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Results for "ZMYND11"

Variant Events: 30

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
ZMYND11     SP0041645chr10:
293299-293299
AGintronicDe novo--Fu2022 E
ZMYND11     MSSNG00390-003chr10:
281974-281974
TCintronicDe novo--Trost2022 G
ZMYND11     1-0595-005chr10:
205686-205687
ACAintronicDe novo--Trost2022 G
Yuen2017 G
ZMYND11     ACGC_GD0141.p1chr10:
287979-287979
GCexonicUnknownnonsynonymous SNVNM_001202465
NM_001202467
NM_001202464
NM_001202466
NM_001202468
NM_006624
NM_212479
c.G595C
c.G688C
c.G688C
c.G685C
c.G850C
c.G850C
c.G847C
p.V199L
p.V230L
p.V230L
p.V229L
p.V284L
p.V284L
p.V283L
36.0-Wang2020 T
ZMYND11     AU006804chr10:
220680-220680
AGintronicDe novo--Yuen2017 G
ZMYND11     TASC_217-14300-4210chr10:
286882-286882
GAexonicUnknownnonsynonymous SNVNM_001202465
NM_001202467
NM_001202464
NM_001202466
NM_001202468
NM_006624
NM_212479
c.G548A
c.G641A
c.G641A
c.G638A
c.G803A
c.G803A
c.G800A
p.R183H
p.R214H
p.R214H
p.R213H
p.R268H
p.R268H
p.R267H
34.0-Wang2020 T
ZMYND11     2-1137-003chr10:
265832-265832
GAintronicDe novo--Trost2022 G
Yuen2016 G
Yuen2017 G
ZMYND11     1-0338-005chr10:
304623-304623
GAintergenicDe novo--Yuen2017 G
ZMYND11     217-14300-4210chr10:
286882-286882
GAexonicUnknownnonsynonymous SNVNM_001202465
NM_001202467
NM_001202464
NM_001202466
NM_001202468
NM_006624
NM_212479
c.G548A
c.G641A
c.G641A
c.G638A
c.G803A
c.G803A
c.G800A
p.R183H
p.R214H
p.R214H
p.R213H
p.R268H
p.R268H
p.R267H
34.0-Stessman2017 T
ZMYND11     SF0032271.p2chr10:
286037-286039
GACGexonicframeshift deletionNM_001202465
NM_001202467
NM_001202464
NM_001202466
NM_001202468
NM_006624
NM_212479
c.485_486del
c.578_579del
c.578_579del
c.575_576del
c.740_741del
c.740_741del
c.737_738del
p.D162fs
p.D193fs
p.D193fs
p.D192fs
p.D247fs
p.D247fs
p.D246fs
--Wang2020 T
ZMYND11     Uddin2014:1chr10:
293337-293337
GAsplicingDe novosplicing26.9-Uddin2014 E
ZMYND11     AU4188302chr10:
187681-187681
TGintronicDe novo--Trost2022 G
Yuen2017 G
ZMYND11     ITAN_1428chr10:
225959-225959
CTexonicMaternalnonsynonymous SNVNM_001202467
NM_001202468
NM_001202464
NM_001202465
NM_001202466
NM_006624
NM_212479
c.C7T
c.C7T
c.C7T
c.C7T
c.C7T
c.C7T
c.C7T
p.R3C
p.R3C
p.R3C
p.R3C
p.R3C
p.R3C
p.R3C
24.5-Wang2020 T
ZMYND11     SSC07968chr10:
293337-293337
GAsplicingDe novosplicing26.9-Antaki2022 GE
Chan2022 G
Fu2022 E
Lim2017 E
Trost2022 G
ZMYND11     TASC_220-9740-202chr10:
225960-225960
GAexonicUnknownnonsynonymous SNVNM_001202467
NM_001202468
NM_001202464
NM_001202465
NM_001202466
NM_006624
NM_212479
c.G8A
c.G8A
c.G8A
c.G8A
c.G8A
c.G8A
c.G8A
p.R3H
p.R3H
p.R3H
p.R3H
p.R3H
p.R3H
p.R3H
33.04.994E-5Wang2020 T
ZMYND11     Gecz4_48414chr10:
225960-225960
GAexonicUnknownnonsynonymous SNVNM_001202467
NM_001202468
NM_001202464
NM_001202465
NM_001202466
NM_006624
NM_212479
c.G8A
c.G8A
c.G8A
c.G8A
c.G8A
c.G8A
c.G8A
p.R3H
p.R3H
p.R3H
p.R3H
p.R3H
p.R3H
p.R3H
33.04.994E-5Wang2020 T
ZMYND11     Gecz4_47533chr10:
225960-225960
GAexonicUnknownnonsynonymous SNVNM_001202467
NM_001202468
NM_001202464
NM_001202465
NM_001202466
NM_006624
NM_212479
c.G8A
c.G8A
c.G8A
c.G8A
c.G8A
c.G8A
c.G8A
p.R3H
p.R3H
p.R3H
p.R3H
p.R3H
p.R3H
p.R3H
33.04.994E-5Wang2020 T
ZMYND11     SJD_44.3chr10:
187296-187296
TCintronicDe novo--Trost2022 G
ZMYND11     AU2296301chr10:
205182-205182
AGintronicDe novo--Trost2022 G
ZMYND11     4-0073-003chr10:
179435-179436
ATTAupstreamDe novo--Trost2022 G
ZMYND11     SP0032272chr10:
286037-286039
GACGexonicDe novoframeshift deletionNM_001202465
NM_001202467
NM_001202464
NM_001202466
NM_001202468
NM_006624
NM_212479
c.485_486del
c.578_579del
c.578_579del
c.575_576del
c.740_741del
c.740_741del
c.737_738del
p.D162fs
p.D193fs
p.D193fs
p.D192fs
p.D247fs
p.D247fs
p.D246fs
--Antaki2022 GE
Fu2022 E
Trost2022 G
Zhou2022 GE
ZMYND11     2-1423-003chr10:
260823-260823
AGintronicDe novo--Trost2022 G
ZMYND11     MSSNG00399-003chr10:
262221-262221
CTintronicDe novo--Trost2022 G
ZMYND11     AU015903chr10:
251958-251958
TGintronicDe novo--Trost2022 G
ZMYND11     MSSNG00361-003chr10:
258652-258652
ACintronicDe novo--Trost2022 G
ZMYND11     MSSNG00356-003chr10:
229865-229865
TCintronicDe novo--Trost2022 G
ZMYND11     13513.p1chr10:
293337-293337
GAsplicingMosaic, De novo, Unknownsplicing26.9-Dou2017 E
Iossifov2012 E
Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Krupp2017 E
Lowther2023 G
O’Roak2014 T
Satterstrom2020 E
Wang2020 T
Wilfert2021 G
Willsey2013 E
Zhou2022 GE
ZMYND11     MSSNG00435-003chr10:
250143-250143
ACintronicDe novo--Trost2022 G
ZMYND11     2-0139-003chr10:
217374-217374
TGintronicDe novo--Trost2022 G
ZMYND11     2-0197-004chr10:
217928-217929
CATGintronicDe novo--Trost2022 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 notesView
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