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Incidental Mutations
53
incidental mutations are currently displayed, and affect
53
genes.
11
are Possibly Damaging.
18
are Probably Damaging.
15
are Probably Benign.
5
are Probably Null.
2
create premature stop codons.
3
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 53 of 53]
10
25
50
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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
396740
0610010F05Rik
0.150
R5156
G1
225
Y
11
23593424
A
G
critical splice donor site
2 bp
Het
probably null
0.949
06/21/2016
2
396752
4921513D11Rik
0.525
R5156
G1
225
N
17
79628209
G
T
intron
Het
probably benign
06/21/2016
3
396736
Apeh
0.000
R5156
G1
225
Y
9
108094287
A29T
C
T
missense
Het
probably damaging
0.999
0.357
phenotype
06/21/2016
4
396721
Arap2
0.000
R5156
G1
225
Y
5
62669181
Y1013*
A
T
nonsense
Het
probably null
0.976
phenotype
06/21/2016
5
396706
Arhgef4
0.000
R5156
G1
225
Y
1
34723274
E537G
A
G
missense
Het
unknown
0.119
phenotype
06/21/2016
6
396734
Asf1b
0.000
R5156
G1
183
Y
8
83955911
F28S
T
C
missense
Het
probably damaging
0.999
0.960
phenotype
06/21/2016
7
396709
Cd46
0.000
R5156
G1
225
Y
1
195085385
I123L
T
A
missense
Het
possibly damaging
0.902
0.179
phenotype
06/21/2016
8
470607
Cdca7
0.144
R5156
G1
225
Y
2
72479026
T48S
A
T
missense
Het
probably damaging
0.996
0.074
phenotype
03/23/2017
9
396753
Cfap53
0.123
R5156
G1
225
Y
18
74359767
T
A
utr 3 prime
Het
probably benign
0.090
phenotype
06/21/2016
10
396719
Clca3a2
0.084
R5156
G1
225
Y
3
144805838
T599S
T
A
missense
Het
probably benign
0.262
0.090
06/21/2016
11
396718
Csf1
0.686
R5156
G1
225
Y
3
107748936
T148S
T
A
missense
Het
probably benign
0.006
0.090
phenotype
06/21/2016
12
396732
Dmbt1
0.266
R5156
G1
225
Y
7
131097670
T
C
critical splice donor site
2 bp
Het
probably null
0.949
phenotype
06/21/2016
13
396728
Dmpk
0.382
R5156
G1
225
N
7
19084125
D44G
A
G
missense
Het
probably damaging
0.999
phenotype
06/21/2016
14
396738
Dnajb12
0.062
R5156
G1
225
Y
10
59892960
N223K
T
A
missense
Het
probably damaging
0.999
0.647
phenotype
06/21/2016
15
396745
Dync1h1
1.000
R5156
G1
225
Y
12
110628830
M1392K
T
A
missense
Het
probably benign
0.001
0.072
phenotype
06/21/2016
16
396733
Edrf1
0.641
R5156
G1
225
Y
7
133660179
A867V
C
T
missense
Het
probably damaging
1.000
0.300
phenotype
06/21/2016
17
396754
Efemp2
1.000
R5156
G1
225
Y
19
5477678
C94S
T
A
missense
Het
possibly damaging
0.931
0.966
phenotype
06/21/2016
18
396720
Epha8
0.000
R5156
G1
225
Y
4
136938726
S373N
C
T
missense
Het
probably benign
0.139
0.089
phenotype
06/21/2016
19
396725
Foxk1
0.667
R5156
G1
211
Y
5
142448833
D284G
A
G
missense
Het
possibly damaging
0.876
0.094
phenotype
06/21/2016
20
396724
Fzd10
0.000
R5156
G1
225
Y
5
128601302
R29S
C
A
missense
Het
possibly damaging
0.679
0.103
phenotype
06/21/2016
21
396712
Gm13991
0.117
R5156
G1
225
Y
2
116528184
T
C
exon
Het
noncoding transcript
0.435
06/21/2016
22
396730
Gm6818
0.173
R5156
G1
225
Y
7
38402047
A
T
exon
Het
noncoding transcript
06/21/2016
23
396735
Hydin
0.678
R5156
G1
225
Y
8
110609701
C5037S
T
A
missense
Het
probably benign
0.003
0.090
phenotype
06/21/2016
24
396739
Ikzf1
0.000
R5156
G1
225
Y
11
11769448
M492K
T
A
missense
Het
probably damaging
0.999
0.963
phenotype
06/21/2016
25
396743
Krt20
0.080
R5156
G1
225
Y
11
99430053
S394R
G
T
missense
Het
possibly damaging
0.917
0.086
phenotype
06/21/2016
26
396716
Lrrc71
0.000
R5156
G1
225
Y
3
87745787
R107S
T
A
missense
Het
probably benign
0.073
0.090
06/21/2016
27
396744
Mia2
0.959
R5156
G1
225
Y
12
59172537
T436A
A
G
missense
Het
possibly damaging
0.944
0.179
phenotype
06/21/2016
28
396750
Muc19
0.144
R5156
G1
225
Y
15
91900420
T
A
exon
Het
noncoding transcript
0.087
phenotype
06/21/2016
29
396708
Neu4
0.000
R5156
G1
225
Y
1
94024455
V182A
T
C
missense
Het
probably damaging
0.999
0.456
phenotype
06/21/2016
30
396717
Notch2
1.000
R5156
G1
225
Y
3
98124310
F1167V
T
G
missense
Het
possibly damaging
0.529
0.095
phenotype
06/21/2016
31
396756
Nrap
0.000
R5156
G1
225
Y
19
56371845
M189T
A
G
missense
Het
possibly damaging
0.938
0.123
06/21/2016
32
396741
Nt5m
0.068
R5156
G1
174
Y
11
59874661
I172F
A
T
missense
Het
probably damaging
0.996
0.359
phenotype
06/21/2016
33
396711
Olfr1138
0.114
R5156
G1
225
Y
2
87737775
P183L
G
A
missense
Het
possibly damaging
0.946
0.408
phenotype
06/21/2016
34
396755
Olfr1474
0.071
R5156
G1
225
Y
19
13471673
K234N
G
T
missense
Het
probably damaging
1.000
0.647
phenotype
06/21/2016
35
396710
Olfr228
0.139
R5156
G1
225
Y
2
86483018
C241*
A
T
nonsense
Het
probably null
0.972
phenotype
06/21/2016
36
396727
Plekha5
0.171
R5156
G1
225
Y
6
140426528
T68M
C
T
missense
Het
probably damaging
1.000
0.647
06/21/2016
37
470608
Ppef2
0.000
R5156
G1
225
Y
5
92244602
A
G
critical splice donor site
2 bp
Het
probably null
phenotype
03/23/2017
38
396729
Ppp1r37
0.214
R5156
G1
90
N
7
19561975
T
C
unclassified
Het
probably benign
06/21/2016
39
470609
Rfx4
1.000
R5156
G1
225
Y
10
84868354
Y238H
T
C
missense
Het
probably damaging
0.999
0.080
phenotype
03/23/2017
40
396726
Sec13
0.957
R5156
G1
225
Y
6
113730876
A161V
G
A
missense
Het
probably benign
0.048
0.183
phenotype
06/21/2016
41
396749
Serhl
0.059
R5156
G1
225
Y
15
83102694
G
A
unclassified
Het
probably benign
06/21/2016
42
396714
Slco4a1
0.131
R5156
G1
225
Y
2
180472779
V588A
T
C
missense
Het
probably benign
0.013
0.090
06/21/2016
43
396715
Slitrk3
0.735
R5156
G1
225
Y
3
73049259
T727A
T
C
missense
Het
probably benign
0.000
0.063
phenotype
06/21/2016
44
470606
Sp100
0.201
R5156
G1
225
Y
1
85673683
D241E
T
A
missense
Het
probably damaging
1.000
0.078
03/23/2017
45
396713
Spata2
0.000
R5156
G1
225
Y
2
167483574
H442N
G
T
missense
Het
probably damaging
0.961
0.083
phenotype
06/21/2016
46
396707
Speg
1.000
R5156
G1
225
Y
1
75428087
V2588A
T
C
missense
Het
probably damaging
0.987
0.063
phenotype
06/21/2016
47
396742
Tnfsf12
0.155
R5156
G1
225
Y
11
69687329
S141P
A
G
missense
Het
probably damaging
1.000
0.663
phenotype
06/21/2016
48
396737
Trank1
0.000
R5156
G1
225
Y
9
111390694
I2166M
A
G
missense
Het
probably damaging
0.998
0.068
06/21/2016
49
396751
Trim10
0.093
R5156
G1
225
Y
17
36877056
V388E
T
A
missense
Het
probably damaging
0.990
0.799
phenotype
06/21/2016
50
396748
Ttc23l
0.072
R5156
G1
225
Y
15
10551550
T30K
G
T
missense
Het
possibly damaging
0.955
0.153
06/21/2016
51
396723
Vmn2r10
0.076
R5156
G1
225
Y
5
108995600
V828A
A
G
missense
Het
probably benign
0.112
0.090
06/21/2016
52
396731
Vmn2r75
0.063
R5156
G1
225
Y
7
86164228
L455F
T
A
missense
Het
possibly damaging
0.510
0.179
06/21/2016
53
396747
Vwa8
0.000
R5156
G1
225
Y
14
78984226
S541T
T
A
missense
Het
probably benign
0.003
0.084
06/21/2016
[records 1 to 53 of 53]