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)
DeletionNM_001009944.3(PKD1):c.12044_12068del (p.Phe4015fs)PKD1Likely pathogenic1621407452140769CAGAGCTCGGCATAATGTCTTGCCAACcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.12061C>T (p.Arg4021Ter)PKD1Pathogenic1621407522140752GAcriteria provided, multiple submitters, no conflicts-
DuplicationNM_001009944.3(PKD1):c.11921_11942dup (p.Ala3981_Gln3982insHisTer)PKD1Likely pathogenic1621409452140946CCGCCACCTGGTCGAAGCTAGTGAcriteria provided, single submitter-
DuplicationNM_001009944.3(PKD1):c.11563dup (p.Thr3855fs)PKD1Likely pathogenic1621415722141573GGTcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.11390A>G (p.Tyr3797Cys)PKD1Likely pathogenic1621420692142069TCcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.11122G>T (p.Glu3708Ter)PKD1Likely pathogenic1621429892142989CAcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.10377C>G (p.Tyr3459Ter)PKD1Likely pathogenic1621473482147348GCcriteria provided, single submitter-
DeletionNM_001009944.3(PKD1):c.10247del (p.Gly3416fs)PKD1Likely pathogenic1621474782147478TCTcriteria provided, single submitter-
DeletionNM_001009944.3(PKD1):c.9826_9829del (p.Thr3276fs)PKD1Likely pathogenic1621499562149959CGAGTCcriteria provided, single submitter-
single nucleotide variantNM_001009944.3(PKD1):c.9431G>C (p.Gly3144Ala)PKD1Likely pathogenic1621505342150534CGcriteria provided, single submitter-