ClinVar Miner

List of variants reported as uncertain significance by Cancer Genomic Medicine Translational Research Lab, Cleveland Clinic Genomic Medicine Institute

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Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_000314.8(PTEN):c.210-39A>G rs370918174 0.00177
NM_000314.8(PTEN):c.493-31A>G rs550267891 0.00006
NM_000314.8(PTEN):c.493-52A>G rs1043121029 0.00003
NM_000314.8(PTEN):c.210-7_210-3del rs587780544
NM_000314.8(PTEN):c.210-8del rs1554897849
NM_000314.8(PTEN):c.254-30dup rs77494260
NM_000314.8(PTEN):c.254-51A>T rs1554898040
NM_000314.8(PTEN):c.254-72A>T rs1554898037
NM_000314.8(PTEN):c.80-3C>G rs1554893746
NM_000314.8(PTEN):c.802-51_802-14del rs557364463

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