Variant Results

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Results for "XRN2"

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
XRN2	39.s2	chr20: 21327102-21327102	G	A	exonic		De novo	nonsynonymous SNV	NM_012255	c.G1579A	p.V527M	32.0	-	An2014 E
XRN2	SSC03520	chr20: 21319718-21319718	A	G	exonic		De novo	nonsynonymous SNV	NM_012255	c.A1270G	p.R424G	13.78	-	Lim2017 E
XRN2	2-1437-003	chr20: 21335653-21335653	C	T	intronic		De novo					-	-	Yuen2017 G
XRN2	1-0862-003	chr20: 21285426-21285426	C	T	intronic		De novo					-	-	Yuen2017 G
XRN2	5-0041-003	chr20: 21372943-21372943	T	C	intergenic		De novo					-	-	Yuen2017 G
XRN2	2-0028-003	chr20: 21296449-21296449	A	G	intronic		De novo					-	-	Yuen2016 G Yuen2017 G
XRN2	11909.p1	chr20: 21319718-21319718	A	G	exonic		Mosaic, De novo	nonsynonymous SNV	NM_012255	c.A1270G	p.R424G	13.78	-	Dou2017 E Iossifov2014 E Ji2016 E Kosmicki2017 E
XRN2	AU3858303	chr20: 21300654-21300654	G	C	intronic		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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