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: 56
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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_002734.4(PRKAR1A):c.*1014A>G rs886053311
NM_002734.4(PRKAR1A):c.*1062A>G rs752303671
NM_002734.4(PRKAR1A):c.*1118dup 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_*175del rs201146882
NM_002734.4(PRKAR1A):c.*1777C>T rs7977
NM_002734.4(PRKAR1A):c.*1835del 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.*587del rs398041821
NM_002734.4(PRKAR1A):c.*587dup 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.1003C>T (p.Arg335Cys) rs1555815121
NM_002734.4(PRKAR1A):c.1014A>C (p.Thr338=) rs1409504061
NM_002734.4(PRKAR1A):c.1024C>T (p.Arg342Cys) rs146383819
NM_002734.4(PRKAR1A):c.1025G>A (p.Arg342His) rs760033566
NM_002734.4(PRKAR1A):c.1029C>T (p.Gly343=) rs1803241
NM_002734.4(PRKAR1A):c.1031C>T (p.Pro344Leu)
NM_002734.4(PRKAR1A):c.1041C>T (p.Cys347=) rs1192354369
NM_002734.4(PRKAR1A):c.1042G>A (p.Val348Ile) rs772571340
NM_002734.4(PRKAR1A):c.1062A>G (p.Arg354=)
NM_002734.4(PRKAR1A):c.1079G>T (p.Gly360Val)
NM_002734.4(PRKAR1A):c.1081C>G (p.Pro361Ala)
NM_002734.4(PRKAR1A):c.1088C>T (p.Ser363Leu) rs1555815165
NM_002734.4(PRKAR1A):c.1143C>G (p.Val381=) rs755043531
NM_017565.4(FAM20A):c.1511C>T (p.Thr504Ile) rs146689929

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