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Incidental Mutations
46
incidental mutations are currently displayed, and affect
46
genes.
6
are Possibly Damaging.
14
are Probably Damaging.
16
are Probably Benign.
8
are Probably Null.
4
create premature stop codons.
3
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 46 of 46]
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
433417
Allc
0.068
R5469
G1
225
N
12
28555306
N331K
A
T
missense
Het
probably benign
0.002
phenotype
10/06/2016
2
433392
Anapc1
1.000
R5469
G1
225
N
2
128675701
S341*
G
T
nonsense
Het
probably null
phenotype
10/06/2016
3
433390
Cacna1e
0.139
R5469
G1
225
N
1
154443937
E1339G
T
C
missense
Het
probably damaging
1.000
phenotype
10/06/2016
4
501081
Cacna2d1
0.385
R5469
G1
225
N
5
16352678
I702N
T
A
missense
Het
probably damaging
0.988
phenotype
12/01/2017
5
433405
Casp2
0.447
R5469
G1
225
N
6
42269334
H209N
C
A
missense
Het
probably benign
0.005
phenotype
10/06/2016
6
433430
Casr
1.000
R5469
G1
225
N
16
36510030
V314A
A
G
missense
Het
probably benign
0.290
phenotype
10/06/2016
7
433395
Ccne2
0.000
R5469
G1
225
N
4
11201353
R294*
A
T
nonsense
Het
probably null
phenotype
10/06/2016
8
433420
Cd180
0.000
R5469
G1
225
N
13
102704834
H129Q
T
A
missense
Het
probably benign
0.374
phenotype
10/06/2016
9
433389
Chst10
0.219
R5469
G1
225
N
1
38865527
Y362N
A
T
missense
Het
probably damaging
1.000
phenotype
10/06/2016
10
433433
Ctnna1
1.000
R5469
G1
225
N
18
35239520
D509E
T
A
missense
Het
probably benign
0.003
phenotype
10/06/2016
11
433412
Ctsh
0.000
R5469
G1
225
N
9
90060511
G
T
critical splice donor site
1 bp
Het
probably null
phenotype
10/06/2016
12
433421
Dhx29
1.000
R5469
G1
225
N
13
112944539
A369V
C
T
missense
Het
possibly damaging
0.936
phenotype
10/06/2016
13
433426
Enox1
0.000
R5469
G1
225
N
14
77592974
T340A
A
G
missense
Het
probably benign
0.001
phenotype
10/06/2016
14
433428
Fam135b
0.000
R5469
G1
225
N
15
71446043
T1357S
T
A
missense
Het
probably benign
0.160
10/06/2016
15
433404
Flt3
0.000
R5469
G1
220
N
5
147355083
S544T
A
T
missense
Het
possibly damaging
0.633
phenotype
10/06/2016
16
433397
Gm12689
0.310
R5469
G1
225
N
4
99296165
I85T
T
C
missense
Het
unknown
0.087
10/06/2016
17
433400
Gsap
0.104
R5469
G1
195
N
5
21290544
Y831F
A
T
missense
Het
possibly damaging
0.917
phenotype
10/06/2016
18
433398
Hnrnpr
0.000
R5469
G1
225
N
4
136319434
T142M
C
T
missense
Het
probably damaging
1.000
phenotype
10/06/2016
19
433410
Jak3
0.721
R5469
G1
225
N
8
71678773
D94G
A
G
missense
Het
probably benign
0.000
0.090
phenotype
10/06/2016
20
433423
Ktn1
0.000
R5469
G1
225
N
14
47690920
E579D
A
T
missense
Het
probably damaging
0.999
phenotype
10/06/2016
21
433414
Lama2
0.356
R5469
G1
225
N
10
27041189
P2247S
G
A
missense
Het
possibly damaging
0.915
phenotype
10/06/2016
22
433394
Lrba
0.000
R5469
G1
225
N
3
86542641
S2089F
C
T
missense
Het
probably damaging
1.000
0.710
phenotype
10/06/2016
23
433419
Map1b
1.000
R5469
G1
225
N
13
99429338
V2292M
C
T
missense
Het
unknown
phenotype
10/06/2016
24
433408
Mphosph10
0.953
R5469
G1
225
N
7
64389445
A
T
critical splice donor site
2 bp
Het
probably null
phenotype
10/06/2016
25
501080
Pappa
0.766
R5469
G1
225
N
4
65205152
T908M
C
T
missense
Het
probably benign
0.006
phenotype
12/01/2017
26
433393
Pdcd10
1.000
R5469
G1
225
N
3
75521057
K150*
T
A
nonsense
Het
probably null
phenotype
10/06/2016
27
433434
Piezo2
1.000
R5469
G1
225
N
18
63027864
I2275N
A
T
missense
Het
probably damaging
0.999
phenotype
10/06/2016
28
501079
Pmvk
0.936
R5469
G1
194
N
3
89467682
T
C
critical splice donor site
2 bp
Het
probably null
phenotype
12/01/2017
29
433415
Pold2
1.000
R5469
G1
98
N
11
5873048
P376S
G
A
missense
Het
probably damaging
0.999
0.959
phenotype
10/06/2016
30
433411
Prtg
0.659
R5469
G1
225
N
9
72891965
Q759L
A
T
missense
Het
probably damaging
0.982
phenotype
10/06/2016
31
457921
Rad51ap1
0.000
R5469
G1
225
N
6
126928227
S107N
C
T
missense
Het
probably damaging
0.957
02/16/2017
32
433435
Rfk
1.000
R5469
G1
225
N
19
17395202
N29K
T
A
missense
Het
probably damaging
1.000
phenotype
10/06/2016
33
433418
Ror2
1.000
R5469
G1
120
N
13
53117339
M315V
T
C
missense
Het
probably benign
0.001
phenotype
10/06/2016
34
433429
Rrn3
1.000
R5469
G1
225
N
16
13813100
E600G
A
G
missense
Het
probably benign
0.008
phenotype
10/06/2016
35
433413
Ryk
1.000
R5469
G1
204
N
9
102906954
Y593C
A
G
missense
Het
possibly damaging
0.761
phenotype
10/06/2016
36
433401
Slc30a3
0.269
R5469
G1
225
N
5
31088660
D193V
T
A
missense
Het
probably damaging
1.000
phenotype
10/06/2016
37
433399
Slc35e2
0.000
R5469
G1
188
N
4
155610026
P10L
C
T
missense
Het
probably benign
0.000
0.090
10/06/2016
38
433432
Srbd1
0.962
R5469
G1
225
N
17
86119942
C421F
C
A
missense
Het
possibly damaging
0.768
10/06/2016
39
433431
Sstr5
0.213
R5469
G1
225
N
17
25492069
V62G
A
C
missense
Het
probably damaging
0.999
phenotype
10/06/2016
40
433402
Tfip11
0.970
R5469
G1
119
N
5
112334325
W483*
G
A
nonsense
Het
probably null
phenotype
10/06/2016
41
433391
Tlk1
0.000
R5469
G1
225
N
2
70721668
H553R
T
C
missense
Het
probably benign
0.146
phenotype
10/06/2016
42
433396
Tnc
0.000
R5469
G1
225
N
4
64013925
T
C
splice site
4 bp
Het
probably null
phenotype
10/06/2016
43
433424
Trav12-1
R5469
G1
225
N
14
53538473
T27A
A
G
missense
Het
probably damaging
0.970
10/06/2016
44
433436
Usp9y
0.064
R5469
G1
222
N
Y
1364714
T1033I
G
A
missense
Het
probably benign
0.011
phenotype
10/06/2016
45
433406
V1ra8
0.105
R5469
G1
225
N
6
90203204
H130Y
C
T
missense
Het
probably benign
0.004
10/06/2016
46
433409
Vmn2r77
0.083
R5469
G1
225
N
7
86802063
M386L
A
T
missense
Het
probably benign
0.013
10/06/2016
[records 1 to 46 of 46]