Variant Results

or

or

Results for "MKL2"

Variant Events: 22

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

MKL2

2-0036-003

chr16:
14180628-14180628

G

T

intronic

De novo

-

-

Yuen2016 G

MKL2

AU4145303

chr16:
14221788-14221788

T

A

intronic

De novo

-

-

Yuen2017 G

MKL2

08C74799

chr16:
14310975-14310975

T

G

intronic

De novo

-

-

Fu2022 E
Satterstrom2020 E

MKL2

2-1314-003

chr16:
14233824-14233824

C

T

intronic

De novo

-

-

Yuen2016 G

MKL2

7-0141-003

chr16:
14358633-14358633

T

A

UTR3

De novo

-

-

Yuen2017 G

MKL2

Li2017:16235

chr16:
14340619-14340619

C

T

exonic

De novo

nonsynonymous SNV

NM_001308142
NM_014048

c.C1502T
c.C1502T

p.S501F
p.S501F

18.86

-

Li2017 T

MKL2

1-0279-004

chr16:
14292999-14292999

T

C

intronic

De novo

-

-

Yuen2017 G

MKL2

10C107875

chr16:
14334157-14334157

C

T

exonic

De novo

nonsynonymous SNV

NM_001308142
NM_014048

c.C895T
c.C895T

p.R299W
p.R299W

19.45

DeRubeis2014 E
Fu2022 E
Kosmicki2017 E
Satterstrom2020 E

MKL2

1-0736-003

chr16:
14246482-14246482

A

G

intronic

De novo

-

-

Yuen2017 G

MKL2

2-1518-003

chr16:
14290375-14290375

A

G

intronic

De novo

-

-

Yuen2017 G

MKL2

7-0119-003

chr16:
14306921-14306921

T

C

intronic

De novo

-

-

Yuen2017 G

MKL2

SP0135020

chr16:
14280861-14280861

T

TGAGG

intronic

De novo

-

-

Fu2022 E

MKL2

13942.p1

chr16:
14381116-14381116

G

T

intergenic

De novo

-

-

Turner2016 G

MKL2

AU1860302

chr16:
14322706-14322706

A

G

intronic

De novo

-

-

Yuen2017 G

MKL2

2-0016-003

chr16:
14180628-14180628

G

T

intronic

De novo

-

-

Yuen2017 G

MKL2

5093_child

chr16:
14334157-14334157

C

T

exonic

De novo

nonsynonymous SNV

NM_001308142
NM_014048

c.C895T
c.C895T

p.R299W
p.R299W

19.45

Neale2012 E

MKL2

12449.p1

chr16:
14238925-14238925

T

C

intronic

De novo

-

-

Turner2016 G

MKL2

AU4242302

chr16:
14378009-14378009

A

G

intergenic

De novo

-

-

Yuen2017 G

MKL2

AU4079301

chr16:
14165378-14165378

A

C

intronic

De novo

-

-

Yuen2017 G

MKL2

2-1431-003

chr16:
14358677-14358677

G

A

UTR3

De novo

-

-

Yuen2016 G

MKL2

1-0009-004

chr16:
14232054-14232054

T

C

intronic

De novo

-

-

Yuen2017 G

MKL2

AU3728301

chr16:
14207354-14207354

C

T

intronic

De novo

-

-

Yuen2017 G

Source Variant Information

, -

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	View
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