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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
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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
396740
0610010F05Rik
0.122
R5156
G1
225
Y
11
23593424 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
0.949
2016-06-21
2
396752
4921513D11Rik
0.469
R5156
G1
225
N
17
79628209 (GRCm38)
G
T
intron
Het
probably benign
2016-06-21
3
396736
Apeh
0.000
R5156
G1
225
Y
9
108094287 (GRCm38)
A29T
C
T
missense
Het
probably damaging
0.999
0.357
phenotype
2016-06-21
4
396721
Arap2
0.000
R5156
G1
225
Y
5
62669181 (GRCm38)
Y1013*
A
T
nonsense
Het
probably null
0.976
phenotype
2016-06-21
5
396706
Arhgef4
0.000
R5156
G1
225
Y
1
34723274 (GRCm38)
E537G
A
G
missense
Het
unknown
0.119
phenotype
2016-06-21
6
396734
Asf1b
0.000
R5156
G1
183
Y
8
83955911 (GRCm38)
F28S
T
C
missense
Het
probably damaging
0.999
0.960
phenotype
2016-06-21
7
396709
Cd46
0.000
R5156
G1
225
Y
1
195085385 (GRCm38)
I123L
T
A
missense
Het
possibly damaging
0.902
0.179
phenotype
2016-06-21
8
470607
Cdca7
0.129
R5156
G1
225
Y
2
72479026 (GRCm38)
T48S
A
T
missense
Het
probably damaging
0.996
0.074
phenotype
2017-03-23
9
396753
Cfap53
0.077
R5156
G1
225
Y
18
74359767 (GRCm38)
T
A
utr 3 prime
Het
probably benign
0.090
phenotype
2016-06-21
10
396719
Clca3a2
0.073
R5156
G1
225
Y
3
144805838 (GRCm38)
T599S
T
A
missense
Het
probably benign
0.262
0.090
2016-06-21
11
396718
Csf1
0.715
R5156
G1
225
Y
3
107748936 (GRCm38)
T148S
T
A
missense
Het
probably benign
0.006
0.090
phenotype
2016-06-21
12
396732
Dmbt1
0.338
R5156
G1
225
Y
7
131097670 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
0.949
phenotype
2016-06-21
13
396728
Dmpk
0.576
R5156
G1
225
N
7
19084125 (GRCm38)
D44G
A
G
missense
Het
probably damaging
0.999
phenotype
2016-06-21
14
396738
Dnajb12
0.065
R5156
G1
225
Y
10
59892960 (GRCm38)
N223K
T
A
missense
Het
probably damaging
0.999
0.647
phenotype
2016-06-21
15
396745
Dync1h1
1.000
R5156
G1
225
Y
12
110628830 (GRCm38)
M1392K
T
A
missense
Het
probably benign
0.001
0.072
phenotype
2016-06-21
16
396733
Edrf1
0.603
R5156
G1
225
Y
7
133660179 (GRCm38)
A867V
C
T
missense
Het
probably damaging
1.000
0.300
phenotype
2016-06-21
17
396754
Efemp2
1.000
R5156
G1
225
Y
19
5477678 (GRCm38)
C94S
T
A
missense
Het
possibly damaging
0.931
0.966
phenotype
2016-06-21
18
396720
Epha8
0.000
R5156
G1
225
Y
4
136938726 (GRCm38)
S373N
C
T
missense
Het
probably benign
0.139
0.089
phenotype
2016-06-21
19
396725
Foxk1
0.551
R5156
G1
211
Y
5
142448833 (GRCm38)
D284G
A
G
missense
Het
possibly damaging
0.876
0.094
phenotype
2016-06-21
20
396724
Fzd10
0.000
R5156
G1
225
Y
5
128601302 (GRCm38)
R29S
C
A
missense
Het
possibly damaging
0.679
0.103
phenotype
2016-06-21
21
396712
Gm13991
0.103
R5156
G1
225
Y
2
116528184 (GRCm38)
T
C
exon
Het
noncoding transcript
0.435
2016-06-21
22
396730
Gm6818
0.141
R5156
G1
225
Y
7
38402047 (GRCm38)
A
T
exon
Het
noncoding transcript
2016-06-21
23
396735
Hydin
0.835
R5156
G1
225
Y
8
110609701 (GRCm38)
C5037S
T
A
missense
Het
probably benign
0.003
0.090
phenotype
2016-06-21
24
396739
Ikzf1
0.000
R5156
G1
225
Y
11
11769448 (GRCm38)
M492K
T
A
missense
Het
probably damaging
0.999
0.963
phenotype
2016-06-21
25
396743
Krt20
0.067
R5156
G1
225
Y
11
99430053 (GRCm38)
S394R
G
T
missense
Het
possibly damaging
0.917
0.086
phenotype
2016-06-21
26
396716
Lrrc71
0.000
R5156
G1
225
Y
3
87745787 (GRCm38)
R107S
T
A
missense
Het
probably benign
0.073
0.090
2016-06-21
27
396744
Mia2
0.948
R5156
G1
225
Y
12
59172537 (GRCm38)
T436A
A
G
missense
Het
possibly damaging
0.944
0.179
phenotype
2016-06-21
28
396750
Muc19
0.280
R5156
G1
225
Y
15
91900420 (GRCm38)
T
A
exon
Het
noncoding transcript
0.087
phenotype
2016-06-21
29
396708
Neu4
0.000
R5156
G1
225
Y
1
94024455 (GRCm38)
V182A
T
C
missense
Het
probably damaging
0.999
0.456
phenotype
2016-06-21
30
396717
Notch2
1.000
R5156
G1
225
Y
3
98124310 (GRCm38)
F1167V
T
G
missense
Het
possibly damaging
0.529
0.095
phenotype
2016-06-21
31
396756
Nrap
0.000
R5156
G1
225
Y
19
56371845 (GRCm38)
M189T
A
G
missense
Het
possibly damaging
0.938
0.123
2016-06-21
32
396741
Nt5m
0.079
R5156
G1
174
Y
11
59874661 (GRCm38)
I172F
A
T
missense
Het
probably damaging
0.996
0.359
phenotype
2016-06-21
33
396711
Olfr1138
0.086
R5156
G1
225
Y
2
87737775 (GRCm38)
P183L
G
A
missense
Het
possibly damaging
0.946
0.408
phenotype
2016-06-21
34
396755
Olfr1474
0.068
R5156
G1
225
Y
19
13471673 (GRCm38)
K234N
G
T
missense
Het
probably damaging
1.000
0.647
phenotype
2016-06-21
35
396710
Olfr228
0.139
R5156
G1
225
Y
2
86483018 (GRCm38)
C241*
A
T
nonsense
Het
probably null
0.972
phenotype
2016-06-21
36
396727
Plekha5
0.217
R5156
G1
225
Y
6
140426528 (GRCm38)
T68M
C
T
missense
Het
probably damaging
1.000
0.647
2016-06-21
37
470608
Ppef2
0.000
R5156
G1
225
Y
5
92244602 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
phenotype
2017-03-23
38
396729
Ppp1r37
0.207
R5156
G1
90
N
7
19561975 (GRCm38)
T
C
unclassified
Het
probably benign
2016-06-21
39
470609
Rfx4
1.000
R5156
G1
225
Y
10
84868354 (GRCm38)
Y238H
T
C
missense
Het
probably damaging
0.999
0.080
phenotype
2017-03-23
40
396726
Sec13
0.959
R5156
G1
225
Y
6
113730876 (GRCm38)
A161V
G
A
missense
Het
probably benign
0.048
0.183
phenotype
2016-06-21
41
396749
Serhl
0.060
R5156
G1
225
Y
15
83102694 (GRCm38)
G
A
unclassified
Het
probably benign
0.085
2016-06-21
42
396714
Slco4a1
0.221
R5156
G1
225
Y
2
180472779 (GRCm38)
V588A
T
C
missense
Het
probably benign
0.013
0.090
2016-06-21
43
396715
Slitrk3
0.622
R5156
G1
225
Y
3
73049259 (GRCm38)
T727A
T
C
missense
Het
probably benign
0.000
0.063
phenotype
2016-06-21
44
470606
Sp100
0.236
R5156
G1
225
Y
1
85673683 (GRCm38)
D241E
T
A
missense
Het
probably damaging
1.000
0.078
2017-03-23
45
396713
Spata2
0.000
R5156
G1
225
Y
2
167483574 (GRCm38)
H442N
G
T
missense
Het
probably damaging
0.961
0.083
phenotype
2016-06-21
46
396707
Speg
1.000
R5156
G1
225
Y
1
75428087 (GRCm38)
V2588A
T
C
missense
Het
probably damaging
0.987
0.063
phenotype
2016-06-21
47
396742
Tnfsf12
0.186
R5156
G1
225
Y
11
69687329 (GRCm38)
S141P
A
G
missense
Het
probably damaging
1.000
0.663
phenotype
2016-06-21
48
396737
Trank1
0.000
R5156
G1
225
Y
9
111390694 (GRCm38)
I2166M
A
G
missense
Het
probably damaging
0.998
0.068
2016-06-21
49
396751
Trim10
0.087
R5156
G1
225
Y
17
36877056 (GRCm38)
V388E
T
A
missense
Het
probably damaging
0.990
0.799
phenotype
2016-06-21
50
396748
Ttc23l
0.070
R5156
G1
225
Y
15
10551550 (GRCm38)
T30K
G
T
missense
Het
possibly damaging
0.955
0.153
2016-06-21
51
396723
Vmn2r10
0.070
R5156
G1
225
Y
5
108995600 (GRCm38)
V828A
A
G
missense
Het
probably benign
0.112
0.090
2016-06-21
52
396731
Vmn2r75
0.076
R5156
G1
225
Y
7
86164228 (GRCm38)
L455F
T
A
missense
Het
possibly damaging
0.510
0.179
2016-06-21
53
396747
Vwa8
0.000
R5156
G1
225
Y
14
78984226 (GRCm38)
S541T
T
A
missense
Het
probably benign
0.003
0.084
2016-06-21
[records 1 to 53 of 53]