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Results for "FBXW11"

Variant Events: 30

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
FBXW11     5-0003-003chr5:
171429993-171429993
GTintronicDe novo--Trost2022 G
Yuen2017 G
FBXW11     5-5014-003chr5:
171303457-171303457
AGexonicDe novosynonymous SNVNM_033645
NM_012300
NM_033644
c.T888C
c.T990C
c.T951C
p.N296N
p.N330N
p.N317N
--Trost2022 G
Zhou2022 GE
FBXW11     2-1383-003chr5:
171317202-171317202
CAintronicDe novo--Trost2022 G
Yuen2017 G
FBXW11     2-1093-003chr5:
171398558-171398571
TTTTTCTGAAATAATintronicDe novo--Trost2022 G
Yuen2017 G
FBXW11     2-1425-004chr5:
171364554-171364554
TCintronicDe novo--Trost2022 G
Yuen2017 G
FBXW11     1-0551-004chr5:
171354974-171354974
CTintronicDe novo--Trost2022 G
Yuen2017 G
FBXW11     G01_GEA518HIchr5:
171303662-171303662
ACintronicDe novo--Fu2022 E
FBXW11     2-1313-003chr5:
171342691-171342691
CTintronicDe novo--Yuen2016 G
FBXW11     AU026412chr5:
171428250-171428257
GCAATCAAGCAAintronicDe novo--Yuen2017 G
FBXW11     1-1137-003chr5:
171345323-171345323
CAintronicDe novo--Trost2022 G
FBXW11     7-0441-003chr5:
171359230-171359230
ATintronicDe novo--Trost2022 G
FBXW11     AU4032307chr5:
171298394-171298394
GAintronicDe novo--Trost2022 G
Yuen2017 G
FBXW11     MSSNG00066-004chr5:
171312178-171312178
CTintronicDe novo--Trost2022 G
FBXW11     13895.p1chr5:
171326970-171326970
GAexonicDe novostopgainNM_033645
NM_012300
NM_033644
c.C406T
c.C508T
c.C469T
p.R136X
p.R170X
p.R157X
17.78-Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Satterstrom2020 E
Zhou2022 GE
FBXW11     SSC09279chr5:
171326970-171326970
GAexonicMosaic, De novostopgainNM_033645
NM_012300
NM_033644
c.C406T
c.C508T
c.C469T
p.R136X
p.R170X
p.R157X
17.78-Lim2017 E
Trost2022 G
FBXW11     MSSNG00355-003chr5:
171313346-171313346
TCintronicDe novo--Trost2022 G
FBXW11     UK10K_SKUSE5080170chr5:
171337706-171337706
GCexonicDe novononsynonymous SNVNM_033645
NM_012300
NM_033644
c.C141G
c.C243G
c.C204G
p.D47E
p.D81E
p.D68E
10.43-DeRubeis2014 E
Fu2022 E
Kosmicki2017 E
Lim2017 E
Satterstrom2020 E
Trost2022 G
Zhou2022 GE
FBXW11     A25chr5:
171366306-171366306
TCintronicDe novo--Wu2018 G
FBXW11     5-0001-003chr5:
171412677-171412677
GAintronicDe novo--Trost2022 G
FBXW11     Mahjani2021:65chr5:
171337639-171337639
GAexonicnonsynonymous SNVNM_033645
NM_012300
NM_033644
c.C208T
c.C310T
c.C271T
p.H70Y
p.H104Y
p.H91Y
32.0-Mahjani2021 E
FBXW11     SP0083539chr5:
171384710-171384710
AGintronicDe novo--Fu2022 E
Trost2022 G
FBXW11     MT_188.3chr5:
171426588-171426588
TGintronicDe novo--Trost2022 G
FBXW11     AU024104chr5:
171370385-171370385
CTintronicDe novo--Yuen2017 G
FBXW11     3-0498-000chr5:
171406716-171406716
TCintronicDe novo--Trost2022 G
FBXW11     4-0002-003chr5:
171407293-171407293
ACintronicDe novo--Trost2022 G
FBXW11     1-0206-003chr5:
171389293-171389302
GGAGGATCATCTTCTGTTAintronicDe novo--Trost2022 G
FBXW11     1-0206-004chr5:
171389293-171389302
GGAGGATCATCTTCTGTTAintronicDe novo--Trost2022 G
FBXW11     2-1093-009chr5:
171398558-171398571
TTTTTCTGAAATAATintronicDe novo--Trost2022 G
Yuen2017 G
FBXW11     AU1542301chr5:
171377912-171377913
ATAintronicDe novo--Trost2022 G
FBXW11     MSSNG00003-003chr5:
171384933-171384933
TCintronicDe 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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