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Results for "RTN3"

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
RTN3     13351.p1chr11:
63520130-63520131
TGTintronicDe novo--Satterstrom2020 E
RTN3     AU002903chr11:
63465432-63465432
GCintronicDe novo--Yuen2017 G
RTN3     AU3190305chr11:
63514884-63514884
AGintronicDe novo--Yuen2017 G
RTN3     2-1212-003chr11:
63487665-63487665
TCexonicDe novononsynonymous SNVNM_001265590
NM_201428
NM_001265589
c.T1355C
c.T1634C
c.T1691C
p.L452P
p.L545P
p.L564P
4.833-Yuen2017 G
RTN3     Codina-Sola2015:ASD_4chr11:
63486837-63486837
CCAGexonicMaternalframeshift insertionNM_001265590
NM_201428
NM_001265589
c.527_528insAG
c.806_807insAG
c.863_864insAG
p.S176fs
p.S269fs
p.S288fs
--Codina-Sola2015 E
RTN3     AU4056301chr11:
63484137-63484137
GTintronicDe novo--Yuen2017 G
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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