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Results for "SHC4"

Variant Events: 9

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
SHC4     AU3057301chr15:
49227644-49227644
GAintronicDe novo--Yuen2017 G
SHC4     5-0071-003chr15:
49271108-49271108
CAintergenicDe novo--Yuen2017 G
SHC4     1-0972-003chr15:
49118291-49118291
GAexonicDe novosynonymous SNVNM_203349c.C1770Tp.V590V--Yuen2017 G
SHC4     2-1105-003chr15:
49204325-49204325
GTintronicDe novo--Yuen2016 G
Yuen2017 G
SHC4     1-0597-003chr15:
49142833-49142833
CGintronicDe novo--Yuen2017 G
SHC4     AU4060306chr15:
49186277-49186277
TCintronicDe novo--Yuen2017 G
SHC4     2-0238-004chr15:
49248249-49248252
GAGAGintronicDe novo--Yuen2017 G
SHC4     AU061104chr15:
49150741-49150741
GAintronicDe novo--Yuen2017 G
SHC4     7-0254-004chr15:
49261707-49261707
TCintergenicDe 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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