Variant Results

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Results for "IL22RA2"

Variant Events: 9

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
IL22RA2	AU049304	chr6: 137503539-137503541	ATT	AT	intergenic		De novo					-	-	Yuen2017 G
IL22RA2	7-0256-003	chr6: 137479239-137479239	G	A	intronic		De novo					-	-	Trost2022 G Yuen2017 G
IL22RA2	mAGRE4041	chr6: 137477960-137477960	G	A	exonic		Maternal	stopgain	NM_052962	c.C229T	p.Q77X	15.39	8.241E-6	Cirnigliaro2023 G
IL22RA2	1-0868-003	chr6: 137491343-137491343	G	C	intronic		De novo					-	-	Trost2022 G Yuen2017 G
IL22RA2	AU043804	chr6: 137512067-137512067	G	A	intergenic		De novo					-	-	Yuen2017 G
IL22RA2	13171.p1	chr6: 137499793-137499793	G	A	intergenic		De novo					-	-	Turner2016 G
IL22RA2	B5X9C-01	chr6: 137468107-137468107	T	G	intronic		De novo					-	-	Trost2022 G
IL22RA2	AU055603	chr6: 137491115-137491115	C	T	intronic		De novo					-	-	Trost2022 G
IL22RA2	MSSNG00206-003	chr6: 137464811-137464811	G	A	downstream		De novo					-	-	Trost2022 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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