Variant Results

or

or

Results for "HNRNPUL2"

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
HNRNPUL2	36862	chr11: 62490296-62490296	C	T	exonic		De novo	nonsynonymous SNV	NM_001079559	c.G971A	p.R324H	15.95	4.143E-5	Fu2022 E Trost2022 G
HNRNPUL2	1989-24099	chr11: 62484506-62484506	G	A	exonic			stopgain	NM_001079559	c.C1936T	p.R646X	39.0	-	Callaghan2019 G
HNRNPUL2	SP0126796	chr11: 62484535-62484536	GA	G	exonic		De novo	frameshift deletion	NM_001079559	c.1906delT	p.S636fs	-	-	Antaki2022 GE Fu2022 E Trost2022 G Zhou2022 GE
HNRNPUL2	SP0094458	chr11: 62482992-62482994	AAT	A	exonic		De novo	frameshift deletion	NM_001079559	c.2141_2142del	p.Y714fs	-	-	Antaki2022 GE Fu2022 E Trost2022 G Zhou2022 GE
HNRNPUL2	14554.p1	chr11: 62490296-62490296	C	T	exonic		De novo	nonsynonymous SNV	NM_001079559	c.G971A	p.R324H	15.95	4.143E-5	Iossifov2014 E Ji2016 E Kosmicki2017 E Krupp2017 E Satterstrom2020 E Zhou2022 GE
HNRNPUL2	SP0119831	chr11: 62487558-62487559	GC	G	exonic		De novo	frameshift deletion	NM_001079559	c.1716delG	p.R572fs	-	-	Antaki2022 GE Fu2022 E Trost2022 G Zhou2022 GE

Source Variant Information

, -

Source:

Paper alias:

No records found.

Paper Information

Title
Authors
Technology
Variant source
Cohorts
Design
URL
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.
Variant event count
Curation notes	View
	More