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Results for "CELF4"
Variant Events: 39
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
CELF4
2-1715-003
chr18:
34864003-34864003
C
CA
intronic
De novo
-
-
Yuen2017
G
CELF4
1-0826-003
chr18:
34987927-34987927
A
G
intronic
De novo
-
-
Yuen2017
G
CELF4
1-0652-004
chr18:
34967430-34967430
A
G
intronic
De novo
-
-
Yuen2017
G
CELF4
AU4336301
chr18:
34844563-34844563
C
T
intronic
De novo
-
-
Yuen2017
G
CELF4
Mahjani2021:142
chr18:
34855146-34855146
C
A
exonic
nonsynonymous SNV
NM_001025087
NM_001025088
NM_001025089
NM_020180
c.G509T
c.G506T
c.G479T
c.G509T
p.R170L
p.R169L
p.R160L
p.R170L
20.4
8.38E-6
Mahjani2021
E
CELF4
2-1644-004
chr18:
34863893-34863893
C
CACTG
intronic
De novo
-
-
Yuen2017
G
CELF4
SSC11202
chr18:
34855162-34855162
C
A
exonic
De novo
stopgain
NM_001025087
NM_001025088
NM_001025089
NM_020180
c.G493T
c.G490T
c.G463T
c.G493T
p.E165X
p.E164X
p.E155X
p.E165X
40.0
-
Antaki2022
G
E
Fu2022
E
Lim2017
E
CELF4
AU079605
chr18:
35032785-35032785
G
A
intronic
De novo
-
-
Yuen2017
G
CELF4
A11
chr18:
34991296-34991296
C
T
intronic
De novo
-
-
Wu2018
G
CELF4
AU4067301
chr18:
34972944-34972946
CCT
C
intronic
De novo
-
-
Yuen2017
G
CELF4
1-0007-003
chr18:
34854815-34854815
C
G
exonic
De novo
nonsynonymous SNV
NM_001025087
NM_001025088
NM_001025089
NM_020180
c.G610C
c.G607C
c.G580C
c.G610C
p.E204Q
p.E203Q
p.E194Q
p.E204Q
22.2
-
Yuen2017
G
CELF4
AU3397302
chr18:
35194548-35194548
C
T
intergenic
De novo
-
-
Yuen2017
G
CELF4
2-1339-003
chr18:
34863975-34863975
A
C
intronic
De novo
-
-
Yuen2017
G
CELF4
2-0286-004
chr18:
35067388-35067388
C
T
intronic
De novo
-
-
Yuen2017
G
CELF4
14214.p1
chr18:
34855162-34855162
C
A
exonic
De novo
stopgain
NM_001025087
NM_001025088
NM_001025089
NM_020180
c.G493T
c.G490T
c.G463T
c.G493T
p.E165X
p.E164X
p.E155X
p.E165X
40.0
-
Ji2016
E
Krumm2015
E
Satterstrom2020
E
Wilfert2021
G
CELF4
1-0541-004
chr18:
34863893-34863893
C
CACACACACTG
intronic
De novo
-
-
Yuen2017
G
CELF4
1-0303-004
chr18:
34863905-34863905
C
CACACACAACATA
intronic
De novo
-
-
Yuen2017
G
CELF4
AU072504
chr18:
34888581-34888581
A
G
intronic
De novo
-
-
Yuen2017
G
CELF4
1-0677-003
chr18:
34844729-34844729
C
T
intronic
De novo
-
-
Yuen2017
G
CELF4
1-0144-004
chr18:
34863893-34863893
C
CACACACACTG
intronic
De novo
-
-
Yuen2017
G
CELF4
7-0191-003
chr18:
34863926-34863926
C
CACATACACACACCAA
intronic
De novo
-
-
Yuen2017
G
CELF4
SP0115698
chr18:
34854796-34854796
T
C
exonic
De novo
nonsynonymous SNV
NM_001025087
NM_001025088
NM_001025089
NM_020180
c.A629G
c.A626G
c.A599G
c.A629G
p.N210S
p.N209S
p.N200S
p.N210S
9.171
-
Fu2022
E
CELF4
08C74427
chr18:
34844598-34844598
G
C
intronic
De novo
-
-
Satterstrom2020
E
CELF4
1-0184-003
chr18:
35009271-35009286
CTGTGTGTGTGTGTGT
CTGTGTGTGTGTGT
intronic
De novo
-
-
Yuen2017
G
CELF4
2-0144-004
chr18:
34863912-34863912
T
TACACACAACATACACACATATACACATAC
intronic
De novo
-
-
Yuen2017
G
CELF4
AU3786301
chr18:
34914809-34914809
A
G
intronic
De novo
-
-
Yuen2017
G
CELF4
1-0112-004
chr18:
34884002-34884002
A
G
intronic
De novo
-
-
Yuen2017
G
CELF4
EGAN00001101315
chr18:
34839080-34839080
C
T
intronic
De novo
-
-
Fu2022
E
Satterstrom2020
E
CELF4
1-0054-004
chr18:
35195983-35195983
T
C
intergenic
De novo
-
-
Yuen2017
G
CELF4
1-0882-003
chr18:
35227611-35227611
G
A
intergenic
De novo
-
-
Yuen2017
G
CELF4
1-0338-005
chr18:
35095862-35095862
G
A
intronic
De novo
-
-
Yuen2017
G
CELF4
G01-GEA-111-HI
chr18:
34846529-34846529
G
A
exonic
De novo
stopgain
NM_001025087
NM_001025088
NM_001025089
NM_020180
c.C1129T
c.C1126T
c.C1102T
c.C1132T
p.Q377X
p.Q376X
p.Q368X
p.Q378X
41.0
-
Fu2022
E
Lim2017
E
Satterstrom2020
E
CELF4
63-343
chr18:
35094644-35094644
G
A
intronic
De novo
-
-
Michaelson2012
G
CELF4
ASC_CA_59_A
chr18:
34854331-34854331
C
A
exonic
De novo
nonsynonymous SNV
NM_001025087
NM_001025088
NM_001025089
NM_020180
c.G744T
c.G741T
c.G714T
c.G744T
p.M248I
p.M247I
p.M238I
p.M248I
19.45
-
Fu2022
E
Satterstrom2020
E
CELF4
iHART1776
chr18:
34846538-34846538
G
C
exonic
De novo
nonsynonymous SNV
NM_001025087
NM_001025088
NM_001025089
NM_020180
c.C1120G
c.C1117G
c.C1093G
c.C1123G
p.P374A
p.P373A
p.P365A
p.P375A
15.25
-
Ruzzo2019
G
CELF4
2-0319-004
chr18:
35029123-35029123
T
C
intronic
De novo
-
-
Yuen2017
G
CELF4
AU2293301
chr18:
35034819-35034819
G
A
intronic
De novo
-
-
Yuen2017
G
CELF4
AU071703
chr18:
34827652-34827652
A
T
intronic
De novo
-
-
Yuen2017
G
CELF4
AU066404
chr18:
34922481-34922481
G
A
intronic
De 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 notes
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