Variant Results

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Results for "TBX22"

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
TBX22	1-0208-003	chrX: 79482543-79482543	G	A	intergenic		De novo					-	-	Yuen2017 G
TBX22	AU3702307	chrX: 79396283-79396283	T	A	intergenic		De novo					-	-	Yuen2017 G
TBX22	AU3053301	chrX: 79337168-79337168	T	C	intergenic		De novo					-	-	Yuen2017 G
TBX22	AU009805	chrX: 79403757-79403757	G	T	intergenic		De novo					-	-	Yuen2017 G
TBX22	1-0804-003	chrX: 79300718-79300718	C	T	intergenic		De novo					-	-	Yuen2017 G
TBX22	14380.p1	chrX: 79277939-79277939	G	T	exonic		De novo	synonymous SNV	NM_016954 NM_001109878	c.G171T c.G171T	p.P57P p.P57P	-	-	Iossifov2014 E Kosmicki2017 E Satterstrom2020 E Wilfert2021 G
TBX22	14261.p1	chrX: 79279657-79279657	G	A	exonic		Mosaic, De novo	nonsynonymous SNV	NM_001303475 NM_016954 NM_001109878 NM_001109879	c.G92A c.G452A c.G452A c.G92A	p.R31H p.R151H p.R151H p.R31H	17.55	-	Dou2017 E Iossifov2014 E Ji2016 E Kosmicki2017 E Satterstrom2020 E Wilfert2021 G
TBX22	ASD005	chrX: 79279657-79279657	G	T	exonic		Inherited	nonsynonymous SNV	NM_001303475 NM_016954 NM_001109878 NM_001109879	c.G92T c.G452T c.G452T c.G92T	p.R31L p.R151L p.R151L p.R31L	18.04	8.0E-5	Tran2020 E Wu2019 E
TBX22	2-1417-003	chrX: 79326582-79326582	G	A	intergenic		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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