Variant Results

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Results for "ANKRD36C"

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
ANKRD36C	ASC_CA_69_A1	chr2: 96578095-96578095	A	G	intronic		De novo					-	-	Satterstrom2020 E Trost2022 G
ANKRD36C	1-0028-003	chr2: 96624563-96624563	C	T	intronic		De novo					-	-	Yuen2017 G
ANKRD36C	SP0063548	chr2: 96648077-96648077	G	T	exonic			nonsynonymous SNV	NM_001310154	c.C520A	p.Q174K	0.849	-	Zhou2022 GE
ANKRD36C	SSC05990	chr2: 96610876-96610876	T	C	exonic		Mosaic	nonsynonymous SNV	NM_001310154	c.A1409G	p.Q470R	3.912	-	Lim2017 E
ANKRD36C	SP0067090	chr2: 96521640-96521640	C	T	exonic			nonsynonymous SNV	NM_001310154	c.G5467A	p.G1823R	0.097	6.0E-4	Zhou2022 GE
ANKRD36C	1-0995-003	chr2: 96618133-96618147	CAGAGAGAGAGAGAG	CAGAGAGAGAGAG	intronic		De novo					-	-	Yuen2017 G
ANKRD36C	AU045514	chr2: 96661488-96661490	CAT	C	intergenic		De novo					-	-	Yuen2017 G
ANKRD36C	5-0042-003	chr2: 96608281-96608281	C	T	intronic		De novo					-	-	Yuen2017 G
ANKRD36C	2-1411-003	chr2: 96639556-96639556	A	G	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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