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Incidental Mutations
32
incidental mutations are currently displayed, and affect
32
genes.
8
are Possibly Damaging.
11
are Probably Damaging.
10
are Probably Benign.
2
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 32 of 32]
10
25
50
100
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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
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
334272
Ascc3
0.966
R4522
G1
225
N
10
50660670
N700D
A
G
missense
Het
probably benign
0.000
0.069
phenotype
08/18/2015
2
334261
Babam2
0.826
R4522
G1
225
N
5
32007242
V287M
G
A
missense
Het
probably damaging
0.998
phenotype
08/18/2015
3
334273
Brip1
0.000
R4522
G1
225
N
11
86189801
I146M
T
C
missense
Het
possibly damaging
0.488
phenotype
08/18/2015
4
334253
Cacna1b
0.000
R4522
G1
225
N
2
24654430
R1248H
C
T
missense
Het
probably damaging
1.000
phenotype
08/18/2015
5
334275
Ccdc88c
0.000
R4522
G1
225
N
12
100913332
S1843R
G
T
missense
Het
possibly damaging
0.484
0.179
phenotype
08/18/2015
6
334277
Chaf1b
0.958
R4522
G1
225
N
16
93901295
A485T
G
A
missense
Het
probably benign
0.047
phenotype
08/18/2015
7
334260
Dock7
0.000
R4522
G1
225
N
4
98962224
R1594G
T
C
missense
Het
probably damaging
0.997
phenotype
08/18/2015
8
334282
Fam122c
0.000
R4522
G1
222
N
X
53293499
R94H
G
A
missense
Het
possibly damaging
0.944
0.179
08/18/2015
9
334263
Fbxo41
0.407
R4522
G1
170
N
6
85484042
I228T
A
G
missense
Het
probably damaging
0.999
0.256
phenotype
08/18/2015
10
334276
Gm3739
0.171
R4522
G1
92
N
14
7299398
K86*
T
A
nonsense
Het
probably null
0.976
08/18/2015
11
334283
Gm7173
0.098
R4522
G1
222
N
X
79509995
N291K
A
T
missense
Het
possibly damaging
0.633
0.127
08/18/2015
12
334280
Mark2
0.901
R4522
G1
225
N
19
7285948
D151E
A
T
missense
Het
probably damaging
1.000
phenotype
08/18/2015
13
334265
Nop2
0.971
R4522
G1
225
N
6
125133552
R47L
G
T
missense
Het
probably damaging
1.000
0.125
phenotype
08/18/2015
14
334269
Nwd1
0.220
R4522
G1
225
N
8
72670951
D606V
A
T
missense
Het
probably damaging
1.000
phenotype
08/18/2015
15
334256
Olfr1132
0.126
R4522
G1
225
N
2
87635151
I199L
T
A
missense
Het
probably benign
0.000
phenotype
08/18/2015
16
334264
Pcbp1
0.929
R4522
G1
225
N
6
86525050
N289S
T
C
missense
Het
probably benign
0.011
phenotype
08/18/2015
17
334281
Plce1
0.633
R4522
G1
225
N
19
38524319
S21P
T
C
missense
Het
possibly damaging
0.462
0.081
phenotype
08/18/2015
18
334247
Ptpn18
0.097
R4522
G1
225
N
1
34472960
L55P
T
C
missense
Het
probably benign
0.000
phenotype
08/18/2015
19
334274
Rpl10l
0.577
R4522
G1
225
N
12
66283738
D207G
T
C
missense
Het
probably benign
0.190
0.063
phenotype
08/18/2015
20
334248
Rufy4
0.256
R4522
G1
225
N
1
74147663
C537R
T
C
missense
Het
probably damaging
0.988
0.860
08/18/2015
21
334257
Sec23b
1.000
R4522
G1
225
N
2
144578366
I450N
T
A
missense
Het
possibly damaging
0.796
phenotype
08/18/2015
22
334249
Speg
1.000
R4522
G1
225
N
1
75428330
E2922G
A
G
missense
Het
probably damaging
1.000
phenotype
08/18/2015
23
500662
Spem1
0.145
R4522
G1
225
N
11
69821805
C
A
critical splice donor site
1 bp
Het
probably null
phenotype
12/01/2017
24
500663
Stxbp3-ps
0.297
R4522
G1
225
N
19
9559110
A
T
critical splice donor site
Het
noncoding transcript
12/01/2017
25
334268
Tmem38a
0.000
R4522
G1
186
N
8
72572161
P20S
C
T
missense
Het
possibly damaging
0.910
0.112
phenotype
08/18/2015
26
334270
Tmod2
0.000
R4522
G1
225
N
9
75592584
T129A
T
C
missense
Het
probably benign
0.101
phenotype
08/18/2015
27
334262
Ttc28
0.000
R4522
G1
205
N
5
111280172
T1845A
A
G
missense
Het
probably benign
0.012
08/18/2015
28
334267
Ubqlnl
0.143
R4522
G1
225
N
7
104149718
V191M
C
T
missense
Het
probably benign
0.003
0.090
phenotype
08/18/2015
29
334252
Ush2a
0.697
R4522
G1
225
N
1
188864625
T3854M
C
T
missense
Het
probably damaging
1.000
phenotype
08/18/2015
30
334266
Vmn2r72
0.083
R4522
G1
225
N
7
85751926
H95L
T
A
missense
Het
probably benign
0.440
0.090
08/18/2015
31
334279
Xdh
0.502
R4522
G1
225
N
17
73898344
G1042V
C
A
missense
Het
probably damaging
1.000
0.959
phenotype
08/18/2015
32
334271
Zfp105
0.149
R4522
G1
225
N
9
122930056
V264E
T
A
missense
Het
possibly damaging
0.878
phenotype
08/18/2015
[records 1 to 32 of 32]