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.56648-1G>ATTNLikely pathogenic2179463790179463790CTcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001267550.2(TTN):c.56347+1G>ATTNLikely pathogenic2179464280179464280CTcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001276345.2(TNNT2):c.294T>A (p.Asp98Glu)TNNT2Likely pathogenic1201334738201334738ATcriteria provided, single submitter-
single nucleotide variantNM_001267550.2(TTN):c.104947C>T (p.Gln34983Ter)TTNLikely pathogenic2179396395179396395GAcriteria provided, single submitter-
single nucleotide variantNM_001267550.2(TTN):c.82525C>T (p.Arg27509Ter)TTNLikely pathogenic2179428334179428334GAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_001267550.2(TTN):c.80950G>T (p.Glu26984Ter)TTNLikely pathogenic2179429909179429909CAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000256.3(MYBPC3):c.773-2A>TMYBPC3Likely pathogenic114736945847369458TAcriteria provided, single submitter-
single nucleotide variantNM_000256.3(MYBPC3):c.622C>T (p.Gln208Ter)MYBPC3Likely pathogenic114737135747371357GAcriteria provided, single submitter-
DeletionNM_020778.5(ALPK3):c.4391del (p.Asn1464fs)ALPK3Pathogenic/Likely pathogenic158540612585406125GAGcriteria provided, multiple submitters, no conflicts-