List of variants in gene PRKAR1A reported as likely benign for bone development disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_002734.5(PRKAR1A):c.87G>A (p.Ala29=)	rs3730349	0.01815
NM_002734.5(PRKAR1A):c.*1837G>T	rs201999343	0.01775
NM_002734.5(PRKAR1A):c.*138C>A	rs28730842	0.00772
NM_002734.5(PRKAR1A):c.*759C>T	rs62087489	0.00683
NM_002734.5(PRKAR1A):c.204G>A (p.Leu68=)	rs74863634	0.00405
NM_002734.5(PRKAR1A):c.*151A>G	rs11540571	0.00340
NM_002734.5(PRKAR1A):c.*847A>G	rs144299673	0.00091
NM_002734.5(PRKAR1A):c.221G>A (p.Arg74His)	rs200069356	0.00036
NM_002734.5(PRKAR1A):c.381T>C (p.Ala127=)	rs372669687	0.00011
NM_002734.5(PRKAR1A):c.103A>G (p.Ile35Val)	rs377513504	0.00009
NM_002734.5(PRKAR1A):c.502+12_502+13del	rs764075585	0.00009
NM_002734.5(PRKAR1A):c.762T>C (p.Ser254=)	rs753621663	0.00003
NM_002734.5(PRKAR1A):c.-6-7C>T	rs373646911	0.00002
NM_002734.5(PRKAR1A):c.172_175del	rs201146882
NM_002734.5(PRKAR1A):c.*1835del	rs138320066
NM_002734.5(PRKAR1A):c.*812A>C	rs116996069
NM_002734.5(PRKAR1A):c.503-13dup	rs138285568

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