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Results for "BRD1"
Variant Events: 27
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
BRD1
13577.p1
chr22:
50170516-50170516
C
T
intronic
Unknown
-
-
Werling2018
G
BRD1
MT_6.3
chr22:
50170811-50170811
T
A
splicing
De novo
splicing
13.84
-
Antaki2022
G
E
Trost2022
G
Zhou2022
G
E
BRD1
1256-20693
chr22:
50181377-50181378
CG
C
exonic
frameshift deletion
NM_001304808
c.2517delC
p.S839fs
-
5.98E-5
Callaghan2019
G
BRD1
1-1155-003
chr22:
50218020-50218020
G
A
intronic
De novo
-
-
Trost2022
G
BRD1
12515.p1
chr22:
50169672-50169672
G
A
intronic
De novo
-
2.0E-4
Satterstrom2020
E
BRD1
SSC11200
chr22:
50192770-50192775
GAGAAC
G
intronic
De novo
-
-
Fu2022
E
Trost2022
G
BRD1
GEA471
chr22:
50170786-50170786
C
T
exonic
De novo
nonsynonymous SNV
NM_001304808
NM_001304809
c.G3017A
c.G2624A
p.R1006Q
p.R875Q
20.7
8.336E-6
Fu2022
E
BRD1
SP0098425
chr22:
50217373-50217373
T
C
exonic
De novo
nonsynonymous SNV
NM_001304808
NM_001304809
c.A593G
c.A593G
p.H198R
p.H198R
13.42
-
Fu2022
E
Trost2022
G
Zhou2022
G
E
BRD1
SP0005093
chr22:
50169467-50169467
C
CCCCCCCGCCCCCCGCAGCTGTGTGAGCCTCCTCAGAACT
intronic
De novo
-
-
Fu2022
E
BRD1
SP0086561
chr22:
50169188-50169188
G
A
intronic
De novo
-
4.4E-5
Fu2022
E
Trost2022
G
BRD1
MT_6.3
chr22:
50170813-50170813
C
T
intronic
De novo
-
3.351E-5
Trost2022
G
Zhou2022
G
E
BRD1
SP0237885
chr22:
50170745-50170745
G
A
exonic
nonsynonymous SNV
NM_001304808
NM_001304809
c.C3058T
c.C2665T
p.R1020C
p.R889C
16.18
1.662E-5
Zhou2022
G
E
BRD1
SP0015245
chr22:
50169479-50169479
C
T
intronic
De novo
-
-
Fu2022
E
BRD1
SP0212560
chr22:
50217127-50217127
G
T
exonic
De novo
nonsynonymous SNV
NM_001304808
NM_001304809
c.C839A
c.C839A
p.A280D
p.A280D
25.0
-
Trost2022
G
Zhou2022
G
E
BRD1
SP0048475
chr22:
50192294-50192294
G
A
exonic
De novo
nonsynonymous SNV
NM_001304808
NM_001304809
c.C1697T
c.C1697T
p.P566L
p.P566L
15.35
-
Trost2022
G
Zhou2022
G
E
BRD1
11301.p1
chr22:
50167925-50167925
G
A
exonic
De novo
nonsynonymous SNV
NM_001304808
NM_001304809
c.C3526T
c.C3133T
p.R1176C
p.R1045C
14.78
2.473E-5
Iossifov2014
E
Ji2016
E
Kosmicki2017
E
Krupp2017
E
Sanders2012
E
Satterstrom2020
E
Trost2022
G
Wilfert2021
G
Zhou2022
G
E
BRD1
14225.p1
chr22:
50192770-50192775
GAGAAC
G
intronic
De novo
-
-
Iossifov2014
E
Kosmicki2017
E
Satterstrom2020
E
Zhou2022
G
E
BRD1
AU3912302
Complex Event; expand row to view variants
De novo
-
-
Trost2022
G
Yuen2017
G
BRD1
11301_p1
chr22:
50167925-50167925
G
A
exonic
De novo
nonsynonymous SNV
NM_001304808
NM_001304809
c.C3526T
c.C3133T
p.R1176C
p.R1045C
14.78
2.473E-5
Fu2022
E
BRD1
1-0158-003
chr22:
50168553-50168555
GCA
G
intronic
De novo
-
-
Trost2022
G
Yuen2017
G
BRD1
MSSNG00254-004
chr22:
50201543-50201543
A
G
intronic
De novo
-
-
Trost2022
G
BRD1
MSSNG00360-003
chr22:
50196633-50196633
C
T
intronic
De novo
-
-
Trost2022
G
BRD1
4-0046-003
chr22:
50193882-50193882
C
T
intronic
De novo
-
-
Trost2022
G
BRD1
SP0246954
chr22:
50191454-50191454
G
A
exonic
De novo
synonymous SNV
NM_001304808
NM_001304809
c.C2097T
c.C2097T
p.D699D
p.D699D
-
4.672E-5
Trost2022
G
BRD1
1-0681-003
chr22:
50183152-50183152
C
T
intronic
De novo
-
-
Trost2022
G
BRD1
MT_27.3
chr22:
50178834-50178834
C
T
intronic
De novo
-
-
Trost2022
G
BRD1
SSC05092
chr22:
50169672-50169672
G
A
intronic
De novo
-
2.0E-4
Trost2022
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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