ClinVar Miner

List of variants in gene PRKAR1A reported as likely benign for Carney complex

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_002734.4(PRKAR1A):c.441-5T>C rs771949207
NM_002734.4(PRKAR1A):c.550-6C>T rs1555814031
NM_002734.4(PRKAR1A):c.892-5T>C rs1181021204
NM_212472.2(PRKAR1A):c.-106G>T rs559757120
NM_212472.2(PRKAR1A):c.-56C>T rs546338099
NM_212472.2(PRKAR1A):c.103A>G (p.Ile35Val) rs377513504
NM_212472.2(PRKAR1A):c.204G>A (p.Leu68=) rs74863634
NM_212472.2(PRKAR1A):c.221G>A (p.Arg74His) rs200069356
NM_212472.2(PRKAR1A):c.303C>T (p.Ser101=) rs1294747986
NM_212472.2(PRKAR1A):c.349-5T>C rs1456043929
NM_212472.2(PRKAR1A):c.360A>G (p.Lys120=) rs1555813428
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.54T>C (p.Cys18=) rs1555811690
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.678C>T (p.Ile226=) rs200592054
NM_212472.2(PRKAR1A):c.693T>C (p.Tyr231=) rs1555814113
NM_212472.2(PRKAR1A):c.87G>A (p.Ala29=) rs3730349

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