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Incidental Mutations
23
incidental mutations are currently displayed, and affect
23
genes.
2
are Possibly Damaging.
12
are Probably Damaging.
8
are Probably Benign.
1
are Probably Null.
0
create premature stop codons.
0
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 23 of 23]
10
25
50
100
500
1000
per page
Full List
ID
Source
UTSW
APN
Gene
E-score
Stock #
Gen
G0
G0'
G1
G2
G3
G3R
F1
F2
F3
C0
C1
C2
C3
D1
HES
IPS
A3
Quality
-
Vld
Y
N
?
Strain
Chr
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
X
Y
Position
Mutation
A
R
N
D
C
E
Q
G
H
I
L
K
M
F
P
S
T
W
Y
V
*
A
R
N
D
C
E
Q
G
H
I
L
K
M
F
P
S
T
W
Y
V
*
Ref
A
C
G
T
-
Var
A
C
G
T
-
Type
makesense
missense
nonsense
start codon destroyed
start gained
synonymous
splice acceptor site
splice donor site
critical splice acceptor site
critical splice donor site
splice site
large deletion
large insertion
rearrangement
small deletion
small insertion
exon
frame shift
intragenic
intron
utr 3 prime
utr 5 prime
unclassified
Exon Dist
Zygosity
Homo
Het
Hemi
Null
Predicted Effect
unknown
probably benign
probably null
possibly damaging
probably damaging
noncoding transcript
silent
not run
no transcript
PPH Score
-
Meta Score
MGI Phenotype
available
none listed
Posted
1
248360
AK157302
0.945
R2378
G1
225
N
13
21495562
I86T
T
C
missense
Het
possibly damaging
0.688
11/11/2014
2
248337
Akr1cl
0.068
R2378
G1
184
N
1
65021988
M124K
A
T
missense
Het
probably benign
0.143
11/11/2014
3
248358
Asap2
0.095
R2378
G1
225
N
12
21254318
L745P
T
C
missense
Het
possibly damaging
0.955
phenotype
11/11/2014
4
248349
B3gnt9
0.102
R2378
G1
225
N
8
105254484
R91C
G
A
missense
Het
probably damaging
1.000
11/11/2014
5
248346
Capg
0.169
R2378
G1
225
N
6
72555491
P13L
C
T
missense
Het
probably benign
0.069
phenotype
11/11/2014
6
248348
Eif3c
0.000
R2378
G1
225
N
7
126552325
R609H
C
T
missense
Het
probably damaging
0.989
phenotype
11/11/2014
7
248361
Ephb3
0.901
R2378
G1
225
N
16
21218243
H152R
A
G
missense
Het
probably benign
0.000
phenotype
11/11/2014
8
248345
Gbp9
0.053
R2378
G1
225
N
5
105080176
D580G
T
C
missense
Het
probably benign
0.023
11/11/2014
9
248356
Gm884
0.140
R2378
G1
225
N
11
103619711
A
G
unclassified
Het
probably benign
11/11/2014
10
248340
Iars2
1.000
R2378
G1
225
N
1
185327721
Y97H
A
G
missense
Het
probably damaging
1.000
phenotype
11/11/2014
11
248352
Ip6k2
0.000
R2378
G1
225
N
9
108796301
A
G
splice site
Het
probably null
phenotype
11/11/2014
12
248341
Itih2
0.122
R2378
G1
225
N
2
10094887
D907V
T
A
missense
Het
probably damaging
0.997
phenotype
11/11/2014
13
248344
Msh4
0.383
R2378
G1
225
N
3
153863477
C732R
A
G
missense
Het
probably damaging
0.994
phenotype
11/11/2014
14
248350
Mtss1l
0.000
R2378
G1
225
N
8
110738349
F474L
T
C
missense
Het
probably damaging
0.999
11/11/2014
15
248354
Nbeal2
0.252
R2378
G1
168
N
9
110630808
E1175G
T
C
missense
Het
probably damaging
0.989
phenotype
11/11/2014
16
248351
Pgm3
0.950
R2378
G1
225
N
9
86562667
C272S
A
T
missense
Het
probably damaging
0.966
phenotype
11/11/2014
17
248364
R3hcc1l
0.000
R2378
G1
225
N
19
42563473
I303N
T
A
missense
Het
probably damaging
0.991
11/11/2014
18
248343
Sla2
0.000
R2378
G1
225
N
2
156875942
R137C
G
A
missense
Het
probably damaging
0.999
0.314
phenotype
11/11/2014
19
248363
Spsb3
0.111
R2378
G1
225
N
17
24886950
A
G
unclassified
Het
probably benign
11/11/2014
20
248355
Tgfbr2
1.000
R2378
G1
225
N
9
116129950
T132I
G
A
missense
Het
probably benign
0.018
phenotype
11/11/2014
21
248336
Tpp2
0.630
R2378
G1
225
N
1
43999765
E223V
A
T
missense
Het
probably damaging
0.992
phenotype
11/11/2014
22
248342
Ttn
1.000
R2378
G1
225
N
2
76889450
T
A
intron
Het
probably benign
0.111
phenotype
11/11/2014
23
248362
Vmn2r102
0.000
R2378
G1
225
N
17
19694668
L832V
T
G
missense
Het
probably damaging
0.999
11/11/2014
[records 1 to 23 of 23]