Knowledge base for genomic medicine in Japanese
肥大型心筋症
Excelでダウンロード
表のタイトル行が青色の項目は、クリックすることでソートすることができます。
TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DeletionNM_000256.3(MYBPC3):c.3799del (p.Arg1267fs)MYBPC3Pathogenic114735363847353638CGCcriteria provided, multiple submitters, no conflicts-
DeletionNM_000256.3(MYBPC3):c.3570_3573del (p.Val1192fs)MYBPC3Pathogenic114735417147354174CCGAGCcriteria provided, single submitter-
DuplicationNM_000256.3(MYBPC3):c.2572_2576dup (p.Ser861fs)MYBPC3Pathogenic114735896747358968AAGGGCTcriteria provided, single submitter-
DeletionNM_000256.3(MYBPC3):c.2438del (p.Lys813fs)MYBPC3Pathogenic114735910647359106CTCcriteria provided, single submitter-
DeletionNM_000256.3(MYBPC3):c.1755del (p.Asp587fs)MYBPC3Pathogenic114736357747363577GCGcriteria provided, single submitter-
IndelNM_000256.3(MYBPC3):c.1440_1441delinsC (p.Glu480fs)MYBPC3Pathogenic114736439747364398CCGcriteria provided, single submitter-
DeletionNM_000256.3(MYBPC3):c.1319_1328del (p.Gly440fs)MYBPC3Pathogenic114736459547364604ACACTTCTCGCAcriteria provided, single submitter-
DeletionNM_000256.3(MYBPC3):c.440del (p.Pro147fs)MYBPC3Pathogenic114737163047371630AGAcriteria provided, single submitter-
single nucleotide variantNM_000257.4(MYH7):c.5594A>C (p.Gln1865Pro)MYH7Pathogenic142388327723883277TGcriteria provided, single submitter-
single nucleotide variantNM_000257.4(MYH7):c.4358T>C (p.Leu1453Pro)MYH7Pathogenic142388652323886523AGcriteria provided, single submitter-