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Results for "NRDE2"

Variant Events: 10

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
NRDE2     1-0534-003chr14:
90827891-90827891
GAintergenicDe novo--Yuen2017 G
NRDE2     2-1132-003chr14:
90791166-90791166
GAintronicDe novo--Yuen2017 G
NRDE2     2-1508-003chr14:
90848596-90848596
CAintergenicDe novo--Yuen2017 G
NRDE2     1-0158-003chr14:
90824227-90824227
TGintergenicDe novo--Yuen2017 G
NRDE2     iHART2788chr14:
90769212-90769212
GCexonicMaternalstopgainNM_017970c.C1263Gp.Y421X40.0-Ruzzo2019 G
NRDE2     AU009904chr14:
90842437-90842437
CTintergenicDe novo--Yuen2017 G
NRDE2     AU075803chr14:
90806859-90806859
CTintergenicDe novo--Yuen2017 G
NRDE2     Cukier2014:37024chr14:
90756862-90756862
CGexonicUnknownnonsynonymous SNVNM_017970c.G1932Cp.L644F16.350.0079Cukier2014 E
NRDE2     2-1170-003chr14:
90765389-90765395
TTTTTTATintronicDe novo--Yuen2017 G
NRDE2     12327.p1chr14:
90756969-90756969
TAintronicDe novo-3.0E-4Satterstrom2020 E
Source Variant Information

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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 notesView
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