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_000256.3(MYBPC3):c.2894_2905+4delMYBPC3Pathogenic114735658947356604CTCACGCAGGATCTCCTCcriteria provided, single submitterClinGen:CA296494
single nucleotide variantNM_000256.3(MYBPC3):c.2893C>T (p.Gln965Ter)MYBPC3Pathogenic114735660547356605GAcriteria provided, multiple submitters, no conflictsClinGen:CA013116
DuplicationNM_000256.3(MYBPC3):c.2792dup (p.Lys932fs)MYBPC3Pathogenic114735670547356706CCAcriteria provided, single submitterClinGen:CA296493
single nucleotide variantNM_000256.3(MYBPC3):c.2748G>A (p.Trp916Ter)MYBPC3Pathogenic/Likely pathogenic114735675047356750CTcriteria provided, multiple submitters, no conflictsClinGen:CA012943
DeletionNM_000256.3(MYBPC3):c.2744del (p.Glu915fs)MYBPC3Pathogenic114735675447356754CTCcriteria provided, single submitterClinGen:CA012927
DeletionNM_000256.3(MYBPC3):c.2739del (p.Ser914fs)MYBPC3Likely pathogenic114735675947356759AGAcriteria provided, single submitterClinGen:CA012918
DeletionNM_000256.3(MYBPC3):c.2737del (p.Cys913fs)MYBPC3Pathogenic114735742847357428CACcriteria provided, single submitterClinGen:CA012912
DeletionNM_000256.3(MYBPC3):c.2709_2719del (p.Tyr904fs)MYBPC3Pathogenic114735744647357456TCCACGCTGTAGTcriteria provided, multiple submitters, no conflictsClinGen:CA012846
DeletionNM_000256.3(MYBPC3):c.2610del (p.Ser871fs)MYBPC3Pathogenic/Likely pathogenic114735755547357555TGTcriteria provided, multiple submitters, no conflictsClinGen:CA012712
DeletionNM_000256.3(MYBPC3):c.2604del (p.Ser871fs)MYBPC3Pathogenic114735756147357561GAGcriteria provided, multiple submitters, no conflictsClinGen:CA012697