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Results for "KDM6B"
Variant Events: 34
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
KDM6B
SP0159366
chr17:
7755119-7755119
G
A
intronic
-
-
Zhou2022
G
E
KDM6B
SP0172698
chr17:
7754424-7754427
AGAT
A
exonic
De novo
nonframeshift deletion
NM_001080424
c.3760_3762del
p.1254_1254del
-
-
Trost2022
G
Zhou2022
G
E
KDM6B
SP0019310
chr17:
7756573-7756573
C
T
exonic
De novo
nonsynonymous SNV
NM_001080424
c.C4783T
p.R1595C
14.86
-
Feliciano2019
E
Fu2022
E
Zhou2022
G
E
KDM6B
Mahjani2021:84
chr17:
7751740-7751740
C
T
exonic
stopgain
NM_001080424
c.C2134T
p.Q712X
39.0
-
Mahjani2021
E
KDM6B
SP0340104
chr17:
7756427-7756427
T
C
exonic
nonsynonymous SNV
NM_001080424
c.T4720C
p.Y1574H
14.42
-
Zhou2022
G
E
KDM6B
TAS_F3039Y
chr17:
7756583-7756584
AC
A
exonic
De novo
frameshift deletion
NM_001080424
c.4794delC
p.Y1598fs
-
-
Fu2022
E
Satterstrom2020
E
Trost2022
G
Zhou2022
G
E
KDM6B
SP0157208
chr17:
7751936-7751936
C
CA
exonic
frameshift insertion
NM_001080424
c.2331dupA
p.P777fs
-
-
Zhou2022
G
E
KDM6B
SP0277638
chr17:
7751090-7751090
G
A
exonic
nonsynonymous SNV
NM_001080424
c.G1484A
p.R495Q
10.82
-
Zhou2022
G
E
KDM6B
SP0103211
chr17:
7753227-7753227
C
T
exonic
nonsynonymous SNV
NM_001080424
c.C3529T
p.P1177S
15.17
-
Zhou2022
G
E
KDM6B
SP0156468
chr17:
7752457-7752457
C
T
exonic
stopgain
NM_001080424
c.C2851T
p.R951X
42.0
-
Zhou2022
G
E
KDM6B
11329.p1
chr17:
7749188-7749188
A
G
splicing
De novo
splicing
13.0
-
Iossifov2014
E
Ji2016
E
Kosmicki2017
E
Lim2017
E
Satterstrom2020
E
Trost2022
G
Wilfert2021
G
Zhou2022
G
E
KDM6B
13675.p1
chr17:
7755287-7755290
ACTT
A
exonic
De novo
nonframeshift deletion
NM_001080424
c.4185_4187del
p.1395_1396del
-
-
Iossifov2014
E
Kosmicki2017
E
Satterstrom2020
E
Trost2022
G
Wilfert2021
G
Zhou2022
G
E
KDM6B
12683.p1
chr17:
7749188-7749188
A
G
splicing
De novo
splicing
13.0
-
Willsey2013
E
KDM6B
12683.p1
Complex Event; expand row to view variants
De novo
frameshift deletion
NM_001080424
NM_001080424
c.575delG
c.576delG
p.R192fs
p.R192fs
-
-
Dong2014
E
Iossifov2012
E
Iossifov2014
E
Ji2016
E
Kosmicki2017
E
Satterstrom2020
E
Wilfert2021
G
Willsey2013
E
Zhou2022
G
E
KDM6B
13446.p1
chr17:
7755659-7755659
G
C
intronic
De novo
-
-
Iossifov2014
E
Kosmicki2017
E
Satterstrom2020
E
Trost2022
G
Zhou2022
G
E
KDM6B
SSC05540
chr17:
7749921-7749922
CG
C
exonic
De novo
frameshift deletion
NM_001080424
c.575delG
p.R192fs
-
-
Fu2022
E
Trost2022
G
KDM6B
DEASD_0146_001
chr17:
7755277-7755277
G
A
exonic
De novo
nonsynonymous SNV
NM_001080424
c.G4174A
p.E1392K
20.3
-
DeRubeis2014
E
Fu2022
E
Kosmicki2017
E
Lim2017
E
Satterstrom2020
E
Trost2022
G
Zhou2022
G
E
KDM6B
MT_48.3
chr17:
7749562-7749562
C
T
exonic
De novo
stopgain
NM_001080424
c.C403T
p.R135X
37.0
-
Antaki2022
G
E
Trost2022
G
Zhou2022
G
E
KDM6B
SSC02193
chr17:
7749188-7749188
A
G
splicing
splicing
13.0
-
Antaki2022
G
E
KDM6B
11329_p1
chr17:
7749188-7749188
A
G
splicing
De novo
splicing
13.0
-
Fu2022
E
KDM6B
C221803
chr17:
7750647-7750666
AACCACCGCCTGCGTGCCTT
A
exonic
De novo
frameshift deletion
NM_001080424
c.1135_1153del
p.T379fs
-
-
Fu2022
E
KDM6B
13446_p1
chr17:
7755659-7755659
G
C
intronic
De novo
-
-
Fu2022
E
KDM6B
mAGRE4510
chr17:
7755606-7755606
G
A
exonic
De novo
nonsynonymous SNV
NM_001080424
c.G4420A
p.A1474T
21.1
-
Cirnigliaro2023
G
KDM6B
13675_p1
chr17:
7755287-7755290
ACTT
A
exonic
De novo
nonframeshift deletion
NM_001080424
c.4185_4187del
p.1395_1396del
-
-
Fu2022
E
KDM6B
SP0037558
chr17:
7756304-7756304
C
T
intronic
De novo
-
-
Fu2022
E
KDM6B
Krgovic2022:040353
chr17:
7752805-7752805
G
GTCAG
exonic
De novo
frameshift insertion
NM_001080424
c.3199_3200insTCAG
p.A1067fs
-
-
Krgovic2022
E
KDM6B
SP0022019
chr17:
7749868-7749868
C
T
intronic
De novo
-
8.335E-6
Fu2022
E
Trost2022
G
KDM6B
SP0052849
chr17:
7749689-7749689
G
GGGCCGGC
intronic
De novo
-
-
Fu2022
E
KDM6B
Hu2022:11
chr17:
7752386-7752400
GGGTGGGCCGGAGTG
G
exonic
Unknown
frameshift deletion
NM_001080424
c.2781_2794del
p.R927fs
-
-
Hu2022
T
KDM6B
AU4359301
chr17:
7757138-7757138
C
CCGG
UTR3
De novo
-
-
Trost2022
G
KDM6B
2-1764-003
chr17:
7755116-7755116
T
A
splicing
De novo
splicing
23.4
-
Trost2022
G
Zhou2022
G
E
KDM6B
DEASD_0129_001
chr17:
7755289-7755289
T
A
exonic
De novo
nonsynonymous SNV
NM_001080424
c.T4186A
p.F1396I
20.1
-
Fu2022
E
Satterstrom2020
E
Trost2022
G
Zhou2022
G
E
KDM6B
SP0197793
chr17:
7750769-7750771
TTG
T
exonic
frameshift deletion
NM_001080424
c.1257_1257del
p.I419fs
-
-
Zhou2022
G
E
KDM6B
SP0125028
chr17:
7749604-7749604
C
T
exonic
stopgain
NM_001080424
c.C445T
p.R149X
37.0
-
Zhou2022
G
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 notes
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