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Incidental Mutations
38
incidental mutations are currently displayed, and affect
38
genes.
6
are Possibly Damaging.
12
are Probably Damaging.
12
are Probably Benign.
7
are Probably Null.
3
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 38 of 38]
10
25
50
100
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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
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
84918
A730049H05Rik
1.000
R1083
G1
225
Y
6
92828065 (GRCm38)
T
C
intron
Het
probably benign
0.090
2013-11-18
2
84923
Adamts17
0.071
R1083
G1
165
Y
7
67147574 (GRCm38)
C986Y
G
A
missense
Het
probably damaging
1.000
0.965
phenotype
2013-11-18
3
84922
AI987944
0.078
R1083
G1
225
Y
7
41375339 (GRCm38)
V75A
A
G
missense
Het
probably benign
0.085
0.090
2013-11-18
4
84925
Arhgap10
0.119
R1083
G1
209
Y
8
77517749 (GRCm38)
Y12C
T
C
missense
Het
probably damaging
0.998
0.208
phenotype
2013-11-18
5
84907
Atp11b
0.260
R1083
G1
225
Y
3
35778013 (GRCm38)
G
A
splice site
Het
probably benign
0.090
phenotype
2013-11-18
6
84932
Ccer1
0.057
R1083
G1
225
Y
10
97694658 (GRCm38)
D394E
T
A
missense
Het
possibly damaging
0.705
0.179
2013-11-18
7
84937
Cdh2
1.000
R1083
G1
225
Y
18
16643959 (GRCm38)
N273S
T
C
missense
Het
possibly damaging
0.607
0.112
phenotype
2013-11-18
8
84904
Cfap65
0.168
R1083
G1
225
Y
1
74918504 (GRCm38)
G
T
splice site
Het
probably benign
phenotype
2013-11-18
9
99138
Crybb3
0.000
R1083
G1
194
Y
5
113080578 (GRCm38)
A
T
utr 5 prime
Het
probably benign
0.090
phenotype
2014-01-10
10
84924
D7Ertd443e
0.000
R1083
G1
225
Y
7
134348934 (GRCm38)
Q337*
G
A
nonsense
Het
probably null
0.964
2013-11-18
11
84928
Dixdc1
0.000
R1083
G1
193
Y
9
50676993 (GRCm38)
C
T
intron
Het
probably benign
0.090
phenotype
2013-11-18
12
84905
Dut
0.969
R1083
G1
152
Y
2
125247828 (GRCm38)
GCGGC
GCGGCCGGC
frame shift
Het
probably null
phenotype
2013-11-18
13
84911
Fbxo2
0.194
R1083
G1
225
Y
4
148165777 (GRCm38)
A
G
splice site
4 bp
Het
probably null
0.976
phenotype
2013-11-18
14
84931
Gm5174
0.079
R1083
G1
225
Y
10
86656108 (GRCm38)
T
C
unclassified
Het
noncoding transcript
0.192
2013-11-18
15
84939
Gpam
0.282
R1083
G1
225
Y
19
55088211 (GRCm38)
A
G
splice site
Het
probably benign
phenotype
2013-11-18
16
84908
Il12a
0.000
R1083
G1
225
Y
3
68695333 (GRCm38)
T112M
C
T
missense
Het
probably damaging
0.999
0.647
phenotype
2013-11-18
17
84919
Itpr1
0.857
R1083
G1
216
Y
6
108510696 (GRCm38)
V2361D
T
A
missense
Het
possibly damaging
0.922
0.179
phenotype
2013-11-18
18
84906
Jag1
1.000
R1083
G1
209
Y
2
137096232 (GRCm38)
L283F
G
A
missense
Het
probably damaging
0.992
0.141
phenotype
2013-11-18
19
84929
Lamb2
0.876
R1083
G1
225
Y
9
108483693 (GRCm38)
D538A
A
C
missense
Het
probably benign
0.000
0.115
phenotype
2013-11-18
20
84926
Map10
0.067
R1083
G1
225
Y
8
125670439 (GRCm38)
C190*
T
A
nonsense
Het
probably null
0.976
2013-11-18
21
84927
Pcnx2
0.000
R1083
G1
225
Y
8
125772104 (GRCm38)
R1552H
C
T
missense
Het
probably damaging
0.999
0.224
phenotype
2013-11-18
22
84936
Phf1
0.000
R1083
G1
225
Y
17
26937270 (GRCm38)
T
C
unclassified
Het
probably benign
phenotype
2013-11-18
23
84909
Pitx2
1.000
R1083
G1
225
Y
3
129218769 (GRCm38)
T276A
A
G
missense
Het
probably damaging
0.998
0.121
phenotype
2013-11-18
24
84920
Pparg
1.000
R1083
G1
225
Y
6
115490146 (GRCm38)
D490G
A
G
missense
Het
probably damaging
0.990
0.148
phenotype
2013-11-18
25
84913
Rnf10
0.526
R1083
G1
225
Y
5
115260104 (GRCm38)
A
T
splice site
Het
probably benign
0.090
phenotype
2013-11-18
26
84935
Sbp
0.062
R1083
G1
225
Y
17
23942730 (GRCm38)
T
C
splice site
Het
probably benign
0.090
2013-11-18
27
84938
Setbp1
0.573
R1083
G1
225
Y
18
78857626 (GRCm38)
L942H
A
T
missense
Het
probably damaging
1.000
0.467
phenotype
2013-11-18
28
84903
Sf3b1
1.000
R1083
G1
225
Y
1
55019395 (GRCm38)
E12Q
C
G
missense
Het
possibly damaging
0.894
0.137
phenotype
2013-11-18
29
84933
Sfmbt1
0.748
R1083
G1
225
Y
14
30787541 (GRCm38)
N326Y
A
T
missense
Het
possibly damaging
0.917
0.179
phenotype
2013-11-18
30
84934
Slx4
1.000
R1083
G1
225
Y
16
3990910 (GRCm38)
Q389*
G
A
nonsense
Het
probably null
0.976
phenotype
2013-11-18
31
84914
Srrm3
0.437
R1083
G1
225
Y
5
135854409 (GRCm38)
V206E
T
A
missense
Het
probably damaging
0.992
0.066
2013-11-18
32
84916
Sspo
0.000
R1083
G1
225
Y
6
48470999 (GRCm38)
D2270E
T
A
missense
Het
possibly damaging
0.906
0.179
2013-11-18
33
84902
Sulf1
0.440
R1083
G1
217
Y
1
12836164 (GRCm38)
AAGGGA
AAGGGAGGGA
frame shift
Het
probably null
0.976
phenotype
2013-11-18
34
84917
Vmn1r14
0.177
R1083
G1
225
Y
6
57234199 (GRCm38)
I210N
T
A
missense
Het
probably damaging
0.998
0.647
2013-11-18
35
84915
Wasf3
0.000
R1083
G1
117
Y
5
146435372 (GRCm38)
L13R
T
G
missense
Het
probably damaging
1.000
0.647
phenotype
2013-11-18
36
84912
Yes1
0.760
R1083
G1
225
Y
5
32651757 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
0.950
phenotype
2013-11-18
37
84910
Zfp292
0.657
R1083
G1
225
Y
4
34807569 (GRCm38)
D1830G
T
C
missense
Het
probably damaging
0.977
0.157
2013-11-18
38
84921
Zfp541
0.728
R1083
G1
216
N
7
16078712 (GRCm38)
N430S
A
G
missense
Het
probably benign
0.164
2013-11-18
[records 1 to 38 of 38]