ClinVar Miner

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

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 109
Download table as spreadsheet
HGVS dbSNP
NM_000244.3(MEN1):c.*104C>T rs886048477
NM_000244.3(MEN1):c.*272T>C rs563783609
NM_000244.3(MEN1):c.*373G>C rs886048476
NM_000244.3(MEN1):c.*392G>A rs886048475
NM_000244.3(MEN1):c.*438C>T rs886048474
NM_000244.3(MEN1):c.*89G>A rs886048478
NM_000244.3(MEN1):c.-94G>A rs886048480
NM_000244.3(MEN1):c.1201-10C>T rs762303621
NM_000244.3(MEN1):c.327A>C (p.Glu109Asp) rs773976527
NM_000244.3(MEN1):c.585G>A (p.Gly195=) rs547249181
NM_000244.3(MEN1):c.956G>A (p.Arg319Gln) rs771645621
NM_000546.6(TP53):c.*1132C>T
NM_000546.6(TP53):c.*144G>A
NM_000546.6(TP53):c.*168C>T
NM_000546.6(TP53):c.*760T>C
NM_000546.6(TP53):c.*761T>C
NM_000546.6(TP53):c.-123C>T
NM_000546.6(TP53):c.-22G>A
NM_000546.6(TP53):c.1093C>T (p.His365Tyr) rs267605075
NM_000546.6(TP53):c.31G>C (p.Glu11Gln) rs201382018
NM_001126112.2(TP53):c.*1160T>G rs886053499
NM_001126112.2(TP53):c.*327C>T rs886053512
NM_001126112.2(TP53):c.*346G>T rs886053511
NM_001126112.2(TP53):c.*347T>C rs886053510
NM_001126112.2(TP53):c.*382C>T rs886053509
NM_001126112.2(TP53):c.*548G>T rs886053508
NM_001126112.2(TP53):c.*565G>T rs886053507
NM_001126112.2(TP53):c.*626C>T rs886053506
NM_001126112.2(TP53):c.*735C>A rs886053505
NM_001126112.2(TP53):c.*747C>T rs886053504
NM_001126112.2(TP53):c.*754C>T rs199729221
NM_001126112.2(TP53):c.*772del rs200757381
NM_001126112.2(TP53):c.*779del rs886053503
NM_001126112.2(TP53):c.*790G>A rs886053502
NM_001126112.2(TP53):c.*806C>A rs886053501
NM_001126112.2(TP53):c.*977G>C rs886053500
NM_001126112.2(TP53):c.*99G>A rs886053513
NM_001126112.2(TP53):c.-70C>A rs886053514
NM_001126112.2(TP53):c.-91C>T rs886053515
NM_001126112.2(TP53):c.-99C>G rs886053516
NM_001126112.2(TP53):c.1015G>A (p.Glu339Lys) rs17882252
NM_001126112.2(TP53):c.145G>A (p.Asp49Asn) rs587780728
NM_001126112.2(TP53):c.145G>C (p.Asp49His) rs587780728
NM_001126112.2(TP53):c.63C>T (p.Asp21=) rs1800369
NM_001126112.2(TP53):c.74+9A>C rs1057517593
NM_001126112.2(TP53):c.782+12C>T rs17881780
NM_001126112.2(TP53):c.96+15T>C rs200053580
NM_001126112.2(TP53):c.993+8G>A rs1060504163
NM_001276290.1(PRKAR1A):c.973+3439G>T
NM_001370259.2(MEN1):c.*245C>T
NM_001370259.2(MEN1):c.*341C>G
NM_001370259.2(MEN1):c.*400G>A
NM_001370259.2(MEN1):c.*470A>G rs778272737
NM_001370259.2(MEN1):c.*693T>C
NM_001370259.2(MEN1):c.1414G>C (p.Gly472Arg)
NM_001370259.2(MEN1):c.1618C>T (p.Pro540Ser) rs745404679
NM_001370259.2(MEN1):c.274C>A (p.Arg92Ser)
NM_001370259.2(MEN1):c.655-6C>G rs77461664
NM_001370259.2(MEN1):c.849G>T (p.Leu283=)
NM_001370259.2(MEN1):c.965T>C (p.Met322Thr)
NM_002734.5(PRKAR1A):c.*1003C>T
NM_002734.5(PRKAR1A):c.*1085G>A
NM_002734.5(PRKAR1A):c.*1111C>G
NM_002734.5(PRKAR1A):c.*1640C>T
NM_002734.5(PRKAR1A):c.*1687T>C
NM_002734.5(PRKAR1A):c.*1838A>T
NM_002734.5(PRKAR1A):c.*1949G>T
NM_002734.5(PRKAR1A):c.*2089A>G
NM_002734.5(PRKAR1A):c.*2114G>A
NM_002734.5(PRKAR1A):c.*2152T>C
NM_002734.5(PRKAR1A):c.*233C>T
NM_002734.5(PRKAR1A):c.*2940G>A
NM_002734.5(PRKAR1A):c.*299T>G
NM_002734.5(PRKAR1A):c.*331G>A
NM_002734.5(PRKAR1A):c.*384C>T
NM_002734.5(PRKAR1A):c.*535T>G
NM_002734.5(PRKAR1A):c.*560G>A
NM_002734.5(PRKAR1A):c.*609C>G
NM_002734.5(PRKAR1A):c.*812A>G
NM_002734.5(PRKAR1A):c.-11C>T
NM_002734.5(PRKAR1A):c.28G>A (p.Glu10Lys)
NM_002734.5(PRKAR1A):c.770-8T>G
NM_212472.2(PRKAR1A):c.*1014A>G rs886053311
NM_212472.2(PRKAR1A):c.*1062A>G rs752303671
NM_212472.2(PRKAR1A):c.*1118dup rs886053312
NM_212472.2(PRKAR1A):c.*1168A>T rs886053313
NM_212472.2(PRKAR1A):c.*1346A>G rs545417998
NM_212472.2(PRKAR1A):c.*1487C>T rs886053314
NM_212472.2(PRKAR1A):c.*156C>T rs535007635
NM_212472.2(PRKAR1A):c.*1839G>A rs886053316
NM_212472.2(PRKAR1A):c.*1842A>T rs886053317
NM_212472.2(PRKAR1A):c.*2018C>T rs540185706
NM_212472.2(PRKAR1A):c.*2067T>C rs886053318
NM_212472.2(PRKAR1A):c.*2072G>A rs886053319
NM_212472.2(PRKAR1A):c.*2196C>T rs886053320
NM_212472.2(PRKAR1A):c.*2197G>A rs533508012
NM_212472.2(PRKAR1A):c.*389T>G rs886053307
NM_212472.2(PRKAR1A):c.*526G>A rs886053308
NM_212472.2(PRKAR1A):c.*587del rs398041821
NM_212472.2(PRKAR1A):c.*704T>G rs886053310
NM_212472.2(PRKAR1A):c.*722A>G rs555951287
NM_212472.2(PRKAR1A):c.*724T>A rs746409603
NM_212472.2(PRKAR1A):c.*893G>C rs186568426
NM_212472.2(PRKAR1A):c.-200T>A
NM_212472.2(PRKAR1A):c.-47C>A rs886053305
NM_212472.2(PRKAR1A):c.-56C>T rs546338099
NM_212472.2(PRKAR1A):c.-84C>T rs886053304
NM_212472.2(PRKAR1A):c.309G>A (p.Glu103=) rs746113372
NM_212472.2(PRKAR1A):c.331G>A (p.Ala111Thr) rs1472324247

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.