Variant Results

or

Results for "MYSM1"

Variant Events: 14

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

MYSM1

UK10K_SKUSE5080234

chr1:
59147575-59147575

T

C

exonic

De novo

nonsynonymous SNV

NM_001085487

c.A1141G

p.I381V

9.507

-

DeRubeis2014 E
Fu2022 E
Kosmicki2017 E
Lim2017 E
Satterstrom2020 E
Trost2022 G
Zhou2022 GE

MYSM1

AU4476302

chr1:
59133826-59133826

C

A

intronic

De novo

-

Trost2022 G
Yuen2017 G

MYSM1

13289.p1

chr1:
59132683-59132683

T

C

intronic

De novo

-

Satterstrom2020 E
Trost2022 G

MYSM1

SP0001510

chr1:
59147934-59147934

T

A

exonic

De novo

nonsynonymous SNV

NM_001085487

c.A782T

p.E261V

7.157

-

Feliciano2019 E
Fu2022 E
Trost2022 G
Zhou2022 GE

MYSM1

MSSNG00121-003

chr1:
59156128-59156128

A

C

intronic

De novo

-

Trost2022 G

MYSM1

9-0010-003

chr1:
59150640-59150640

C

G

intronic

De novo

-

Trost2022 G

MYSM1

AU2165301

chr1:
59231867-59231867

G

A

intergenic

De novo

-

Yuen2017 G

MYSM1

SP0087800

chr1:
59165690-59165690

C

T

exonic

De novo

nonsynonymous SNV

NM_001085487

c.G35A

p.G12E

20.5

-

Trost2022 G

MYSM1

1-0271-003

chr1:
59205757-59205757

T

G

intergenic

De novo

-

Yuen2017 G

MYSM1

5-5011-003

chr1:
59140750-59140750

T

TA

intronic

De novo

-

Trost2022 G

MYSM1

1-0213-004

chr1:
59174680-59174680

T

G

intergenic

De novo

-

Yuen2017 G

MYSM1

7-0055-003

chr1:
59210962-59210962

C

T

intergenic

De novo

-

Yuen2017 G

MYSM1

7-0135-003

chr1:
59154127-59154127

T

C

intronic

De novo

-

Trost2022 G
Yuen2017 G

MYSM1

AU3764302

chr1:
59149548-59149548

G

A

intronic

De novo

-

Trost2022 G
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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