List of variants in gene RB1 reported as uncertain significance for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000321.3(RB1):c.59C>T (p.Pro20Leu)	rs587778637	0.00011
NM_000321.3(RB1):c.2360G>A (p.Arg787Gln)	rs748094394	0.00006
NM_000321.3(RB1):c.1814+11T>C	rs771369373	0.00004
NM_000321.3(RB1):c.2626C>T (p.Arg876Cys)	rs143105337	0.00003
NM_000321.3(RB1):c.2491A>G (p.Ile831Val)	rs761068783	0.00002
NM_000321.3(RB1):c.-149G>T	rs1014776340	0.00001
NM_000321.3(RB1):c.1024A>T (p.Thr342Ser)	rs751263356	0.00001
NM_000321.3(RB1):c.1489A>G (p.Thr497Ala)	rs776531398	0.00001
NM_000321.3(RB1):c.2242G>A (p.Glu748Lys)	rs121913297	0.00001
NM_000321.3(RB1):c.2393G>A (p.Arg798Gln)	rs374523971	0.00001
NM_000321.3(RB1):c.1111C>T (p.Pro371Ser)	rs1952727399
NM_000321.3(RB1):c.13A>C (p.Thr5Pro)	rs898303682
NM_000321.3(RB1):c.1462G>A (p.Ala488Thr)
NM_000321.3(RB1):c.1753C>T (p.His585Tyr)	rs1401332173
NM_000321.3(RB1):c.1861C>T (p.Arg621Cys)	rs367578442

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