ClinVar Miner

List of variants in gene FAM20A, PRKAR1A studied for Carney complex

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
Download table as spreadsheet
HGVS dbSNP
NC_000017.10:g.(?_66508520)_(66526600_?)del
NC_000017.10:g.(?_66511535)_(66526596_?)del
NC_000017.11:g.(?_68512379)_(68533431_?)del
NC_000017.11:g.(?_68528870)_(68530449_?)del
NM_017565.4(FAM20A):c.1511C>T (p.Thr504Ile) rs146689929
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.*1212T>G rs8905
NM_212472.2(PRKAR1A):c.*1244T>C rs9925
NM_212472.2(PRKAR1A):c.*1346A>G rs545417998
NM_212472.2(PRKAR1A):c.*138C>A rs28730842
NM_212472.2(PRKAR1A):c.*1487C>T rs886053314
NM_212472.2(PRKAR1A):c.*151A>G rs11540571
NM_212472.2(PRKAR1A):c.*156C>T rs535007635
NM_212472.2(PRKAR1A):c.*1606A>G rs144632545
NM_212472.2(PRKAR1A):c.*172_*175del rs201146882
NM_212472.2(PRKAR1A):c.*1777C>T rs7977
NM_212472.2(PRKAR1A):c.*1835del rs138320066
NM_212472.2(PRKAR1A):c.*1837G>T rs201999343
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.*2188C>G rs6958
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.*587dup rs398041821
NM_212472.2(PRKAR1A):c.*672T>C rs546125048
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.*759C>T rs62087489
NM_212472.2(PRKAR1A):c.*795G>T rs150031305
NM_212472.2(PRKAR1A):c.*812A>C rs116996069
NM_212472.2(PRKAR1A):c.*847A>G rs144299673
NM_212472.2(PRKAR1A):c.*870G>A rs8082254
NM_212472.2(PRKAR1A):c.*893G>C rs186568426
NM_212472.2(PRKAR1A):c.1003C>T (p.Arg335Cys) rs1555815121
NM_212472.2(PRKAR1A):c.1024C>T (p.Arg342Cys) rs146383819
NM_212472.2(PRKAR1A):c.1025G>A (p.Arg342His) rs760033566
NM_212472.2(PRKAR1A):c.1031C>T (p.Pro344Leu)
NM_212472.2(PRKAR1A):c.1042G>A (p.Val348Ile) rs772571340
NM_212472.2(PRKAR1A):c.1062A>G (p.Arg354=)
NM_212472.2(PRKAR1A):c.1079G>T (p.Gly360Val)
NM_212472.2(PRKAR1A):c.1081C>G (p.Pro361Ala)
NM_212472.2(PRKAR1A):c.1088C>T (p.Ser363Leu) rs1555815165
NM_212472.2(PRKAR1A):c.1143C>G (p.Val381=) rs755043531

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.