ClinVar Miner

List of variants reported as likely benign for Cushing syndrome by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (24):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NM_000546.5(TP53):c.*1070C>T rs114831472
NM_000546.5(TP53):c.*1175A>C rs78378222
NM_000546.5(TP53):c.*205G>A rs16956880
NM_000546.5(TP53):c.*485G>A rs4968187
NM_000546.5(TP53):c.*569_*570delGT rs1555523911
NM_000546.5(TP53):c.*613C>A rs17879353
NM_000546.5(TP53):c.*826G>A rs17884306
NM_000546.5(TP53):c.*936A>G rs55817367
NM_000546.5(TP53):c.108G>A (p.Pro36=) rs1800370
NM_000546.5(TP53):c.639A>G (p.Arg213=) rs1800372
NM_000546.5(TP53):c.91G>A (p.Val31Ile) rs201753350
NM_000546.5(TP53):c.97-6C>T rs35117667
NM_000546.5(TP53):c.993+12T>C rs1800899
NM_001126113.2(TP53):c.*1422G>C rs17883782
NM_002734.4(PRKAR1A):c.*1346A>G rs545417998
NM_002734.4(PRKAR1A):c.*138C>A rs28730842
NM_002734.4(PRKAR1A):c.*151A>G rs11540571
NM_002734.4(PRKAR1A):c.*156C>T rs535007635
NM_002734.4(PRKAR1A):c.*1606A>G rs144632545
NM_002734.4(PRKAR1A):c.*172_*175delCTAA rs201146882
NM_002734.4(PRKAR1A):c.*1835delA rs138320066
NM_002734.4(PRKAR1A):c.*1837G>T rs201999343
NM_002734.4(PRKAR1A):c.*2018C>T rs540185706
NM_002734.4(PRKAR1A):c.*2197G>A rs533508012
NM_002734.4(PRKAR1A):c.*672T>C rs546125048
NM_002734.4(PRKAR1A):c.*722A>G rs555951287
NM_002734.4(PRKAR1A):c.*759C>T rs62087489
NM_002734.4(PRKAR1A):c.*795G>T rs150031305
NM_002734.4(PRKAR1A):c.*812A>C rs116996069
NM_002734.4(PRKAR1A):c.*847A>G rs144299673
NM_002734.4(PRKAR1A):c.*893G>C rs186568426
NM_002734.4(PRKAR1A):c.-25C>T rs546338099
NM_002734.4(PRKAR1A):c.-75G>T rs559757120
NM_002734.4(PRKAR1A):c.103A>G (p.Ile35Val) rs377513504
NM_002734.4(PRKAR1A):c.204G>A (p.Leu68=) rs74863634
NM_002734.4(PRKAR1A):c.221G>A (p.Arg74His) rs200069356
NM_002734.4(PRKAR1A):c.546G>A (p.Thr182=) rs117639566
NM_002734.4(PRKAR1A):c.678C>T (p.Ile226=) rs200592054
NM_002734.4(PRKAR1A):c.87G>A (p.Ala29=) rs3730349
NM_017565.4(FAM20A):c.1511C>T (p.Thr504Ile) rs146689929
NM_018081.2(WRAP53):c.-206G>A rs17551150
NM_018081.2(WRAP53):c.-245G>C rs17883670
NM_018081.2(WRAP53):c.31C>T (p.Pro11Ser) rs17880282
NM_018081.2(WRAP53):c.407C>G (p.Pro136Arg) rs34067256
NM_018081.2(WRAP53):c.450C>T (p.Phe150=) rs2287498

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