List of variants reported as uncertain significance for small cell lung carcinoma by Fulgent Genetics, Fulgent Genetics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000321.3(RB1):c.850A>G (p.Asn284Asp)	rs761609284	0.00002
NM_000321.3(RB1):c.1174G>A (p.Ala392Thr)	rs181988132	0.00001
NM_000321.3(RB1):c.269G>T (p.Gly90Val)	rs554727080	0.00001
NM_000321.3(RB1):c.352A>T (p.Thr118Ser)	rs1429553692	0.00001
NM_000321.3(RB1):c.752G>A (p.Arg251Gln)	rs772678500	0.00001
NM_000321.3(RB1):c.1376C>T (p.Ser459Phe)	rs1593455667
NM_000321.3(RB1):c.276T>G (p.Ile92Met)	rs1555282772

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