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)
single nucleotide variantNM_001267550.2(TTN):c.94405A>T (p.Lys31469Ter)TTNLikely pathogenic2179411847179411847TAcriteria provided, multiple submitters, no conflictsClinGen:CA349474274
single nucleotide variantNM_001267550.2(TTN):c.67897G>T (p.Glu22633Ter)TTNLikely pathogenic2179443860179443860CAcriteria provided, single submitterClinGen:CA349422569
IndelNM_001267550.2(TTN):c.73324_73328delinsC (p.Ala24442fs)TTNLikely pathogenic2179437531179437535CAGGCGcriteria provided, single submitterClinGen:CA658796035
single nucleotide variantNM_001267550.2(TTN):c.82350T>G (p.Tyr27450Ter)TTNLikely pathogenic2179428509179428509ACcriteria provided, single submitterClinGen:CA349573976
single nucleotide variantNM_001267550.2(TTN):c.60307A>T (p.Arg20103Ter)TTNLikely pathogenic2179456145179456145TAcriteria provided, multiple submitters, no conflictsClinGen:CA349485552
DeletionNM_001267550.2(TTN):c.56741del (p.Ser18914fs)TTNLikely pathogenic2179463696179463696AGAcriteria provided, multiple submitters, no conflictsClinGen:CA658796055
single nucleotide variantNM_001267550.2(TTN):c.58874G>A (p.Trp19625Ter)TTNLikely pathogenic2179458061179458061CTcriteria provided, single submitterClinGen:CA349501161
DuplicationNM_001267550.2(TTN):c.48369dup (p.Glu16124fs)TTNLikely pathogenic2179480458179480459CCTcriteria provided, single submitterClinGen:CA658796073
DuplicationNM_001267550.2(TTN):c.57035dup (p.Leu19013fs)TTNLikely pathogenic2179463308179463309TTGcriteria provided, single submitterClinGen:CA658796048
DeletionNM_001267550.2(TTN):c.51525del (p.Ser17177fs)TTNPathogenic/Likely pathogenic2179474625179474625CTCcriteria provided, multiple submitters, no conflictsClinGen:CA658795993