List of variants in gene BCOR 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001123385.2(BCOR):c.3802A>G (p.Arg1268Gly)	rs140897453	0.00058
NM_001123385.2(BCOR):c.3974A>G (p.Lys1325Arg)	rs187172641	0.00027
NM_001123385.2(BCOR):c.365T>C (p.Met122Thr)	rs369585835	0.00014
NM_001123385.2(BCOR):c.3277G>A (p.Glu1093Lys)	rs144736705	0.00013
NM_001123385.2(BCOR):c.4766G>A (p.Arg1589His)	rs367859441	0.00009
NM_001123385.2(BCOR):c.2129G>A (p.Arg710His)	rs200732803	0.00007
NM_001123385.2(BCOR):c.4014A>C (p.Glu1338Asp)	rs142866108	0.00006
NM_001123385.2(BCOR):c.2954A>T (p.Tyr985Phe)	rs587778093	0.00005
NM_001123385.2(BCOR):c.5234A>C (p.His1745Pro)	rs587778100	0.00002
NM_001123385.2(BCOR):c.2509C>G (p.Pro837Ala)	rs587778098	0.00001
NM_001123385.2(BCOR):c.254C>T (p.Pro85Leu)	rs121434618	0.00001
NM_001123385.2(BCOR):c.305G>C (p.Arg102Pro)	rs587778099	0.00001
NM_001123385.2(BCOR):c.11C>T (p.Ala4Val)	rs587778092
NM_001123385.2(BCOR):c.3440C>T (p.Thr1147Ile)	rs587778101
NM_001123385.2(BCOR):c.4173+2T>C	rs2147028921

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