Variant Results

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Results for "BCOR"

Variant Events: 7

Gene Gene symbol on which the variant is located	ID Subject Identifier from the original study	Location Genomic location of the reference allele	REF Reference allele	ALT Alternate allele	Context Variant functional categories	Variant validation performed by an orthogonal method and reported	Inheritance Reported inheritance status	Effects Variant effect on transcript per Annovar	Transcript Transcript used for the cDNA/Protein mutation	cDNA cDNA variant notation	Protein Protein variant notation	CADD-Phred v1.0 CADD phred-like score. This is phred-like rank score based on whole genome CADD raw scores	ExAC v0.3 ExAC population frequency (version 0.3)	Sources Source(s) where variants from this event are reported
BCOR	SP0024125	chrX: 39933215-39933215	C	A	exonic			nonsynonymous SNV	NM_001123383 NM_001123384 NM_001123385 NM_017745	c.G1384T c.G1384T c.G1384T c.G1384T	p.A462S p.A462S p.A462S p.A462S	13.89	-	Zhou2022 GE
BCOR	1-0464-003	chrX: 40110644-40110644	C	G	intergenic		De novo					-	-	Yuen2017 G
BCOR	AU4006302	chrX: 39998636-39998638	TAA	TA	intronic		De novo					-	-	Yuen2017 G
BCOR	AU3889305	chrX: 40068701-40068701	C	T	intergenic		De novo					-	-	Yuen2017 G
BCOR	Valentino2021:4	chrX: 39933823-39933823	G	A	exonic		De novo	nonsynonymous SNV	NM_001123383 NM_001123384 NM_001123385 NM_017745	c.C776T c.C776T c.C776T c.C776T	p.S259L p.S259L p.S259L p.S259L	19.31	-	Valentino2021 E
BCOR	2H596	chrX: 39933651-39933651	G	A	exonic		De novo	synonymous SNV	NM_001123383 NM_001123384 NM_001123385 NM_017745	c.C948T c.C948T c.C948T c.C948T	p.P316P p.P316P p.P316P p.P316P	-	-	Satterstrom2020 E Trost2022 G Zhou2022 GE
BCOR	AU3760302	chrX: 39911312-39911312	T	A	UTR3		De novo					-	-	Yuen2017 G

Source Variant Information

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Paper Information

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Pubmed
Subject count	The number of subjects for this study could not be determined directly from the variant data; the value given is that reported by the authors in the publication.
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