List of variants reported as uncertain significance for Hepatocellular carcinoma

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_198253.3(TERT):c.887A>C (p.His296Pro)	rs778187343	0.00007
NM_000038.6(APC):c.2527A>G (p.Ser843Gly)	rs536223189	0.00006
NM_000038.6(APC):c.8332G>T (p.Ala2778Ser)	rs587778046	0.00006
NM_000876.4(IGF2R):c.5691C>T (p.Thr1897=)	rs139019277	0.00001
NM_000876.4(IGF2R):c.50G>C (p.Arg17Pro)	rs2115160662
NM_003502.4(AXIN1):c.1118G>A (p.Arg373His)
NM_003502.4(AXIN1):c.2167C>T (p.Arg723Ter)
NM_198253.3(TERT):c.578C>T (p.Pro193Leu)	rs751762765

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