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_000256.3(MYBPC3):c.2258dup (p.Lys754fs)MYBPC3Pathogenic114736012047360121CCAcriteria provided, multiple submitters, no conflictsClinGen:CA5975367
single nucleotide variantNM_000256.3(MYBPC3):c.1927G>T (p.Glu643Ter)MYBPC3Pathogenic114736255447362554CAcriteria provided, single submitterClinGen:CA380323208
IndelNM_000256.3(MYBPC3):c.1827_1846delinsTACAGC (p.Asp610fs)MYBPC3Pathogenic114736274047362759AGCTGTAGTCAGCCTCGTCGGCTGTAcriteria provided, single submitterClinGen:CA658797629
DeletionNM_000256.3(MYBPC3):c.1570_1594del (p.His524fs)MYBPC3Pathogenic114736415947364183CCCCCGCTAGTGCACAGTGCATAGTGCcriteria provided, multiple submitters, no conflictsClinGen:CA658797633
DeletionNM_000256.3(MYBPC3):c.1483del (p.Arg495fs)MYBPC3Pathogenic114736427047364270CGCcriteria provided, single submitterClinGen:CA658797635
DuplicationNM_000256.3(MYBPC3):c.1103_1107dup (p.Glu370fs)MYBPC3Pathogenic114736515847365159CCCAGCTcriteria provided, multiple submitters, no conflictsClinGen:CA658797638
single nucleotide variantNM_000256.3(MYBPC3):c.660T>G (p.Tyr220Ter)MYBPC3Pathogenic114737008747370087ACcriteria provided, single submitterClinGen:CA380336488
DeletionNM_000256.3(MYBPC3):c.505_505+7delMYBPC3Pathogenic114737155847371565ACACTCACCAcriteria provided, single submitterClinGen:CA658797645
DeletionNM_000256.3(MYBPC3):c.480del (p.Pro161fs)MYBPC3Pathogenic114737159047371590GCGcriteria provided, multiple submitters, no conflictsClinGen:CA658797646
DuplicationNM_000256.3(MYBPC3):c.405dup (p.Gly136fs)MYBPC3Pathogenic114737205347372054CCTcriteria provided, single submitterClinGen:CA658797647