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Results for "MAP4"
Variant Events: 51
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
MAP4
SP0025562
chr3:
48014784-48014784
G
C
UTR3
De novo
-
-
Fu2022
E
MAP4
SP0114472
chr3:
47908750-47908750
G
A
exonic
De novo
nonsynonymous SNV
NM_001134364
NM_002375
c.C3052T
c.C3052T
p.P1018S
p.P1018S
24.5
-
Fu2022
E
Trost2022
G
Zhou2022
G
E
MAP4
PN400455
chr3:
47933504-47933504
G
A
intronic
Unknown
36.0
-
Leblond2019
E
MAP4
2-1719-003
Complex Event; expand row to view variants
De novo
-
-
Trost2022
G
Yuen2017
G
MAP4
SJD_71.3
chr3:
47958644-47958644
C
G
exonic
De novo
nonsynonymous SNV
NM_001134364
NM_002375
c.G673C
c.G673C
p.E225Q
p.E225Q
12.82
-
Trost2022
G
Zhou2022
G
E
MAP4
2-1272-003A
chr3:
47957453-47957453
T
C
exonic
nonsynonymous SNV
NM_001134364
NM_002375
c.A1864G
c.A1864G
p.M622V
p.M622V
1.269
-
Zhou2022
G
E
MAP4
11842.p1
chr3:
47918907-47918907
C
T
exonic
Mosaic
synonymous SNV
NM_001134364
NM_002375
c.G2106A
c.G2106A
p.K702K
p.K702K
14.09
-
Krupp2017
E
MAP4
2-1456-004
chr3:
47964033-47964037
AAGAC
A
intronic
De novo
-
-
Trost2022
G
Yuen2017
G
MAP4
AU4186302
chr3:
48166474-48166474
C
T
intergenic
De novo
-
-
Yuen2017
G
MAP4
1-1005-005A
chr3:
47945355-47945355
A
T
intronic
De novo
-
-
Trost2022
G
MAP4
AU059903
chr3:
47977332-47977332
G
T
intronic
De novo
-
-
Yuen2017
G
MAP4
MSSNG00437-003
chr3:
47959856-47959856
T
C
intronic
De novo
-
-
Trost2022
G
MAP4
T2T9E-01
chr3:
47915662-47915662
A
T
intronic
De novo
-
-
Trost2022
G
MAP4
A19
chr3:
48143560-48143560
G
A
intergenic
De novo
-
-
Wu2018
G
MAP4
SP0199562
chr3:
47934207-47934207
C
T
intronic
De novo
-
-
Trost2022
G
MAP4
08C73330
chr3:
47953165-47953165
T
G
intronic
De novo
12.79
-
Fu2022
E
MAP4
2-1272-003
chr3:
47957453-47957453
T
C
exonic
De novo
nonsynonymous SNV
NM_001134364
NM_002375
c.A1864G
c.A1864G
p.M622V
p.M622V
1.269
-
Jiang2013
G
Yuen2016
G
Zhou2022
G
E
MAP4
7-0095-003
chr3:
47973545-47973545
C
T
intronic
De novo
-
-
Trost2022
G
Yuen2017
G
MAP4
4890
chr3:
47969769-47969769
C
A
exonic
De novo
nonsynonymous SNV
NM_001134364
NM_002375
c.G364T
c.G364T
p.D122Y
p.D122Y
13.89
-
Fu2022
E
Trost2022
G
MAP4
2-1733-003
chr3:
47907557-47907557
A
G
intronic
De novo
-
-
Trost2022
G
MAP4
5-0040-003
chr3:
48020701-48020701
T
AC
intronic
De novo
-
-
Trost2022
G
MAP4
5-0040-003
chr3:
48020705-48020705
T
A
intronic
De novo
-
-
Trost2022
G
MAP4
08C74627
chr3:
48028831-48028831
C
T
intronic
De novo
-
-
Satterstrom2020
E
Trost2022
G
MAP4
7-0286-003A
chr3:
48000467-48000467
C
T
intronic
De novo
-
-
Trost2022
G
MAP4
3-0548-000
chr3:
48001887-48001887
T
A
intronic
De novo
-
-
Trost2022
G
MAP4
5-5127-003
chr3:
47976145-47976145
C
T
intronic
De novo
-
-
Trost2022
G
MAP4
REACH000653
chr3:
47981079-47981079
T
A
intronic
De novo
-
-
Trost2022
G
MAP4
7-0130-003
chr3:
47960705-47960705
A
G
intronic
De novo
-
-
Trost2022
G
MAP4
70523
chr3:
47963210-47963210
T
A
intronic
De novo
-
5.086E-5
Trost2022
G
MAP4
AU005213
chr3:
47972138-47972138
G
A
intronic
De novo
-
-
Trost2022
G
Yuen2017
G
MAP4
5-5165-003
chr3:
48100834-48100834
G
C
intronic
De novo
-
-
Trost2022
G
MAP4
3-0430-000
chr3:
48113350-48113350
C
G
intronic
De novo
-
-
Trost2022
G
MAP4
5-0040-003
chr3:
48020707-48020711
CCTGT
C
intronic
De novo
-
-
Trost2022
G
MAP4
SJD_49.4
chr3:
48092988-48092989
TA
T
intronic
De novo
-
-
Trost2022
G
MAP4
3-0391-000
chr3:
48023582-48023582
C
A
intronic
De novo
-
-
Yuen2017
G
MAP4
PN400178
chr3:
47933504-47933504
G
A
intronic
Unknown
36.0
-
Leblond2019
E
MAP4
PN400386
chr3:
47933504-47933504
G
A
intronic
Unknown
36.0
-
Leblond2019
E
MAP4
2-1644-003
chr3:
48000678-48000678
G
A
intronic
De novo
-
-
Trost2022
G
Yuen2017
G
MAP4
AU3698301
chr3:
47912800-47912800
A
G
intronic
De novo
-
8.247E-6
Trost2022
G
Yuen2017
G
MAP4
Lim2017:4890
chr3:
47969769-47969769
C
A
exonic
De novo
nonsynonymous SNV
NM_001134364
NM_002375
c.G364T
c.G364T
p.D122Y
p.D122Y
13.89
-
Lim2017
E
MAP4
14496.p1
chr3:
48024445-48024445
T
G
intronic
De novo
-
-
Turner2016
G
MAP4
7-0024-005
chr3:
47996165-47996165
A
G
intronic
De novo
-
-
Trost2022
G
Yuen2017
G
MAP4
14496.p1
chr3:
47899083-47899083
T
G
intronic
De novo
-
-
Turner2016
G
MAP4
2-0090-003
chr3:
48079351-48079351
G
C
intronic
De novo
-
-
Trost2022
G
Yuen2017
G
MAP4
PN400190
chr3:
47933504-47933504
G
A
intronic
Unknown
36.0
-
Leblond2019
E
MAP4
2-1300-003
chr3:
47972018-47972018
A
T
intronic
De novo
-
-
Yuen2016
G
MAP4
1-0531-003
chr3:
48189939-48189939
G
A
intergenic
De novo
-
-
Yuen2016
G
Yuen2017
G
MAP4
13822.p1
chr3:
47969769-47969769
C
A
exonic
De novo
nonsynonymous SNV
NM_001134364
NM_002375
c.G364T
c.G364T
p.D122Y
p.D122Y
13.89
-
Iossifov2014
E
Ji2016
E
Kosmicki2017
E
Krupp2017
E
O’Roak2012b
E
Satterstrom2020
E
Wilfert2021
G
Zhou2022
G
E
MAP4
1-0965-003
chr3:
48191255-48191255
C
T
intergenic
De novo
-
-
Yuen2017
G
MAP4
AU031403
chr3:
47973812-47973812
C
A
intronic
De novo
-
-
Yuen2017
G
MAP4
14518.p1
chr3:
47963210-47963210
T
A
intronic
De novo
-
5.086E-5
Satterstrom2020
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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