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)
DeletionNM_000256.3(MYBPC3):c.3662del (p.Leu1221fs)MYBPC3Pathogenic/Likely pathogenic114735377547353775CACcriteria provided, multiple submitters, no conflictsClinGen:CA279321
DuplicationNM_000256.3(MYBPC3):c.3414dup (p.Val1139fs)MYBPC3Likely pathogenic114735444047354441CCGcriteria provided, multiple submitters, no conflictsClinGen:CA279290
single nucleotide variantNM_000256.3(MYBPC3):c.3300C>A (p.Tyr1100Ter)MYBPC3Pathogenic/Likely pathogenic114735477547354775GTcriteria provided, multiple submitters, no conflictsClinGen:CA279299
DuplicationNM_000256.3(MYBPC3):c.2670dup (p.Arg891fs)MYBPC3Likely pathogenic114735749447357495GGCcriteria provided, single submitterClinGen:CA279270
DeletionNM_000256.3(MYBPC3):c.2550del (p.Asn850fs)MYBPC3Likely pathogenic114735899447358994CGCcriteria provided, single submitterClinGen:CA279283
single nucleotide variantNM_000256.3(MYBPC3):c.2376G>A (p.Trp792Ter)MYBPC3Pathogenic/Likely pathogenic114735927847359278CTcriteria provided, multiple submitters, no conflictsClinGen:CA279280
single nucleotide variantNM_000256.3(MYBPC3):c.2371C>T (p.Gln791Ter)MYBPC3Pathogenic/Likely pathogenic114735928347359283GAcriteria provided, multiple submitters, no conflictsClinGen:CA279318
DeletionNM_000256.3(MYBPC3):c.306del (p.Met103fs)MYBPC3Likely pathogenic114737215347372153TGTcriteria provided, single submitterClinGen:CA279289
DuplicationNM_000256.3(MYBPC3):c.227dup (p.Ser78fs)MYBPC3Likely pathogenic114737285447372855CCTcriteria provided, single submitterClinGen:CA279311
single nucleotide variantNM_000257.4(MYH7):c.3358G>A (p.Glu1120Lys)MYH7Likely pathogenic142388942223889422CTcriteria provided, single submitterClinGen:CA279329