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)
single nucleotide variantNM_001267550.2(TTN):c.2089A>T (p.Lys697Ter)TTNLikely pathogenic2179650856179650856TAcriteria provided, single submitterClinGen:CA349502198
DeletionNM_000256.3(MYBPC3):c.3627+2delMYBPC3Pathogenic114735411547354115TATcriteria provided, multiple submitters, no conflictsClinGen:CA658797619
single nucleotide variantNM_000256.3(MYBPC3):c.3491-2A>CMYBPC3Likely pathogenic114735425547354255TGcriteria provided, single submitterClinGen:CA380312951
single nucleotide variantNM_000256.3(MYBPC3):c.3331-1G>CMYBPC3Pathogenic/Likely pathogenic114735452547354525CGcriteria provided, multiple submitters, no conflictsClinGen:CA380313881
single nucleotide variantNM_000256.3(MYBPC3):c.3330+1G>TMYBPC3Pathogenic/Likely pathogenic114735474447354744CAcriteria provided, multiple submitters, no conflictsClinGen:CA380314001
single nucleotide variantNM_000256.3(MYBPC3):c.3294G>A (p.Trp1098Ter)MYBPC3Pathogenic114735478147354781CTcriteria provided, multiple submitters, no conflictsClinGen:CA053346
InsertionNM_000256.3(MYBPC3):c.3228_3229insT (p.Ala1077fs)MYBPC3Pathogenic114735484647354847CCAcriteria provided, single submitterClinGen:CA658797620
InsertionNM_000256.3(MYBPC3):c.2604_2605insA (p.Pro869fs)MYBPC3Pathogenic114735756047357561GGTcriteria provided, single submitterClinGen:CA658797622
DeletionNM_000256.3(MYBPC3):c.2451del (p.Trp818fs)MYBPC3Pathogenic114735909347359093ACAcriteria provided, single submitterClinGen:CA658797624
DeletionNM_000256.3(MYBPC3):c.2310del (p.Asp770fs)MYBPC3Pathogenic114735934447359344CGCcriteria provided, single submitterClinGen:CA658797627