Knowledge base for genomic medicine in Japanese
肥大型心筋症
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DuplicationNM_001267550.2(TTN):c.71202dup (p.Lys23735fs)TTNPathogenic/Likely pathogenic2179439656179439657TTGcriteria provided, multiple submitters, no conflictsClinGen:CA430257756
DeletionNM_001267550.2(TTN):c.60902del (p.Ser20301fs)TTNLikely pathogenic2179455550179455550ACAcriteria provided, multiple submitters, no conflictsClinGen:CA658657141
DeletionNM_001267550.2(TTN):c.57849del (p.Val19284fs)TTNLikely pathogenic2179459372179459372CACcriteria provided, multiple submitters, no conflictsClinGen:CA1992974
single nucleotide variantNM_000256.3(MYBPC3):c.2738-1G>AMYBPC3Likely pathogenic114735676147356761CTcriteria provided, single submitterClinGen:CA380316885
single nucleotide variantNM_000256.3(MYBPC3):c.2526C>A (p.Tyr842Ter)MYBPC3Pathogenic114735901847359018GTcriteria provided, multiple submitters, no conflictsClinGen:CA380318189
single nucleotide variantNM_000256.3(MYBPC3):c.2067+1G>AMYBPC3Pathogenic114736120147361201CTcriteria provided, multiple submitters, no conflictsClinGen:CA380321286
single nucleotide variantNM_000257.4(MYH7):c.1052A>C (p.Lys351Thr)MYH7Likely pathogenic142389907023899070TGcriteria provided, multiple submitters, no conflictsClinGen:CA389051463
single nucleotide variantNM_020778.5(ALPK3):c.2407C>T (p.Gln803Ter)ALPK3Likely pathogenic158540037685400376CTcriteria provided, single submitterClinGen:CA393357038
single nucleotide variantNM_001276345.2(TNNT2):c.565T>G (p.Ser189Ala)TNNT2Likely pathogenic1201332459201332459ACcriteria provided, single submitterClinGen:CA35420183
DeletionNM_001267550.2(TTN):c.99588_99595del (p.Phe33196fs)TTNLikely pathogenic2179402339179402346CCAGGATGGCcriteria provided, single submitterClinGen:CA658657126