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Results for "FAM214B"
Variant Events: 12
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
FAM214B
SSC05135
chr9:
35106325-35106325
C
T
exonic
De novo
nonsynonymous SNV
NM_025182
c.G1142A
p.C381Y
19.62
-
Fu2022
E
Lim2017
E
Trost2022
G
FAM214B
1-0265-004
chr9:
35129308-35129310
CTA
C
intergenic
De novo
-
-
Yuen2017
G
FAM214B
1-0265-003
chr9:
35129308-35129310
CTA
C
intergenic
De novo
-
-
Yuen2017
G
FAM214B
2-1207-003
chr9:
35111031-35111031
T
C
intronic
De novo
-
-
Yuen2016
G
Yuen2017
G
FAM214B
AU4145303
chr9:
35146508-35146508
G
C
intergenic
De novo
-
-
Yuen2017
G
FAM214B
13395.p1
chr9:
35107352-35107352
G
A
intronic
De novo
-
2.554E-5
Satterstrom2020
E
Trost2022
G
FAM214B
2-1183-003
chr9:
35114253-35114253
C
T
intronic
De novo
-
-
Trost2022
G
Yuen2017
G
FAM214B
AU045514
chr9:
35118375-35118375
T
G
intergenic
De novo
-
-
Yuen2017
G
FAM214B
SP0037507
chr9:
35106669-35106669
T
G
intronic
De novo
-
-
Trost2022
G
FAM214B
SP0088794
chr9:
35106669-35106669
T
G
intronic
De novo
-
-
Trost2022
G
FAM214B
SP0033571
chr9:
35106669-35106669
T
G
intronic
De novo
-
-
Trost2022
G
FAM214B
12232.p1
chr9:
35106325-35106325
C
T
exonic
De novo
nonsynonymous SNV
NM_025182
c.G1142A
p.C381Y
19.62
-
Iossifov2014
E
Ji2016
E
Kosmicki2017
E
Satterstrom2020
E
Zhou2022
G
E
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 notes
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