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_000297.4(PKD2):c.603G>A (p.Trp201Ter)PKD2Pathogenic48894061788940617GAcriteria provided, single submitterClinGen:CA357628188
single nucleotide variantNM_000297.4(PKD2):c.596-1G>TPKD2Pathogenic48894060988940609GTcriteria provided, single submitter-
DuplicationNM_000297.4(PKD2):c.538dup (p.Leu180fs)PKD2Pathogenic48892941888929419TTCcriteria provided, single submitter-
DeletionNM_000297.4(PKD2):c.514del (p.Asp172fs)PKD2Pathogenic48892939688929396CGCcriteria provided, multiple submitters, no conflictsClinGen:CA658657391
DeletionNM_000297.4(PKD2):c.481_502del (p.Gly161fs)PKD2Pathogenic48892936288929383ACCAGGGCCCGCCGTGCCCCAGCAcriteria provided, single submitterClinGen:CA645509147
DeletionNM_000297.4(PKD2):c.473del (p.Glu158fs)PKD2Pathogenic48892935888929358GAGcriteria provided, single submitter-
DeletionNM_000297.4(PKD2):c.443del (p.Gly148fs)PKD2Pathogenic48892932688929326CGCcriteria provided, single submitter-
IndelNM_000297.4(PKD2):c.357_364delinsTAGGACG (p.Pro120fs)PKD2Pathogenic48892924288929249CCCGGGCATAGGACGcriteria provided, single submitterClinGen:CA16043405
DuplicationNM_000297.4(PKD2):c.203dup (p.Ala69fs)PKD2Pathogenic48892908288929083AACcriteria provided, multiple submitters, no conflictsClinGen:CA658657390,OMIM:173910.0007
single nucleotide variantNM_000297.4(PKD2):c.181C>T (p.Gln61Ter)PKD2Likely pathogenic48892906688929066CTcriteria provided, single submitter-