ClinVar Miner

List of variants in gene PRC1 reported as uncertain significance for breast disorder

Included ClinVar conditions (69):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_003981.4(PRC1):c.1792-828T>C rs12910825 0.56832
NM_003981.4(PRC1):c.1350+35C>G rs12898311 0.52787
NM_003981.4(PRC1):c.*769A>G rs7601 0.46627
NM_003981.4(PRC1):c.970+436G>A rs6496742 0.39225
NM_003981.4(PRC1):c.12-2765T>C rs8028856 0.38070
NM_003981.4(PRC1):c.282G>A (p.Thr94=) rs2301826 0.37356
NM_003981.4(PRC1):c.268-107G>A rs11857612 0.15952
NM_003981.4(PRC1):c.268-203A>G rs11855081 0.12736
NM_003981.4(PRC1):c.1351-3C>T rs17636091 0.09389
NM_003981.4(PRC1):c.*627T>C rs14280 0.08057
NM_003981.4(PRC1):c.*441C>A rs3743450 0.05570
NM_003981.4(PRC1):c.1532A>G (p.Tyr511Cys) rs12911192 0.04874
NM_003981.4(PRC1):c.*919G>T rs15172 0.04817
NM_003981.4(PRC1):c.971-441G>A rs59025289 0.00503
NM_003981.4(PRC1):c.*342A>G rs112187198 0.00059
NM_003981.4(PRC1):c.*733G>A rs112770009 0.00025
NM_003981.4(PRC1):c.971-466T>C rs190852637 0.00002
NM_003981.4(PRC1):c.971-375A>G rs186031385 0.00001
NM_003981.3(PRC1):c.1351-124_1351-123insoAC068831.17:g.63209_63266

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