ClinVar Miner

List of variants in gene TSC1 reported as likely benign by Invitae

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Gene type:
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Total variants: 183
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HGVS dbSNP
NM_000368.4(TSC1):c.1006C>A (p.Arg336=) rs118203483
NM_000368.4(TSC1):c.1029+8G>A rs1036865129
NM_000368.4(TSC1):c.1038T>C (p.Leu346=) rs753360364
NM_000368.4(TSC1):c.1050T>C (p.Ser350=) rs150777389
NM_000368.4(TSC1):c.106+9A>G rs1554820969
NM_000368.4(TSC1):c.1107G>A (p.Leu369=) rs909737447
NM_000368.4(TSC1):c.110G>A (p.Arg37His) rs750441497
NM_000368.4(TSC1):c.1110A>T (p.Ser370=) rs371648887
NM_000368.4(TSC1):c.1113C>T (p.His371=) rs771217333
NM_000368.4(TSC1):c.1141+10T>C rs367601694
NM_000368.4(TSC1):c.1142-9G>A rs1554817169
NM_000368.4(TSC1):c.114C>G (p.Gly38=) rs776158461
NM_000368.4(TSC1):c.1163T>C (p.Leu388Pro) rs377598226
NM_000368.4(TSC1):c.1167A>C (p.Gly389=) rs876660723
NM_000368.4(TSC1):c.1178C>T (p.Thr393Ile) rs201452238
NM_000368.4(TSC1):c.1191A>G (p.Pro397=) rs370281825
NM_000368.4(TSC1):c.1194C>G (p.Ala398=) rs1060504861
NM_000368.4(TSC1):c.1200C>G (p.Leu400=) rs767514820
NM_000368.4(TSC1):c.1248C>T (p.Val416=) rs777823426
NM_000368.4(TSC1):c.1251A>G (p.Thr417=) rs147127442
NM_000368.4(TSC1):c.1257C>A (p.Pro419=) rs369642207
NM_000368.4(TSC1):c.1257C>G (p.Pro419=) rs369642207
NM_000368.4(TSC1):c.1257C>T (p.Pro419=) rs369642207
NM_000368.4(TSC1):c.1263+6_1263+8dup rs751182565
NM_000368.4(TSC1):c.1263+9C>T rs761837376
NM_000368.4(TSC1):c.1269G>A (p.Glu423=) rs1272450087
NM_000368.4(TSC1):c.1296A>C (p.Leu432=) rs1554816406
NM_000368.4(TSC1):c.1302A>G (p.Arg434=) rs907840461
NM_000368.4(TSC1):c.1305A>G (p.Gln435=) rs1334781311
NM_000368.4(TSC1):c.1317G>C (p.Leu439=) rs770692313
NM_000368.4(TSC1):c.1332A>G (p.Ser444=) rs773003016
NM_000368.4(TSC1):c.1338G>A (p.Glu446=) rs1410493156
NM_000368.4(TSC1):c.133T>C (p.Leu45=) rs755226092
NM_000368.4(TSC1):c.1344T>C (p.Pro448=) rs530908428
NM_000368.4(TSC1):c.1344T>G (p.Pro448=) rs530908428
NM_000368.4(TSC1):c.1439-10T>A rs1060504852
NM_000368.4(TSC1):c.1443A>C (p.Ala481=) rs1554816081
NM_000368.4(TSC1):c.1443A>G (p.Ala481=) rs1554816081
NM_000368.4(TSC1):c.1476A>C (p.Ala492=) rs1554816067
NM_000368.4(TSC1):c.1491G>A (p.Val497=) rs1554816056
NM_000368.4(TSC1):c.1503A>C (p.Gly501=) rs201810746
NM_000368.4(TSC1):c.1530C>T (p.Asp510=) rs1554816033
NM_000368.4(TSC1):c.1539A>G (p.Pro513=) rs755055358
NM_000368.4(TSC1):c.153A>C (p.Glu51Asp) rs118203342
NM_000368.4(TSC1):c.1563G>A (p.Ser521=) rs1554816005
NM_000368.4(TSC1):c.1581G>A (p.Gln527=) rs1554815989
NM_000368.4(TSC1):c.1584C>T (p.Gly528=) rs149439187
NM_000368.4(TSC1):c.159C>T (p.Ser53=) rs756335238
NM_000368.4(TSC1):c.1611C>T (p.His537=) rs898271020
NM_000368.4(TSC1):c.1614C>T (p.Ser538=) rs878853961
NM_000368.4(TSC1):c.1617C>T (p.Ser539=) rs1554815969
NM_000368.4(TSC1):c.1626G>A (p.Lys542=) rs756935981
NM_000368.4(TSC1):c.1631G>A (p.Gly544Glu) rs770570830
NM_000368.4(TSC1):c.1674C>T (p.Pro558=) rs878853962
NM_000368.4(TSC1):c.168G>A (p.Pro56=) rs781483110
NM_000368.4(TSC1):c.1701G>C (p.Ala567=) rs35478675
NM_000368.4(TSC1):c.171A>G (p.Ala57=) rs1060504853
NM_000368.4(TSC1):c.1775C>T (p.Thr592Met) rs775869914
NM_000368.4(TSC1):c.1779A>G (p.Arg593=) rs964191879
NM_000368.4(TSC1):c.1794C>T (p.Ser598=) rs766438395
NM_000368.4(TSC1):c.1809G>A (p.Pro603=) rs112434645
NM_000368.4(TSC1):c.181C>T (p.Leu61=) rs752047592
NM_000368.4(TSC1):c.1848C>T (p.Ala616=) rs752286096
NM_000368.4(TSC1):c.1863C>T (p.Ile621=) rs898222579
NM_000368.4(TSC1):c.1869G>A (p.Lys623=) rs778556382
NM_000368.4(TSC1):c.1878G>A (p.Glu626=) rs753424167
NM_000368.4(TSC1):c.1879C>T (p.Leu627=) rs1171110012
NM_000368.4(TSC1):c.1882T>C (p.Leu628=) rs375534013
NM_000368.4(TSC1):c.1884A>G (p.Leu628=) rs1038140620
NM_000368.4(TSC1):c.1944G>A (p.Val648=) rs1554815720
NM_000368.4(TSC1):c.1954C>T (p.Leu652=) rs747452647
NM_000368.4(TSC1):c.1997+9C>T rs371043832
NM_000368.4(TSC1):c.2031C>A (p.Thr677=) rs1060504855
NM_000368.4(TSC1):c.2064C>T (p.Ile688=) rs878853963
NM_000368.4(TSC1):c.211-10del rs1060504859
NM_000368.4(TSC1):c.2115G>A (p.Glu705=) rs142662480
NM_000368.4(TSC1):c.2136T>C (p.His712=) rs1554815286
NM_000368.4(TSC1):c.2148C>T (p.Asn716=) rs1554815274
NM_000368.4(TSC1):c.2196T>C (p.His732=) rs776441369
NM_000368.4(TSC1):c.21C>T (p.Val7=) rs145987906
NM_000368.4(TSC1):c.2208+10G>T rs945077563
NM_000368.4(TSC1):c.2226A>G (p.Leu742=) rs397514878
NM_000368.4(TSC1):c.2235G>A (p.Lys745=) rs753265422
NM_000368.4(TSC1):c.2286T>C (p.Asn762=) rs1554815010
NM_000368.4(TSC1):c.231C>T (p.Asn77=) rs397514809
NM_000368.4(TSC1):c.2322G>A (p.Lys774=) rs772038670
NM_000368.4(TSC1):c.2391+8C>T rs1554814904
NM_000368.4(TSC1):c.2392-7T>C rs1554814693
NM_000368.4(TSC1):c.2394G>A (p.Thr798=) rs1060504860
NM_000368.4(TSC1):c.2412G>A (p.Arg804=) rs1554814676
NM_000368.4(TSC1):c.2472T>G (p.Thr824=) rs762811821
NM_000368.4(TSC1):c.249C>T (p.Ala83=) rs145783693
NM_000368.4(TSC1):c.2508A>C (p.Ser836=) rs1554814456
NM_000368.4(TSC1):c.2511C>T (p.Asn837=) rs1554814448
NM_000368.4(TSC1):c.2517G>A (p.Glu839=) rs1554814437
NM_000368.4(TSC1):c.2520G>A (p.Ser840=) rs547498792
NM_000368.4(TSC1):c.2556G>C (p.Leu852=) rs770381040
NM_000368.4(TSC1):c.255T>C (p.Thr85=) rs1060504856
NM_000368.4(TSC1):c.2604C>T (p.Asn868=) rs147163264
NM_000368.4(TSC1):c.2613A>G (p.Ser871=) rs1031508405
NM_000368.4(TSC1):c.2626-3dup rs1554813639
NM_000368.4(TSC1):c.2626-4T>C rs777386691
NM_000368.4(TSC1):c.2626-4_2626-3insTC rs1554813651
NM_000368.4(TSC1):c.2654G>A (p.Arg885Gln) rs200514807
NM_000368.4(TSC1):c.2658A>G (p.Lys886=) rs368212910
NM_000368.4(TSC1):c.2682T>C (p.His894=) rs771479673
NM_000368.4(TSC1):c.273G>C (p.Ser91=) rs115097221
NM_000368.4(TSC1):c.2760C>T (p.Asp920=) rs1226490074
NM_000368.4(TSC1):c.2766T>G (p.Leu922=) rs546119844
NM_000368.4(TSC1):c.2778G>A (p.Gln926=) rs1554813423
NM_000368.4(TSC1):c.2781G>A (p.Lys927=) rs118203733
NM_000368.4(TSC1):c.2814-7C>T rs1060504851
NM_000368.4(TSC1):c.2814-9A>G rs878853965
NM_000368.4(TSC1):c.2904G>A (p.Arg968=) rs1554813280
NM_000368.4(TSC1):c.2922C>T (p.Leu974=) rs769389702
NM_000368.4(TSC1):c.2932C>G (p.Leu978Val) rs397514859
NM_000368.4(TSC1):c.2934T>C (p.Leu978=) rs1554813253
NM_000368.4(TSC1):c.2940A>G (p.Glu980=) rs557674294
NM_000368.4(TSC1):c.2964A>G (p.Ala988=) rs1057520482
NM_000368.4(TSC1):c.2968G>A (p.Glu990Lys) rs200398750
NM_000368.4(TSC1):c.2976-8T>G rs1060504858
NM_000368.4(TSC1):c.2982C>T (p.Asp994=) rs199919348
NM_000368.4(TSC1):c.3005A>T (p.Asp1002Val) rs202121327
NM_000368.4(TSC1):c.3060C>T (p.Thr1020=) rs1380396209
NM_000368.4(TSC1):c.3072C>T (p.Ser1024=) rs1554812912
NM_000368.4(TSC1):c.3075C>T (p.Ser1025=) rs765753157
NM_000368.4(TSC1):c.3079C>T (p.Arg1027Trp) rs375394001
NM_000368.4(TSC1):c.3120C>T (p.Ser1040=) rs1289954163
NM_000368.4(TSC1):c.3125G>T (p.Ser1042Ile) rs148931779
NM_000368.4(TSC1):c.3144A>C (p.Pro1048=) rs1554812826
NM_000368.4(TSC1):c.3159C>T (p.His1053=) rs778413037
NM_000368.4(TSC1):c.3195G>A (p.Thr1065=) rs118203746
NM_000368.4(TSC1):c.3207A>G (p.Glu1069=) rs878853966
NM_000368.4(TSC1):c.3228C>T (p.Thr1076=) rs140622357
NM_000368.4(TSC1):c.3237C>T (p.Gly1079=) rs749995749
NM_000368.4(TSC1):c.3321C>T (p.Asp1107=) rs118203752
NM_000368.4(TSC1):c.3361C>T (p.Leu1121=) rs769478982
NM_000368.4(TSC1):c.3363G>C (p.Leu1121=) rs1060504857
NM_000368.4(TSC1):c.3373T>C (p.Leu1125=) rs1157060310
NM_000368.4(TSC1):c.3381G>A (p.Val1127=) rs773586317
NM_000368.4(TSC1):c.3396C>G (p.Pro1132=) rs774980129
NM_000368.4(TSC1):c.3396C>T (p.Pro1132=) rs774980129
NM_000368.4(TSC1):c.3420G>A (p.Pro1140=) rs763931959
NM_000368.4(TSC1):c.3426C>T (p.Pro1142=) rs758286878
NM_000368.4(TSC1):c.3429G>A (p.Pro1143=) rs759431801
NM_000368.4(TSC1):c.3429G>C (p.Pro1143=) rs759431801
NM_000368.4(TSC1):c.3453A>G (p.Leu1151=) rs1554812550
NM_000368.4(TSC1):c.3489C>T (p.His1163=) rs1554812527
NM_000368.4(TSC1):c.364-7C>T rs775465260
NM_000368.4(TSC1):c.375C>T (p.Asp125=) rs560863078
NM_000368.4(TSC1):c.378C>T (p.Val126=) rs373173550
NM_000368.4(TSC1):c.45C>T (p.Asp15=) rs1457262106
NM_000368.4(TSC1):c.509-10C>T rs780670013
NM_000368.4(TSC1):c.51C>G (p.Pro17=) rs768175095
NM_000368.4(TSC1):c.531C>T (p.Leu177=) rs752615412
NM_000368.4(TSC1):c.540C>T (p.Leu180=) rs201562103
NM_000368.4(TSC1):c.549T>C (p.Ser183=) rs774398322
NM_000368.4(TSC1):c.555C>T (p.Tyr185=) rs118203398
NM_000368.4(TSC1):c.593A>G (p.Asn198Ser) rs577983115
NM_000368.4(TSC1):c.597C>T (p.Phe199=) rs202242304
NM_000368.4(TSC1):c.72C>T (p.Asp24=) rs376527838
NM_000368.4(TSC1):c.737+10C>T rs1554819375
NM_000368.4(TSC1):c.738-10C>A rs768158324
NM_000368.4(TSC1):c.771C>T (p.Ile257=) rs1060504854
NM_000368.4(TSC1):c.774G>A (p.Glu258=) rs1554817678
NM_000368.4(TSC1):c.798C>T (p.Pro266=) rs770704462
NM_000368.4(TSC1):c.804A>G (p.Glu268=) rs753895570
NM_000368.4(TSC1):c.813T>C (p.Tyr271=) rs118203452
NM_000368.4(TSC1):c.852C>T (p.Arg284=) rs769706203
NM_000368.4(TSC1):c.870C>T (p.Ala290=) rs779155575
NM_000368.4(TSC1):c.879C>T (p.Thr293=) rs1554817584
NM_000368.4(TSC1):c.914-10T>C rs1554817441
NM_000368.4(TSC1):c.942G>A (p.Thr314=) rs144208203
NM_000368.4(TSC1):c.951G>A (p.Leu317=) rs1554817419
NM_000368.4(TSC1):c.960A>G (p.Leu320=) rs770183315
NM_000368.4(TSC1):c.976C>T (p.Leu326=) rs1554817396
NM_000368.4(TSC1):c.978A>G (p.Leu326=) rs1060504862
NM_000368.4(TSC1):c.99C>T (p.Leu33=) rs757216373
NM_001162426.2(TSC1):c.1436-20_1436-9del rs1064792996
NM_001162426.2(TSC1):c.1995-11dup rs1388433086
NM_001162426.2(TSC1):c.2389-8_2389-7del rs1554814696
NM_001162426.2(TSC1):c.2499+8_2499+10del rs762882968
NM_001162426.2(TSC1):c.3109_3111AGC[8] (p.Ser1041_Ser1042dup) rs2234980

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