ClinVar Miner

List of variants reported as uncertain significance for adrenal gland disease by Mendelics

Included ClinVar conditions (124):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 71
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HGVS dbSNP
NM_000244.3(MEN1):c.1180C>T (p.Arg394Trp) rs566593066
NM_000244.3(MEN1):c.1421A>C (p.Glu474Ala) rs1565638407
NM_000244.3(MEN1):c.1558C>T (p.Pro520Ser)
NM_000244.3(MEN1):c.1609G>T (p.Gly537Cys) rs587780843
NM_000244.3(MEN1):c.1633C>T (p.Pro545Ser) rs745404679
NM_000244.3(MEN1):c.1652C>T (p.Pro551Leu) rs779413959
NM_000244.3(MEN1):c.203C>T (p.Ala68Val) rs1319371332
NM_000244.3(MEN1):c.236C>G (p.Pro79Arg) rs1555166557
NM_000244.3(MEN1):c.343C>G (p.Arg115Gly) rs1565651402
NM_000244.3(MEN1):c.409C>T (p.Arg137Trp) rs1208267598
NM_000244.3(MEN1):c.670-6C>G rs77461664
NM_000244.3(MEN1):c.818A>G (p.Tyr273Cys) rs773500082
NM_000546.5(TP53):c.1069A>G (p.Lys357Glu) rs1567541856
NM_000546.5(TP53):c.234_263del (p.Ala79_Ala88del) rs754312472
NM_000546.5(TP53):c.285T>G (p.Ser95=) rs876658696
NM_000546.5(TP53):c.28G>A (p.Val10Ile) rs535274413
NM_000546.5(TP53):c.31G>C (p.Glu11Gln) rs201382018
NM_000546.5(TP53):c.320A>G (p.Tyr107Cys) rs587782447
NM_000546.5(TP53):c.417G>T (p.Lys139Asn) rs1567554121
NM_000546.5(TP53):c.467G>A (p.Arg156His) rs371524413
NM_000546.5(TP53):c.623A>G (p.Asp208Gly) rs1464727668
NM_000546.5(TP53):c.642T>G (p.His214Gln) rs587781386
NM_000546.5(TP53):c.66A>G (p.Leu22=) rs748527030
NM_000546.5(TP53):c.869G>A (p.Arg290His) rs55819519
NM_000546.5(TP53):c.91G>A (p.Val31Ile) rs201753350
NM_000546.5(TP53):c.935C>G (p.Thr312Ser) rs145151284
NM_000546.5(TP53):c.997C>T (p.Arg333Cys) rs769934890
NM_001126113.2(TP53):c.1028T>A (p.Ile343Lys) rs1567545268
NM_020975.6(RET):c.1013C>T (p.Thr338Ile) rs377767433
NM_020975.6(RET):c.1063+9G>A rs765463636
NM_020975.6(RET):c.1183G>C (p.Val395Leu) rs1452469572
NM_020975.6(RET):c.134C>T (p.Ala45Val) rs763526874
NM_020975.6(RET):c.1377G>T (p.Glu459Asp) rs1564494424
NM_020975.6(RET):c.1423C>T (p.Arg475Trp)
NM_020975.6(RET):c.1448A>G (p.Tyr483Cys) rs752322996
NM_020975.6(RET):c.1462A>T (p.Thr488Ser) rs753733901
NM_020975.6(RET):c.1466A>T (p.Asp489Val)
NM_020975.6(RET):c.1467C>A (p.Asp489Glu) rs372648203
NM_020975.6(RET):c.1531G>A (p.Glu511Lys) rs201553718
NM_020975.6(RET):c.1567A>C (p.Lys523Gln) rs766278774
NM_020975.6(RET):c.1642G>A (p.Gly548Ser) rs374461212
NM_020975.6(RET):c.1678C>T (p.Pro560Ser) rs748852160
NM_020975.6(RET):c.1760-3C>T rs587781734
NM_020975.6(RET):c.1876C>A (p.Gln626Lys) rs1255575160
NM_020975.6(RET):c.1907C>T (p.Thr636Met) rs1035958105
NM_020975.6(RET):c.1946C>T (p.Ser649Leu) rs148935214
NM_020975.6(RET):c.2081G>A (p.Arg694Gln) rs141185224
NM_020975.6(RET):c.2116G>A (p.Val706Met) rs137855422
NM_020975.6(RET):c.2129A>G (p.Lys710Arg)
NM_020975.6(RET):c.2166G>T (p.Lys722Asn) rs527726480
NM_020975.6(RET):c.2234A>T (p.His745Leu)
NM_020975.6(RET):c.2330A>G (p.Asn777Ser) rs377767415
NM_020975.6(RET):c.2371T>A (p.Tyr791Asn) rs377767417
NM_020975.6(RET):c.2432C>G (p.Ser811Cys) rs587778657
NM_020975.6(RET):c.2527G>A (p.Glu843Lys) rs755837568
NM_020975.6(RET):c.2531G>A (p.Arg844Gln) rs55947360
NM_020975.6(RET):c.2611G>A (p.Val871Ile) rs145170911
NM_020975.6(RET):c.2834T>C (p.Val945Ala) rs1408196943
NM_020975.6(RET):c.2931C>G (p.Ser977Arg) rs375414982
NM_020975.6(RET):c.3052C>T (p.Leu1018Phe) rs766330880
NM_020975.6(RET):c.3149G>A (p.Arg1050Gln) rs200956659
NM_020975.6(RET):c.3314C>T (p.Ala1105Val) rs532862288
NM_020975.6(RET):c.405C>T (p.Gly135=) rs142345108
NM_020975.6(RET):c.428C>T (p.Ala143Val) rs1564490082
NM_020975.6(RET):c.44_46TGC[8] (p.Leu17_Leu19dup) rs768132465
NM_020975.6(RET):c.452A>G (p.Asn151Ser) rs150261092
NM_020975.6(RET):c.652C>T (p.Pro218Ser)
NM_020975.6(RET):c.785T>C (p.Val262Ala) rs139790943
NM_020975.6(RET):c.874G>A (p.Val292Met) rs34682185
NM_020975.6(RET):c.961G>A (p.Gly321Arg) rs377767388
NM_020975.6(RET):c.973G>A (p.Ala325Thr) rs779719517

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