or
or
Exact

Results for "Vaags2012"

Variant Events: 8

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
CNTN3     F1-003chr3:
74334560-74334560
CTexonicPaternalnonsynonymous SNVNM_020872c.G2600Ap.R867Q9.9220.0318Vaags2012 E
EP300     F1-003chr22:
41513727-41513727
GAexonicPaternalnonsynonymous SNVNM_001429c.G631Ap.G211S17.30.0054Vaags2012 E
CNTNAP3     F1-003chr9:
39171471-39171471
CTexonicPaternalnonsynonymous SNVNM_033655c.G1228Ap.G410S1.8610.0362Vaags2012 E
FBXO40     F2-003chr3:
121340620-121340620
TGexonicPaternalnonsynonymous SNVNM_016298c.T344Gp.I115S12.234.0E-4Vaags2012 E
CNTNAP5     F2-003chr2:
125669092-125669092
GAexonicPaternalnonsynonymous SNVNM_130773c.G3701Ap.R1234Q11.911.0E-4Vaags2012 E
PRUNE2     F2-003chr9:
79324017-79324017
TCexonicPaternalnonsynonymous SNVNM_001308047
NM_001308048
NM_015225
c.A3173G
c.A3173G
c.A3173G
p.E1058G
p.E1058G
p.E1058G
17.52-Vaags2012 E
PDE1C     F2-003chr7:
32209524-32209524
GCexonicPaternalnonsynonymous SNVNM_001191058c.C181Gp.L61V18.882.608E-5Vaags2012 E
ARNT2     F2-003chr15:
80847464-80847464
GAexonicPaternalnonsynonymous SNVNM_014862c.G1148Ap.R383H19.994.135E-5Vaags2012 E
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