ClinVar Miner

List of variants in gene TSC1 reported as benign for Tuberous sclerosis syndrome

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Gene type:
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Total variants: 21
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HGVS dbSNP
NM_000368.4(TSC1):c.*1275T>G rs2809244
NM_000368.4(TSC1):c.*1322C>T rs2809243
NM_000368.4(TSC1):c.*1372T>G rs58612431
NM_000368.4(TSC1):c.*1487C>T rs79277527
NM_000368.4(TSC1):c.*1488C>T rs739442
NM_000368.4(TSC1):c.*1507G>A rs739441
NM_000368.4(TSC1):c.*1934A>G rs10491534
NM_000368.4(TSC1):c.*2558A>G rs115516164
NM_000368.4(TSC1):c.*289del rs11323835
NM_000368.4(TSC1):c.*3679G>A rs1050700
NM_000368.4(TSC1):c.*376C>T rs114064768
NM_000368.4(TSC1):c.*4437G>A rs11553763
NM_000368.4(TSC1):c.*4763T>C rs79470094
NM_000368.4(TSC1):c.*4898G>A rs79220715
NM_000368.4(TSC1):c.*682C>T rs75252898
NM_000368.4(TSC1):c.1335A>G (p.Glu445=) rs7862221
NM_000368.4(TSC1):c.1760A>G (p.Lys587Arg) rs118203576
NM_000368.4(TSC1):c.2829C>T (p.Ala943=) rs4962081
NM_000368.4(TSC1):c.3324C>T (p.Gly1108=) rs35593170
NM_000368.4(TSC1):c.965T>C (p.Met322Thr) rs1073123
NM_001162426.2(TSC1):c.2623-4del rs5901000

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