List of variants reported as likely pathogenic for bone cancer by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000535.7(PMS2):c.137G>T (p.Ser46Ile)	rs121434629	0.00018
NM_004260.4(RECQL4):c.1717C>T (p.Gln573Ter)	rs1483085748	0.00003
NM_004364.5(CEBPA):c.324C>G (p.Tyr108Ter)	rs1555742221

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