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
61
incidental mutations are currently displayed, and affect
61
genes.
5
are Possibly Damaging.
26
are Probably Damaging.
19
are Probably Benign.
7
are Probably Null.
2
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 61 of 61]
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
351061
2010111I01Rik
0.093
R4616
G1
225
Y
13
63298751 (GRCm38)
E123K
G
A
missense
Het
probably damaging
1.000
0.403
phenotype
2015-10-08
2
351040
4931417E11Rik
0.102
R4616
G1
225
Y
6
73469269 (GRCm38)
V99A
A
G
missense
Het
probably benign
0.021
0.090
2015-10-08
3
351062
Acod1
0.000
R4616
G1
225
Y
14
103055345 (GRCm38)
T435M
C
T
missense
Het
probably benign
0.097
0.090
phenotype
2015-10-08
4
351069
Adgrf5
0.000
R4616
G1
225
Y
17
43452440 (GRCm38)
F1078L
T
C
missense
Het
probably benign
0.376
0.189
phenotype
2015-10-08
5
351031
Adh6a
0.129
R4616
G1
225
Y
3
138324947 (GRCm38)
N110I
A
T
missense
Het
probably damaging
1.000
0.872
2015-10-08
6
351043
Aldh16a1
0.000
R4616
G1
225
Y
7
45148788 (GRCm38)
T
C
intron
Het
probably benign
0.090
phenotype
2015-10-08
7
351045
Arhgef17
0.000
R4616
G1
225
Y
7
100882485 (GRCm38)
F1302S
A
G
missense
Het
probably damaging
0.999
0.933
2015-10-08
8
351051
Bcl2a1a
0.103
R4616
G1
225
Y
9
88957453 (GRCm38)
R135W
C
T
missense
Het
probably damaging
0.999
0.647
phenotype
2015-10-08
9
351023
Bpifa6
0.060
R4616
G1
225
Y
2
153982988 (GRCm38)
S28P
T
C
missense
Het
possibly damaging
0.473
0.179
2015-10-08
10
351063
C9
0.000
R4616
G1
225
Y
15
6491463 (GRCm38)
D51G
A
G
missense
Het
probably damaging
0.991
0.647
phenotype
2015-10-08
11
351068
Cfb
0.000
R4616
G1
225
Y
17
34859068 (GRCm38)
H962L
T
A
missense
Het
probably benign
0.287
0.090
phenotype
2015-10-08
12
351038
Chn2
0.172
R4616
G1
225
Y
6
54290403 (GRCm38)
M292I
G
A
missense
Het
probably damaging
0.997
0.110
phenotype
2015-10-08
13
351066
Clec16a
0.132
R4616
G1
225
Y
16
10644883 (GRCm38)
T
A
critical splice donor site
2 bp
Het
probably null
0.950
phenotype
2015-10-08
14
351049
Cyp1a1
0.096
R4616
G1
225
Y
9
57701756 (GRCm38)
S307P
T
C
missense
Het
probably benign
0.091
0.127
phenotype
2015-10-08
15
351072
Dsg3
0.470
R4616
G1
225
Y
18
20531559 (GRCm38)
V538A
T
C
missense
Het
probably benign
0.000
0.090
phenotype
2015-10-08
16
351053
Erbb3
1.000
R4616
G1
225
Y
10
128572770 (GRCm38)
Q815*
G
A
nonsense
Het
probably null
0.975
phenotype
2015-10-08
17
351048
Fam90a1a
0.082
R4616
G1
216
Y
8
21963846 (GRCm38)
Q406K
C
A
missense
Het
possibly damaging
0.483
0.179
2015-10-08
18
351033
Frmd3
0.367
R4616
G1
225
Y
4
74187872 (GRCm38)
V585A
T
C
missense
Het
probably benign
0.149
0.102
phenotype
2015-10-08
19
351078
Gm7102
0.133
R4616
G1
225
Y
19
61175926 (GRCm38)
G24R
C
T
missense
Het
unknown
0.109
2015-10-08
20
351020
Gm8214
0.228
R4616
G1
225
Y
1
183681897 (GRCm38)
T
C
exon
Het
noncoding transcript
0.087
2015-10-08
21
351060
Gpld1
0.000
R4616
G1
225
Y
13
24984816 (GRCm38)
G771D
G
A
missense
Het
probably damaging
1.000
0.266
phenotype
2015-10-08
22
351064
Gpr20
0.000
R4616
G1
225
Y
15
73695736 (GRCm38)
N268S
T
C
missense
Het
probably benign
0.000
0.090
2015-10-08
23
351027
Gria2
0.482
R4616
G1
225
Y
3
80706897 (GRCm38)
I612N
A
T
missense
Het
probably damaging
0.998
0.874
phenotype
2015-10-08
24
351076
Ifit1bl1
0.000
R4616
G1
135
Y
19
34594610 (GRCm38)
E149G
T
C
missense
Het
probably damaging
1.000
0.832
2015-10-08
25
351058
Ighv1-82
0.213
R4616
G1
225
Y
12
115952660 (GRCm38)
T77A
T
C
missense
Het
probably benign
0.057
0.090
2015-10-08
26
351057
Ighv2-9
0.125
R4616
G1
225
Y
12
113879219 (GRCm38)
T76K
G
T
missense
Het
probably damaging
0.991
0.647
2015-10-08
27
470265
Igkv6-13
0.103
R4616
G1
225
N
6
70458035 (GRCm38)
M1K
A
T
start codon destroyed
Het
probably null
0.948
2017-03-08
28
351039
Igkv8-21
0.143
R4616
G1
225
Y
6
70315157 (GRCm38)
S34T
A
T
missense
Het
probably benign
0.051
0.090
2015-10-08
29
386331
Itpr1
0.857
R4616
G1
225
Y
6
108481223 (GRCm38)
N1985D
A
G
missense
Het
probably damaging
0.997
0.489
phenotype
2016-05-11
30
351071
Lama3
1.000
R4616
G1
225
Y
18
12504397 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
0.948
phenotype
2015-10-08
31
351019
Lamc2
0.707
R4616
G1
225
Y
1
153166169 (GRCm38)
Y73C
T
C
missense
Het
probably damaging
1.000
0.693
phenotype
2015-10-08
32
386333
Maff
0.000
R4616
G1
54
Y
15
79357698 (GRCm38)
D105G
A
G
missense
Het
probably damaging
0.998
0.949
phenotype
2016-05-11
33
351070
Mep1a
0.000
R4616
G1
225
Y
17
43486241 (GRCm38)
V312M
C
T
missense
Het
possibly damaging
0.807
0.200
phenotype
2015-10-08
34
351054
Mfap4
0.000
R4616
G1
174
Y
11
61485509 (GRCm38)
C
A
unclassified
Het
probably benign
0.090
phenotype
2015-10-08
35
351025
Mrgbp
0.629
R4616
G1
225
Y
2
180585314 (GRCm38)
A
T
synonymous
Het
silent
2015-10-08
36
386332
Mtmr4
0.172
R4616
G1
225
Y
11
87610935 (GRCm38)
L548S
T
C
missense
Het
probably damaging
0.992
0.063
2016-05-11
37
351073
Myo7b
0.000
R4616
G1
225
Y
18
32003487 (GRCm38)
T
C
splice site
4 bp
Het
probably null
0.976
phenotype
2015-10-08
38
351050
Myo9a
0.000
R4616
G1
225
Y
9
59821649 (GRCm38)
I596T
T
C
missense
Het
probably damaging
1.000
0.792
phenotype
2015-10-08
39
351037
Olfr38
0.077
R4616
G1
225
Y
6
42762418 (GRCm38)
R122L
G
T
missense
Het
probably benign
0.066
0.220
phenotype
2015-10-08
40
351046
Olfr594
0.084
R4616
G1
225
Y
7
103220422 (GRCm38)
R235*
C
T
nonsense
Het
probably null
0.976
phenotype
2015-10-08
41
351075
Pcsk5
1.000
R4616
G1
225
Y
19
17560750 (GRCm38)
Q904H
T
G
missense
Het
probably benign
0.001
0.162
phenotype
2015-10-08
42
351041
Pdzrn3
0.771
R4616
G1
225
Y
6
101152009 (GRCm38)
H565Q
G
T
missense
Het
probably damaging
0.994
0.074
phenotype
2015-10-08
43
351047
Phkg2
0.582
R4616
G1
225
Y
7
127577620 (GRCm38)
R61W
C
T
missense
Het
probably damaging
0.999
0.282
phenotype
2015-10-08
44
351077
Pkd2l1
0.091
R4616
G1
225
Y
19
44154134 (GRCm38)
A490S
C
A
missense
Het
probably damaging
0.991
0.421
phenotype
2015-10-08
45
351034
Pomgnt1
0.000
R4616
G1
225
Y
4
116154890 (GRCm38)
I337N
T
A
missense
Het
probably damaging
1.000
0.929
phenotype
2015-10-08
46
351055
Psmd3
0.948
R4616
G1
192
Y
11
98682926 (GRCm38)
V66A
T
C
missense
Het
probably benign
0.003
0.062
phenotype
2015-10-08
47
351032
Ptger3
0.060
R4616
G1
213
Y
3
157567294 (GRCm38)
S93P
T
C
missense
Het
probably damaging
0.997
0.732
phenotype
2015-10-08
48
351074
Rbm27
0.000
R4616
G1
225
Y
18
42301775 (GRCm38)
D301E
T
A
missense
Het
probably damaging
0.964
0.481
2015-10-08
49
351052
Rdh16
0.000
R4616
G1
225
Y
10
127801513 (GRCm38)
A
T
splice site
3 bp
Het
probably null
0.976
2015-10-08
50
351067
Slc35a5
0.119
R4616
G1
225
Y
16
45144292 (GRCm38)
F193I
A
T
missense
Het
probably benign
0.124
0.071
phenotype
2015-10-08
51
351036
Slc4a4
1.000
R4616
G1
225
Y
5
89038561 (GRCm38)
K167R
A
G
missense
Het
probably damaging
0.999
0.089
phenotype
2015-10-08
52
351029
Sort1
0.791
R4616
G1
225
Y
3
108355541 (GRCm38)
T772S
A
T
missense
Het
possibly damaging
0.659
0.179
phenotype
2015-10-08
53
351022
Sptbn5
0.272
R4616
G1
203
Y
2
120048757 (GRCm38)
T
A
exon
Het
noncoding transcript
2015-10-08
54
351044
Stard5
0.000
R4616
G1
225
Y
7
83633281 (GRCm38)
G
T
intron
Het
probably benign
phenotype
2015-10-08
55
351065
Tbc1d22a
0.000
R4616
G1
225
Y
15
86235685 (GRCm38)
T61A
A
G
missense
Het
probably damaging
1.000
0.185
2015-10-08
56
351024
Tox2
0.000
R4616
G1
225
N
2
163320647 (GRCm38)
L479P
T
C
missense
Het
probably damaging
1.000
0.426
2015-10-08
57
351030
Usp53
0.233
R4616
G1
225
Y
3
122959120 (GRCm38)
M80K
A
T
missense
Het
probably damaging
0.996
0.222
phenotype
2015-10-08
58
351059
Vmn1r209
0.124
R4616
G1
225
Y
13
22805965 (GRCm38)
L185Q
A
T
missense
Het
probably damaging
0.998
0.647
2015-10-08
59
351042
Vmn2r59
0.066
R4616
G1
225
Y
7
42012438 (GRCm38)
I651T
A
G
missense
Het
probably benign
0.000
0.090
2015-10-08
60
351079
Vsig1
0.062
R4616
G1
222
Y
X
140926386 (GRCm38)
A95S
G
T
missense
Het
probably benign
0.011
0.090
phenotype
2015-10-08
61
351026
Zfhx4
0.622
R4616
G1
225
Y
3
5413067 (GRCm38)
S3556P
T
C
missense
Het
possibly damaging
0.659
0.060
2015-10-08
[records 1 to 61 of 61]