Variant Results

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Results for "FOPNL"

Variant Events: 6

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
FOPNL	3-0284-000	chr16: 15973352-15973352	T	A	intronic		De novo					-	-	Trost2022 G
FOPNL	SP0201404	chr16: 15977972-15977972	C	T	exonic		De novo	nonsynonymous SNV	NM_001304497 NM_001304498 NM_001304499 NM_001304502 NM_144600	c.G119A c.G119A c.G119A c.G119A c.G119A	p.R40H p.R40H p.R40H p.R40H p.R40H	13.58	8.241E-6	Trost2022 G
FOPNL	AU2718301	chr16: 15962060-15962060	A	G	intronic		De novo					-	-	Trost2022 G
FOPNL	A18	chr16: 16005030-16005030	G	A	intergenic		De novo					-	-	Wu2018 G
FOPNL	2-0285-003	chr16: 15985644-15985644	T	A	intergenic		De novo					-	-	Yuen2017 G
FOPNL	AU4149301	chr16: 16036452-16036452	A	C	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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