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Incidental Mutations
50
incidental mutations are currently displayed, and affect
50
genes.
6
are Possibly Damaging.
22
are Probably Damaging.
21
are Probably Benign.
1
are Probably Null.
1
create premature stop codons.
0
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 50 of 50]
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
157329
Abca8b
0.000
R1371
G1
225
Y
11
109953553 (GRCm38)
D884V
T
A
missense
Het
probably damaging
0.988
0.647
phenotype
2014-02-18
2
157301
Acvr2a
0.000
R1371
G1
225
Y
2
48899616 (GRCm38)
T457M
C
T
missense
Het
probably damaging
1.000
0.647
phenotype
2014-02-18
3
157309
Akr1b10
0.068
R1371
G1
225
Y
6
34392459 (GRCm38)
T208I
C
T
missense
Het
probably benign
0.276
0.090
2014-02-18
4
157315
Aldh16a1
0.000
R1371
G1
128
Y
7
45147250 (GRCm38)
T275K
G
T
missense
Het
possibly damaging
0.780
0.434
phenotype
2014-02-18
5
157308
Alkbh2
0.000
R1371
G1
215
Y
5
114124226 (GRCm38)
E148K
C
T
missense
Het
probably damaging
0.979
0.223
phenotype
2014-02-18
6
157327
Asgr1
0.000
R1371
G1
225
Y
11
70056097 (GRCm38)
C56W
T
G
missense
Het
probably benign
0.037
0.588
phenotype
2014-02-18
7
157303
Atp11b
0.285
R1371
G1
225
Y
3
35806769 (GRCm38)
I335T
T
C
missense
Het
probably damaging
0.973
0.186
phenotype
2014-02-18
8
157338
BC061237
0.073
R1371
G1
221
Y
14
44504305 (GRCm38)
A
G
splice site
Het
probably benign
0.090
2014-02-18
9
157343
Bdh1
0.115
R1371
G1
217
Y
16
31456902 (GRCm38)
K280N
G
T
missense
Het
probably benign
0.004
0.273
phenotype
2014-02-18
10
157340
Bmp1
1.000
R1371
G1
225
Y
14
70492466 (GRCm38)
C466Y
C
T
missense
Het
probably damaging
1.000
0.973
phenotype
2014-02-18
11
157298
Ccdc181
0.000
R1371
G1
225
Y
1
164280603 (GRCm38)
E285G
A
G
missense
Het
probably benign
0.337
0.069
2014-02-18
12
157319
Ces1f
0.073
R1371
G1
222
Y
8
93279649 (GRCm38)
G18R
C
T
missense
Het
probably damaging
0.981
0.647
2014-02-18
13
157346
Cfap43
0.141
R1371
G1
225
Y
19
47835606 (GRCm38)
I109L
T
A
missense
Het
possibly damaging
0.951
0.179
phenotype
2014-02-18
14
157339
Cma2
0.071
R1371
G1
225
Y
14
55972826 (GRCm38)
L56S
T
C
missense
Het
probably damaging
1.000
0.760
2014-02-18
15
157320
Edc4
1.000
R1371
G1
225
Y
8
105890750 (GRCm38)
A
G
unclassified
Het
probably benign
0.090
phenotype
2014-02-18
16
157306
F3
0.087
R1371
G1
225
Y
3
121732510 (GRCm38)
C241R
T
C
missense
Het
probably damaging
1.000
0.963
phenotype
2014-02-18
17
157305
Fhdc1
0.332
R1371
G1
225
Y
3
84445003 (GRCm38)
S972C
T
A
missense
Het
probably damaging
0.996
0.198
2014-02-18
18
157325
H2afy2
0.396
R1371
G1
225
Y
10
61749333 (GRCm38)
D177E
A
T
missense
Het
possibly damaging
0.705
0.079
phenotype
2014-02-18
19
157331
Heatr1
0.962
R1371
G1
225
Y
13
12417632 (GRCm38)
I1086R
T
G
missense
Het
possibly damaging
0.800
0.290
2014-02-18
20
157317
Hsh2d
0.054
R1371
G1
145
Y
8
72196894 (GRCm38)
A
T
splice site
Het
probably benign
phenotype
2014-02-18
21
157335
Ice1
0.951
R1371
G1
225
Y
13
70596221 (GRCm38)
Y2081C
T
C
missense
Het
probably damaging
1.000
0.213
2014-02-18
22
157296
Il1rl1
0.000
R1371
G1
225
Y
1
40442713 (GRCm38)
N194D
A
G
missense
Het
probably damaging
0.958
0.191
phenotype
2014-02-18
23
157323
Ip6k1
0.376
R1371
G1
141
Y
9
108045823 (GRCm38)
V385M
G
A
missense
Het
probably damaging
0.959
0.779
phenotype
2014-02-18
24
157312
Lig1
1.000
R1371
G1
211
Y
7
13288685 (GRCm38)
R147Q
G
A
missense
Het
probably damaging
0.997
0.115
phenotype
2014-02-18
25
157300
Lrp1b
0.000
R1371
G1
225
Y
2
40647153 (GRCm38)
V41I
C
T
missense
Het
probably damaging
0.998
0.647
phenotype
2014-02-18
26
157322
Mst1r
0.277
R1371
G1
122
Y
9
107917225 (GRCm38)
V1201E
T
A
missense
Het
probably damaging
0.997
0.924
phenotype
2014-02-18
27
157345
Myof
0.000
R1371
G1
225
Y
19
37903668 (GRCm38)
T
C
splice site
Het
probably benign
0.090
phenotype
2014-02-18
28
157330
Nbas
1.000
R1371
G1
225
Y
12
13482378 (GRCm38)
G
T
splice site
Het
probably benign
phenotype
2014-02-18
29
157344
Ndst1
1.000
R1371
G1
225
Y
18
60707647 (GRCm38)
I321T
A
G
missense
Het
possibly damaging
0.900
0.910
phenotype
2014-02-18
30
157337
Nek10
0.000
R1371
G1
225
Y
14
14850983 (GRCm38)
G343R
G
A
missense
Het
probably damaging
0.975
0.229
2014-02-18
31
157310
Olfr13
0.540
R1371
G1
225
Y
6
43174300 (GRCm38)
T105S
A
T
missense
Het
probably benign
0.014
0.090
phenotype
2014-02-18
32
157326
Olfr1385
0.072
R1371
G1
225
Y
11
49494823 (GRCm38)
C97S
T
A
missense
Het
probably damaging
0.998
0.828
phenotype
2014-02-18
33
157328
Olfr462
0.836
R1371
G1
225
Y
11
87889296 (GRCm38)
I200N
A
T
missense
Het
probably damaging
1.000
0.416
phenotype
2014-02-18
34
157336
Pde4d
0.000
R1371
G1
131
Y
13
109117061 (GRCm38)
S141P
T
C
missense
Het
probably benign
0.003
0.107
phenotype
2014-02-18
35
157299
Pigm
1.000
R1371
G1
187
Y
1
172376814 (GRCm38)
Q39L
A
T
missense
Het
probably damaging
1.000
0.653
phenotype
2014-02-18
36
157333
Prl7a2
0.060
R1371
G1
225
Y
13
27662767 (GRCm38)
I88F
T
A
missense
Het
probably benign
0.009
0.090
2014-02-18
37
157332
Prss16
0.000
R1371
G1
225
Y
13
22008686 (GRCm38)
T
A
unclassified
Het
probably benign
0.090
phenotype
2014-02-18
38
157313
Psmc4
1.000
R1371
G1
225
Y
7
28042797 (GRCm38)
G
A
splice site
Het
probably benign
phenotype
2014-02-18
39
157307
Ptger3
0.067
R1371
G1
95
Y
3
157567728 (GRCm38)
C237*
T
A
nonsense
Het
probably null
0.976
phenotype
2014-02-18
40
157311
Recql
0.345
R1371
G1
225
Y
6
142372875 (GRCm38)
T214M
G
A
missense
Het
probably damaging
0.986
0.647
phenotype
2014-02-18
41
157321
Rfx7
0.933
R1371
G1
225
Y
9
72619575 (GRCm38)
V1349D
T
A
missense
Het
probably damaging
1.000
0.108
phenotype
2014-02-18
42
157324
Ros1
0.156
R1371
G1
225
Y
10
52087945 (GRCm38)
S1740P
A
G
missense
Het
probably damaging
0.979
0.173
phenotype
2014-02-18
43
157342
Rrm2b
0.632
R1371
G1
225
Y
15
37946809 (GRCm38)
S83T
A
T
missense
Het
probably benign
0.059
0.090
phenotype
2014-02-18
44
157302
Sall4
1.000
R1371
G1
225
Y
2
168756474 (GRCm38)
Y149H
A
G
missense
Het
probably benign
0.096
0.073
phenotype
2014-02-18
45
157318
Smad1
1.000
R1371
G1
225
Y
8
79349578 (GRCm38)
A
G
splice site
Het
probably benign
phenotype
2014-02-18
46
157316
Snrnp70
0.962
R1371
G1
225
Y
7
45380705 (GRCm38)
T
C
unclassified
Het
probably benign
phenotype
2014-02-18
47
157341
Spef2
0.093
R1371
G1
225
Y
15
9725108 (GRCm38)
C
A
splice site
Het
probably benign
0.090
phenotype
2014-02-18
48
157334
Sptlc1
1.000
R1371
G1
123
Y
13
53351624 (GRCm38)
T253A
T
C
missense
Het
probably benign
0.000
0.083
phenotype
2014-02-18
49
157304
Zbbx
0.053
R1371
G1
225
Y
3
75052477 (GRCm38)
Y595C
T
C
missense
Het
possibly damaging
0.585
0.118
2014-02-18
50
157314
Zfp382
0.179
R1371
G1
225
Y
7
30133689 (GRCm38)
V255A
T
C
missense
Het
probably benign
0.362
0.090
phenotype
2014-02-18
[records 1 to 50 of 50]