206del (p.Tyr3734fs)PKD1Pathogenic1621425442142550TGGACGTATcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001009944.3(PKD1):c.10724G>A (p.Trp3575Ter)PKD1Pathogenic1621439092143909CTcriteria provided, multiple submitters, no conflicts-
DeletionNM_001009944.3(PKD1):c.10552_10585del (p.Glu3518fs)PKD1Pathogenic1621441262144159TCCCAGTTCAGGCCTGGGCTGGGTGGCCCCAGCTCTcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.10540C>T (p.Gln3514Ter)PKD1Pathogenic1621441712144171GAcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.8590G>T (p.Glu2864Ter)PKD1Pathogenic1621534682153468CAcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.8560C>T (p.Gln2854Ter)PKD1Pathogenic1621534982153498GAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001009944.3(PKD1):c.7987C>T (p.Gln2663Ter)PKD1Pathogenic1621553522155352GAcriteria provided, multiple submitters, no conflicts-
DeletionNM_001009944.3(PKD1):c.7751_7754del (p.Leu2584fs)PKD1Pathogenic1621559752155978TGTGATcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.7666C>T (p.Gln2556Ter)PKD1Pathogenic1621561292156129GAcriteria provided, multiple submitters, no conflicts-