ClinVar Miner

List of variants in gene RET reported as uncertain significance for adrenal carcinoma

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 123
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HGVS dbSNP
NM_020630.4(RET):c.1264-55dupG rs193922698
NM_020630.4(RET):c.2080C>T (p.Arg694Trp) rs193922700
NM_020630.4(RET):c.2081G>A (p.Arg694Gln) rs141185224
NM_020630.4(RET):c.2452G>A (p.Glu818Lys) rs377767420
NM_020630.4(RET):c.2454G>A (p.Glu818=) rs794727131
NM_020630.4(RET):c.2522C>T (p.Pro841Leu) rs149891333
NM_020630.4(RET):c.2543T>A (p.Met848Lys) rs201101792
NM_020630.4(RET):c.2982A>C (p.Lys994Asn) rs199718928
NM_020630.4(RET):c.3116C>T (p.Pro1039Leu) rs79853121
NM_020630.4(RET):c.509C>T (p.Thr170Ile) rs200547906
NM_020630.4(RET):c.539G>A (p.Arg180Gln) rs370736139
NM_020630.5(RET):c.1183G>C (p.Val395Leu)
NM_020630.5(RET):c.1377G>T (p.Glu459Asp)
NM_020630.5(RET):c.1466A>T (p.Asp489Val)
NM_020630.5(RET):c.1942G>A (p.Val648Ile) rs77711105
NM_020630.5(RET):c.2234A>T (p.His745Leu)
NM_020630.5(RET):c.2372A>T (p.Tyr791Phe) rs77724903
NM_020630.5(RET):c.2611G>A (p.Val871Ile) rs145170911
NM_020630.5(RET):c.2834T>C (p.Val945Ala)
NM_020630.5(RET):c.428C>T (p.Ala143Val)
NM_020630.5(RET):c.652C>T (p.Pro218Ser)
NM_020630.5(RET):c.874G>A (p.Val292Met) rs34682185
NM_020630.5(RET):c.961G>A (p.Gly321Arg) rs377767388
NM_020975.4(RET):c.1018G>T (p.Val340Phe) rs367737920
NM_020975.4(RET):c.1063+9G>A rs765463636
NM_020975.4(RET):c.1150C>G (p.Pro384Ala) rs536298339
NM_020975.4(RET):c.1151C>G (p.Pro384Arg) rs771679592
NM_020975.4(RET):c.1187C>T (p.Ser396Leu) rs781646869
NM_020975.4(RET):c.1354C>A (p.Leu452Ile) rs151148041
NM_020975.4(RET):c.139G>A (p.Gly47Ser) rs529018971
NM_020975.4(RET):c.1531G>A (p.Glu511Lys) rs201553718
NM_020975.4(RET):c.1538C>T (p.Ala513Val) rs149238501
NM_020975.4(RET):c.1597G>A (p.Gly533Ser) rs75873440
NM_020975.4(RET):c.1702G>A (p.Gly568Ser) rs140464432
NM_020975.4(RET):c.1724C>T (p.Thr575Ile) rs587780808
NM_020975.4(RET):c.1777G>A (p.Gly593Arg) rs878855059
NM_020975.4(RET):c.1878G>A (p.Gln626=) rs147692872
NM_020975.4(RET):c.1891G>A (p.Asp631Asn) rs377767406
NM_020975.4(RET):c.1897C>G (p.Leu633Val) rs267607010
NM_020975.4(RET):c.1915G>A (p.Ala639Thr) rs777122776
NM_020975.4(RET):c.1921G>A (p.Ala641Thr) rs377767411
NM_020975.4(RET):c.1946C>T (p.Ser649Leu) rs148935214
NM_020975.4(RET):c.2071G>A (p.Gly691Ser) rs1799939
NM_020975.4(RET):c.2110G>T (p.Val704Phe) rs927029236
NM_020975.4(RET):c.2225C>T (p.Thr742Met) rs773256580
NM_020975.4(RET):c.2261C>T (p.Thr754Met) rs181856591
NM_020975.4(RET):c.2348A>C (p.Asn783Thr) rs587778656
NM_020975.4(RET):c.2449C>T (p.Arg817Cys) rs142318626
NM_020975.4(RET):c.2477A>C (p.Tyr826Ser) rs34617196
NM_020975.4(RET):c.2488G>A (p.Gly830Arg) rs200127630
NM_020975.4(RET):c.2497C>T (p.Arg833Cys) rs377767422
NM_020975.4(RET):c.2530C>T (p.Arg844Trp) rs377767424
NM_020975.4(RET):c.2531G>T (p.Arg844Leu) rs55947360
NM_020975.4(RET):c.2556C>G (p.Ile852Met) rs377767426
NM_020975.4(RET):c.2607+4C>T rs200634990
NM_020975.4(RET):c.2607+5G>A rs143862573
NM_020975.4(RET):c.262A>G (p.Ile88Val) rs141679950
NM_020975.4(RET):c.2641C>G (p.Leu881Val) rs377767427
NM_020975.4(RET):c.2833G>A (p.Val945Met) rs587780811
NM_020975.4(RET):c.2875C>T (p.Arg959Trp) rs587778658
NM_020975.4(RET):c.2887C>A (p.Leu963Ile) rs864622603
NM_020975.4(RET):c.2939+6C>T rs181245759
NM_020975.4(RET):c.2944C>T (p.Arg982Cys) rs17158558
NM_020975.4(RET):c.308A>G (p.His103Arg) rs375390467
NM_020975.4(RET):c.3142C>G (p.Leu1048Val) rs774347808
NM_020975.4(RET):c.3182T>C (p.Leu1061Pro) rs536486113
NM_020975.4(RET):c.3185A>G (p.Tyr1062Cys) rs587778659
NM_020975.4(RET):c.334C>T (p.Arg112Cys) rs762626209
NM_020975.4(RET):c.335G>A (p.Arg112His) rs587780814
NM_020975.4(RET):c.431G>A (p.Arg144His) rs551142665
NM_020975.4(RET):c.604G>A (p.Val202Met) rs751572082
NM_020975.4(RET):c.667G>A (p.Val223Met) rs587780815
NM_020975.4(RET):c.785T>C (p.Val262Ala) rs139790943
NM_020975.4(RET):c.832A>G (p.Thr278Ala) rs541929171
NM_020975.4(RET):c.835G>A (p.Ala279Thr) rs777221273
NM_020975.4(RET):c.938G>A (p.Arg313Gln) rs77702891
NM_020975.4(RET):c.972G>C (p.Trp324Cys) rs758298916
NM_020975.4(RET):c.977A>G (p.Gln326Arg) rs863224778
NM_020975.5(RET):c.1013C>T (p.Thr338Ile) rs377767433
NM_020975.5(RET):c.1016C>T (p.Ser339Leu) rs774829203
NM_020975.5(RET):c.1083C>A (p.Asn361Lys) rs770587835
NM_020975.5(RET):c.1267G>A (p.Gly423Arg) rs767601598
NM_020975.5(RET):c.1312G>A (p.Val438Ile) rs774474422
NM_020975.5(RET):c.134C>T (p.Ala45Val) rs763526874
NM_020975.5(RET):c.1423C>T (p.Arg475Trp)
NM_020975.5(RET):c.1441C>G (p.Leu481Val) rs767210575
NM_020975.5(RET):c.1448A>G (p.Tyr483Cys) rs752322996
NM_020975.5(RET):c.1462A>T (p.Thr488Ser) rs753733901
NM_020975.5(RET):c.1467C>A (p.Asp489Glu) rs372648203
NM_020975.5(RET):c.1567A>C (p.Lys523Gln) rs766278774
NM_020975.5(RET):c.1642G>A (p.Gly548Ser) rs374461212
NM_020975.5(RET):c.1678C>T (p.Pro560Ser) rs748852160
NM_020975.5(RET):c.1760-3C>T rs587781734
NM_020975.5(RET):c.1876C>A (p.Gln626Lys) rs1255575160
NM_020975.5(RET):c.1894G>A (p.Glu632Lys) rs377767407
NM_020975.5(RET):c.1907C>T (p.Thr636Met) rs1035958105
NM_020975.5(RET):c.2116G>A (p.Val706Met) rs137855422
NM_020975.5(RET):c.2129A>G (p.Lys710Arg)
NM_020975.5(RET):c.2166G>T (p.Lys722Asn) rs527726480
NM_020975.5(RET):c.2330A>G (p.Asn777Ser) rs377767415
NM_020975.5(RET):c.2371T>A (p.Tyr791Asn) rs377767417
NM_020975.5(RET):c.2392+19T>C rs778745375
NM_020975.5(RET):c.2432C>G (p.Ser811Cys) rs587778657
NM_020975.5(RET):c.2527G>A (p.Glu843Lys) rs755837568
NM_020975.5(RET):c.2531G>A (p.Arg844Gln) rs55947360
NM_020975.5(RET):c.2931C>G (p.Ser977Arg) rs375414982
NM_020975.5(RET):c.2945G>A (p.Arg982His) rs368550200
NM_020975.5(RET):c.3052C>T (p.Leu1018Phe) rs766330880
NM_020975.5(RET):c.3149G>A (p.Arg1050Gln) rs200956659
NM_020975.5(RET):c.3176A>G (p.Asn1059Ser) rs772395752
NM_020975.5(RET):c.3188-2A>G rs1554820302
NM_020975.5(RET):c.3188-9C>T rs551159582
NM_020975.5(RET):c.3199C>T (p.Pro1067Ser) rs775583354
NM_020975.5(RET):c.3206G>C (p.Trp1069Ser) rs776615468
NM_020975.5(RET):c.3253A>G (p.Thr1085Ala) rs756465544
NM_020975.5(RET):c.3314C>T (p.Ala1105Val) rs532862288
NM_020975.5(RET):c.405C>T (p.Gly135=) rs142345108
NM_020975.5(RET):c.406G>A (p.Glu136Lys) rs79014735
NM_020975.5(RET):c.433G>A (p.Val145Ile)
NM_020975.5(RET):c.452A>G (p.Asn151Ser) rs150261092
NM_020975.5(RET):c.50_58dup (p.Leu19_Pro20insLeuLeuLeu) rs768132465
NM_020975.5(RET):c.973G>A (p.Ala325Thr) rs779719517
NM_020975.6(RET):c.1438G>A (p.Glu480Lys) rs537874538

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