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Results for "PPP1R21"

Variant Events: 7

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
PPP1R21     5-0125-003chr2:
48671557-48671557
CGintronicDe novo--Trost2022 G
Yuen2017 G
PPP1R21     SP0041950chr2:
48685366-48685366
AATTTTTTGAAGCTGATGAGCAGCACAAGCATexonicDe novononframeshift insertionNM_001135629
NM_001193475
NM_152994
c.375_376insTTTTTTGAAGCTGATGAGCAGCACAAGCAT
c.375_376insTTTTTTGAAGCTGATGAGCAGCACAAGCAT
c.375_376insTTTTTTGAAGCTGATGAGCAGCACAAGCAT
p.Q125delinsQFFEADEQHKH
p.Q125delinsQFFEADEQHKH
p.Q125delinsQFFEADEQHKH
--Fu2022 E
PPP1R21     AU207Achr2:
48692688-48692688
GAexonicDe novosynonymous SNVNM_001135629
NM_001193475
NM_152994
c.G804A
c.G804A
c.G804A
p.T268T
p.T268T
p.T268T
-8.243E-6DeRubeis2014 E
Fu2022 E
Kosmicki2017 E
Lim2017 E
Satterstrom2020 E
Trost2022 G
Zhou2022 GE
PPP1R21     MSSNG00087-003chr2:
48741533-48741533
CTintronicDe novo--Trost2022 G
PPP1R21     SJD_61.3chr2:
48722114-48722114
AGintronicDe novo--Trost2022 G
PPP1R21     1-1175-003chr2:
48720608-48720608
TGintronicDe novo--Trost2022 G
PPP1R21     1-0375-003chr2:
48691902-48691902
ACintronicDe novo--Trost2022 G
Yuen2017 G
Source Variant Information

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Source:

Paper alias:

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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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