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Incidental Mutations
73
incidental mutations are currently displayed, and affect
72
genes.
14
are Possibly Damaging.
23
are Probably Damaging.
24
are Probably Benign.
10
are Probably Null.
4
create premature stop codons.
2
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
507660
4930504O13Rik
0.067
R6276
G1
225.01
Y
11
58446366 (GRCm38)
I94L
T
A
missense
Het
possibly damaging
0.511
0.179
2018-03-15
2
507640
4931406P16Rik
0.000
R6276
G1
141.01
Y
7
34242377 (GRCm38)
Y627*
A
T
nonsense
Het
probably null
0.976
2018-03-15
3
507615
Actr3
1.000
R6276
G1
225.01
Y
1
125395137 (GRCm38)
D364E
A
T
missense
Het
probably benign
0.000
0.058
phenotype
2018-03-15
4
507630
Adra2c
0.391
R6276
G1
148.01
Y
5
35280079 (GRCm38)
T65I
C
T
missense
Het
probably damaging
0.980
phenotype
2018-03-15
5
507657
Agap2
0.312
R6276
G1
225.01
Y
10
127089360 (GRCm38)
T
A
critical splice donor site
2 bp
Het
probably null
phenotype
2018-03-15
6
507678
Ager
0.098
R6276
G1
225.01
Y
17
34598754 (GRCm38)
V126A
T
C
missense
Het
possibly damaging
0.859
phenotype
2018-03-15
7
507673
Arhgap39
0.146
R6276
G1
225.01
Y
15
76737536 (GRCm38)
I288M
T
C
missense
Het
probably benign
0.058
0.090
2018-03-15
8
507655
Arhgap45
0.000
R6276
G1
225.01
Y
10
80026234 (GRCm38)
S541C
A
T
missense
Het
probably benign
0.252
0.083
2018-03-15
9
507634
Asb4
0.177
R6276
G1
225.01
Y
6
5431043 (GRCm38)
Y426C
A
G
missense
Het
probably damaging
1.000
0.293
phenotype
2018-03-15
10
507653
Azi2
0.103
R6276
G1
225.01
Y
9
118049338 (GRCm38)
T82I
C
T
missense
Het
probably damaging
0.965
0.066
phenotype
2018-03-15
11
507619
Baz2b
0.412
R6276
G1
225.01
Y
2
59948223 (GRCm38)
R764S
T
A
missense
Het
probably damaging
0.998
0.151
phenotype
2018-03-15
12
507628
Ccdc146
0.000
R6276
G1
225.01
Y
5
21301340 (GRCm38)
I701S
A
C
missense
Het
probably damaging
0.982
2018-03-15
13
507616
Cd55b
0.000
R6276
G1
225.01
Y
1
130418166 (GRCm38)
I172F
T
A
missense
Het
probably damaging
0.995
0.384
phenotype
2018-03-15
14
507627
Cdk11b
1.000
R6276
G1
225.01
Y
4
155634190 (GRCm38)
E199G
A
G
missense
Het
probably benign
0.112
0.095
phenotype
2018-03-15
15
507651
Cntnap4
0.079
R6276
G1
225.01
Y
8
112752289 (GRCm38)
T216S
A
T
missense
Het
possibly damaging
0.942
0.158
phenotype
2018-03-15
16
507631
D5Ertd579e
0.243
R6276
G1
225.01
Y
5
36604514 (GRCm38)
N1336K
A
T
missense
Het
possibly damaging
0.663
0.093
2018-03-15
17
507669
Dlg5
1.000
R6276
G1
91.01
Y
14
24164568 (GRCm38)
N649S
T
C
missense
Het
probably damaging
1.000
0.537
phenotype
2018-03-15
18
507685
Dmxl1
0.958
R6276
G1
225.01
Y
18
49846586 (GRCm38)
E96G
A
G
missense
Het
probably benign
0.000
0.060
phenotype
2018-03-15
19
507652
Dscaml1
0.602
R6276
G1
222.01
Y
9
45668160 (GRCm38)
T335I
C
T
missense
Het
possibly damaging
0.622
phenotype
2018-03-15
20
507654
Epb41l2
0.313
R6276
G1
225.01
Y
10
25502124 (GRCm38)
G695C
G
T
missense
Het
probably damaging
0.979
phenotype
2018-03-15
21
507614
Erbb4
1.000
R6276
G1
225.01
Y
1
68560576 (GRCm38)
R114H
C
T
missense
Het
probably damaging
1.000
0.647
phenotype
2018-03-15
22
507666
F2rl1
0.000
R6276
G1
225.01
Y
13
95513938 (GRCm38)
Y145*
G
T
nonsense
Het
probably null
phenotype
2018-03-15
23
507663
Fam58b
1.000
R6276
G1
225.01
Y
11
78751230 (GRCm38)
K145E
T
C
missense
Het
probably damaging
1.000
0.647
phenotype
2018-03-15
24
507620
Fsip2
0.076
R6276
G1
225.01
Y
2
82980441 (GRCm38)
Y2368F
A
T
missense
Het
possibly damaging
0.907
phenotype
2018-03-15
25
507648
Galnt7
0.719
R6276
G1
225.01
Y
8
57536578 (GRCm38)
C
T
splice site
5 bp
Het
probably null
0.976
phenotype
2018-03-15
26
507675
Gm6811
0.068
R6276
G1
225.01
Y
17
21093983 (GRCm38)
T
A
intron
Het
noncoding transcript
0.087
2018-03-15
27
507676
Gm6811
0.068
R6276
G1
225.01
Y
17
21094690 (GRCm38)
T
G
intron
Het
noncoding transcript
0.087
2018-03-15
28
507679
H2-M1
0.054
R6276
G1
225.01
Y
17
36671710 (GRCm38)
T86M
G
A
missense
Het
possibly damaging
0.794
2018-03-15
29
507636
Hk2
1.000
R6276
G1
225.01
Y
6
82743366 (GRCm38)
D170G
T
C
missense
Het
probably benign
0.049
0.231
phenotype
2018-03-15
30
507617
Hmcn1
0.000
R6276
G1
225.01
Y
1
150738681 (GRCm38)
A1325T
C
T
missense
Het
possibly damaging
0.688
0.188
phenotype
2018-03-15
31
507625
Insrr
0.329
R6276
G1
225.01
Y
3
87800519 (GRCm38)
Y89*
T
A
nonsense
Het
probably null
phenotype
2018-03-15
32
507668
Itga1
0.393
R6276
G1
221.01
Y
13
114980852 (GRCm38)
E871G
T
C
missense
Het
probably benign
0.000
0.090
phenotype
2018-03-15
33
507646
Kat6a
1.000
R6276
G1
225.01
Y
8
22939405 (GRCm38)
L1592P
T
C
missense
Het
possibly damaging
0.956
0.073
phenotype
2018-03-15
34
507645
Kndc1
0.000
R6276
G1
225.01
Y
7
139921063 (GRCm38)
A756E
C
A
missense
Het
probably benign
0.000
0.143
phenotype
2018-03-15
35
507664
Krt12
0.166
R6276
G1
225.01
Y
11
99421902 (GRCm38)
C105*
A
T
nonsense
Het
probably null
0.976
phenotype
2018-03-15
36
507680
Lama1
1.000
R6276
G1
156.01
Y
17
67784088 (GRCm38)
G
A
splice site
5 bp
Het
probably null
phenotype
2018-03-15
37
507681
Lama3
1.000
R6276
G1
225.01
Y
18
12506949 (GRCm38)
N67S
A
G
missense
Het
probably benign
0.024
0.090
phenotype
2018-03-15
38
507641
Lrrk1
1.000
R6276
G1
225.01
Y
7
66306839 (GRCm38)
A
G
splice site
6 bp
Het
probably null
0.976
phenotype
2018-03-15
39
507613
Map2
0.659
R6276
G1
225.01
Y
1
66399419 (GRCm38)
V34A
T
C
missense
Het
probably damaging
1.000
0.074
phenotype
2018-03-15
40
507672
Mroh6
0.103
R6276
G1
225.01
Y
15
75885700 (GRCm38)
L487P
A
G
missense
Het
probably damaging
0.993
0.179
2018-03-15
41
507632
Myo18b
1.000
R6276
G1
225.01
Y
5
112811642 (GRCm38)
S1430T
A
T
missense
Het
probably benign
0.311
phenotype
2018-03-15
42
507677
Notch3
0.000
R6276
G1
225.01
Y
17
32154749 (GRCm38)
T495I
G
A
missense
Het
probably benign
0.100
phenotype
2018-03-15
43
507661
Olfr391-ps
0.076
R6276
G1
225.01
Y
11
73799403 (GRCm38)
M118K
A
T
missense
Het
probably damaging
0.997
0.685
phenotype
2018-03-15
44
507649
Palld
1.000
R6276
G1
225.01
Y
8
61513423 (GRCm38)
A980T
C
T
missense
Het
probably damaging
1.000
0.148
phenotype
2018-03-15
45
507629
Paxip1
1.000
R6276
G1
225.01
Y
5
27761668 (GRCm38)
I620N
A
T
missense
Het
probably damaging
1.000
phenotype
2018-03-15
46
507682
Pcdha6
0.130
R6276
G1
225.01
Y
18
36969767 (GRCm38)
A
G
splice site
Het
probably null
0.611
phenotype
2018-03-15
47
507683
Pcdhb11
0.069
R6276
G1
225.01
Y
18
37421760 (GRCm38)
V48M
G
A
missense
Het
probably benign
0.363
0.090
2018-03-15
48
507684
Pcdhga6
0.122
R6276
G1
225.01
Y
18
37707644 (GRCm38)
E139G
A
G
missense
Het
probably benign
0.279
0.144
phenotype
2018-03-15
49
507622
Pck1
1.000
R6276
G1
225.01
Y
2
173157319 (GRCm38)
V426A
T
C
missense
Het
probably damaging
1.000
0.772
phenotype
2018-03-15
50
507671
Pck2
0.292
R6276
G1
225.01
Y
14
55542624 (GRCm38)
I110N
T
A
missense
Het
probably damaging
1.000
phenotype
2018-03-15
51
507633
Peg10
1.000
R6276
G1
149.47
Y
6
4756449 (GRCm38)
GAT
GATCAT
small insertion
Het
probably benign
0.090
phenotype
2018-03-15
52
507623
Phactr3
0.093
R6276
G1
197.01
Y
2
178279019 (GRCm38)
E222K
G
A
missense
Het
probably damaging
0.986
0.106
phenotype
2018-03-15
53
507621
Ppip5k1
0.473
R6276
G1
124.01
Y
2
121323203 (GRCm38)
A
T
unclassified
Het
probably benign
0.059
phenotype
2018-03-15
54
507639
Prodh2
0.151
R6276
G1
225.01
Y
7
30506651 (GRCm38)
H278R
A
G
missense
Het
probably benign
0.072
0.081
phenotype
2018-03-15
55
507650
Rspry1
0.477
R6276
G1
225.01
Y
8
94623258 (GRCm38)
H91Q
T
A
missense
Het
probably damaging
0.995
0.077
phenotype
2018-03-15
56
507662
Slc13a2
0.000
R6276
G1
217.47
Y
11
78403480 (GRCm38)
CGTTATCTGT
CGT
critical splice acceptor site
Het
probably benign
0.090
phenotype
2018-03-15
57
507667
Smn1
1.000
R6276
G1
225.01
Y
13
100127995 (GRCm38)
N78S
A
G
missense
Het
possibly damaging
0.658
0.099
phenotype
2018-03-15
58
507618
Spta1
0.826
R6276
G1
225.01
Y
1
174218512 (GRCm38)
I1614N
T
A
missense
Het
probably damaging
1.000
0.473
phenotype
2018-03-15
59
507644
Syt17
0.000
R6276
G1
225.01
Y
7
118434290 (GRCm38)
D165G
T
C
missense
Het
probably damaging
0.984
0.065
2018-03-15
60
507626
Tbck
0.324
R6276
G1
225.01
Y
3
132743005 (GRCm38)
Y593C
A
G
missense
Het
probably damaging
1.000
0.744
phenotype
2018-03-15
61
507635
Tcaf2
0.102
R6276
G1
225.01
Y
6
42629753 (GRCm38)
F422L
G
C
missense
Het
probably benign
0.038
0.090
2018-03-15
62
507647
Tex15
0.304
R6276
G1
225.01
Y
8
33577189 (GRCm38)
F2216I
T
A
missense
Het
possibly damaging
0.928
0.179
phenotype
2018-03-15
63
507624
Trpc4
0.207
R6276
G1
225.01
Y
3
54318020 (GRCm38)
E846G
A
G
missense
Het
probably benign
0.247
0.065
phenotype
2018-03-15
64
507656
Ttc41
0.146
R6276
G1
225.01
Y
10
86744449 (GRCm38)
I753T
T
C
missense
Het
probably benign
0.006
0.090
2018-03-15
65
507659
Vdac1
0.755
R6276
G1
225.01
Y
11
52376482 (GRCm38)
T70M
C
T
missense
Het
possibly damaging
0.843
0.455
phenotype
2018-03-15
66
507638
Vmn1r124
0.066
R6276
G1
191.01
N
7
21260179 (GRCm38)
F147V
A
C
missense
Het
probably benign
0.030
2018-03-15
67
507665
Vmn1r220
0.185
R6276
G1
225.01
Y
13
23184295 (GRCm38)
D77G
T
C
missense
Het
probably damaging
0.999
0.647
2018-03-15
68
507637
Vmn2r28
0.093
R6276
G1
225.01
Y
7
5490731 (GRCm38)
H72R
T
C
missense
Het
probably benign
0.015
0.090
2018-03-15
69
507643
Vmn2r78
0.067
R6276
G1
225.01
Y
7
86921110 (GRCm38)
I279L
A
T
missense
Het
probably benign
0.001
0.090
2018-03-15
70
507674
Vmn2r95
0.085
R6276
G1
225.01
Y
17
18451470 (GRCm38)
A490S
G
T
missense
Het
possibly damaging
0.956
0.179
2018-03-15
71
507670
Wdfy4
0.000
R6276
G1
225.01
Y
14
33109525 (GRCm38)
A915T
C
T
missense
Het
possibly damaging
0.544
2018-03-15
72
507658
Zmiz2
1.000
R6276
G1
162.01
N
11
6395604 (GRCm38)
G
T
splice site
Het
probably null
phenotype
2018-03-15
73
507642
Zscan2
0.000
R6276
G1
225.01
N
7
80875809 (GRCm38)
N426S
A
G
missense
Het
probably benign
0.000
phenotype
2018-03-15
[records 1 to 73 of 73]