ClinVar Miner

List of variants reported as uncertain significance for Cushing syndrome by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (23):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NM_000546.5(TP53):c.*1160T>G rs886053499
NM_000546.5(TP53):c.*327C>T rs886053512
NM_000546.5(TP53):c.*346G>T rs886053511
NM_000546.5(TP53):c.*347T>C rs886053510
NM_000546.5(TP53):c.*382C>T rs886053509
NM_000546.5(TP53):c.*548G>T rs886053508
NM_000546.5(TP53):c.*565G>T rs886053507
NM_000546.5(TP53):c.*626C>T rs886053506
NM_000546.5(TP53):c.*735C>A rs886053505
NM_000546.5(TP53):c.*747C>T rs886053504
NM_000546.5(TP53):c.*754C>T rs199729221
NM_000546.5(TP53):c.*772delT rs200757381
NM_000546.5(TP53):c.*779delC rs886053503
NM_000546.5(TP53):c.*790G>A rs886053502
NM_000546.5(TP53):c.*806C>A rs886053501
NM_000546.5(TP53):c.*977G>C rs886053500
NM_000546.5(TP53):c.*99G>A rs886053513
NM_000546.5(TP53):c.-73C>A rs886053514
NM_000546.5(TP53):c.63C>T (p.Asp21=) rs1800369
NM_002734.4(PRKAR1A):c.*1014A>G rs886053311
NM_002734.4(PRKAR1A):c.*1062A>G rs752303671
NM_002734.4(PRKAR1A):c.*1118dupT rs886053312
NM_002734.4(PRKAR1A):c.*1168A>T rs886053313
NM_002734.4(PRKAR1A):c.*1487C>T rs886053314
NM_002734.4(PRKAR1A):c.*1839G>A rs886053316
NM_002734.4(PRKAR1A):c.*1842A>T rs886053317
NM_002734.4(PRKAR1A):c.*2067T>C rs886053318
NM_002734.4(PRKAR1A):c.*2072G>A rs886053319
NM_002734.4(PRKAR1A):c.*2196C>T rs886053320
NM_002734.4(PRKAR1A):c.*389T>G rs886053307
NM_002734.4(PRKAR1A):c.*526G>A rs886053308
NM_002734.4(PRKAR1A):c.*587delT rs398041821
NM_002734.4(PRKAR1A):c.*704T>G rs886053310
NM_002734.4(PRKAR1A):c.*724T>A rs746409603
NM_002734.4(PRKAR1A):c.-16C>A rs886053305
NM_002734.4(PRKAR1A):c.-53C>T rs886053304
NM_002734.4(PRKAR1A):c.-6-7C>T rs373646911
NM_002734.4(PRKAR1A):c.309G>A (p.Glu103=) rs746113372

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