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Results for "DHX9"

Variant Events: 11

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
DHX9     12773.p1chr1:
182852665-182852665
GAexonicDe novononsynonymous SNVNM_001357c.G3155Ap.R1052Q33.0-Iossifov2012 E
Iossifov2014 E
Ji2016 E
Kosmicki2017 E
DHX9     AU082104chr1:
182852662-182852662
CTexonicUnknownnonsynonymous SNVNM_001357c.C3152Tp.T1051I27.2-Stessman2017 T
DHX9     7-0247-003chr1:
182813207-182813207
CTintronicDe novo--Yuen2017 G
DHX9     2-1188-003chr1:
182831440-182831440
GTintronicDe novo--Yuen2017 G
DHX9     AU1459301chr1:
182822497-182822497
CTexonicDe novostopgainNM_001357c.C421Tp.R141X21.3-Stessman2017 T
Stessman2017 T
DHX9     AU2495301chr1:
182836532-182836532
ACintronicDe novo--Yuen2017 G
DHX9     SSC05600chr1:
182852665-182852665
GAexonicDe novononsynonymous SNVNM_001357c.G3155Ap.R1052Q33.0-Lim2017 E
DHX9     109056-200chr1:
182841496-182841496
CTexonicUnknownnonsynonymous SNVNM_001357c.C1582Tp.R528C19.488.295E-6Stessman2017 T
DHX9     217-14168-2730chr1:
182823301-182823301
CTexonicUnknownnonsynonymous SNVNM_001357c.C614Tp.P205L25.6-Stessman2017 T
DHX9     M23690chr1:
182850520-182850520
GAexonicPaternalnonsynonymous SNVNM_001357c.G2746Ap.V916I31.0-Guo2018 T
Wang2016 T
DHX9     2-0002-005chr1:
182853904-182853904
TCexonicDe novosynonymous SNVNM_001357c.T3417Cp.S1139S--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 notesView
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