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Results for "PATJ"
Variant Events: 33
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
PATJ
AU3053302
chr1:
62378948-62378948
C
G
intronic
De novo
-
-
Yuen2017
G
PATJ
SP0044098
chr1:
62374032-62374032
T
G
intronic
De novo
-
-
Fu2022
E
PATJ
SP0034904
chr1:
62588733-62588733
A
G
intronic
De novo
-
-
Fu2022
E
PATJ
2-1154-003
chr1:
62658407-62658407
T
G
intergenic
De novo
-
-
Yuen2017
G
PATJ
AU0636303
chr1:
62325251-62325251
T
C
intronic
De novo
-
-
Yuen2017
G
PATJ
SP0078543
chr1:
62614103-62614103
C
A
intronic
De novo
-
-
Fu2022
E
PATJ
1-0219-003
chr1:
62291136-62291136
A
G
intronic
De novo
-
-
Yuen2017
G
PATJ
1-0458-003
chr1:
62624277-62624277
C
A
intronic
De novo
-
-
Yuen2017
G
PATJ
1-0144-004
chr1:
62655471-62655471
C
T
intergenic
De novo
-
-
Yuen2017
G
PATJ
1-0079-008
chr1:
62535179-62535179
G
A
intronic
De novo
-
-
Yuen2017
G
PATJ
Kenny2014:1
chr1:
62321741-62321742
TC
T
exonic
Unknown
frameshift deletion
NM_176877
c.2153delC
p.S718fs
-
-
Kenny2014
T
PATJ
1-0007-003
chr1:
62604323-62604323
C
T
intronic
De novo
-
-
Yuen2017
G
PATJ
5111007080051-C
chr1:
62232230-62232230
C
T
intronic
De novo
-
-
Fu2022
E
PATJ
AU2089302
chr1:
62585855-62585855
G
A
intronic
De novo
-
-
Yuen2017
G
PATJ
PN400341
chr1:
62574145-62574145
G
C
exonic
Unknown
nonsynonymous SNV
NM_176877
c.G4414C
p.A1472P
29.9
2.498E-5
Leblond2019
E
PATJ
AU2569301
chr1:
62579917-62579917
C
T
exonic
De novo
stopgain
NM_176877
c.C4654T
p.R1552X
44.0
5.012E-5
Yuen2017
G
PATJ
11402.p1
chr1:
62374072-62374072
C
T
exonic
Mosaic
nonsynonymous SNV
NM_176877
c.C3410T
p.S1137L
19.79
-
Dou2017
E
PATJ
5-0055-003
chr1:
62228363-62228363
G
T
intronic
De novo
-
-
Yuen2017
G
PATJ
7-0141-003
chr1:
62588653-62588653
T
G
intronic
De novo
-
-
Yuen2017
G
PATJ
AU3786301
chr1:
62427926-62427934
ATGTCTTGT
ATGT
intronic
De novo
-
-
Yuen2017
G
PATJ
AU003403
chr1:
62311337-62311337
A
G
intronic
De novo
-
-
Yuen2017
G
PATJ
1-0551-004
chr1:
62561747-62561747
A
G
intronic
De novo
-
-
Yuen2017
G
PATJ
1-0197-004
chr1:
62657831-62657831
T
C
intergenic
De novo
-
-
Yuen2017
G
PATJ
2-1168-003
chr1:
62445134-62445134
G
A
intronic
De novo
-
-
Yuen2017
G
PATJ
Cukier2014:17122
chr1:
62582847-62582847
C
G
exonic
Unknown
nonsynonymous SNV
NM_176877
c.C4847G
p.A1616G
18.62
0.013
Cukier2014
E
PATJ
1-0261-004
chr1:
62596547-62596547
C
T
intronic
De novo
-
-
Yuen2017
G
PATJ
1-0169-003
chr1:
62499320-62499320
A
C
intronic
De novo
-
-
Yuen2017
G
PATJ
iHART1751
chr1:
62614060-62614064
AGAGT
A
exonic
Paternal
frameshift deletion
NM_176877
c.5377_5378del
p.E1793fs
-
4.969E-5
Ruzzo2019
G
PATJ
11490.p1
chr1:
62327208-62327208
G
T
intronic
De novo
-
-
Krumm2015
E
PATJ
AU4327303
chr1:
62656499-62656503
CCTCT
CCT
intergenic
De novo
-
-
Yuen2017
G
PATJ
iHART1912
chr1:
62366953-62366953
G
A
splicing
Paternal
splicing
23.0
8.667E-6
Ruzzo2019
G
PATJ
iHART1754
chr1:
62614060-62614064
AGAGT
A
exonic
Paternal
frameshift deletion
NM_176877
c.5377_5378del
p.E1793fs
-
4.969E-5
Ruzzo2019
G
PATJ
iHART2411
chr1:
62241004-62241004
C
T
exonic
Maternal
stopgain
NM_176877
c.C847T
p.R283X
39.0
8.27E-6
Ruzzo2019
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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