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Incidental Mutations
39
incidental mutations are currently displayed, and affect
38
genes.
8
are Possibly Damaging.
11
are Probably Damaging.
17
are Probably Benign.
3
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 39 of 39]
10
25
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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
162266
Abcc10
0.116
R1426
G1
225
Y
17
46324435
V214E
A
T
missense
Het
probably damaging
0.970
0.076
phenotype
03/14/2014
2
162240
Adh1
0.000
R1426
G1
225
Y
3
138286795
D224G
A
G
missense
Het
probably damaging
0.999
0.281
phenotype
03/14/2014
3
162267
Arhgap28
0.000
R1426
G1
224
Y
17
67857464
Q554H
C
A
missense
Het
probably damaging
0.995
0.140
phenotype
03/14/2014
4
162260
Atp8a2
0.304
R1426
G1
98
Y
14
59860270
K770E
T
C
missense
Het
probably benign
0.006
0.083
phenotype
03/14/2014
5
162244
Brat1
0.152
R1426
G1
215
Y
5
140718013
V674I
G
A
missense
Het
probably benign
0.001
0.090
phenotype
03/14/2014
6
162265
Brd2
1.000
R1426
G1
217
Y
17
34114007
ATCTTCTTC
ATCTTC
utr 3 prime
Het
probably benign
0.090
phenotype
03/14/2014
7
262801
Ccdc162
0.077
R1426
G1
87
N
10
41553182
D438G
T
C
missense
Het
possibly damaging
0.890
02/04/2015
8
162243
Cyp4x1
0.125
R1426
G1
225
Y
4
115112791
T
A
splice site
Het
probably benign
phenotype
03/14/2014
9
162250
Dip2a
0.000
R1426
G1
175
Y
10
76279820
T
C
unclassified
Het
probably benign
phenotype
03/14/2014
10
162256
Eif2s1
1.000
R1426
G1
225
Y
12
78881168
D206G
A
G
missense
Het
probably benign
0.008
0.473
phenotype
03/14/2014
11
162259
Elovl7
0.183
R1426
G1
225
Y
13
108282494
I220N
T
A
missense
Het
possibly damaging
0.658
0.180
03/14/2014
12
162271
Gsto1
0.000
R1426
G1
225
Y
19
47857942
E76G
A
G
missense
Het
probably damaging
1.000
0.467
phenotype
03/14/2014
13
162238
Hspa14
0.238
R1426
G1
181
Y
2
3508821
W12R
A
T
missense
Het
probably damaging
0.999
0.086
03/14/2014
14
162261
L3mbtl2
1.000
R1426
G1
202
Y
15
81676317
C260S
T
A
missense
Het
possibly damaging
0.951
0.773
phenotype
03/14/2014
15
162268
Lama3
1.000
R1426
G1
225
Y
18
12481098
G
T
critical splice donor site
1 bp
Het
probably null
0.949
phenotype
03/14/2014
16
250614
Lrrc34
0.068
R1426
G1
29
Y
3
30643579
T
A
unclassified
Het
probably benign
0.090
11/26/2014
17
162253
Lrrc45
0.183
R1426
G1
225
Y
11
120720013
Q525L
A
T
missense
Het
probably benign
0.002
0.072
03/14/2014
18
162251
Lss
1.000
R1426
G1
221
Y
10
76536303
I164T
T
C
missense
Het
probably damaging
0.979
0.793
phenotype
03/14/2014
19
162262
Myh11
1.000
R1426
G1
225
Y
16
14205931
K1527*
T
A
nonsense
Het
probably null
0.975
phenotype
03/14/2014
20
250616
Naip2
0.084
R1426
G1
64
Y
13
100161854
E558G
T
C
missense
Het
probably benign
0.000
0.090
phenotype
11/26/2014
21
250617
Naip2
0.084
R1426
G1
50
Y
13
100161860
G556D
C
T
missense
Het
probably benign
0.001
0.090
phenotype
11/26/2014
22
162254
Ncoa1
0.000
R1426
G1
166
Y
12
4270737
T
A
splice site
Het
probably benign
0.090
phenotype
03/14/2014
23
162270
Olfr262
0.083
R1426
G1
225
Y
19
12241182
Q160K
G
T
missense
Het
possibly damaging
0.807
0.401
phenotype
03/14/2014
24
162252
Olfr768
0.068
R1426
G1
225
Y
10
129093690
C95S
A
T
missense
Het
probably damaging
1.000
0.647
phenotype
03/14/2014
25
162248
Pafah1b3
0.000
R1426
G1
225
Y
7
25297135
E41G
T
C
missense
Het
possibly damaging
0.910
0.116
phenotype
03/14/2014
26
162247
Pnmal1
0.097
R1426
G1
225
Y
7
16960984
P255S
C
T
missense
Het
possibly damaging
0.559
0.179
03/14/2014
27
162255
Prkar2b
0.528
R1426
G1
225
Y
12
31962988
A
T
splice site
Het
probably benign
0.090
phenotype
03/14/2014
28
162239
Rbck1
0.000
R1426
G1
225
Y
2
152327241
A
T
unclassified
Het
probably benign
0.090
phenotype
03/14/2014
29
162269
Rcor2
0.815
R1426
G1
194
Y
19
7271030
S137G
A
G
missense
Het
possibly damaging
0.823
0.111
phenotype
03/14/2014
30
250615
Slc25a48
0.113
R1426
G1
59
Y
13
56448991
T
A
splice site
Het
probably benign
11/26/2014
31
162263
Slc7a4
0.561
R1426
G1
192
Y
16
17573944
A
G
critical splice donor site
2 bp
Het
probably null
0.949
03/14/2014
32
162258
Tert
0.678
R1426
G1
225
Y
13
73642353
T
C
splice site
Het
probably benign
phenotype
03/14/2014
33
162264
Traf7
0.668
R1426
G1
225
Y
17
24511681
I344N
A
T
missense
Het
probably damaging
0.996
0.665
phenotype
03/14/2014
34
162257
Vmn1r194
0.063
R1426
G1
225
Y
13
22245066
F284L
T
A
missense
Het
probably damaging
0.987
0.647
03/14/2014
35
162246
Xpc
0.332
R1426
G1
225
Y
6
91493238
M699T
A
G
missense
Het
probably damaging
0.998
0.545
phenotype
03/14/2014
36
162241
Zbtb5
0.000
R1426
G1
225
Y
4
44993968
H472R
T
C
missense
Het
possibly damaging
0.951
0.060
03/14/2014
37
162245
Zfp786
0.075
R1426
G1
223
Y
6
47825079
V88A
A
G
missense
Het
probably benign
0.165
0.090
03/14/2014
38
162249
Zkscan7
0.000
R1426
G1
225
Y
9
122895163
I399T
T
C
missense
Het
probably benign
0.000
0.090
03/14/2014
39
162242
Zyg11b
0.552
R1426
G1
204
Y
4
108250812
R466C
G
A
missense
Het
probably damaging
0.996
0.647
03/14/2014
[records 1 to 39 of 39]