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Results for "IPCEF1"

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
IPCEF1     PN400284chr6:
154489119-154489119
CTexonicUnknownnonsynonymous SNVNM_001130700
NM_015553
NM_001130699
c.G1040A
c.G1037A
c.G1040A
p.R347Q
p.R346Q
p.R347Q
35.0-Leblond2019 E
IPCEF1     AU2100302chr6:
154607885-154607885
CTintronicDe novo--Trost2022 G
Yuen2017 G
IPCEF1     1-0593-003chr6:
154722487-154722498
TTCTCTCTCTCTTTCTCTCTCTintergenicDe novo--Yuen2017 G
IPCEF1     1-0329-003chr6:
154621212-154621212
AGintronicDe novo--Yuen2017 G
IPCEF1     1-0673-003chr6:
154681163-154681164
GAGintergenicDe novo--Yuen2017 G
IPCEF1     1-0043-003chr6:
154641493-154641493
TCintronicDe novo--Trost2022 G
Yuen2017 G
IPCEF1     5020chr6:
154481044-154481044
CGexonicDe novosynonymous SNVNM_001130700
NM_015553
NM_001130699
c.G1236C
c.G1233C
c.G1236C
p.S412S
p.S411S
p.S412S
-3.0E-4Trost2022 G
IPCEF1     1-0859-003chr6:
154524339-154524339
TAintronicDe novo--Trost2022 G
Trost2022 G
IPCEF1     AU005214chr6:
154624617-154624617
CAintronicDe novo--Trost2022 G
Yuen2017 G
IPCEF1     2-1342-003chr6:
154529109-154529109
CTintronicDe novo--Yuen2016 G
IPCEF1     REACH000405chr6:
154634867-154634867
CCTintronicDe novo--Trost2022 G
IPCEF1     MSSNG00011-003chr6:
154643693-154643694
CACintronicDe novo--Trost2022 G
IPCEF1     3-0548-000chr6:
154612728-154612728
AATGintronicDe novo--Trost2022 G
IPCEF1     2-1811-003chr6:
154616128-154616128
CAintronicDe novo--Trost2022 G
IPCEF1     14637.p1chr6:
154664402-154664402
TGintronicDe novo--Turner2016 G
IPCEF1     3-0485-000Achr6:
154597929-154597929
TCintronicDe novo--Trost2022 G
IPCEF1     MSSNG00032-003chr6:
154606518-154606518
GTintronicDe novo--Trost2022 G
IPCEF1     1-1115-003chr6:
154529618-154529618
AGintronicDe novo--Trost2022 G
Trost2022 G
IPCEF1     12449.p1chr6:
154525242-154525242
CTintronicDe novo--Turner2016 G
IPCEF1     11414.p1chr6:
154481044-154481044
CGexonicDe novosynonymous SNVNM_001130700
NM_015553
NM_001130699
c.G1236C
c.G1233C
c.G1236C
p.S412S
p.S411S
p.S412S
-3.0E-4Satterstrom2020 E
IPCEF1     1-1071-003chr6:
154562138-154562138
GCintronicDe novo--Trost2022 G
Trost2022 G
IPCEF1     2-1811-003chr6:
154675585-154675585
ATintronicDe novo--Trost2022 G
IPCEF1     AU4467302chr6:
154724556-154724557
ATAintergenicDe novo--Trost2022 G
IPCEF1     2-1811-003chr6:
154675573-154675573
TAintronicDe novo--Trost2022 G
IPCEF1     2-0215-003chr6:
154517303-154517303
CTintronicDe novo--Trost2022 G
Yuen2017 G
IPCEF1     7-0292-004Achr6:
154675583-154675583
CTintronicDe novo--Trost2022 G
IPCEF1     2-0057-004chr6:
154500634-154500634
CAintronicDe novo--Yuen2017 G
IPCEF1     10-0007-003chr6:
154666061-154666061
CCCTATCTCCAACCTATintronicDe novo--Trost2022 G
IPCEF1     2-1811-003chr6:
154675571-154675571
TCintronicDe novo--Trost2022 G
IPCEF1     2-0205-003chr6:
154654547-154654547
GAintronicDe novo--Trost2022 G
IPCEF1     REACH000345chr6:
154664759-154664759
AGintronicDe novo--Trost2022 G
IPCEF1     AU031003chr6:
154558466-154558466
TAintronicDe novo--Trost2022 G
Trost2022 G
Yuen2017 G
IPCEF1     1-0045-004chr6:
154573855-154573855
GAintronicDe novo--Trost2022 G
Yuen2017 G
IPCEF1     A24chr6:
154621573-154621573
CTintronicDe novo--Wu2018 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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