ClinVar Miner

List of variants in gene RB1 reported as likely benign for Hereditary cancer-predisposing syndrome

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Total variants: 21
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HGVS dbSNP
NM_000321.2(RB1):c.1129A>T (p.Thr377Ser) rs146897002
NM_000321.2(RB1):c.113G>A (p.Gly38Asp) rs766529534
NM_000321.2(RB1):c.1140C>T (p.Asn380=) rs117865557
NM_000321.2(RB1):c.1318G>A (p.Glu440Lys) rs1060503078
NM_000321.2(RB1):c.1410T>C (p.Ile470=) rs578226820
NM_000321.2(RB1):c.1464G>A (p.Ala488=) rs753520981
NM_000321.2(RB1):c.1596C>T (p.Ile532=) rs770728170
NM_000321.2(RB1):c.1632A>G (p.Arg544=) rs143948310
NM_000321.2(RB1):c.1707A>G (p.Leu569=) rs3092895
NM_000321.2(RB1):c.1770T>C (p.Cys590=) rs145310579
NM_000321.2(RB1):c.1800C>T (p.His600=) rs1555293650
NM_000321.2(RB1):c.207T>C (p.His69=) rs759594127
NM_000321.2(RB1):c.2244G>A (p.Glu748=) rs1131690911
NM_000321.2(RB1):c.2455C>G (p.Leu819Val) rs375751988
NM_000321.2(RB1):c.2455C>T (p.Leu819=) rs375751988
NM_000321.2(RB1):c.2463A>G (p.Thr821=) rs370088029
NM_000321.2(RB1):c.2559T>C (p.Cys853=) rs148327780
NM_000321.2(RB1):c.42C>T (p.Ala14=) rs148980395
NM_000321.2(RB1):c.69G>A (p.Pro23=) rs746662122
NM_000321.2(RB1):c.920C>T (p.Thr307Ile) rs183898408
NM_000321.2(RB1):c.929G>A (p.Gly310Glu) rs200844292

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