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Results for "GOLGA4"

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
GOLGA4     12420.p1chr3:
37369172-37369172
TCexonicDe novononsynonymous SNVNM_002078
NM_001172713
c.T5795C
c.T5861C
p.L1932S
p.L1954S
15.83-Iossifov2012 E
Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Satterstrom2020 E
GOLGA4     AU3847302chr3:
37362388-37362388
TGintronicDe novo--Yuen2017 G
GOLGA4     SSC04693chr3:
37369172-37369172
TCexonicDe novononsynonymous SNVNM_002078
NM_001172713
c.T5795C
c.T5861C
p.L1932S
p.L1954S
15.83-Lim2017 E
GOLGA4     12653.p1chr3:
37360735-37360735
CGintronicDe novo--Satterstrom2020 E
GOLGA4     AU4306302chr3:
37413021-37413021
AGintergenicDe novo--Yuen2017 G
GOLGA4     1-0261-003chr3:
37415457-37415457
AGintergenicDe novo--Yuen2017 G
GOLGA4     AU4394302chr3:
37367412-37367412
GCexonicDe novononsynonymous SNVNM_002078
NM_001172713
c.G4035C
c.G4101C
p.K1345N
p.K1367N
16.02-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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