Variant Results

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Results for "OLFML2B"

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
OLFML2B	SP0040281	chr1: 161989852-161989852	T	A	exonic		De novo	stopgain	NM_001297713 NM_015441	c.A295T c.A295T	p.K99X p.K99X	38.0	-	Fu2022 E
OLFML2B	2-1242-003	chr1: 162023971-162023971	C	T	intergenic		De novo					-	-	Yuen2017 G
OLFML2B	11818.p1	chr1: 161973172-161973172	G	A	intronic		De novo					-	-	Wilfert2021 G
OLFML2B	DEASD_0097_001	chr1: 161989809-161989809	G	A	exonic		De novo	nonsynonymous SNV	NM_001297713 NM_015441	c.C338T c.C338T	p.S113L p.S113L	12.93	1.0E-4	DeRubeis2014 E Fu2022 E Kosmicki2017 E Satterstrom2020 E
OLFML2B	08C78430	chr1: 161953699-161953699	G	A	exonic		De novo	synonymous SNV	NM_001297713 NM_015441	c.C2022T c.C2019T	p.Y674Y p.Y673Y	-	-	Fu2022 E Satterstrom2020 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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