Knowledge base for genomic medicine in Japanese
網膜芽細胞腫
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DeletionNM_000321.3(RB1):c.1024del (p.Thr342fs)RB1Pathogenic134894171148941711TATcriteria provided, single submitterClinGen:CA026358
single nucleotide variantNM_000321.3(RB1):c.1049+1G>ARB1Pathogenic/Likely pathogenic134894174048941740GAcriteria provided, multiple submitters, no conflictsClinGen:CA026360
single nucleotide variantNM_000321.3(RB1):c.1216-1G>ARB1Pathogenic134895105348951053GAcriteria provided, single submitterClinGen:CA026368
single nucleotide variantNM_000321.3(RB1):c.1332+1G>ARB1Pathogenic134895117148951171GAcriteria provided, multiple submitters, no conflictsClinGen:CA026369
single nucleotide variantNM_000321.3(RB1):c.1363C>T (p.Arg455Ter)RB1Pathogenic134895376048953760CTcriteria provided, multiple submitters, no conflictsClinGen:CA026373
DeletionNM_000321.3(RB1):c.1456_1457del (p.Leu486fs)RB1Pathogenic134895433448954335CTTCcriteria provided, single submitterClinGen:CA026378
single nucleotide variantNM_000321.3(RB1):c.1654C>T (p.Arg552Ter)RB1Pathogenic134895553848955538CTcriteria provided, multiple submitters, no conflictsClinGen:CA026383
DeletionNM_000321.3(RB1):c.1421+12_1421+32delRB1Likely pathogenic134895422348954243TAAATTTTTTACTTTTAGTAAATcriteria provided, single submitterClinGen:CA269950
DeletionNM_000321.3(RB1):c.54_79del (p.Glu19fs)RB1Pathogenic134887809448878119TGCCGCCGCGGAACCCCCGGCACCGCCTcriteria provided, multiple submitters, no conflictsClinGen:CA026461
DeletionNM_000321.3(RB1):c.1191del (p.Glu398fs)RB1Pathogenic134894760448947604CACcriteria provided, multiple submitters, no conflictsClinGen:CA026366