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Results for "ACACB"

Variant Events: 45

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
ACACB     SP0042363chr12:
109631424-109631424
GAintronicDe novo--Fu2022 E
ACACB     SP0032493chr12:
109609582-109609582
CGintronicDe novo--Fu2022 E
ACACB     SP0092140chr12:
109684210-109684210
ATexonicnonsynonymous SNVNM_001093c.A5528Tp.H1843L15.1-Zhou2022 GE
ACACB     SP0104241chr12:
109639562-109639562
CTintronicDe novo--Fu2022 E
Trost2022 G
ACACB     3-0515-000chr12:
109577653-109577660
CCAAAGAACexonicDe novoframeshift deletionNM_001093c.444_450delp.S148fs--Trost2022 G
Zhou2022 GE
ACACB     1-0346-004chr12:
109671468-109671468
GAintronicDe novo--Trost2022 G
Yuen2017 G
ACACB     SP0035635chr12:
109577236-109577236
GAexonicDe novononsynonymous SNVNM_001093c.G26Ap.C9Y13.532.482E-5Fu2022 E
Trost2022 G
Zhou2022 GE
ACACB     5-0043-003chr12:
109705671-109705671
GAUTR3De novo--Trost2022 G
ACACB     SP0082648chr12:
109675039-109675039
CGexonicDe novononsynonymous SNVNM_001093c.C4516Gp.R1506G23.2-Fu2022 E
Trost2022 G
Zhou2022 GE
ACACB     AU145Achr12:
109644616-109644616
CTexonicDe novosynonymous SNVNM_001093c.C3015Tp.N1005N-0.0365DeRubeis2014 E
Kosmicki2017 E
ACACB     1-0090-003chr12:
109690903-109690903
CTexonicDe novosynonymous SNVNM_001093c.C5985Tp.T1995T-6.665E-5Trost2022 G
Zhou2022 GE
ACACB     ASC_CA_204_Achr12:
109683954-109683954
AGintronicDe novo--Satterstrom2020 E
Trost2022 G
ACACB     150653chr12:
109684055-109684055
CTexonicDe novosynonymous SNVNM_001093c.C5373Tp.I1791I-4.946E-5Fu2022 E
ACACB     EGAN00001100988chr12:
109704162-109704162
ACexonicDe novononsynonymous SNVNM_001093c.A7372Cp.T2458P16.562.597E-5Fu2022 E
ACACB     14135_p1chr12:
109677728-109677728
CTexonicDe novononsynonymous SNVNM_001093c.C4756Tp.R1586C26.54.946E-5Fu2022 E
ACACB     14574.p1chr12:
109625794-109625794
CTintronicDe novo-8.348E-6Iossifov2014 E
Kosmicki2017 E
Satterstrom2020 E
ACACB     SSC07902chr12:
109577549-109577549
AAGexonicDe novoframeshift insertionNM_001093c.340dupGp.P113fs--Fu2022 E
Trost2022 G
ACACB     14135.p1chr12:
109677728-109677728
CTexonicDe novononsynonymous SNVNM_001093c.C4756Tp.R1586C26.54.946E-5Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Krupp2017 E
Lim2017 E
Satterstrom2020 E
Trost2022 G
Wilfert2021 G
Zhou2022 GE
ACACB     ASC_CA_179_Achr12:
109614036-109614036
AGexonicDe novononsynonymous SNVNM_001093c.A1405Gp.S469G14.85-Fu2022 E
Satterstrom2020 E
Trost2022 G
Zhou2022 GE
ACACB     iHART2507chr12:
109684020-109684020
CTexonicPaternalstopgainNM_001093c.C5338Tp.Q1780X42.08.253E-6Ruzzo2019 G
ACACB     iHART1991chr12:
109629570-109629570
TCsplicingMaternalsplicing19.358.266E-6Ruzzo2019 G
ACACB     iHART3265chr12:
109623546-109623546
GCsplicingPaternalsplicing16.158.394E-6Ruzzo2019 G
ACACB     iHART1212chr12:
109660325-109660325
GGCexonicMaternalframeshift insertionNM_001093c.3579dupCp.G1193fs-1.0E-4Ruzzo2019 G
ACACB     13585.p1 Complex Event; expand row to view variants  De novoframeshift insertionNM_001093
NM_001093
c.340dupG
c.340dupG
p.P113fs
p.E114fs
--Dong2014 E
Iossifov2012 E
Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Satterstrom2020 E
Wilfert2021 G
Willsey2013 E
Zhou2022 GE
ACACB     7-0129-003chr12:
109644596-109644596
GAexonicDe novononsynonymous SNVNM_001093c.G2995Ap.V999I11.332.0E-4Trost2022 G
Yuen2017 G
Zhou2022 GE
ACACB     iHART2158chr12:
109629751-109629751
GTexonicPaternalstopgainNM_001093c.G2395Tp.E799X40.0-Ruzzo2019 G
ACACB     mAGRE4334chr12:
109684016-109684026
GACCCAGGAGTGexonicMaternalframeshift deletionNM_001093c.5335_5344delp.T1779fs--Cirnigliaro2023 G
ACACB     mAGRE1212chr12:
109660325-109660325
GGCexonicMaternalframeshift insertionNM_001093c.3579dupCp.G1193fs-1.0E-4Cirnigliaro2023 G
ACACB     mAGRE2158chr12:
109629751-109629751
GTexonicPaternalstopgainNM_001093c.G2395Tp.E799X40.0-Cirnigliaro2023 G
ACACB     mAGRE1991chr12:
109629570-109629570
TCsplicingMaternalsplicing19.358.266E-6Cirnigliaro2023 G
ACACB     AU4033305chr12:
109623546-109623546
GCsplicingPaternalsplicing16.158.394E-6Cirnigliaro2023 G
ACACB     mAGRE1944chr12:
109623382-109623382
AGsplicingPaternalsplicing21.5-Cirnigliaro2023 G
ACACB     mAGRE4743chr12:
109577305-109577307
TCATexonicMaternalframeshift deletionNM_001093c.96_97delp.I32fs--Cirnigliaro2023 G
ACACB     1-0757-003chr12:
109643725-109643725
GAintronicDe novo--Trost2022 G
Yuen2017 G
ACACB     1-0935-003chr12:
109644607-109644607
CAexonicDe novononsynonymous SNVNM_001093c.C3006Ap.N1002K2.441-Trost2022 G
Yuen2017 G
Zhou2022 GE
ACACB     5-5101-003chr12:
109617932-109617932
TGintronicDe novo--Trost2022 G
ACACB     REACH000182chr12:
109700802-109700802
TAintronicDe novo--Trost2022 G
ACACB     1-1005-004chr12:
109702843-109702843
AGintronicDe novo--Trost2022 G
ACACB     SP0204789chr12:
109687851-109687851
CGexonicDe novostopgainNM_001093c.C5732Gp.S1911X44.0-Trost2022 G
ACACB     7-0167-003chr12:
109578380-109578380
TGintronicDe novo--Trost2022 G
Yuen2017 G
ACACB     5-5180-003chr12:
109695036-109695036
GAintronicDe novo--Trost2022 G
ACACB     2-1407-003chr12:
109647701-109647701
TCintronicDe novo--Trost2022 G
ACACB     MSSNG00063-003chr12:
109653622-109653622
TCintronicDe novo--Trost2022 G
ACACB     37411chr12:
109625794-109625794
CTintronicDe novo-8.348E-6Trost2022 G
ACACB     2-1407-003chr12:
109647694-109647694
AGintronicDe novo--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 notesView
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