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.363+1G>ATSC1Likely pathogenic9135800973135800973CTcriteria provided, single submitterClinGen:CA007428,Tuberous sclerosis database (TSC1):TSC1_00396
single nucleotide variantNM_000368.5(TSC1):c.363+1G>TTSC1Likely pathogenic9135800973135800973CAcriteria provided, multiple submitters, no conflictsClinGen:CA007434,Tuberous sclerosis database (TSC1):TSC1_00018
single nucleotide variantNM_000368.5(TSC1):c.362A>T (p.Lys121Met)TSC1Likely pathogenic9135800975135800975TAcriteria provided, single submitterClinGen:CA16612651
single nucleotide variantNM_000368.5(TSC1):c.325C>T (p.Gln109Ter)TSC1Pathogenic9135801012135801012GAcriteria provided, multiple submitters, no conflictsClinGen:CA007276,Tuberous sclerosis database (TSC1):TSC1_00522
single nucleotide variantNM_000368.5(TSC1):c.309G>A (p.Trp103Ter)TSC1Pathogenic9135801028135801028CTcriteria provided, single submitterClinGen:CA007158,Tuberous sclerosis database (TSC1):TSC1_00015
single nucleotide variantNM_000368.5(TSC1):c.308G>A (p.Trp103Ter)TSC1Pathogenic9135801029135801029CTcriteria provided, single submitterClinGen:CA007151,Tuberous sclerosis database (TSC1):TSC1_00014
DuplicationNM_000368.5(TSC1):c.276dup (p.Leu93fs)TSC1Pathogenic9135801060135801061GGTcriteria provided, single submitterClinGen:CA262319,Tuberous sclerosis database (TSC1):TSC1_00202
DeletionNM_000368.5(TSC1):c.271del (p.Ser91fs)TSC1Pathogenic9135801066135801066GAGcriteria provided, single submitter-
DuplicationNM_000368.5(TSC1):c.261dup (p.Ser88fs)TSC1Pathogenic9135801075135801076AATcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000368.5(TSC1):c.260T>G (p.Leu87Ter)TSC1Pathogenic9135801077135801077ACcriteria provided, single submitterClinGen:CA006706,Tuberous sclerosis database (TSC1):TSC1_00650