Knowledge base for genomic medicine in Japanese
結節性硬化症
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
single nucleotide variantNM_000368.5(TSC1):c.555C>G (p.Tyr185Ter)TSC1Pathogenic9135797314135797314GCcriteria provided, single submitter-
single nucleotide variantNM_000368.5(TSC1):c.569G>C (p.Arg190Pro)TSC1Likely pathogenic9135797300135797300CGcriteria provided, single submitterClinGen:CA007774,Tuberous sclerosis database (TSC1):TSC1_00028
single nucleotide variantNM_000368.5(TSC1):c.572T>C (p.Leu191Pro)TSC1Likely pathogenic9135797297135797297AGcriteria provided, single submitterClinGen:CA16618779
single nucleotide variantNM_000368.5(TSC1):c.572T>G (p.Leu191Arg)TSC1Pathogenic9135797297135797297ACcriteria provided, single submitterClinGen:CA007790,Tuberous sclerosis database (TSC1):TSC1_00248
single nucleotide variantNM_000368.5(TSC1):c.572T>A (p.Leu191His)TSC1Likely pathogenic9135797297135797297ATcriteria provided, single submitterClinGen:CA007782,UniProtKB:Q92574#VAR_009399,Tuberous sclerosis database (TSC1):TSC1_00029
DeletionNM_000368.5(TSC1):c.587del (p.Pro196fs)TSC1Pathogenic9135797282135797282AGAcriteria provided, multiple submitters, no conflictsClinGen:CA319327
DeletionNM_000368.5(TSC1):c.590_594del (p.Cys197fs)TSC1Pathogenic9135797275135797279AGTTGCAcriteria provided, single submitterClinGen:CA16618778
DuplicationNM_000368.5(TSC1):c.599dup (p.Ser201fs)TSC1Pathogenic9135797269135797270GGAcriteria provided, single submitterClinGen:CA262380,Tuberous sclerosis database (TSC1):TSC1_00446
DuplicationNM_000368.5(TSC1):c.637dup (p.Leu213fs)TSC1Pathogenic9135797231135797232AAGcriteria provided, single submitterClinGen:CA645369461
DeletionNM_000368.5(TSC1):c.647_648del (p.Thr215_Phe216insTer)TSC1Pathogenic9135797221135797222CAACcriteria provided, multiple submitters, no conflictsClinGen:CA007920,Tuberous sclerosis database (TSC1):TSC1_00031