Variant Results

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Results for "UBE2O"

Variant Events: 8

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
UBE2O	SP0031728	chr17: 74387802-74387802	C	A	intronic		De novo					-	-	Fu2022 E
UBE2O	AU2248302	chr17: 74422021-74422021	T	C	intronic		De novo					-	-	Yuen2017 G
UBE2O	11292.p1	chr17: 74392476-74392476	T	C	exonic		De novo	nonsynonymous SNV	NM_022066	c.A2542G	p.T848A	19.16	-	Satterstrom2020 E
UBE2O	AU079605	chr17: 74412072-74412072	T	C	intronic		De novo					-	-	Yuen2017 G
UBE2O	G01-GEA-148-HI	chr17: 74392127-74392127	C	CACCCT	intronic		De novo					-	-	Satterstrom2020 E
UBE2O	SP0115628	chr17: 74394609-74394609	C	T	exonic		De novo	nonsynonymous SNV	NM_022066	c.G1840A	p.G614S	24.8	8.242E-6	Fu2022 E
UBE2O	SSC00482	chr17: 74392476-74392476	T	C	exonic		De novo	nonsynonymous SNV	NM_022066	c.A2542G	p.T848A	19.16	-	Fu2022 E
UBE2O	JASD_Fam0254	chr17: 74392872-74392872	C	G	exonic		De novo	nonsynonymous SNV	NM_022066	c.G2146C	p.E716Q	13.49	-	Takata2018 E

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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