ClinVar Miner

List of variants reported as likely benign for Carney complex

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 71
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HGVS dbSNP
NM_002734.5(PRKAR1A):c.-11C>T
NM_002734.5(PRKAR1A):c.-6-4G>C rs190803359
NM_002734.5(PRKAR1A):c.-6-5C>T rs750536611
NM_002734.5(PRKAR1A):c.1098C>T (p.Leu366=) rs1600496468
NM_002734.5(PRKAR1A):c.1110C>T (p.Ile370=) rs62638722
NM_002734.5(PRKAR1A):c.237G>A (p.Glu79=) rs1197286957
NM_002734.5(PRKAR1A):c.378C>T (p.Ala126=) rs199974368
NM_002734.5(PRKAR1A):c.522C>T (p.Phe174=) rs148109898
NM_002734.5(PRKAR1A):c.769+10A>T rs375239425
NM_002734.5(PRKAR1A):c.810A>G (p.Ala270=) rs778165219
NM_002734.5(PRKAR1A):c.825G>A (p.Gln275=) rs1267422534
NM_002734.5(PRKAR1A):c.837G>C (p.Gly279=) rs1600492307
NM_002734.5(PRKAR1A):c.892-6T>C rs1600494784
NM_017565.4(FAM20A):c.1511C>T (p.Thr504Ile) rs146689929
NM_212472.2(PRKAR1A):c.*138C>A rs28730842
NM_212472.2(PRKAR1A):c.*151A>G rs11540571
NM_212472.2(PRKAR1A):c.*172_*175del rs201146882
NM_212472.2(PRKAR1A):c.*1835del rs138320066
NM_212472.2(PRKAR1A):c.*1837G>T rs201999343
NM_212472.2(PRKAR1A):c.*759C>T rs62087489
NM_212472.2(PRKAR1A):c.*812A>C rs116996069
NM_212472.2(PRKAR1A):c.*847A>G rs144299673
NM_212472.2(PRKAR1A):c.-6-4G>A rs190803359
NM_212472.2(PRKAR1A):c.-6-7C>T rs373646911
NM_212472.2(PRKAR1A):c.103A>G (p.Ile35Val) rs377513504
NM_212472.2(PRKAR1A):c.1041C>T (p.Cys347=) rs1192354369
NM_212472.2(PRKAR1A):c.1143C>G (p.Val381=) rs755043531
NM_212472.2(PRKAR1A):c.132G>A (p.Glu44=) rs145590804
NM_212472.2(PRKAR1A):c.135A>G (p.Arg45=) rs1060504125
NM_212472.2(PRKAR1A):c.178-8T>G rs771192586
NM_212472.2(PRKAR1A):c.189A>G (p.Lys63=) rs1060504126
NM_212472.2(PRKAR1A):c.18C>T (p.Thr6=) rs755978926
NM_212472.2(PRKAR1A):c.221G>A (p.Arg74His) rs200069356
NM_212472.2(PRKAR1A):c.280A>C (p.Arg94=) rs1443738914
NM_212472.2(PRKAR1A):c.303C>T (p.Ser101=) rs1294747986
NM_212472.2(PRKAR1A):c.306T>C (p.Ala102=) rs757511127
NM_212472.2(PRKAR1A):c.309G>A (p.Glu103=) rs746113372
NM_212472.2(PRKAR1A):c.318G>A (p.Thr106=) rs113994213
NM_212472.2(PRKAR1A):c.330G>A (p.Ala110=) rs371834376
NM_212472.2(PRKAR1A):c.349-5T>C rs1456043929
NM_212472.2(PRKAR1A):c.360A>G (p.Lys120=) rs1555813428
NM_212472.2(PRKAR1A):c.381T>C (p.Ala127=) rs372669687
NM_212472.2(PRKAR1A):c.441-5T>C rs771949207
NM_212472.2(PRKAR1A):c.441-5del rs777677808
NM_212472.2(PRKAR1A):c.477C>T (p.Ile159=) rs372389205
NM_212472.2(PRKAR1A):c.483A>G (p.Gly161=) rs141518491
NM_212472.2(PRKAR1A):c.525T>C (p.Tyr175=) rs1168113151
NM_212472.2(PRKAR1A):c.528G>A (p.Val176=) rs752927621
NM_212472.2(PRKAR1A):c.546G>A (p.Thr182=) rs117639566
NM_212472.2(PRKAR1A):c.549+10A>C rs751413552
NM_212472.2(PRKAR1A):c.54T>C (p.Cys18=) rs1555811690
NM_212472.2(PRKAR1A):c.550-6C>T rs1555814031
NM_212472.2(PRKAR1A):c.550-8C>T rs375936679
NM_212472.2(PRKAR1A):c.567A>G (p.Glu189=) rs767405408
NM_212472.2(PRKAR1A):c.591A>G (p.Gly197=) rs991638429
NM_212472.2(PRKAR1A):c.606A>G (p.Glu202=) rs878884422
NM_212472.2(PRKAR1A):c.630G>A (p.Pro210=) rs756720013
NM_212472.2(PRKAR1A):c.63C>T (p.Tyr21=) rs777110464
NM_212472.2(PRKAR1A):c.675C>A (p.Gly225=) rs150244650
NM_212472.2(PRKAR1A):c.693T>C (p.Tyr231=) rs1555814113
NM_212472.2(PRKAR1A):c.709-6T>C rs1060504127
NM_212472.2(PRKAR1A):c.727C>A (p.Arg243=) rs770136522
NM_212472.2(PRKAR1A):c.762T>C (p.Ser254=) rs753621663
NM_212472.2(PRKAR1A):c.798G>A (p.Thr266=) rs201774040
NM_212472.2(PRKAR1A):c.798G>T (p.Thr266=) rs201774040
NM_212472.2(PRKAR1A):c.852G>A (p.Val284=) rs771167809
NM_212472.2(PRKAR1A):c.858A>G (p.Gly286=) rs746582369
NM_212472.2(PRKAR1A):c.87G>A (p.Ala29=) rs3730349
NM_212472.2(PRKAR1A):c.892-5T>C rs1181021204
NM_212472.2(PRKAR1A):c.894G>C (p.Gly298=) rs933520060
NM_212472.2(PRKAR1A):c.974-10C>T rs774715675

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