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Results for "CENPW"

Variant Events: 9

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
CENPW     3-0216-000chr6:
126693529-126693531
GTTGTintergenicDe novo--Yuen2017 G
CENPW     AU050603chr6:
126706539-126706539
TGintergenicDe novo--Yuen2017 G
CENPW     AU3913301chr6:
126714143-126714143
GTintergenicDe novo--Yuen2017 G
CENPW     MSSNG00239-003chr6:
126667302-126667302
TGintronicDe novo--Trost2022 G
CENPW     MSSNG00336-003chr6:
126669065-126669065
AGintronicDe novo--Trost2022 G
CENPW     2-0298-003chr6:
126714772-126714772
TCintergenicDe novo--Yuen2017 G
CENPW     1-0052-004chr6:
126740919-126740919
CAintergenicDe novo--Yuen2017 G
CENPW     111316chr6:
126661511-126661511
CGexonicnonsynonymous SNVNM_001012507
NM_001286524
NM_001286525
c.C92G
c.C92G
c.C92G
p.P31R
p.P31R
p.P31R
20.68.238E-6Woodbury-Smith2022 E
CENPW     1-0923-003chr6:
126691053-126691053
GCintergenicDe novo--Yuen2017 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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