ClinVar Miner

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

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Gene type:
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Total variants: 89
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HGVS dbSNP
NM_000368.4(TSC1):c.*1000A>G rs886063610
NM_000368.4(TSC1):c.*106A>G rs886063620
NM_000368.4(TSC1):c.*1089G>A rs886063609
NM_000368.4(TSC1):c.*1508A>G rs552190342
NM_000368.4(TSC1):c.*1519C>T rs886063608
NM_000368.4(TSC1):c.*1519delC rs886063607
NM_000368.4(TSC1):c.*1541dupT rs748099884
NM_000368.4(TSC1):c.*1612C>A rs886063605
NM_000368.4(TSC1):c.*1969T>C rs886063604
NM_000368.4(TSC1):c.*1970G>A rs886063603
NM_000368.4(TSC1):c.*2022G>T rs568052856
NM_000368.4(TSC1):c.*2213C>A rs539030496
NM_000368.4(TSC1):c.*2364T>A rs886063602
NM_000368.4(TSC1):c.*2439C>A rs886063601
NM_000368.4(TSC1):c.*2475C>A rs886063600
NM_000368.4(TSC1):c.*2576T>C rs886063599
NM_000368.4(TSC1):c.*2615C>A rs886063598
NM_000368.4(TSC1):c.*2632A>G rs886063597
NM_000368.4(TSC1):c.*2644G>T rs886063596
NM_000368.4(TSC1):c.*2647C>T rs886063595
NM_000368.4(TSC1):c.*2658G>T rs886063594
NM_000368.4(TSC1):c.*2679T>C rs886063593
NM_000368.4(TSC1):c.*2691A>T rs886063592
NM_000368.4(TSC1):c.*2829A>G rs886063591
NM_000368.4(TSC1):c.*2893dupA rs143549363
NM_000368.4(TSC1):c.*2897A>G rs886063589
NM_000368.4(TSC1):c.*2949A>T rs886063588
NM_000368.4(TSC1):c.*298A>G rs886063619
NM_000368.4(TSC1):c.*3047C>A rs886063587
NM_000368.4(TSC1):c.*3063A>T rs886063586
NM_000368.4(TSC1):c.*3238T>C rs886063585
NM_000368.4(TSC1):c.*3239G>T rs886063584
NM_000368.4(TSC1):c.*3240G>T rs886063583
NM_000368.4(TSC1):c.*3248_*3250delCAG rs886063582
NM_000368.4(TSC1):c.*3284C>A rs886063581
NM_000368.4(TSC1):c.*3285G>T rs886063580
NM_000368.4(TSC1):c.*3330G>T rs553475307
NM_000368.4(TSC1):c.*333C>A rs886063618
NM_000368.4(TSC1):c.*3531G>T rs886063579
NM_000368.4(TSC1):c.*3543C>A rs886063578
NM_000368.4(TSC1):c.*3565C>T rs771494783
NM_000368.4(TSC1):c.*3658G>A rs886063577
NM_000368.4(TSC1):c.*3737C>A rs886063576
NM_000368.4(TSC1):c.*3924G>T rs886063575
NM_000368.4(TSC1):c.*3987A>G rs886063574
NM_000368.4(TSC1):c.*4072G>A rs886063573
NM_000368.4(TSC1):c.*4128G>A rs886063572
NM_000368.4(TSC1):c.*4159G>T rs886063571
NM_000368.4(TSC1):c.*4167C>A rs886063570
NM_000368.4(TSC1):c.*4193A>C rs886063569
NM_000368.4(TSC1):c.*4233G>T rs886063568
NM_000368.4(TSC1):c.*4248C>A rs886063567
NM_000368.4(TSC1):c.*4248C>T rs886063567
NM_000368.4(TSC1):c.*4356C>T rs886063566
NM_000368.4(TSC1):c.*4447C>T rs112968492
NM_000368.4(TSC1):c.*448G>A rs886063617
NM_000368.4(TSC1):c.*4515G>A rs886063565
NM_000368.4(TSC1):c.*4622G>A rs886063564
NM_000368.4(TSC1):c.*4631dupT rs60000611
NM_000368.4(TSC1):c.*4826A>C rs886063563
NM_000368.4(TSC1):c.*4845G>T rs886063562
NM_000368.4(TSC1):c.*548C>A rs886063616
NM_000368.4(TSC1):c.*583C>A rs886063615
NM_000368.4(TSC1):c.*817G>T rs886063614
NM_000368.4(TSC1):c.*824C>T rs886063613
NM_000368.4(TSC1):c.*859G>T rs886063612
NM_000368.4(TSC1):c.*920C>A rs886063611
NM_000368.4(TSC1):c.-166A>G rs886063626
NM_000368.4(TSC1):c.-174A>T rs886063627
NM_000368.4(TSC1):c.-214C>T rs886063628
NM_000368.4(TSC1):c.-227G>A rs886063629
NM_000368.4(TSC1):c.-35G>A rs370122384
NM_000368.4(TSC1):c.-80-10T>C rs886063625
NM_000368.4(TSC1):c.108C>T (p.Asp36=) rs886063624
NM_000368.4(TSC1):c.1438+6G>A rs118203530
NM_000368.4(TSC1):c.1745C>T (p.Thr582Ile) rs886063623
NM_000368.4(TSC1):c.1882T>C (p.Leu628=) rs375534013
NM_000368.4(TSC1):c.2209-3T>C rs368309229
NM_000368.4(TSC1):c.2209-9C>G rs118203660
NM_000368.4(TSC1):c.231C>T (p.Asn77=) rs397514809
NM_000368.4(TSC1):c.2556G>C (p.Leu852=) rs770381040
NM_000368.4(TSC1):c.2626-3_2626-2insTA rs760737807
NM_000368.4(TSC1):c.2626-3delC rs886063622
NM_000368.4(TSC1):c.2626-4_2626-3dupTC rs1554813638
NM_000368.4(TSC1):c.2626-6_2626-4dupTTT rs5901000
NM_000368.4(TSC1):c.3123C>G (p.Ser1041Arg) rs753374839
NM_000368.4(TSC1):c.3252A>C (p.Ser1084=) rs886063621
NM_000368.4(TSC1):c.3428C>T (p.Pro1143Leu) rs201867031
NM_000368.4(TSC1):c.346T>G (p.Leu116Val) rs199620268

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