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Incidental Mutations
49
incidental mutations are currently displayed, and affect
49
genes.
9
are Possibly Damaging.
16
are Probably Damaging.
16
are Probably Benign.
6
are Probably Null.
4
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 49 of 49]
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
ABI
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
294156
0610009O20Rik
0.285
IGL02456
18
38261124 (GRCm38)
L458Q
T
A
missense
Het
probably damaging
1.000
2015-04-16
2
294166
4921511C20Rik
IGL02456
X
127394961 (GRCm38)
Y174*
T
A
nonsense
Het
probably null
2015-04-16
3
294164
Apc
0.970
IGL02456
18
34313882 (GRCm38)
S1243*
C
A
nonsense
Het
probably null
phenotype
2015-04-16
4
294186
Atp8b5
0.074
IGL02456
4
43365578 (GRCm38)
T731A
A
G
missense
Het
probably benign
0.163
2015-04-16
5
294149
Bcl2a1c
0.297
IGL02456
9
114330390 (GRCm38)
F79I
T
A
missense
Het
probably damaging
1.000
2015-04-16
6
294184
Brip1
0.000
IGL02456
11
86065099 (GRCm38)
L863I
G
T
missense
Het
possibly damaging
0.707
phenotype
2015-04-16
7
294152
Cbx4
1.000
IGL02456
11
119082112 (GRCm38)
K146*
T
A
nonsense
Het
probably null
phenotype
2015-04-16
8
294179
Ccdc36
0.127
IGL02456
9
108406621 (GRCm38)
T208K
G
T
missense
Het
probably benign
0.001
2015-04-16
9
294170
Ces1a
0.000
IGL02456
8
93039498 (GRCm38)
V163I
C
T
missense
Het
possibly damaging
0.565
2015-04-16
10
294189
Ces5a
0.125
IGL02456
8
93528644 (GRCm38)
C
T
splice site
Het
probably benign
phenotype
2015-04-16
11
294176
Cfhr1
0.072
IGL02456
1
139556393 (GRCm38)
N128K
A
C
missense
Het
possibly damaging
0.877
phenotype
2015-04-16
12
294158
Clcn3
0.527
IGL02456
8
60941357 (GRCm38)
D46G
T
C
missense
Het
probably damaging
0.998
phenotype
2015-04-16
13
294174
Cntnap1
0.270
IGL02456
11
101178129 (GRCm38)
I166S
T
G
missense
Het
probably benign
0.305
phenotype
2015-04-16
14
294194
Cntnap3
0.055
IGL02456
13
64799058 (GRCm38)
A
T
splice site
Het
probably benign
phenotype
2015-04-16
15
294196
Cntnap5c
0.066
IGL02456
17
58407744 (GRCm38)
T
A
splice site
Het
probably benign
2015-04-16
16
294159
Ddx23
1.000
IGL02456
15
98647549 (GRCm38)
V626E
A
T
missense
Het
probably damaging
0.999
phenotype
2015-04-16
17
294175
Gcm2
0.677
IGL02456
13
41103001 (GRCm38)
Y424C
T
C
missense
Het
probably benign
0.015
phenotype
2015-04-16
18
294183
Gm9964
0.180
IGL02456
11
79296370 (GRCm38)
F84L
A
G
missense
Het
probably damaging
0.985
2015-04-16
19
294172
Grn
0.494
IGL02456
11
102436104 (GRCm38)
D509E
T
A
missense
Het
probably benign
0.007
phenotype
2015-04-16
20
294162
Kdm5c
IGL02456
X
152246318 (GRCm38)
D343N
G
A
missense
Het
probably damaging
1.000
phenotype
2015-04-16
21
294188
Ly75
0.000
IGL02456
2
60293781 (GRCm38)
M1717I
C
T
missense
Het
probably benign
0.090
phenotype
2015-04-16
22
294163
Map1a
0.311
IGL02456
2
121298653 (GRCm38)
P133T
C
A
missense
Het
probably damaging
1.000
phenotype
2015-04-16
23
294157
Mpp2
0.000
IGL02456
11
102059373 (GRCm38)
A552S
C
A
missense
Het
possibly damaging
0.716
phenotype
2015-04-16
24
294178
Mtr
1.000
IGL02456
13
12199094 (GRCm38)
I897M
T
C
missense
Het
probably damaging
0.981
phenotype
2015-04-16
25
294173
Npas3
0.920
IGL02456
12
54048767 (GRCm38)
I337F
A
T
missense
Het
probably damaging
0.993
phenotype
2015-04-16
26
294191
Nup85
1.000
IGL02456
11
115581865 (GRCm38)
T
C
unclassified
Het
probably benign
phenotype
2015-04-16
27
294151
Olfr118
0.057
IGL02456
17
37672449 (GRCm38)
M142K
T
A
missense
Het
possibly damaging
0.903
phenotype
2015-04-16
28
294153
Olfr325
0.059
IGL02456
11
58581198 (GRCm38)
L118H
T
A
missense
Het
possibly damaging
0.482
phenotype
2015-04-16
29
294160
Olfr517
0.115
IGL02456
7
108869050 (GRCm38)
Y35H
A
G
missense
Het
probably benign
0.190
phenotype
2015-04-16
30
294171
Olfr630
0.088
IGL02456
7
103755493 (GRCm38)
I31F
T
A
missense
Het
possibly damaging
0.938
phenotype
2015-04-16
31
294154
Olfr683
0.083
IGL02456
7
105143759 (GRCm38)
N178S
T
C
missense
Het
probably damaging
0.989
phenotype
2015-04-16
32
294169
Pdia4
0.000
IGL02456
6
47803495 (GRCm38)
D301E
A
T
missense
Het
probably benign
0.190
phenotype
2015-04-16
33
294180
Phf2
0.334
IGL02456
13
48828846 (GRCm38)
G134C
C
A
missense
Het
unknown
phenotype
2015-04-16
34
294168
Polr2h
1.000
IGL02456
16
20720602 (GRCm38)
L76H
T
A
missense
Het
probably damaging
1.000
phenotype
2015-04-16
35
294185
Rbm47
0.229
IGL02456
5
66027021 (GRCm38)
R80C
G
A
missense
Het
probably damaging
1.000
phenotype
2015-04-16
36
294155
Sfmbt1
0.748
IGL02456
14
30785880 (GRCm38)
S286P
T
C
missense
Het
probably damaging
0.994
phenotype
2015-04-16
37
294197
Slc5a12
0.135
IGL02456
2
110616834 (GRCm38)
T
C
splice site
Het
probably benign
phenotype
2015-04-16
38
294167
Tacc2
0.000
IGL02456
7
130626261 (GRCm38)
S1559P
T
C
missense
Het
probably benign
0.350
phenotype
2015-04-16
39
294181
Tbc1d16
0.000
IGL02456
11
119210546 (GRCm38)
H46P
T
G
missense
Het
probably damaging
1.000
2015-04-16
40
294193
Tbck
0.324
IGL02456
3
132734714 (GRCm38)
A
G
splice site
Het
probably benign
phenotype
2015-04-16
41
294192
Tmtc4
0.000
IGL02456
14
122925962 (GRCm38)
A
T
critical splice donor site
2 bp
Het
probably null
2015-04-16
42
294190
Ttc13
0.000
IGL02456
8
124690361 (GRCm38)
T
C
critical splice acceptor site
Het
probably null
2015-04-16
43
294195
Ttc17
0.528
IGL02456
2
94362785 (GRCm38)
T
C
splice site
Het
probably benign
2015-04-16
44
294150
Vmn1r121
0.070
IGL02456
7
21098513 (GRCm38)
M1L
T
A
start codon destroyed
Het
possibly damaging
0.924
2015-04-16
45
294182
Vps13c
0.000
IGL02456
9
67952976 (GRCm38)
S2825P
T
C
missense
Het
probably damaging
1.000
phenotype
2015-04-16
46
294177
Zan
0.078
IGL02456
5
137446844 (GRCm38)
S1718A
A
C
missense
Het
unknown
phenotype
2015-04-16
47
294165
Zfp39
0.211
IGL02456
11
58902800 (GRCm38)
Y37*
G
T
nonsense
Het
probably null
phenotype
2015-04-16
48
294161
Zfp407
1.000
IGL02456
18
84558641 (GRCm38)
N1449S
T
C
missense
Het
probably damaging
0.996
phenotype
2015-04-16
49
294187
Zhx2
0.310
IGL02456
15
57823639 (GRCm38)
D801E
C
A
missense
Het
possibly damaging
0.720
phenotype
2015-04-16
[records 1 to 49 of 49]