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Incidental Mutations
32
incidental mutations are currently displayed, and affect
32
genes.
8
are Possibly Damaging.
10
are Probably Damaging.
9
are Probably Benign.
4
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 32 of 32]
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
330267
0610040J01Rik
0.145
R4464
G1
186
Y
5
63898839
G
T
unclassified
Het
probably benign
0.169
07/21/2015
2
330278
Abcc3
0.000
R4464
G1
199
Y
11
94358786
V1111A
A
G
missense
Het
probably benign
0.006
0.090
phenotype
07/21/2015
3
330284
Acot10
0.178
R4464
G1
225
Y
15
20665744
R304*
G
A
nonsense
Het
probably null
0.976
07/21/2015
4
330276
Aldh8a1
0.077
R4464
G1
225
Y
10
21388941
C
A
intron
Het
probably benign
0.090
phenotype
07/21/2015
5
330268
Alms1
0.000
R4464
G1
225
Y
6
85620021
T1079A
A
G
missense
Het
possibly damaging
0.659
0.179
phenotype
07/21/2015
6
330259
Armc3
0.083
R4464
G1
225
Y
2
19248659
Y204H
T
C
missense
Het
probably damaging
0.994
0.182
phenotype
07/21/2015
7
330257
Asnsd1
0.137
R4464
G1
225
Y
1
53352527
C
A
splice site
3 bp
Het
probably null
0.976
07/21/2015
8
330277
Atad5
1.000
R4464
G1
225
Y
11
80100311
T
A
splice site
Het
probably null
0.976
phenotype
07/21/2015
9
330263
Cst12
0.060
R4464
G1
225
Y
2
148789517
V53I
G
A
missense
Het
possibly damaging
0.889
0.179
07/21/2015
10
330265
Cylc2
0.052
R4464
G1
225
Y
4
51229651
T331R
C
G
missense
Het
unknown
0.087
07/21/2015
11
330261
Dennd1a
0.799
R4464
G1
225
Y
2
38243390
A
T
splice site
Het
probably benign
0.090
phenotype
07/21/2015
12
377809
Fam213a
0.106
R4464
G1
225
Y
14
40997875
K127N
T
A
missense
Het
probably damaging
0.991
0.370
phenotype
04/07/2016
13
330287
Gm7535
0.224
R4464
G1
225
Y
17
17911662
C
A
intron
Het
probably benign
0.298
07/21/2015
14
330260
Gpr158
0.000
R4464
G1
225
Y
2
21826999
M970K
T
A
missense
Het
probably damaging
0.988
0.142
07/21/2015
15
330275
Ifngr1
0.000
R4464
G1
225
Y
10
19597517
V72I
G
A
missense
Het
possibly damaging
0.748
0.432
phenotype
07/21/2015
16
330258
Kifap3
1.000
R4464
G1
225
Y
1
163817895
Q269K
C
A
missense
Het
probably benign
0.001
0.069
phenotype
07/21/2015
17
330286
Krt86
0.065
R4464
G1
225
Y
15
101473914
D122N
G
A
missense
Het
probably damaging
0.993
0.621
phenotype
07/21/2015
18
330264
Lrrcc1
0.000
R4464
G1
225
Y
3
14557318
K694E
A
G
missense
Het
probably damaging
1.000
0.142
07/21/2015
19
330269
Mbd4
0.191
R4464
G1
225
Y
6
115849502
L155S
A
G
missense
Het
probably damaging
0.988
0.647
phenotype
07/21/2015
20
330283
Nalcn
1.000
R4464
G1
225
Y
14
123323350
N772D
T
C
missense
Het
probably benign
0.000
0.075
phenotype
07/21/2015
21
330288
Olfr109
0.071
R4464
G1
225
Y
17
37466851
S215F
C
T
missense
Het
probably damaging
1.000
0.439
phenotype
07/21/2015
22
330271
Psg29
0.059
R4464
G1
225
Y
7
17210650
N362Y
A
T
missense
Het
possibly damaging
0.609
0.179
07/21/2015
23
330274
Ptpn23
1.000
R4464
G1
225
Y
9
110386813
T1325I
G
A
missense
Het
probably damaging
0.996
0.866
phenotype
07/21/2015
24
330270
Rad51ap1
0.000
R4464
G1
225
Y
6
126934768
N52S
T
C
missense
Het
possibly damaging
0.944
0.079
07/21/2015
25
330282
Rb1
1.000
R4464
G1
225
Y
14
73199198
C
A
splice site
Het
probably null
0.778
phenotype
07/21/2015
26
330266
Slc34a2
1.000
R4464
G1
225
Y
5
53069182
L490P
T
C
missense
Het
probably damaging
0.992
0.283
phenotype
07/21/2015
27
330279
Sost
0.171
R4464
G1
225
N
11
101966844
P44S
G
A
missense
Het
probably damaging
0.968
0.394
phenotype
07/21/2015
28
330273
St3gal2
0.000
R4464
G1
225
Y
8
110967502
N207D
A
G
missense
Het
probably benign
0.093
0.073
phenotype
07/21/2015
29
330256
Stat1
0.000
R4464
G1
225
Y
1
52137416
D257E
T
G
missense
Het
possibly damaging
0.520
0.290
phenotype
07/21/2015
30
330281
Tkt
1.000
R4464
G1
225
Y
14
30568274
T165A
A
G
missense
Het
possibly damaging
0.859
0.088
phenotype
07/21/2015
31
330272
Trim66
0.203
R4464
G1
225
Y
7
109477690
S347R
A
T
missense
Het
possibly damaging
0.511
0.080
07/21/2015
32
330280
Zfp429
0.079
R4464
G1
225
Y
13
67390498
I276V
T
C
missense
Het
probably benign
0.132
0.090
07/21/2015
[records 1 to 32 of 32]