List of variants in gene RB1 reported as not provided

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: 21

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HGVS	dbSNP	gnomAD frequency
NM_000321.3(RB1):c.1574C>G (p.Ala525Gly)	rs4151539	0.00623
NM_000321.3(RB1):c.920C>T (p.Thr307Ile)	rs183898408	0.00079
NM_000321.3(RB1):c.59C>T (p.Pro20Leu)	rs587778637	0.00011
NM_000321.3(RB1):c.1862G>A (p.Arg621His)	rs373601944	0.00009
NM_000321.3(RB1):c.1573G>A (p.Ala525Thr)	rs587778640	0.00004
NM_000321.3(RB1):c.173C>T (p.Thr58Ile)	rs138574644	0.00004
NM_000321.3(RB1):c.1898C>T (p.Thr633Ile)	rs587778641	0.00002
NM_000321.3(RB1):c.1981C>T (p.Arg661Trp)	rs137853294	0.00002
NM_000321.3(RB1):c.1268G>A (p.Gly423Glu)	rs748635133	0.00001
NM_000321.3(RB1):c.2318C>T (p.Ser773Phe)	rs267603841	0.00001
NM_000321.3(RB1):c.1215+1G>T	rs587776783
NM_000321.3(RB1):c.1389+5G>C	rs1131690859
NM_000321.3(RB1):c.1677A>T (p.Glu559Asp)	rs587778639
NM_000321.3(RB1):c.1814+2T>A	rs1131690899
NM_000321.3(RB1):c.1861C>A (p.Arg621Ser)	rs367578442
NM_000321.3(RB1):c.2211+5G>T	rs1593538236
NM_000321.3(RB1):c.2260G>C (p.Val754Leu)	rs587778642
NM_000321.3(RB1):c.2325+1G>A	rs1131690882
NM_000321.3(RB1):c.2489+1G>C	rs764754259
NM_000321.3(RB1):c.43G>C (p.Ala15Pro)	rs587778638
NM_000321.3(RB1):c.45_53del (p.Ala16_Ala18del)	rs572454921

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