Home
Phenotypic Mutations
Incidental Mutations
Engineered Mutations
Candidate Explorer
Protocols
Mutation Statistics
About
Contact
Links
Request Mice
Beutler Lab
APN
Strains @ MMRRC
Search Phenotypes
NEW
Candidate Explorer
Staff Login
Download
Incidental Mutations
30
incidental mutations are currently displayed, and affect
30
genes.
5
are Possibly Damaging.
14
are Probably Damaging.
7
are Probably Benign.
4
are Probably Null.
1
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 30 of 30]
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
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
260361
1700014D04Rik
0.050
R2882
G1
225
N
13
59742943
Q354H
C
A
missense
Het
probably benign
0.003
01/23/2015
2
260350
AF529169
0.000
R2882
G1
225
N
9
89602802
V181I
C
T
missense
Het
possibly damaging
0.857
01/23/2015
3
260341
Atp9a
0.000
R2882
G1
225
N
2
168706214
Y7C
T
C
missense
Het
probably damaging
1.000
01/23/2015
4
260360
Atxn3
0.000
R2882
G1
225
N
12
101937411
L178F
C
A
missense
Het
probably damaging
0.998
phenotype
01/23/2015
5
260358
Cep112
0.475
R2882
G1
225
N
11
108519212
S211P
T
C
missense
Het
possibly damaging
0.935
phenotype
01/23/2015
6
260352
Csl
0.642
R2882
G1
225
N
10
99758925
F93L
A
G
missense
Het
probably damaging
0.999
01/23/2015
7
260364
Cyp4f40
0.056
R2882
G1
225
N
17
32668073
I173V
A
G
missense
Het
probably benign
0.053
phenotype
01/23/2015
8
260339
Dcaf17
0.539
R2882
G1
225
N
2
71082027
I319V
A
G
missense
Het
possibly damaging
0.956
phenotype
01/23/2015
9
260362
Dock5
0.584
R2882
G1
225
N
14
67839620
Y258C
T
C
missense
Het
probably damaging
0.993
phenotype
01/23/2015
10
260336
Dpp10
0.000
R2882
G1
225
N
1
123445203
E236G
T
C
missense
Het
probably damaging
1.000
phenotype
01/23/2015
11
260342
Dpyd
0.000
R2882
G1
225
N
3
119065030
D631G
A
G
missense
Het
probably damaging
0.992
phenotype
01/23/2015
12
260354
Ewsr1
1.000
R2882
G1
225
N
11
5078523
C
A
unclassified
Het
probably benign
phenotype
01/23/2015
13
260356
Fat2
0.000
R2882
G1
225
N
11
55311305
L314F
C
A
missense
Het
probably damaging
0.965
phenotype
01/23/2015
14
260363
Gsdmc
0.050
R2882
G1
225
N
15
63779795
I259V
T
C
missense
Het
probably benign
0.241
01/23/2015
15
260348
Hydin
0.695
R2882
G1
225
N
8
110566923
L3501F
C
T
missense
Het
possibly damaging
0.921
phenotype
01/23/2015
16
260367
Kdm2a
0.965
R2882
G1
225
N
19
4331184
A
G
critical splice donor site
2 bp
Het
probably null
phenotype
01/23/2015
17
260345
Klra1
0.049
R2882
G1
225
N
6
130377863
A
T
splice site
Het
probably null
01/23/2015
18
260355
Kremen1
0.131
R2882
G1
157
N
11
5201791
CGGG
CGGGGGG
unclassified
Het
probably benign
phenotype
01/23/2015
19
260359
Mlh3
0.000
R2882
G1
225
N
12
85267566
H615Q
A
T
missense
Het
probably damaging
0.999
phenotype
01/23/2015
20
260349
Mmp12
0.163
R2882
G1
225
N
9
7358236
Y374C
A
G
missense
Het
probably damaging
1.000
phenotype
01/23/2015
21
260357
Mpp2
0.000
R2882
G1
225
N
11
102064633
E97G
T
C
missense
Het
probably benign
0.002
phenotype
01/23/2015
22
260344
Oasl2
0.000
R2882
G1
225
N
5
114911023
R175C
C
T
missense
Het
probably damaging
1.000
01/23/2015
23
260338
Olfr348
0.058
R2882
G1
225
N
2
36787190
I222F
A
T
missense
Het
probably damaging
0.998
phenotype
01/23/2015
24
260365
Pcdhac2
0.000
R2882
G1
225
N
18
37145812
Q615L
A
T
missense
Het
probably damaging
0.998
phenotype
01/23/2015
25
260353
Ppm1h
0.062
R2882
G1
225
N
10
122941334
Y502N
T
A
missense
Het
probably damaging
0.988
01/23/2015
26
260346
Slc5a11
0.064
R2882
G1
217
N
7
123239372
GGTGC
G
frame shift
Het
probably null
phenotype
01/23/2015
27
260347
Tex15
0.554
R2882
G1
225
N
8
33574907
L1455*
T
A
nonsense
Het
probably null
phenotype
01/23/2015
28
260340
Tgm6
0.000
R2882
G1
225
N
2
130137439
V163A
T
C
missense
Het
probably benign
0.036
phenotype
01/23/2015
29
260337
Tlr5
0.252
R2882
G1
225
N
1
182973893
T240M
C
T
missense
Het
probably damaging
0.996
phenotype
01/23/2015
30
260351
Washc4
0.891
R2882
G1
225
N
10
83579501
I785T
T
C
missense
Het
possibly damaging
0.931
phenotype
01/23/2015
[records 1 to 30 of 30]