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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.p1chr22:
50170516-50170516
CTintronicUnknown--Werling2018 G
BRD1     MT_6.3chr22:
50170811-50170811
TAsplicingDe novosplicing13.84-Antaki2022 GE
Trost2022 G
Zhou2022 GE
BRD1     1256-20693chr22:
50181377-50181378
CGCexonicframeshift deletionNM_001304808c.2517delCp.S839fs-5.98E-5Callaghan2019 G
BRD1     1-1155-003chr22:
50218020-50218020
GAintronicDe novo--Trost2022 G
BRD1     12515.p1chr22:
50169672-50169672
GAintronicDe novo-2.0E-4Satterstrom2020 E
BRD1     SSC11200chr22:
50192770-50192775
GAGAACGintronicDe novo--Fu2022 E
Trost2022 G
BRD1     GEA471chr22:
50170786-50170786
CTexonicDe novononsynonymous SNVNM_001304808
NM_001304809
c.G3017A
c.G2624A
p.R1006Q
p.R875Q
20.78.336E-6Fu2022 E
BRD1     SP0098425chr22:
50217373-50217373
TCexonicDe novononsynonymous SNVNM_001304808
NM_001304809
c.A593G
c.A593G
p.H198R
p.H198R
13.42-Fu2022 E
Trost2022 G
Zhou2022 GE
BRD1     SP0005093chr22:
50169467-50169467
CCCCCCCCGCCCCCCGCAGCTGTGTGAGCCTCCTCAGAACTintronicDe novo--Fu2022 E
BRD1     SP0086561chr22:
50169188-50169188
GAintronicDe novo-4.4E-5Fu2022 E
Trost2022 G
BRD1     MT_6.3chr22:
50170813-50170813
CTintronicDe novo-3.351E-5Trost2022 G
Zhou2022 GE
BRD1     SP0237885chr22:
50170745-50170745
GAexonicnonsynonymous SNVNM_001304808
NM_001304809
c.C3058T
c.C2665T
p.R1020C
p.R889C
16.181.662E-5Zhou2022 GE
BRD1     SP0015245chr22:
50169479-50169479
CTintronicDe novo--Fu2022 E
BRD1     SP0212560chr22:
50217127-50217127
GTexonicDe novononsynonymous SNVNM_001304808
NM_001304809
c.C839A
c.C839A
p.A280D
p.A280D
25.0-Trost2022 G
Zhou2022 GE
BRD1     SP0048475chr22:
50192294-50192294
GAexonicDe novononsynonymous SNVNM_001304808
NM_001304809
c.C1697T
c.C1697T
p.P566L
p.P566L
15.35-Trost2022 G
Zhou2022 GE
BRD1     11301.p1chr22:
50167925-50167925
GAexonicDe novononsynonymous SNVNM_001304808
NM_001304809
c.C3526T
c.C3133T
p.R1176C
p.R1045C
14.782.473E-5Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Krupp2017 E
Sanders2012 E
Satterstrom2020 E
Trost2022 G
Wilfert2021 G
Zhou2022 GE
BRD1     14225.p1chr22:
50192770-50192775
GAGAACGintronicDe novo--Iossifov2014 E
Kosmicki2017 E
Satterstrom2020 E
Zhou2022 GE
BRD1     AU3912302 Complex Event; expand row to view variants  De novo--Trost2022 G
Yuen2017 G
BRD1     11301_p1chr22:
50167925-50167925
GAexonicDe novononsynonymous SNVNM_001304808
NM_001304809
c.C3526T
c.C3133T
p.R1176C
p.R1045C
14.782.473E-5Fu2022 E
BRD1     1-0158-003chr22:
50168553-50168555
GCAGintronicDe novo--Trost2022 G
Yuen2017 G
BRD1     MSSNG00254-004chr22:
50201543-50201543
AGintronicDe novo--Trost2022 G
BRD1     MSSNG00360-003chr22:
50196633-50196633
CTintronicDe novo--Trost2022 G
BRD1     4-0046-003chr22:
50193882-50193882
CTintronicDe novo--Trost2022 G
BRD1     SP0246954chr22:
50191454-50191454
GAexonicDe novosynonymous SNVNM_001304808
NM_001304809
c.C2097T
c.C2097T
p.D699D
p.D699D
-4.672E-5Trost2022 G
BRD1     1-0681-003chr22:
50183152-50183152
CTintronicDe novo--Trost2022 G
BRD1     MT_27.3chr22:
50178834-50178834
CTintronicDe novo--Trost2022 G
BRD1     SSC05092chr22:
50169672-50169672
GAintronicDe novo-2.0E-4Trost2022 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 notesView
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