List of variants in gene combination BCOR, LOC126863239 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001123385.2(BCOR):c.946C>T (p.Pro316Ser)	rs200052076	0.00034
NM_001123385.2(BCOR):c.519C>T (p.Ser173=)	rs138917640	0.00013
NM_001123385.2(BCOR):c.759C>T (p.Val253=)	rs373674220	0.00010
NM_001123385.2(BCOR):c.837C>T (p.Leu279=)	rs753531268	0.00010
NM_001123385.2(BCOR):c.651G>A (p.Met217Ile)	rs368939471	0.00002
NM_001123385.2(BCOR):c.1026A>G (p.Arg342=)
NM_001123385.2(BCOR):c.1083T>C (p.Tyr361=)
NM_001123385.2(BCOR):c.1563T>A (p.Asn521Lys)
NM_001123385.2(BCOR):c.777G>A (p.Ser259=)

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