List of variants in gene BCOR 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001123385.2(BCOR):c.4488A>C (p.Ala1496=)	rs138741225	0.00076
NM_001123385.2(BCOR):c.2035G>A (p.Val679Ile)	rs144722432	0.00053
NM_001123385.2(BCOR):c.4320T>C (p.Pro1440=)	rs753786462	0.00011
NM_001123385.2(BCOR):c.4292C>A (p.Ser1431Tyr)	rs369432845	0.00004
NM_001123385.2(BCOR):c.4902C>T (p.Ser1634=)	rs747409134	0.00003
NM_001123385.2(BCOR):c.1805C>T (p.Pro602Leu)	rs766045784
NM_001123385.2(BCOR):c.2199G>T (p.Thr733=)	rs140693978
NM_001123385.2(BCOR):c.3305T>C (p.Val1102Ala)	rs111622737
NM_001123385.2(BCOR):c.3340G>C (p.Glu1114Gln)	rs757991049
NM_001123385.2(BCOR):c.4523G>C (p.Gly1508Ala)	rs1569142538

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