Variant Results

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Results for "CDC16"

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
CDC16	Codina-Sola2015:ASD_12	chr13: 115027416-115027421	AAACTT	A	exonic		Maternal	frameshift deletion	NM_001078645 NM_003903	c.1370_1374del c.1370_1374del	p.K457fs p.K457fs	-	2.478E-5	Codina-Sola2015 E
CDC16	2-0244-003	chr13: 115001356-115001356	A	CCT	intronic		De novo					-	-	Trost2022 G
CDC16	REACH000714	chr13: 115008560-115008560	G	A	intronic		De novo					-	-	Trost2022 G
CDC16	SP0192085	chr13: 115004821-115004821	G	A	intronic		De novo					-	-	Trost2022 G
CDC16	MSSNG00011-004	chr13: 115008136-115008136	G	A	intronic		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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