ClinVar Miner

List of variants in gene RB1 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_000321.2(RB1):c.1128-5del rs886038280
NM_000321.2(RB1):c.1131T>C (p.Thr377=) rs1414284893
NM_000321.2(RB1):c.1140C>T (p.Asn380=) rs117865557
NM_000321.2(RB1):c.1390-11A>G rs200658795
NM_000321.2(RB1):c.1390-16A>T rs781419356
NM_000321.2(RB1):c.1491A>T (p.Thr497=) rs150115447
NM_000321.2(RB1):c.1764T>A (p.Ser588=) rs542783532
NM_000321.2(RB1):c.1770T>C (p.Cys590=) rs145310579
NM_000321.2(RB1):c.1961-12T>C rs201697122
NM_000321.2(RB1):c.2212-16T>A rs201258424
NM_000321.2(RB1):c.2325+10A>G rs763525092
NM_000321.2(RB1):c.2455C>T (p.Leu819=) rs375751988
NM_000321.2(RB1):c.2521-9A>C rs949077145
NM_000321.2(RB1):c.264+20G>A rs200985890
NM_000321.2(RB1):c.380+10C>G rs187110786
NM_000321.2(RB1):c.380+12T>C rs3092881
NM_000321.2(RB1):c.42C>T (p.Ala14=) rs148980395
NM_000321.2(RB1):c.628G>T (p.Asp210Tyr) rs148992508
NM_000321.2(RB1):c.862-15C>A rs115108608
NM_000321.2(RB1):c.920C>T (p.Thr307Ile) rs183898408
NM_000321.2(RB1):c.929G>A (p.Gly310Glu) rs200844292

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