Knowledge base for genomic medicine in Japanese
皮質下梗塞と白質脳症を伴う常染色体優性脳動脈症
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
single nucleotide variantNM_000435.3(NOTCH3):c.2953C>T (p.Arg985Cys)NOTCH3Pathogenic/Likely pathogenic191529181315291813GAcriteria provided, multiple submitters, no conflictsClinGen:CA404514605
single nucleotide variantNM_000435.3(NOTCH3):c.2956T>G (p.Cys986Gly)NOTCH3Likely pathogenic191529181015291810ACcriteria provided, single submitter-
single nucleotide variantNM_000435.3(NOTCH3):c.2989T>G (p.Cys997Gly)NOTCH3Pathogenic191529177715291777ACcriteria provided, single submitterClinGen:CA404514458
single nucleotide variantNM_000435.3(NOTCH3):c.3011G>A (p.Cys1004Tyr)NOTCH3Pathogenic191529162315291623CTcriteria provided, multiple submitters, no conflictsClinGen:CA404514396
single nucleotide variantNM_000435.3(NOTCH3):c.3016C>T (p.Arg1006Cys)NOTCH3Pathogenic191529161815291618GAcriteria provided, multiple submitters, no conflictsClinGen:CA404514381
single nucleotide variantNM_000435.3(NOTCH3):c.3026G>A (p.Cys1009Tyr)NOTCH3Pathogenic191529160815291608CTcriteria provided, single submitter-
single nucleotide variantNM_000435.3(NOTCH3):c.3040C>T (p.Arg1014Cys)NOTCH3Pathogenic191529159415291594GAcriteria provided, single submitterClinGen:CA404514328
single nucleotide variantNM_000435.3(NOTCH3):c.3062A>G (p.Tyr1021Cys)NOTCH3Pathogenic/Likely pathogenic191529157215291572TCcriteria provided, multiple submitters, no conflictsClinGen:CA404514283
single nucleotide variantNM_000435.3(NOTCH3):c.3065G>T (p.Cys1022Phe)NOTCH3Pathogenic191529156915291569CAcriteria provided, single submitterClinGen:CA404514274
single nucleotide variantNM_000435.3(NOTCH3):c.3091C>T (p.Arg1031Cys)NOTCH3Pathogenic191529154315291543GAcriteria provided, multiple submitters, no conflictsClinGen:CA404514218