ClinVar Miner

List of variants studied for Carney complex, type 1 by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 52
Download table as spreadsheet
HGVS dbSNP
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.*1212T>G rs8905
NM_002734.4(PRKAR1A):c.*1244T>C rs9925
NM_002734.4(PRKAR1A):c.*1346A>G rs545417998
NM_002734.4(PRKAR1A):c.*138C>A rs28730842
NM_002734.4(PRKAR1A):c.*1487C>T rs886053314
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.*1777C>T rs7977
NM_002734.4(PRKAR1A):c.*1835delA rs138320066
NM_002734.4(PRKAR1A):c.*1837G>T rs201999343
NM_002734.4(PRKAR1A):c.*1839G>A rs886053316
NM_002734.4(PRKAR1A):c.*1842A>T rs886053317
NM_002734.4(PRKAR1A):c.*2018C>T rs540185706
NM_002734.4(PRKAR1A):c.*2067T>C rs886053318
NM_002734.4(PRKAR1A):c.*2072G>A rs886053319
NM_002734.4(PRKAR1A):c.*2188C>G rs6958
NM_002734.4(PRKAR1A):c.*2196C>T rs886053320
NM_002734.4(PRKAR1A):c.*2197G>A rs533508012
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.*587dupT rs398041821
NM_002734.4(PRKAR1A):c.*672T>C rs546125048
NM_002734.4(PRKAR1A):c.*704T>G rs886053310
NM_002734.4(PRKAR1A):c.*722A>G rs555951287
NM_002734.4(PRKAR1A):c.*724T>A rs746409603
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.*870G>A rs8082254
NM_002734.4(PRKAR1A):c.*893G>C rs186568426
NM_002734.4(PRKAR1A):c.-16C>A rs886053305
NM_002734.4(PRKAR1A):c.-25C>T rs546338099
NM_002734.4(PRKAR1A):c.-53C>T rs886053304
NM_002734.4(PRKAR1A):c.-6-7C>T rs373646911
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.309G>A (p.Glu103=) rs746113372
NM_002734.4(PRKAR1A):c.349-5dupT rs3841514
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

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.