Variant Results

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Results for "TTC26"

Variant Events: 5

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
TTC26	1-0978-003	chr7: 138874424-138874424	C	T	UTR3		De novo					-	-	Yuen2017 G
TTC26	AU3912302	chr7: 138842085-138842085	G	T	intronic		De novo					-	-	Yuen2017 G
TTC26	5-0146-003	chr7: 138833067-138833067	G	A	exonic		De novo	nonsynonymous SNV	NM_001144923 NM_001144920 NM_001287513 NM_024926	c.G568A c.G661A c.G346A c.G661A	p.A190T p.A221T p.A116T p.A221T	35.0	8.237E-6	Yuen2017 G
TTC26	EGAN00001100925	chr7: 138864271-138864271	A	G	intronic		De novo					-	-	Satterstrom2020 E
TTC26	Codina-Sola2015:ASD_36	chr7: 138854056-138854056	C	T	exonic		Paternal	stopgain	NM_001287512 NM_001144923 NM_001144920 NM_001287513 NM_024926	c.C634T c.C934T c.C1027T c.C712T c.C1027T	p.Q212X p.Q312X p.Q343X p.Q238X p.Q343X	36.0	-	Codina-Sola2015 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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