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Incidental Mutations
60
incidental mutations are currently displayed, and affect
58
genes.
8
are Possibly Damaging.
20
are Probably Damaging.
25
are Probably Benign.
6
are Probably Null.
1
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 60 of 60]
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
438203
0610010F05Rik
0.191
R5615
G1
225
N
11
23606759 (GRCm38)
L407H
A
T
missense
Het
probably damaging
0.961
2016-10-26
2
438166
Abca12
1.000
R5615
G1
225
N
1
71307059 (GRCm38)
L884H
A
T
missense
Het
probably damaging
1.000
phenotype
2016-10-26
3
438207
Ahr
0.960
R5615
G1
225
N
12
35503885 (GRCm38)
V745A
A
G
missense
Het
probably benign
0.012
phenotype
2016-10-26
4
438180
Ankrd17
1.000
R5615
G1
225
N
5
90283436 (GRCm38)
S830T
A
T
missense
Het
possibly damaging
0.877
phenotype
2016-10-26
5
438165
Aox1
0.000
R5615
G1
225
N
1
58096966 (GRCm38)
T1123A
A
G
missense
Het
probably benign
0.000
phenotype
2016-10-26
6
438175
Arhgef11
0.000
R5615
G1
122
N
3
87722485 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
phenotype
2016-10-26
7
438206
Bcas3
0.762
R5615
G1
225
N
11
85470761 (GRCm38)
C250S
T
A
missense
Het
probably damaging
0.998
2016-10-26
8
438193
Bckdk
0.121
R5615
G1
213
N
7
127907317 (GRCm38)
I272T
T
C
missense
Het
probably damaging
0.999
phenotype
2016-10-26
9
501161
Cacna1e
0.204
R5615
G1
225
N
1
154412170 (GRCm38)
K1897E
T
C
missense
Het
probably damaging
0.996
phenotype
2017-12-01
10
438211
Cd180
0.000
R5615
G1
225
N
13
102706203 (GRCm38)
I586F
A
T
missense
Het
probably benign
0.336
phenotype
2016-10-26
11
438201
Cep290
0.902
R5615
G1
206
N
10
100531150 (GRCm38)
D1121G
A
G
missense
Het
probably damaging
0.997
phenotype
2016-10-26
12
438189
Clasrp
1.000
R5615
G1
156
N
7
19586447 (GRCm38)
A
G
utr 3 prime
Het
probably benign
phenotype
2016-10-26
13
501162
Col27a1
1.000
R5615
G1
225
N
4
63281114 (GRCm38)
K912N
G
T
missense
Het
probably damaging
0.959
phenotype
2017-12-01
14
438208
Dock4
0.120
R5615
G1
225
N
12
40649480 (GRCm38)
R231L
G
T
missense
Het
probably benign
0.215
phenotype
2016-10-26
15
438196
Ell
1.000
R5615
G1
225
N
8
70590732 (GRCm38)
S505N
G
A
missense
Het
probably benign
0.044
phenotype
2016-10-26
16
438181
Ephb6
0.517
R5615
G1
225
N
6
41619291 (GRCm38)
T833A
A
G
missense
Het
probably benign
0.000
phenotype
2016-10-26
17
438199
Hemk1
0.176
R5615
G1
225
N
9
107330824 (GRCm38)
T
A
critical splice acceptor site
Het
probably null
2016-10-26
18
501160
Hjurp
0.941
R5615
G1
217
N
1
88266524 (GRCm38)
GT
GTT
nonsense
Het
probably null
0.976
2017-12-01
19
438224
Hspa12a
0.256
R5615
G1
225
N
19
58804650 (GRCm38)
I368V
T
C
missense
Het
possibly damaging
0.564
2016-10-26
20
438185
Igkv3-3
0.211
R5615
G1
225
N
6
70687230 (GRCm38)
T19S
A
T
missense
Het
probably benign
0.001
2016-10-26
21
438187
Itpr1
0.888
R5615
G1
225
N
6
108488600 (GRCm38)
A2158T
G
A
missense
Het
possibly damaging
0.710
phenotype
2016-10-26
22
438183
Lancl2
0.000
R5615
G1
225
N
6
57722511 (GRCm38)
Y104H
T
C
missense
Het
probably damaging
1.000
2016-10-26
23
438188
Leng8
0.966
R5615
G1
225
N
7
4144958 (GRCm38)
E634*
G
T
nonsense
Het
probably null
2016-10-26
24
438192
Lrrk1
1.000
R5615
G1
200
N
7
66287615 (GRCm38)
C930S
A
T
missense
Het
probably damaging
1.000
phenotype
2016-10-26
25
438221
Lvrn
0.543
R5615
G1
225
N
18
46850328 (GRCm38)
S46L
C
T
missense
Het
possibly damaging
0.553
2016-10-26
26
438212
Mcidas
0.000
R5615
G1
225
N
13
112997425 (GRCm38)
V148I
G
A
missense
Het
probably benign
0.007
phenotype
2016-10-26
27
438205
Mprip
0.617
R5615
G1
202
N
11
59758487 (GRCm38)
T1006S
A
T
missense
Het
probably benign
0.081
2016-10-26
28
438191
Mrgprb3
0.086
R5615
G1
225
N
7
48643486 (GRCm38)
M106L
T
A
missense
Het
probably benign
0.006
2016-10-26
29
438169
Mroh2a
0.948
R5615
G1
207
N
1
88232257 (GRCm38)
GCCC
GC
frame shift
Het
probably null
phenotype
2016-10-26
30
501163
Mtor
1.000
R5615
G1
225
N
4
148538276 (GRCm38)
V1938I
G
A
missense
Het
possibly damaging
0.954
phenotype
2017-12-01
31
438195
Muc2
0.082
R5615
G1
225
N
7
141691203 (GRCm38)
D46G
A
G
missense
Het
probably damaging
1.000
phenotype
2016-10-26
32
438223
Nfkb2
0.569
R5615
G1
218
N
19
46307567 (GRCm38)
E170D
G
T
missense
Het
probably benign
0.017
0.084
phenotype
2016-10-26
33
438172
Olfr1113
0.055
R5615
G1
225
N
2
87213739 (GRCm38)
F282L
T
A
missense
Het
probably benign
0.001
phenotype
2016-10-26
34
458003
Olfr811
0.056
R5615
G1
225
N
10
129801767 (GRCm38)
C253S
A
T
missense
Het
probably damaging
1.000
phenotype
2017-02-16
35
438202
Osbp2
0.102
R5615
G1
225
N
11
3863356 (GRCm38)
G171D
C
T
missense
Het
probably benign
0.001
phenotype
2016-10-26
36
438178
Otud6b
0.086
R5615
G1
225
N
4
14818187 (GRCm38)
M238K
A
T
missense
Het
possibly damaging
0.522
phenotype
2016-10-26
37
438218
Pcdhac2
0.000
R5615
G1
225
N
18
37146423 (GRCm38)
G819R
G
A
missense
Het
probably benign
0.221
phenotype
2016-10-26
38
438219
Pcdhac2
0.000
R5615
G1
225
N
18
37146424 (GRCm38)
G819V
G
T
missense
Het
probably benign
0.000
phenotype
2016-10-26
39
438220
Pcdhga12
0.235
R5615
G1
225
N
18
37768079 (GRCm38)
S655A
T
G
missense
Het
probably damaging
0.984
phenotype
2016-10-26
40
438197
Pkd1l3
0.000
R5615
G1
90
N
8
109630210 (GRCm38)
I756V
A
G
missense
Het
probably benign
0.000
phenotype
2016-10-26
41
438209
Plekhd1
0.054
R5615
G1
206
N
12
80720590 (GRCm38)
S251T
T
A
missense
Het
probably damaging
0.998
2016-10-26
42
438215
Ppp2r1a
1.000
R5615
G1
225
N
17
20958987 (GRCm38)
T96S
A
T
missense
Het
probably benign
0.001
phenotype
2016-10-26
43
438173
Qser1
0.541
R5615
G1
225
N
2
104789694 (GRCm38)
S258A
A
C
missense
Het
possibly damaging
0.778
2016-10-26
44
438200
Rsph4a
0.150
R5615
G1
225
N
10
33909328 (GRCm38)
A412T
G
A
missense
Het
probably benign
0.316
phenotype
2016-10-26
45
438177
Sass6
0.958
R5615
G1
225
N
3
116607486 (GRCm38)
C159S
T
A
missense
Het
probably benign
0.000
phenotype
2016-10-26
46
438214
Scaf4
0.698
R5615
G1
225
N
16
90251960 (GRCm38)
Q322R
T
C
missense
Het
unknown
phenotype
2016-10-26
47
438174
Sema6d
0.000
R5615
G1
157
N
2
124656901 (GRCm38)
H244Y
C
T
missense
Het
probably damaging
0.966
phenotype
2016-10-26
48
438194
Sigirr
0.073
R5615
G1
225
N
7
141092719 (GRCm38)
L163F
T
G
missense
Het
probably damaging
0.992
phenotype
2016-10-26
49
438210
Spata31d1c
0.000
R5615
G1
225
N
13
65035264 (GRCm38)
L207I
C
A
missense
Het
possibly damaging
0.613
2016-10-26
50
438184
Tacstd2
0.206
R5615
G1
225
N
6
67535049 (GRCm38)
F220L
A
G
missense
Het
probably damaging
0.998
phenotype
2016-10-26
51
438176
Tdpoz4
0.828
R5615
G1
225
N
3
93797499 (GRCm38)
T368S
A
T
missense
Het
probably benign
0.070
0.090
2016-10-26
52
438217
Tnxb
0.000
R5615
G1
225
N
17
34683418 (GRCm38)
Q1082K
C
A
missense
Het
probably damaging
0.997
phenotype
2016-10-26
53
438204
Trim41
0.366
R5615
G1
215
N
11
48807365 (GRCm38)
GCCTAGGCGCCCA
G
unclassified
Het
probably benign
phenotype
2016-10-26
54
438222
Trpm6
1.000
R5615
G1
171
N
19
18829933 (GRCm38)
R1014C
C
T
missense
Het
probably damaging
0.963
phenotype
2016-10-26
55
438168
Ugt1a10
0.116
R5615
G1
217
N
1
88216158 (GRCm38)
TTCATCA
TTCA
small deletion
Het
probably benign
2016-10-26
56
501164
Vmn2r114
0.108
R5615
G1
144
N
17
23290932 (GRCm38)
ATTT
ATT
makesense
Het
probably null
2017-12-01
57
458002
Vmn2r61
0.128
R5615
G1
225
N
7
42300493 (GRCm38)
E779G
A
G
missense
Het
probably damaging
1.000
2017-02-16
58
438190
Vmn2r61
0.128
R5615
G1
225
N
7
42267253 (GRCm38)
M430K
T
A
missense
Het
probably benign
0.001
2016-10-26
59
438198
Zfp599
0.074
R5615
G1
225
N
9
22253869 (GRCm38)
D70G
T
C
missense
Het
probably benign
0.000
2016-10-26
60
438179
Zmym1
0.225
R5615
G1
225
N
4
127049398 (GRCm38)
I301N
A
T
missense
Het
probably damaging
0.999
2016-10-26
[records 1 to 60 of 60]