or
or
Exact

Results for "ASB4"

Variant Events: 7

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
ASB4     1-0300-004chr7:
95125761-95125761
ATintronicDe novo--Yuen2017 G
ASB4     AU3984301chr7:
95198330-95198330
GAintergenicDe novo--Yuen2017 G
ASB4     1-0595-004chr7:
95182129-95182129
GAintergenicDe novo--Yuen2017 G
ASB4     DEASD_0382_001chr7:
95157379-95157379
CTexonicDe novostopgainNM_016116
NM_145872
c.C742T
c.C742T
p.R248X
p.R248X
24.7-DeRubeis2014 E
Kosmicki2017 E
Lim2017 E
Satterstrom2020 E
ASB4     AU3777302chr7:
95144506-95144506
TAintronicDe novo--Yuen2017 G
ASB4     11341.p1chr7:
95180956-95180956
CAintergenicDe novo--Turner2016 G
ASB4     AU049304chr7:
95159838-95159838
AGintronicDe 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 notesView
More