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Incidental Mutations
39
incidental mutations are currently displayed, and affect
39
genes.
3
are Possibly Damaging.
17
are Probably Damaging.
16
are Probably Benign.
3
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 39 of 39]
10
25
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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
156034
4930548H24Rik
0.049
R1366
G1
225
Y
5
31487517
C205S
T
A
missense
Het
probably benign
0.073
0.090
02/11/2014
2
156035
Aasdh
0.171
R1366
G1
225
Y
5
76888804
S297T
A
T
missense
Het
probably benign
0.105
0.187
phenotype
02/11/2014
3
156040
Acsm1
0.000
R1366
G1
225
Y
7
119658288
T
C
splice site
Het
probably benign
0.090
02/11/2014
4
156019
Ankar
0.077
R1366
G1
225
Y
1
72698649
N125Y
T
A
missense
Het
probably damaging
1.000
0.273
02/11/2014
5
156029
Chd1l
0.207
R1366
G1
225
Y
3
97581149
D517G
T
C
missense
Het
probably damaging
0.989
0.268
phenotype
02/11/2014
6
156023
Cir1
1.000
R1366
G1
225
Y
2
73306413
A
T
splice site
Het
probably benign
0.090
02/11/2014
7
156025
Cpxm1
0.446
R1366
G1
200
Y
2
130396122
R136W
G
A
missense
Het
probably damaging
1.000
0.805
phenotype
02/11/2014
8
156050
Cyhr1
0.367
R1366
G1
185
Y
15
76648969
R190G
T
C
missense
Het
probably damaging
0.963
0.069
02/11/2014
9
156037
Dnah10
0.000
R1366
G1
225
Y
5
124753326
E761D
A
T
missense
Het
probably benign
0.411
0.099
phenotype
02/11/2014
10
156051
Fam186a
0.064
R1366
G1
225
Y
15
99943389
E1658V
T
A
missense
Het
possibly damaging
0.893
0.179
02/11/2014
11
156054
Fam98a
0.706
R1366
G1
225
Y
17
75539386
A
G
splice site
Het
probably benign
0.090
02/11/2014
12
156041
Fanca
0.557
R1366
G1
158
Y
8
123304281
G
A
splice site
Het
probably benign
0.090
phenotype
02/11/2014
13
156046
Frmd6
0.000
R1366
G1
225
Y
12
70887889
T
C
splice site
Het
probably benign
02/11/2014
14
156049
Gmpr2
0.291
R1366
G1
225
Y
14
55676743
T
C
splice site
Het
probably benign
0.090
02/11/2014
15
156026
Hck
0.394
R1366
G1
225
Y
2
153138295
G348D
G
A
missense
Het
probably damaging
0.999
0.647
phenotype
02/11/2014
16
156030
Ifnab
0.064
R1366
G1
225
Y
4
88691100
Q43L
T
A
missense
Het
possibly damaging
0.539
0.461
02/11/2014
17
156020
Ilkap
0.232
R1366
G1
147
Y
1
91387215
I142T
A
G
missense
Het
possibly damaging
0.580
0.092
phenotype
02/11/2014
18
156022
Lamc3
0.000
R1366
G1
174
Y
2
31928847
S1206P
T
C
missense
Het
probably damaging
1.000
0.204
phenotype
02/11/2014
19
156055
Mfsd13a
0.454
R1366
G1
225
Y
19
46366504
T40I
C
T
missense
Het
probably benign
0.224
0.096
02/11/2014
20
247295
Mid1
0.000
R1366
G1
42
Y
X
169986094
N215H
A
C
missense
Het
probably damaging
1.000
0.647
phenotype
11/04/2014
21
156038
Mkrn1
0.000
R1366
G1
225
Y
6
39405917
T134A
T
C
missense
Het
probably benign
0.023
0.068
phenotype
02/11/2014
22
156027
Mmp9
0.000
R1366
G1
209
Y
2
164953342
V628E
T
A
missense
Het
probably damaging
1.000
0.536
phenotype
02/11/2014
23
156045
Msi2
1.000
R1366
G1
159
Y
11
88716580
V67D
A
T
missense
Het
probably damaging
1.000
0.950
phenotype
02/11/2014
24
156042
Ncapd3
0.961
R1366
G1
225
Y
9
27057940
V630E
T
A
missense
Het
probably damaging
1.000
0.860
phenotype
02/11/2014
25
156031
Nkain1
0.171
R1366
G1
225
Y
4
130537316
V73A
A
G
missense
Het
probably damaging
0.999
0.542
phenotype
02/11/2014
26
156033
Nphp4
0.198
R1366
G1
225
Y
4
152502926
D245E
T
A
missense
Het
probably damaging
0.957
0.142
phenotype
02/11/2014
27
156024
Olfr1014
0.087
R1366
G1
225
Y
2
85777004
C140Y
G
A
missense
Het
probably benign
0.350
0.090
phenotype
02/11/2014
28
156052
Olfr114
0.060
R1366
G1
225
Y
17
37589764
I196M
T
C
missense
Het
probably benign
0.026
0.090
phenotype
02/11/2014
29
156043
Olfr57
0.068
R1366
G1
225
Y
10
79035042
M82R
T
G
missense
Het
probably damaging
0.996
0.399
phenotype
02/11/2014
30
156044
Pkd1l1
1.000
R1366
G1
225
Y
11
8941038
T
C
splice site
Het
probably benign
0.090
phenotype
02/11/2014
31
156036
Plcxd1
0.085
R1366
G1
225
Y
5
110102230
I184L
A
C
missense
Het
probably damaging
0.999
0.284
02/11/2014
32
156048
Prl3b1
0.086
R1366
G1
225
Y
13
27243865
A53T
G
A
missense
Het
probably benign
0.001
0.090
02/11/2014
33
247294
Rasl10b
0.150
R1366
G1
42
Y
11
83417839
G
A
splice site
Het
probably null
0.976
phenotype
11/04/2014
34
156039
Scube2
0.473
R1366
G1
204
Y
7
109804614
Y890H
A
G
missense
Het
probably damaging
1.000
0.300
phenotype
02/11/2014
35
156021
Slco6c1
0.000
R1366
G1
225
Y
1
97128203
T
A
start gained
Het
probably null
0.976
02/11/2014
36
156047
Tnfaip2
0.000
R1366
G1
126
Y
12
111449322
F485V
T
G
missense
Het
probably benign
0.001
0.090
phenotype
02/11/2014
37
156028
Tpd52
0.098
R1366
G1
182
Y
3
8963933
D17G
T
C
missense
Het
probably damaging
0.991
0.085
02/11/2014
38
156032
Ube4b
1.000
R1366
G1
166
Y
4
149335149
D1034G
T
C
missense
Het
probably damaging
0.982
0.491
phenotype
02/11/2014
39
156053
Vmn2r118
0.197
R1366
G1
225
Y
17
55593237
Q556*
G
A
nonsense
Het
probably null
0.976
02/11/2014
[records 1 to 39 of 39]