ClinVar Miner

List of variants reported as likely benign for adrenal carcinoma by Counsyl

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NM_020630.5(RET):c.2372A>T (p.Tyr791Phe) rs77724903
NM_020975.5(RET):c.2137-16del rs1409965349
NM_020975.6(RET):c.1017G>A (p.Ser339=) rs369810881
NM_020975.6(RET):c.1095G>A (p.Ser365=) rs201992974
NM_020975.6(RET):c.1118C>T (p.Ala373Val) rs546866208
NM_020975.6(RET):c.1182C>T (p.Asn394=) rs376465385
NM_020975.6(RET):c.1188G>A (p.Ser396=) rs758510657
NM_020975.6(RET):c.1197G>A (p.Pro399=) rs148371113
NM_020975.6(RET):c.1264-4C>T rs587780806
NM_020975.6(RET):c.1336G>C (p.Gly446Arg) rs115423919
NM_020975.6(RET):c.1437C>T (p.Ala479=) rs576806356
NM_020975.6(RET):c.1522+35C>T rs377130948
NM_020975.6(RET):c.1530C>T (p.Ala510=) rs553492964
NM_020975.6(RET):c.1648+24G>A rs1057517640
NM_020975.6(RET):c.1649-4G>A rs369769303
NM_020975.6(RET):c.1760-12G>A rs377767392
NM_020975.6(RET):c.1879+13C>T rs375573788
NM_020975.6(RET):c.1879+14G>A rs532810255
NM_020975.6(RET):c.1879+17C>T rs369920430
NM_020975.6(RET):c.1893C>T (p.Asp631=) rs55846256
NM_020975.6(RET):c.1946C>T (p.Ser649Leu) rs148935214
NM_020975.6(RET):c.2070C>T (p.Ser690=) rs201550433
NM_020975.6(RET):c.2136+15G>A rs751183869
NM_020975.6(RET):c.2226G>A (p.Thr742=) rs762876946
NM_020975.6(RET):c.225G>A (p.Thr75=) rs151267865
NM_020975.6(RET):c.2284+54C>A rs566375223
NM_020975.6(RET):c.2285-4T>G rs376601566
NM_020975.6(RET):c.2298G>A (p.Pro766=) rs140658743
NM_020975.6(RET):c.2393-9C>T rs567543719
NM_020975.6(RET):c.2409C>T (p.Ile803=) rs535051804
NM_020975.6(RET):c.2523G>A (p.Pro841=) rs56195026
NM_020975.6(RET):c.2715C>T (p.Tyr905=) rs755023496
NM_020975.6(RET):c.2802-4G>T rs878855061
NM_020975.6(RET):c.2988G>A (p.Pro996=) rs145798106
NM_020975.6(RET):c.3040-11C>G rs1057517646
NM_020975.6(RET):c.3057G>A (p.Ala1019=) rs369579749
NM_020975.6(RET):c.3112A>G (p.Thr1038Ala) rs201740483
NM_020975.6(RET):c.3243T>C (p.Asp1081=) rs144192900
NM_020975.6(RET):c.337+11C>T rs754967305
NM_020975.6(RET):c.337+12G>A rs200468424
NM_020975.6(RET):c.337+29G>A rs578158807
NM_020975.6(RET):c.337+34C>T rs368088467
NM_020975.6(RET):c.693C>T (p.Arg231=) rs576806329
NM_020975.6(RET):c.73+9278G>A rs537638504
NM_020975.6(RET):c.785T>C (p.Val262Ala) rs139790943

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