ClinVar Miner

List of variants reported as uncertain significance for adrenal carcinoma by Counsyl

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 84
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HGVS dbSNP
NM_020975.6(RET):c.1016C>T (p.Ser339Leu) rs774829203
NM_020975.6(RET):c.1018G>T (p.Val340Phe) rs367737920
NM_020975.6(RET):c.1063+9G>A rs765463636
NM_020975.6(RET):c.1083C>A (p.Asn361Lys) rs770587835
NM_020975.6(RET):c.1150C>G (p.Pro384Ala) rs536298339
NM_020975.6(RET):c.1187C>T (p.Ser396Leu) rs781646869
NM_020975.6(RET):c.1267G>A (p.Gly423Arg) rs767601598
NM_020975.6(RET):c.1312G>A (p.Val438Ile) rs774474422
NM_020975.6(RET):c.134C>T (p.Ala45Val) rs763526874
NM_020975.6(RET):c.1354C>A (p.Leu452Ile) rs151148041
NM_020975.6(RET):c.139G>A (p.Gly47Ser) rs529018971
NM_020975.6(RET):c.1438G>A (p.Glu480Lys) rs537874538
NM_020975.6(RET):c.1441C>G (p.Leu481Val) rs767210575
NM_020975.6(RET):c.1531G>A (p.Glu511Lys) rs201553718
NM_020975.6(RET):c.1538C>T (p.Ala513Val) rs149238501
NM_020975.6(RET):c.1597G>A (p.Gly533Ser) rs75873440
NM_020975.6(RET):c.1642G>A (p.Gly548Ser) rs374461212
NM_020975.6(RET):c.1702G>A (p.Gly568Ser) rs140464432
NM_020975.6(RET):c.1724C>T (p.Thr575Ile) rs587780808
NM_020975.6(RET):c.1760-3C>T rs587781734
NM_020975.6(RET):c.1777G>A (p.Gly593Arg) rs878855059
NM_020975.6(RET):c.1876C>A (p.Gln626Lys) rs1255575160
NM_020975.6(RET):c.1878G>A (p.Gln626=) rs147692872
NM_020975.6(RET):c.1894G>A (p.Glu632Lys) rs377767407
NM_020975.6(RET):c.1897C>G (p.Leu633Val) rs267607010
NM_020975.6(RET):c.1915G>A (p.Ala639Thr) rs777122776
NM_020975.6(RET):c.1921G>A (p.Ala641Thr) rs377767411
NM_020975.6(RET):c.1942G>A (p.Val648Ile) rs77711105
NM_020975.6(RET):c.2080C>T (p.Arg694Trp) rs193922700
NM_020975.6(RET):c.2081G>A (p.Arg694Gln) rs141185224
NM_020975.6(RET):c.2110G>T (p.Val704Phe) rs927029236
NM_020975.6(RET):c.2116G>A (p.Val706Met) rs137855422
NM_020975.6(RET):c.2225C>T (p.Thr742Met) rs773256580
NM_020975.6(RET):c.2261C>T (p.Thr754Met) rs181856591
NM_020975.6(RET):c.2348A>C (p.Asn783Thr) rs587778656
NM_020975.6(RET):c.2371T>A (p.Tyr791Asn) rs377767417
NM_020975.6(RET):c.2392+19T>C rs778745375
NM_020975.6(RET):c.2449C>T (p.Arg817Cys) rs142318626
NM_020975.6(RET):c.2452G>A (p.Glu818Lys) rs377767420
NM_020975.6(RET):c.2477A>C (p.Tyr826Ser) rs34617196
NM_020975.6(RET):c.2488G>A (p.Gly830Arg) rs200127630
NM_020975.6(RET):c.2497C>T (p.Arg833Cys) rs377767422
NM_020975.6(RET):c.2522C>T (p.Pro841Leu) rs149891333
NM_020975.6(RET):c.2530C>T (p.Arg844Trp) rs377767424
NM_020975.6(RET):c.2531G>A (p.Arg844Gln) rs55947360
NM_020975.6(RET):c.2531G>T (p.Arg844Leu) rs55947360
NM_020975.6(RET):c.2543T>A (p.Met848Lys) rs201101792
NM_020975.6(RET):c.2556C>G (p.Ile852Met) rs377767426
NM_020975.6(RET):c.2607+4C>T rs200634990
NM_020975.6(RET):c.2607+5G>A rs143862573
NM_020975.6(RET):c.2611G>A (p.Val871Ile) rs145170911
NM_020975.6(RET):c.262A>G (p.Ile88Val) rs141679950
NM_020975.6(RET):c.2641C>G (p.Leu881Val) rs377767427
NM_020975.6(RET):c.2833G>A (p.Val945Met) rs587780811
NM_020975.6(RET):c.2875C>T (p.Arg959Trp) rs587778658
NM_020975.6(RET):c.2887C>A (p.Leu963Ile) rs864622603
NM_020975.6(RET):c.2931C>G (p.Ser977Arg) rs375414982
NM_020975.6(RET):c.2939+6C>T rs181245759
NM_020975.6(RET):c.2982A>C (p.Lys994Asn) rs199718928
NM_020975.6(RET):c.308A>G (p.His103Arg) rs375390467
NM_020975.6(RET):c.3116C>T (p.Pro1039Leu) rs79853121
NM_020975.6(RET):c.3142C>G (p.Leu1048Val) rs774347808
NM_020975.6(RET):c.3176A>G (p.Asn1059Ser) rs772395752
NM_020975.6(RET):c.3182T>C (p.Leu1061Pro) rs536486113
NM_020975.6(RET):c.3185A>G (p.Tyr1062Cys) rs587778659
NM_020975.6(RET):c.3188-2A>G rs1554820302
NM_020975.6(RET):c.3188-9C>T rs551159582
NM_020975.6(RET):c.3199C>T (p.Pro1067Ser) rs775583354
NM_020975.6(RET):c.3206G>C (p.Trp1069Ser) rs776615468
NM_020975.6(RET):c.3253A>G (p.Thr1085Ala) rs756465544
NM_020975.6(RET):c.3314C>T (p.Ala1105Val) rs532862288
NM_020975.6(RET):c.334C>T (p.Arg112Cys) rs762626209
NM_020975.6(RET):c.335G>A (p.Arg112His) rs587780814
NM_020975.6(RET):c.406G>A (p.Glu136Lys) rs79014735
NM_020975.6(RET):c.431G>A (p.Arg144His) rs551142665
NM_020975.6(RET):c.509C>T (p.Thr170Ile) rs200547906
NM_020975.6(RET):c.539G>A (p.Arg180Gln) rs370736139
NM_020975.6(RET):c.604G>A (p.Val202Met) rs751572082
NM_020975.6(RET):c.667G>A (p.Val223Met) rs587780815
NM_020975.6(RET):c.832A>G (p.Thr278Ala) rs541929171
NM_020975.6(RET):c.835G>A (p.Ala279Thr) rs777221273
NM_020975.6(RET):c.938G>A (p.Arg313Gln) rs77702891
NM_020975.6(RET):c.972G>C (p.Trp324Cys) rs758298916
NM_020975.6(RET):c.977A>G (p.Gln326Arg) rs863224778

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