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Results for "MIOS"
Variant Events: 12
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
MIOS
iHART3087
chr7:
7646706-7646706
G
T
exonic
Maternal
stopgain
NM_019005
c.G2611T
p.E871X
43.0
-
Ruzzo2019
G
MIOS
AU4392302
chr7:
7632141-7632141
C
A
intronic
De novo
-
-
Trost2022
G
Yuen2017
G
MIOS
14153.p1
chr7:
7625250-7625250
C
A
intronic
De novo
-
-
Iossifov2014
E
Kosmicki2017
E
Turner2016
G
MIOS
2-1605-004
chr7:
7652838-7652838
A
G
intergenic
De novo
-
-
Yuen2017
G
MIOS
13582.p1
chr7:
7625488-7625488
T
C
intronic
De novo
-
-
Satterstrom2020
E
MIOS
1-0092-004
chr7:
7613252-7613252
T
A
exonic
De novo
nonsynonymous SNV
NM_019005
c.T1146A
p.N382K
1.375
-
Trost2022
G
Yuen2015
G
Yuen2017
G
Zhou2022
G
E
MIOS
MT_151.4
chr7:
7641308-7641308
A
G
intronic
De novo
-
-
Trost2022
G
MIOS
SP0048038
chr7:
7613221-7613221
G
A
exonic
De novo
nonsynonymous SNV
NM_019005
c.G1115A
p.R372H
19.61
4.974E-5
Trost2022
G
MIOS
SSC08351
chr7:
7625488-7625488
T
C
intronic
De novo
-
-
Trost2022
G
MIOS
AU0039303
chr7:
7614946-7614946
G
A
intronic
De novo
-
-
Trost2022
G
Yuen2017
G
MIOS
AU3154302
chr7:
7646706-7646706
G
T
exonic
Maternal
stopgain
NM_019005
c.G2611T
p.E871X
43.0
-
Cirnigliaro2023
G
MIOS
2-1561-003
chr7:
7665856-7665856
T
C
intergenic
De 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 notes
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