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Results for "ZC3H11A"

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
ZC3H11A       AU3765303chr1:
203797851-203797851
GTintronicDe novo--Yuen2017 G
ZC3H11A       AU242Achr1:
203816590-203816590
ATexonicDe novostopgainNM_014827c.A1321Tp.K441X41.0-DeRubeis2014 E
Kosmicki2017 E
Lim2017 E
Satterstrom2020 E
ZC3H11A       1-0271-003chr1:
203804197-203804197
AGintronicDe novo--Yuen2017 G
ZC3H11A       1-0395-003chr1:
203814235-203814236
ACAintronicDe novo--Yuen2017 G
ZC3H11A       2-0202-004chr1:
203809295-203809295
GCintronicDe novo--Yuen2017 G
ZC3H11A       AU3997301chr1:
203818458-203818458
TCintronicDe novo--Yuen2017 G
ZC3H11A       1-0344-003chr1:
203809025-203809025
GAintronicDe novo--Yuen2017 G
ZC3H11A       1-0395-004chr1:
203814235-203814236
ACAintronicDe novo--Yuen2017 G
ZC3H11A       Lim2017:70524chr1:
203816493-203816493
GTexonicDe novononsynonymous SNVNM_014827c.G1224Tp.E408D20.1-Lim2017 E
ZC3H11A       14581.p1chr1:
203816493-203816493
GTexonicDe novononsynonymous SNVNM_014827c.G1224Tp.E408D20.1-Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Satterstrom2020 E
Wilfert2021 G
ZC3H11A       2-1306-003chr1:
203810338-203810338
AATintronicDe 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 notesView
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