ClinVar Miner

List of variants in gene combination FAM20A, PRKAR1A reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP
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.*1487C>T rs886053314
NM_002734.4(PRKAR1A):c.*1839G>A rs886053316
NM_002734.4(PRKAR1A):c.*1842A>T rs886053317
NM_002734.4(PRKAR1A):c.*2067T>C rs886053318
NM_002734.4(PRKAR1A):c.*2072G>A rs886053319
NM_002734.4(PRKAR1A):c.*2196C>T rs886053320
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.*704T>G rs886053310
NM_002734.4(PRKAR1A):c.*724T>A rs746409603
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.1031C>T (p.Pro344Leu)
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

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