Home
Publications
Statistics
Downloads
About
Documentation
Gene Symbol:
Submit
or
Region:
Submit
or
Sample:
Exact
Submit
Home
Search by gene
Results for "DCX"
Variant Events: 8
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
DCX
AU1261301
chrX:
110653469-110653469
T
C
exonic
Unknown
nonsynonymous SNV
NM_000555
NM_001195553
NM_178151
NM_178152
NM_178153
c.A401G
c.A158G
c.A158G
c.A158G
c.A158G
p.K134R
p.K53R
p.K53R
p.K53R
p.K53R
16.25
-
Chahrour2012
E
DCX
07C64767
chrX:
110644366-110644366
C
A
exonic
Inherited
nonsynonymous SNV
NM_000555
NM_001195553
NM_178151
NM_178152
NM_178153
c.G800T
c.G557T
c.G557T
c.G557T
c.G557T
p.R267L
p.R186L
p.R186L
p.R186L
p.R186L
33.0
-
Stessman2017
T
DCX
AU030104
chrX:
110559321-110559321
A
T
intronic
De novo
-
-
Yuen2017
G
DCX
Hu2022:84
chrX:
110574270-110574270
C
G
splicing
Unknown
splicing
18.07
-
Hu2022
T
DCX
5-0050-004
chrX:
110598458-110598458
G
A
intronic
De novo
-
-
Yuen2017
G
DCX
2-0022-004
chrX:
110710376-110710376
G
T
intergenic
De novo
-
-
Yuen2017
G
DCX
2-1329-003
chrX:
110721103-110721104
AT
A
intergenic
De novo
-
-
Yuen2017
G
DCX
215-13041-0503
chrX:
110653511-110653511
C
T
exonic
Inherited
nonsynonymous SNV
NM_000555
NM_001195553
NM_178151
NM_178152
NM_178153
c.G359A
c.G116A
c.G116A
c.G116A
c.G116A
p.R120Q
p.R39Q
p.R39Q
p.R39Q
p.R39Q
35.0
-
Stessman2017
T
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