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Results for "FRMPD4"
Variant Events: 20
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
FRMPD4
14058.p1
chrX:
12481792-12481792
A
ATG
intronic
Maternal
-
-
Wilfert2021
G
FRMPD4
13150.p1
chrX:
12481792-12481792
A
ATG
intronic
Inherited
-
-
Wilfert2021
G
FRMPD4
1-0139-003
chrX:
12245853-12245853
G
A
intronic
De novo
-
-
Yuen2017
G
FRMPD4
AU0786305
chrX:
12664767-12664767
A
G
intronic
De novo
-
-
Yuen2017
G
FRMPD4
1-0009-004
chrX:
12709963-12709963
C
T
intronic
De novo
-
-
Yuen2017
G
FRMPD4
AU1848302
chrX:
12272012-12272012
T
A
intronic
De novo
-
-
Yuen2017
G
FRMPD4
7-0219-003
chrX:
12704250-12704250
C
T
exonic
De novo
nonsynonymous SNV
NM_014728
c.C608T
p.P203L
29.4
-
Yuen2017
G
Zhou2022
G
E
FRMPD4
AU3891302
chrX:
12336056-12336056
A
G
intronic
De novo
-
-
Yuen2017
G
FRMPD4
13890.p1
chrX:
12587847-12587847
T
C
intronic
De novo
-
-
Wilfert2021
G
FRMPD4
AU3903302
chrX:
12718937-12718937
A
G
intronic
De novo
-
-
Yuen2017
G
FRMPD4
1-0305-004
chrX:
12754127-12754127
C
G
intergenic
De novo
-
-
Yuen2017
G
FRMPD4
AU047704
chrX:
12727485-12727485
C
T
intronic
De novo
-
-
Yuen2017
G
FRMPD4
12296.p1
chrX:
12627964-12627964
A
G
exonic
De novo
nonsynonymous SNV
NM_014728
c.A283G
p.S95G
18.84
-
Ji2016
E
Krumm2015
E
FRMPD4
2-1169-003
chrX:
12542694-12542694
C
T
intronic
De novo
-
-
Yuen2017
G
FRMPD4
AU4006302
chrX:
12434223-12434223
T
C
intronic
De novo
-
-
Yuen2017
G
FRMPD4
Codina-Sola2015:ASD_16
chrX:
12632966-12632966
G
A
exonic
Maternal
nonsynonymous SNV
NM_014728
c.G388A
p.A130T
9.644
9.0E-4
Codina-Sola2015
E
FRMPD4
12493.p1
chrX:
12535571-12535571
C
T
intronic
De novo
-
-
Turner2016
G
FRMPD4
B0435
chrX:
12736216-12736216
C
G
exonic
Maternal
nonsynonymous SNV
NM_014728
c.C3271G
p.Q1091E
18.94
3.0E-4
Xiong2019
E
T
FRMPD4
2-0007-004
chrX:
12630930-12630930
T
C
intronic
De novo
-
-
Yuen2017
G
FRMPD4
2-1518-003
chrX:
12697046-12697046
A
G
intronic
De 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 notes
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