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)
DuplicationNM_000256.3(MYBPC3):c.1168dup (p.His390fs)MYBPC3Likely pathogenic114736509747365098TTGcriteria provided, single submitter-
DuplicationNM_000256.3(MYBPC3):c.1101_1129dup (p.Lys377delinsArgSerTrpSerArgProThrArgTer)MYBPC3Likely pathogenic114736513647365137TTTGCTCACCTGGTAGGCCGGCTCCAGCTTCcriteria provided, single submitter-
single nucleotide variantNM_000256.3(MYBPC3):c.711C>G (p.Tyr237Ter)MYBPC3Pathogenic114737003647370036GCcriteria provided, single submitter-
single nucleotide variantNM_005159.5(ACTC1):c.740G>A (p.Gly247Asp)ACTC1Pathogenic/Likely pathogenic153508435935084359CTcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000363.5(TNNI3):c.485G>T (p.Arg162Leu)TNNI3Likely pathogenic195566546255665462CAcriteria provided, single submitter-
IndelNM_001267550.2(TTN):c.54382-12_54387delinsCTTTNLikely pathogenic2179469027179469044CCAGATCTAGAAATTAGAAGcriteria provided, single submitter-
DeletionNM_000256.3(MYBPC3):c.2766del (p.Gly922_Leu923insTer)MYBPC3Pathogenic114735673247356732GCGcriteria provided, multiple submitters, no conflicts-
DuplicationNM_000257.4(MYH7):c.3985dup (p.Leu1329fs)MYH7Likely pathogenic142388760223887603AAGcriteria provided, single submitter-
single nucleotide variantNM_000257.4(MYH7):c.195T>G (p.Tyr65Ter)MYH7Pathogenic142390274723902747ACcriteria provided, single submitter-
single nucleotide variantNM_001267550.2(TTN):c.49287C>A (p.Asn16429Lys)TTNLikely pathogenic2179478837179478837GTcriteria provided, single submitter-