ClinVar Miner

List of variants in gene TG reported as benign by Invitae

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Gene type:
ClinVar version:
Total variants: 123
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HGVS dbSNP gnomAD frequency
NM_003235.5(TG):c.3082A>G (p.Met1028Val) rs853326 0.60247
NM_003235.5(TG):c.2334T>C (p.Pro778=) rs2069550 0.59900
NM_003235.5(TG):c.7589G>A (p.Arg2530Gln) rs1133076 0.56572
NM_003235.5(TG):c.4506T>C (p.Ala1502=) rs853304 0.55069
NM_003235.5(TG):c.7920C>T (p.Tyr2640=) rs2294024 0.49806
NM_003235.5(TG):c.3848-20T>C rs2261147 0.47593
NM_003235.5(TG):c.3935A>G (p.Asp1312Gly) rs2069556 0.47427
NM_003235.5(TG):c.5512G>A (p.Asp1838Asn) rs2069561 0.39534
NM_003235.5(TG):c.5995C>T (p.Arg1999Trp) rs2076740 0.37641
NM_003235.5(TG):c.5921T>C (p.Met1974Thr) rs56230101 0.13536
NM_003235.5(TG):c.5119C>T (p.Pro1707Ser) rs61744678 0.07252
NM_003235.5(TG):c.5234-10T>C rs4736614 0.06877
NM_003235.5(TG):c.5549-9C>A rs77157347 0.05272
NM_003235.5(TG):c.5862A>G (p.Lys1954=) rs16904799 0.05269
NM_003235.5(TG):c.3217+11A>C rs79594547 0.04535
NM_003235.5(TG):c.6395C>T (p.Ser2132Leu) rs61741457 0.04126
NM_003235.5(TG):c.5907G>A (p.Pro1969=) rs17693031 0.03986
NM_003235.5(TG):c.7578T>A (p.Phe2526Leu) rs12114109 0.03807
NM_003235.5(TG):c.2443G>A (p.Gly815Arg) rs16904774 0.03645
NM_003235.5(TG):c.3933G>A (p.Ala1311=) rs16904786 0.03224
NM_003235.5(TG):c.5122A>G (p.Ile1708Val) rs61744679 0.02642
NM_003235.5(TG):c.5186A>C (p.Asp1729Ala) rs61744749 0.02641
NM_003235.5(TG):c.1332C>T (p.Ile444=) rs61741629 0.02324
NM_003235.5(TG):c.6055+7A>G rs73353474 0.02313
NM_003235.5(TG):c.6984C>G (p.Leu2328=) rs61745590 0.02022
NM_003235.5(TG):c.1821C>T (p.Thr607=) rs61742713 0.02018
NM_003235.5(TG):c.6669G>A (p.Lys2223=) rs61743268 0.01777
NM_003235.5(TG):c.1543C>G (p.Gln515Glu) rs180222 0.01589
NM_003235.5(TG):c.5370A>G (p.Ile1790Met) rs73710715 0.01452
NM_003235.5(TG):c.5299_5301del (p.Asp1767del) rs112749206 0.01445
NM_003235.5(TG):c.353C>T (p.Pro118Leu) rs114322847 0.01424
NM_003235.5(TG):c.6272A>G (p.Asp2091Gly) rs61743198 0.01391
NM_003235.5(TG):c.3494A>G (p.Tyr1165Cys) rs61746583 0.01329
NM_003235.5(TG):c.1958G>A (p.Gly653Asp) rs2069548 0.01198
NM_003235.5(TG):c.4365C>T (p.Asp1455=) rs57453794 0.01068
NM_003235.5(TG):c.199G>A (p.Gly67Ser) rs116340633 0.00924
NM_003235.5(TG):c.3187C>A (p.Leu1063Met) rs11992497 0.00903
NM_003235.5(TG):c.2761+14T>C rs76286566 0.00834
NM_003235.5(TG):c.1890A>G (p.Gln630=) rs2228590 0.00831
NM_003235.5(TG):c.5219C>A (p.Thr1740Lys) rs16904791 0.00801
NM_003235.5(TG):c.1434G>A (p.Val478=) rs116254142 0.00692
NM_003235.5(TG):c.2520T>C (p.Pro840=) rs116489694 0.00543
NM_003235.5(TG):c.7755-9T>G rs190979363 0.00473
NM_003235.5(TG):c.1296G>A (p.Gln432=) rs61741609 0.00444
NM_003235.5(TG):c.2793T>C (p.Arg931=) rs61736710 0.00443
NM_003235.5(TG):c.3313G>A (p.Val1105Ile) rs115670342 0.00443
NM_003235.5(TG):c.3906G>A (p.Pro1302=) rs2294003 0.00435
NM_003235.5(TG):c.5856G>A (p.Arg1952=) rs115476696 0.00430
NM_003235.5(TG):c.1269C>T (p.Arg423=) rs115916398 0.00412
NM_003235.5(TG):c.2561G>A (p.Arg854Gln) rs115361039 0.00408
NM_003235.5(TG):c.7135C>T (p.Arg2379Cys) rs61742878 0.00381
NM_003235.5(TG):c.325A>G (p.Ile109Val) rs35301433 0.00350
NM_003235.5(TG):c.3129C>T (p.His1043=) rs112300885 0.00347
NM_003235.5(TG):c.144C>T (p.Tyr48=) rs114436500 0.00345
NM_003235.5(TG):c.4484T>C (p.Val1495Ala) rs61740825 0.00330
NM_003235.5(TG):c.6783-3C>T rs143075252 0.00297
NM_003235.5(TG):c.6200-7T>A rs79724982 0.00240
NM_003235.5(TG):c.7083G>T (p.Ala2361=) rs116723711 0.00239
NM_003235.5(TG):c.2610G>T (p.Gln870His) rs2229843 0.00229
NM_003235.5(TG):c.7665C>T (p.Arg2555=) rs115139074 0.00214
NM_003235.5(TG):c.537A>G (p.Ser179=) rs114875802 0.00203
NM_003235.5(TG):c.3583G>A (p.Gly1195Arg) rs138469414 0.00197
NM_003235.5(TG):c.3647C>T (p.Pro1216Leu) rs142335537 0.00182
NM_003235.5(TG):c.6646A>G (p.Ile2216Val) rs138690529 0.00179
NM_003235.5(TG):c.6351T>G (p.Thr2117=) rs145367055 0.00172
NM_003235.5(TG):c.3665C>T (p.Ser1222Leu) rs12549018 0.00164
NM_003235.5(TG):c.3035C>T (p.Pro1012Leu) rs115936153 0.00159
NM_003235.5(TG):c.4493C>T (p.Thr1498Met) rs74590117 0.00151
NM_003235.5(TG):c.4003-4G>A rs7824402 0.00143
NM_003235.5(TG):c.4193G>A (p.Arg1398His) rs115263899 0.00143
NM_003235.5(TG):c.2859G>A (p.Leu953=) rs114356482 0.00137
NM_003235.5(TG):c.1075+8T>G rs184523779 0.00133
NM_003235.5(TG):c.3804C>T (p.Ser1268=) rs61747461 0.00130
NM_003235.5(TG):c.3057C>T (p.Ser1019=) rs116032324 0.00120
NM_003235.5(TG):c.426C>T (p.Asp142=) rs114477962 0.00113
NM_003235.5(TG):c.7737T>C (p.Ala2579=) rs145611717 0.00098
NM_003235.5(TG):c.6199+8C>A rs139957020 0.00095
NM_003235.5(TG):c.4323G>A (p.Ser1441=) rs769654694 0.00085
NM_003235.5(TG):c.4563G>A (p.Leu1521=) rs115981067 0.00054
NM_003235.5(TG):c.4859C>T (p.Thr1620Met) rs115902639 0.00044
NM_003235.5(TG):c.8026C>T (p.Arg2676Trp) rs114613744 0.00038
NM_003235.5(TG):c.3351G>A (p.Leu1117=) rs772475658 0.00025
NM_003235.5(TG):c.60T>C (p.Asn20=) rs140030312 0.00024
NM_003235.5(TG):c.6324G>A (p.Arg2108=) rs186519521 0.00020
NM_003235.5(TG):c.5071C>T (p.Arg1691Cys) rs375968742 0.00015
NM_003235.5(TG):c.5863+14G>A rs758834729 0.00014
NM_003235.5(TG):c.5864-8C>T rs189500765 0.00014
NM_003235.5(TG):c.4257G>A (p.Ala1419=) rs116314916 0.00013
NM_003235.5(TG):c.7020C>T (p.Phe2340=) rs756155224 0.00011
NM_003235.5(TG):c.7640T>A (p.Leu2547Gln) rs2979042 0.00008
NM_003235.5(TG):c.555G>A (p.Ala185=) rs374108215 0.00002
NM_003235.5(TG):c.1834C>A (p.Pro612Thr) rs552359043 0.00001
NM_003235.5(TG):c.2200T>G (p.Ser734Ala) rs180223
NM_003235.5(TG):c.2581A>G (p.Ile861Val) rs527511755
NM_003235.5(TG):c.274+17G>A
NM_003235.5(TG):c.2761+10C>T
NM_003235.5(TG):c.2761+11G>T rs77660463
NM_003235.5(TG):c.2762-4del
NM_003235.5(TG):c.2963G>A (p.Arg988His) rs16893332
NM_003235.5(TG):c.2963G>C (p.Arg988Pro) rs16893332
NM_003235.5(TG):c.3001+19A>G
NM_003235.5(TG):c.3218-11C>G
NM_003235.5(TG):c.3330+11G>A
NM_003235.5(TG):c.3634+16del
NM_003235.5(TG):c.3766G>A (p.Val1256Met)
NM_003235.5(TG):c.4379-5dup
NM_003235.5(TG):c.4529-18T>C
NM_003235.5(TG):c.4529-19G>C
NM_003235.5(TG):c.478+15G>A rs141561325
NM_003235.5(TG):c.478+16C>T
NM_003235.5(TG):c.4817-19C>T
NM_003235.5(TG):c.4932+19G>A
NM_003235.5(TG):c.4933-18G>A
NM_003235.5(TG):c.5402-16A>T
NM_003235.5(TG):c.5468-10_5468-9del
NM_003235.5(TG):c.5468-9dup
NM_003235.5(TG):c.5760C>T (p.Thr1920=)
NM_003235.5(TG):c.6200-10del
NM_003235.5(TG):c.6397+8del
NM_003235.5(TG):c.6933T>C (p.Ser2311=)
NM_003235.5(TG):c.7157G>A (p.Arg2386His)
NM_003235.5(TG):c.7847A>G (p.Asn2616Ser) rs10091530
NM_003235.5(TG):c.7847A>T (p.Asn2616Ile) rs10091530

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