Knowledge base for genomic medicine in Japanese
血管型エーラス・ダンロス症候群
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
single nucleotide variantNM_000090.4(COL3A1):c.134G>A (p.Trp45Ter)COL3A1Pathogenic2189849540189849540GAcriteria provided, single submitter-
DeletionNM_000090.4(COL3A1):c.81del (p.Val28fs)COL3A1Pathogenic2189849487189849487CTCcriteria provided, single submitterClinGen:CA16610629
single nucleotide variantNM_000090.4(COL3A1):c.80-1G>CCOL3A1Likely pathogenic2189849485189849485GCcriteria provided, single submitter-
DuplicationNC_000002.11:g.(?_189839196)_(189839314_?)dupCOL3A1Pathogenic2189839196189839314nanacriteria provided, single submitter-
DeletionNC_000002.12:g.(?_188974470)_(189580480_?)delCOL3A1Pathogenic2189839196190445206nanacriteria provided, single submitter-