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)
DeletionNM_001267550.2(TTN):c.52576_52603del (p.Asn17525_Ala17526insTer)TTNLikely pathogenic2179473007179473034AATAAGCCATCTACATTGGCTTTCAAGGCAcriteria provided, multiple submitters, no conflictsClinGen:CA16610476
single nucleotide variantNM_001267550.2(TTN):c.15496+1G>TTTNPathogenic/Likely pathogenic2179599054179599054CAcriteria provided, multiple submitters, no conflictsClinGen:CA16610517
DeletionNC_000011.10:g.(?_47349774)_(47351505_?)delMYBPC3Pathogenic114737132547373056nanacriteria provided, single submitter-
DeletionNC_000011.10:g.(?_47331845)_(47336011_?)delMYBPC3Pathogenic114735339647357562nanacriteria provided, single submitter-
DeletionNM_000256.3(MYBPC3):c.3665del (p.Gly1222fs)MYBPC3Pathogenic114735377247353772TCTcriteria provided, single submitterClinGen:CA16613340
DeletionNM_000256.3(MYBPC3):c.3617del (p.Gly1206fs)MYBPC3Pathogenic114735412747354127ACAcriteria provided, multiple submitters, no conflictsClinGen:CA16613343
InsertionNM_000256.3(MYBPC3):c.2572_2573insAA (p.Ser858fs)MYBPC3Pathogenic114735897147358972CCTTcriteria provided, single submitterClinGen:CA16613382
DeletionNM_000256.3(MYBPC3):c.2279del (p.Asp760fs)MYBPC3Pathogenic114736010047360100GTGcriteria provided, single submitterClinGen:CA16613383
IndelNM_000256.3(MYBPC3):c.257_259delinsGGAGG (p.Ser86fs)MYBPC3Pathogenic114737282347372825TGGCCTCCcriteria provided, single submitterClinGen:CA16613417
DeletionNC_000012.12:g.(?_110910819)_(110911175_?)delMYL2Pathogenic12111348623111348979nanacriteria provided, single submitter-