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Results for "MDM2"

Variant Events: 4

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
MDM2     Lim2017:4893chr12:
69233432-69233432
GAexonicDe novononsynonymous SNVNM_001145340
NM_001278462
NM_001145339
NM_001145337
NM_002392
c.G691A
c.G769A
c.G1132A
c.G1138A
c.G1297A
p.E231K
p.E257K
p.E378K
p.E380K
p.E433K
14.92-Lim2017 E
MDM2     7-0059-003chr12:
69203948-69203948
CTintronicDe novo--Yuen2017 G
MDM2     11947.p1chr12:
69233432-69233432
GAexonicDe novononsynonymous SNVNM_001145340
NM_001278462
NM_001145339
NM_001145337
NM_002392
c.G691A
c.G769A
c.G1132A
c.G1138A
c.G1297A
p.E231K
p.E257K
p.E378K
p.E380K
p.E433K
14.92-Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Krupp2017 E
O’Roak2012b E
Satterstrom2020 E
Wilfert2021 G
MDM2     NDAR_INVWL738LDP_wes1chr12:
69210702-69210702
ACexonicDe novosynonymous SNVNM_001145337
NM_001145339
NM_002392
c.A267C
c.A285C
c.A285C
p.P89P
p.P95P
p.P95P
--DeRubeis2014 E
Kosmicki2017 E
Lim2017 E
Satterstrom2020 E
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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