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Incidental Mutations
73
incidental mutations are currently displayed, and affect
73
genes.
8
are Possibly Damaging.
31
are Probably Damaging.
27
are Probably Benign.
4
are Probably Null.
1
create premature stop codons.
3
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 73 of 73]
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
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
384548
3425401B19Rik
0.062
R4972
G1
225
Y
14
32661404 (GRCm38)
I868N
A
T
missense
Het
possibly damaging
0.734
0.179
2016-04-27
2
384489
A730013G03Rik
0.121
R4972
G1
146
Y
1
192833773 (GRCm38)
C
G
exon
Het
noncoding transcript
0.087
2016-04-27
3
384534
Actl11
0.074
R4972
G1
225
Y
9
107929956 (GRCm38)
T493A
A
G
missense
Het
probably benign
0.073
0.090
2016-04-27
4
384543
Actn1
0.466
R4972
G1
225
Y
12
80173039 (GRCm38)
D686G
T
C
missense
Het
probably benign
0.346
0.268
phenotype
2016-04-27
5
384552
Adamts1
0.000
R4972
G1
225
Y
16
85795945 (GRCm38)
T525I
G
A
missense
Het
probably damaging
1.000
0.202
phenotype
2016-04-27
6
384488
Adcy10
0.300
R4972
G1
225
Y
1
165556862 (GRCm38)
L1064H
T
A
missense
Het
probably damaging
1.000
0.647
phenotype
2016-04-27
7
384554
AI661453
0.064
R4972
G1
225
Y
17
47466399 (GRCm38)
A
T
intron
Het
probably benign
0.089
2016-04-27
8
384558
Apba1
0.000
R4972
G1
225
Y
19
23912536 (GRCm38)
S433T
T
A
missense
Het
probably benign
0.236
0.087
phenotype
2016-04-27
9
444548
Arid4b
1.000
R4972
G1
225
Y
13
14160272 (GRCm38)
N355K
T
A
missense
Het
probably benign
0.069
0.229
phenotype
2016-11-15
10
384535
Bsn
0.271
R4972
G1
225
Y
9
108115178 (GRCm38)
M1125K
A
T
missense
Het
probably damaging
0.998
0.256
phenotype
2016-04-27
11
384516
C2cd5
0.605
R4972
G1
187
Y
6
143013224 (GRCm38)
M1003K
A
T
missense
Het
probably damaging
0.987
0.316
2016-04-27
12
384511
Ccdc18
0.000
R4972
G1
154
Y
5
108192003 (GRCm38)
M805V
A
G
missense
Het
probably benign
0.000
0.090
2016-04-27
13
384518
Cep89
0.153
R4972
G1
178
N
7
35432552 (GRCm38)
L637R
T
G
missense
Het
probably damaging
1.000
2016-04-27
14
384502
Col24a1
0.000
R4972
G1
225
Y
3
145509684 (GRCm38)
I1444F
A
T
missense
Het
probably benign
0.418
0.089
phenotype
2016-04-27
15
384530
Commd4
0.374
R4972
G1
197
Y
9
57155448 (GRCm38)
S175T
A
T
missense
Het
probably benign
0.001
0.062
2016-04-27
16
384523
Coq7
1.000
R4972
G1
225
Y
7
118510117 (GRCm38)
V236A
A
G
missense
Het
unknown
0.087
phenotype
2016-04-27
17
444547
Dctn2
1.000
R4972
G1
225
Y
10
127276703 (GRCm38)
R176C
C
T
missense
Het
probably damaging
1.000
0.569
phenotype
2016-11-15
18
384492
Ddx31
0.888
R4972
G1
225
Y
2
28860770 (GRCm38)
F389L
T
C
missense
Het
probably damaging
1.000
0.125
phenotype
2016-04-27
19
384494
Dgkz
0.000
R4972
G1
197
Y
2
91945702 (GRCm38)
R72H
C
T
missense
Het
probably benign
0.002
0.099
phenotype
2016-04-27
20
384525
Dpysl4
0.092
R4972
G1
179
Y
7
139090290 (GRCm38)
D24G
A
G
missense
Het
probably damaging
1.000
0.972
phenotype
2016-04-27
21
384549
Dydc1
0.079
R4972
G1
225
Y
14
41082338 (GRCm38)
T106A
A
G
missense
Het
probably benign
0.060
0.090
phenotype
2016-04-27
22
384486
F13b
0.000
R4972
G1
225
Y
1
139510923 (GRCm38)
Y355C
A
G
missense
Het
probably damaging
1.000
0.635
phenotype
2016-04-27
23
384501
Fcrl5
0.051
R4972
G1
225
Y
3
87454650 (GRCm38)
M407V
A
G
missense
Het
probably benign
0.001
0.090
phenotype
2016-04-27
24
384484
Fzd5
1.000
R4972
G1
225
Y
1
64736012 (GRCm38)
V197L
C
A
missense
Het
probably benign
0.058
0.060
phenotype
2016-04-27
25
384544
Galnt16
0.085
R4972
G1
225
Y
12
80572329 (GRCm38)
E70*
G
T
nonsense
Het
probably null
0.976
2016-04-27
26
384521
Gm8979
0.110
R4972
G1
225
Y
7
106083314 (GRCm38)
T
C
exon
Het
noncoding transcript
0.087
2016-04-27
27
384500
Gpr171
0.051
R4972
G1
225
Y
3
59097965 (GRCm38)
F130I
A
T
missense
Het
probably damaging
1.000
0.406
2016-04-27
28
384505
Grin3a
0.000
R4972
G1
225
Y
4
49770484 (GRCm38)
N763D
T
C
missense
Het
probably damaging
0.999
0.652
phenotype
2016-04-27
29
384533
Gsta2
0.184
R4972
G1
225
N
9
78337679 (GRCm38)
M51K
A
T
missense
Het
probably damaging
0.977
2016-04-27
30
384531
Hacd3
0.114
R4972
G1
225
Y
9
64990436 (GRCm38)
I298N
A
T
missense
Het
probably damaging
0.985
0.630
2016-04-27
31
384482
Il18r1
0.000
R4972
G1
92
Y
1
40491064 (GRCm38)
P317L
C
T
missense
Het
probably benign
0.387
0.090
phenotype
2016-04-27
32
384513
Iscu
0.953
R4972
G1
196
Y
5
113776976 (GRCm38)
T
A
intron
Het
probably benign
0.090
phenotype
2016-04-27
33
384555
Kif6
0.099
R4972
G1
225
Y
17
49707619 (GRCm38)
D250G
A
G
missense
Het
probably damaging
1.000
0.855
phenotype
2016-04-27
34
384519
Klk14
0.000
R4972
G1
225
Y
7
43692077 (GRCm38)
C51Y
G
A
missense
Het
probably damaging
1.000
0.793
phenotype
2016-04-27
35
384491
Lcn6
0.081
R4972
G1
163
Y
2
25680067 (GRCm38)
C82S
T
A
missense
Het
probably damaging
1.000
0.851
phenotype
2016-04-27
36
384483
Mob4
0.961
R4972
G1
225
Y
1
55151002 (GRCm38)
L135V
C
G
missense
Het
possibly damaging
0.956
0.515
phenotype
2016-04-27
37
384528
Mpzl3
0.068
R4972
G1
151
Y
9
45062256 (GRCm38)
T
A
intron
Het
probably benign
phenotype
2016-04-27
38
384524
Mvp
0.000
R4972
G1
225
Y
7
126989798 (GRCm38)
D599G
T
C
missense
Het
probably damaging
0.988
0.311
phenotype
2016-04-27
39
384541
Myo1a
0.142
R4972
G1
225
Y
10
127716309 (GRCm38)
Y766H
T
C
missense
Het
probably benign
0.312
0.104
phenotype
2016-04-27
40
384556
Myo5b
0.780
R4972
G1
225
Y
18
74627193 (GRCm38)
H260R
A
G
missense
Het
probably damaging
0.984
0.944
phenotype
2016-04-27
41
384499
Nbea
1.000
R4972
G1
225
Y
3
56085246 (GRCm38)
R313H
C
T
missense
Het
probably damaging
0.993
0.174
phenotype
2016-04-27
42
384503
Necab1
0.127
R4972
G1
225
Y
4
14978216 (GRCm38)
D211V
T
A
missense
Het
probably damaging
0.995
0.140
2016-04-27
43
384550
Nefl
0.000
R4972
G1
225
Y
14
68086763 (GRCm38)
G
T
intron
Het
probably benign
0.072
phenotype
2016-04-27
44
384504
Nfx1
0.590
R4972
G1
225
Y
4
40976375 (GRCm38)
D16E
T
A
missense
Het
probably benign
0.361
0.061
phenotype
2016-04-27
45
384517
Nlrp9a
0.072
R4972
G1
225
Y
7
26570539 (GRCm38)
C797F
G
T
missense
Het
probably damaging
0.996
0.647
2016-04-27
46
384495
Olfr1280
0.255
R4972
G1
225
N
2
111315818 (GRCm38)
V113E
T
A
missense
Het
probably damaging
0.999
phenotype
2016-04-27
47
384522
Olfr467
0.076
R4972
G1
225
Y
7
107814746 (GRCm38)
Q56R
A
G
missense
Het
probably benign
0.101
0.090
phenotype
2016-04-27
48
384512
Pde6b
0.000
R4972
G1
225
Y
5
108425264 (GRCm38)
D500G
A
G
missense
Het
probably benign
0.001
0.070
phenotype
2016-04-27
49
384542
Pgs1
1.000
R4972
G1
148
Y
11
118005893 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
0.950
2016-04-27
50
384539
Polr3b
1.000
R4972
G1
225
Y
10
84638124 (GRCm38)
I189N
T
A
missense
Het
probably damaging
0.999
0.867
phenotype
2016-04-27
51
384546
Ppwd1
0.956
R4972
G1
225
Y
13
104220108 (GRCm38)
S300T
A
T
missense
Het
probably benign
0.002
0.058
2016-04-27
52
384545
Prl2c2
0.148
R4972
G1
225
Y
13
13002170 (GRCm38)
N55K
A
C
missense
Het
possibly damaging
0.742
0.179
2016-04-27
53
384557
Prpf19
1.000
R4972
G1
225
Y
19
10899345 (GRCm38)
C
T
intron
Het
probably benign
phenotype
2016-04-27
54
384553
Prph2
0.000
R4972
G1
225
Y
17
46910807 (GRCm38)
L37F
G
T
missense
Het
possibly damaging
0.940
0.179
phenotype
2016-04-27
55
384547
Ptprg
0.000
R4972
G1
225
Y
14
12226427 (GRCm38)
R565L
G
T
missense
Het
possibly damaging
0.937
0.179
phenotype
2016-04-27
56
384527
Rab8a
0.740
R4972
G1
225
Y
8
72171275 (GRCm38)
T74M
C
T
missense
Het
probably damaging
1.000
0.647
phenotype
2016-04-27
57
384538
Rexo1
0.339
R4972
G1
225
Y
10
80549693 (GRCm38)
F510L
A
T
missense
Het
probably damaging
0.962
0.082
2016-04-27
58
384529
Rexo2
1.000
R4972
G1
225
Y
9
48479389 (GRCm38)
T51K
G
T
missense
Het
probably damaging
1.000
0.962
phenotype
2016-04-27
59
384508
Sh3d21
0.095
R4972
G1
225
Y
4
126152416 (GRCm38)
K147R
T
C
missense
Het
possibly damaging
0.645
0.075
2016-04-27
60
384507
Skint6
0.053
R4972
G1
225
Y
4
112835068 (GRCm38)
I1062T
A
G
missense
Het
probably benign
0.000
0.090
2016-04-27
61
384485
Spag16
0.166
R4972
G1
225
Y
1
70724928 (GRCm38)
R636W
C
T
missense
Het
probably damaging
0.998
0.647
phenotype
2016-04-27
62
384498
Spata16
0.123
R4972
G1
225
Y
3
26840723 (GRCm38)
I307T
T
C
missense
Het
possibly damaging
0.931
0.280
phenotype
2016-04-27
63
384510
Speer4f2
0.140
R4972
G1
225
Y
5
17374425 (GRCm38)
I74S
T
G
missense
Het
probably benign
0.268
0.090
2016-04-27
64
384506
Svep1
1.000
R4972
G1
225
Y
4
58087778 (GRCm38)
Y1767F
T
A
missense
Het
possibly damaging
0.707
0.251
phenotype
2016-04-27
65
384487
Swt1
0.173
R4972
G1
222
Y
1
151423542 (GRCm38)
S7G
T
C
missense
Het
probably benign
0.215
0.090
2016-04-27
66
384532
Tex9
0.061
R4972
G1
135
Y
9
72478338 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
0.949
2016-04-27
67
444546
Thsd7b
0.121
R4972
G1
48
Y
1
130188572 (GRCm38)
P1354H
C
A
missense
Het
probably damaging
0.974
0.358
2016-11-15
68
384520
Ticrr
0.943
R4972
G1
225
Y
7
79669668 (GRCm38)
D467G
A
G
missense
Het
probably damaging
0.982
0.069
phenotype
2016-04-27
69
384496
Tmco5b
0.055
R4972
G1
225
Y
2
113296993 (GRCm38)
D303A
A
C
missense
Het
probably damaging
0.994
0.647
2016-04-27
70
384497
Trpm7
1.000
R4972
G1
225
Y
2
126824058 (GRCm38)
V876A
A
G
missense
Het
probably damaging
0.996
0.473
phenotype
2016-04-27
71
384536
Ttc21a
0.157
R4972
G1
225
Y
9
119944961 (GRCm38)
E245K
G
A
missense
Het
probably benign
0.002
0.073
2016-04-27
72
384540
Vezt
1.000
R4972
G1
217
Y
10
94000350 (GRCm38)
C
T
critical splice donor site
1 bp
Het
probably null
0.959
phenotype
2016-04-27
73
384509
Zscan20
0.290
R4972
G1
225
Y
4
128592359 (GRCm38)
P183S
G
A
missense
Het
probably benign
0.394
0.090
2016-04-27
[records 1 to 73 of 73]