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Incidental Mutations
60
incidental mutations are currently displayed, and affect
59
genes.
11
are Possibly Damaging.
26
are Probably Damaging.
17
are Probably Benign.
1
are Probably Null.
1
create premature stop codons.
0
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 60 of 60]
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
449085
Aadacl4
0.062
R5817
G1
225
Y
4
144622927 (GRCm38)
I251M
A
G
missense
Het
probably benign
0.035
0.090
2016-12-20
2
449130
Abcf3
0.094
R5817
G1
225
Y
16
20549083 (GRCm38)
V63A
T
C
missense
Het
possibly damaging
0.950
0.248
2016-12-20
3
449132
Agpat4
0.000
R5817
G1
206
Y
17
12215210 (GRCm38)
C
T
intron
Het
probably benign
phenotype
2016-12-20
4
449090
Ahcyl2
0.781
R5817
G1
225
Y
6
29890721 (GRCm38)
V292M
G
A
missense
Het
probably damaging
0.999
0.630
phenotype
2016-12-20
5
449120
Ahnak2
0.067
R5817
G1
225
Y
12
112774003 (GRCm38)
F406I
A
T
missense
Het
probably damaging
1.000
0.228
2016-12-20
6
449082
Aqp7
0.069
R5817
G1
225
Y
4
41035510 (GRCm38)
T115I
G
A
missense
Het
probably benign
0.003
0.090
phenotype
2016-12-20
7
449092
Arhgef5
0.000
R5817
G1
225
Y
6
43275104 (GRCm38)
D930N
G
A
missense
Het
probably benign
0.149
0.090
phenotype
2016-12-20
8
449077
Casc4
0.000
R5817
G1
225
Y
2
121906044 (GRCm38)
S231T
T
A
missense
Het
probably benign
0.302
0.079
phenotype
2016-12-20
9
449087
Cc2d2a
0.867
R5817
G1
225
Y
5
43712418 (GRCm38)
R887Q
G
A
missense
Het
probably damaging
1.000
0.114
phenotype
2016-12-20
10
449098
Ceacam18
0.053
R5817
G1
225
Y
7
43641841 (GRCm38)
T236A
A
G
missense
Het
probably benign
0.072
0.090
2016-12-20
11
449104
Chst15
0.065
R5817
G1
225
Y
7
132269144 (GRCm38)
Y221N
A
T
missense
Het
probably damaging
0.994
0.151
phenotype
2016-12-20
12
449105
Chst15
0.065
R5817
G1
225
Y
7
132269147 (GRCm38)
L220F
G
A
missense
Het
probably damaging
0.994
0.167
phenotype
2016-12-20
13
501950
Cntn2
0.215
R5817
G1
76
Y
1
132518748 (GRCm38)
T784I
G
A
missense
Het
probably benign
0.213
0.090
phenotype
2018-01-26
14
449079
D630003M21Rik
0.063
R5817
G1
155
Y
2
158196493 (GRCm38)
L1011P
A
G
missense
Het
probably damaging
1.000
0.470
2016-12-20
15
449107
Dync2h1
1.000
R5817
G1
225
Y
9
6996905 (GRCm38)
D3894V
T
A
missense
Het
probably damaging
1.000
0.947
phenotype
2016-12-20
16
449131
E330017A01Rik
0.070
R5817
G1
225
Y
16
58636793 (GRCm38)
I89V
T
C
missense
Het
probably benign
0.223
0.090
2016-12-20
17
449134
Fam13b
0.179
R5817
G1
225
Y
18
34457797 (GRCm38)
M443V
T
C
missense
Het
possibly damaging
0.931
0.076
2016-12-20
18
449115
Fam20a
0.000
R5817
G1
225
Y
11
109673418 (GRCm38)
Q503L
T
A
missense
Het
possibly damaging
0.805
0.093
phenotype
2016-12-20
19
449116
Gm11677
0.112
R5817
G1
225
Y
11
111724711 (GRCm38)
C
T
exon
Het
noncoding transcript
0.087
2016-12-20
20
449119
Gm21319
0.151
R5817
G1
225
Y
12
87773431 (GRCm38)
D119E
G
T
missense
Het
probably benign
0.010
0.090
2016-12-20
21
449123
Gm5454
0.417
R5817
G1
225
Y
13
103356632 (GRCm38)
T
A
exon
Het
noncoding transcript
0.192
2016-12-20
22
449095
Gm5581
0.076
R5817
G1
225
Y
6
131167169 (GRCm38)
A
G
unclassified
Het
noncoding transcript
0.087
2016-12-20
23
449096
Gm6619
0.104
R5817
G1
225
Y
6
131486437 (GRCm38)
I6V
A
G
missense
Het
unknown
0.087
2016-12-20
24
449093
Gmcl1
0.301
R5817
G1
225
Y
6
86714248 (GRCm38)
M255T
A
G
missense
Het
probably damaging
0.996
0.829
phenotype
2016-12-20
25
449117
Gprc5c
0.271
R5817
G1
225
Y
11
114863624 (GRCm38)
C42*
T
A
nonsense
Het
probably null
0.975
phenotype
2016-12-20
26
449072
Hmcn1
0.000
R5817
G1
225
Y
1
150737524 (GRCm38)
E1384V
T
A
missense
Het
possibly damaging
0.774
0.122
phenotype
2016-12-20
27
449086
Il6
0.407
R5817
G1
225
Y
5
30018008 (GRCm38)
I91V
A
G
missense
Het
probably benign
0.000
0.090
phenotype
2016-12-20
28
501951
Kmt2d
1.000
R5817
G1
79
Y
15
98862363 (GRCm38)
S1005T
A
T
missense
Het
unknown
0.060
phenotype
2018-01-26
29
449076
Map1a
0.367
R5817
G1
225
Y
2
121298910 (GRCm38)
H143L
A
T
missense
Het
possibly damaging
0.810
0.181
phenotype
2016-12-20
30
449103
Mical2
0.432
R5817
G1
225
Y
7
112323659 (GRCm38)
T624S
A
T
missense
Het
probably benign
0.000
0.058
phenotype
2016-12-20
31
449122
Msh3
0.287
R5817
G1
225
Y
13
92286000 (GRCm38)
N549K
A
T
missense
Het
possibly damaging
0.855
0.065
phenotype
2016-12-20
32
449097
Ncr1
0.049
R5817
G1
225
Y
7
4340895 (GRCm38)
I164N
T
A
missense
Het
possibly damaging
0.586
0.179
phenotype
2016-12-20
33
449083
Olfr1333
0.112
R5817
G1
225
Y
4
118830099 (GRCm38)
T115P
T
G
missense
Het
probably damaging
0.961
0.647
phenotype
2016-12-20
34
449101
Olfr554
0.158
R5817
G1
225
Y
7
102640378 (GRCm38)
N44S
A
G
missense
Het
probably damaging
0.999
0.508
phenotype
2016-12-20
35
449102
Olfr586
0.151
R5817
G1
225
Y
7
103121908 (GRCm38)
M292K
A
T
missense
Het
possibly damaging
0.936
0.179
phenotype
2016-12-20
36
449108
Olfr926
0.069
R5817
G1
225
Y
9
38877377 (GRCm38)
D67G
A
G
missense
Het
probably damaging
1.000
0.318
phenotype
2016-12-20
37
449081
Palmd
0.078
R5817
G1
225
Y
3
116918623 (GRCm38)
I541M
T
C
missense
Het
probably benign
0.009
0.090
2016-12-20
38
449109
Pcsk7
0.000
R5817
G1
225
Y
9
45926033 (GRCm38)
M552L
A
T
missense
Het
probably benign
0.014
0.074
phenotype
2016-12-20
39
449133
Plekhh2
0.121
R5817
G1
145
Y
17
84571726 (GRCm38)
E626G
A
G
missense
Het
possibly damaging
0.858
0.069
2016-12-20
40
449089
Pole
1.000
R5817
G1
225
Y
5
110312972 (GRCm38)
D1176N
G
A
missense
Het
probably damaging
0.999
0.585
phenotype
2016-12-20
41
449127
Polr2f
1.000
R5817
G1
225
Y
15
79151669 (GRCm38)
I110T
T
C
missense
Het
probably damaging
0.980
0.275
phenotype
2016-12-20
42
449073
Pomt1
0.083
R5817
G1
225
Y
2
32248679 (GRCm38)
I436F
A
T
missense
Het
probably damaging
0.970
0.690
phenotype
2016-12-20
43
449106
Prag1
0.000
R5817
G1
225
Y
8
36103703 (GRCm38)
Q480P
A
C
missense
Het
probably damaging
0.997
0.116
phenotype
2016-12-20
44
449110
Qars
0.965
R5817
G1
225
Y
9
108510242 (GRCm38)
C
T
unclassified
Het
probably benign
2016-12-20
45
449078
Ralgapa2
0.215
R5817
G1
225
Y
2
146333486 (GRCm38)
S1797L
G
A
missense
Het
probably damaging
1.000
0.224
phenotype
2016-12-20
46
449126
Rbm26
0.686
R5817
G1
225
Y
14
105128603 (GRCm38)
T832A
T
C
missense
Het
probably damaging
0.998
0.094
2016-12-20
47
449100
Rnf169
0.187
R5817
G1
225
Y
7
99925769 (GRCm38)
S540P
A
G
missense
Het
probably benign
0.017
0.060
2016-12-20
48
449080
Serpini1
0.093
R5817
G1
225
Y
3
75613324 (GRCm38)
M76K
T
A
missense
Het
probably benign
0.074
0.344
phenotype
2016-12-20
49
449094
Shq1
0.955
R5817
G1
225
Y
6
100573720 (GRCm38)
L419S
A
G
missense
Het
probably damaging
0.957
0.556
phenotype
2016-12-20
50
449128
Slc25a17
0.269
R5817
G1
225
Y
15
81327060 (GRCm38)
T225M
G
A
missense
Het
probably damaging
0.974
0.299
phenotype
2016-12-20
51
449099
Slc6a5
1.000
R5817
G1
225
Y
7
49956491 (GRCm38)
L716I
C
A
missense
Het
probably benign
0.004
0.096
phenotype
2016-12-20
52
449129
Smc1b
0.551
R5817
G1
225
Y
15
85067783 (GRCm38)
V1149A
A
G
missense
Het
probably damaging
0.993
0.305
phenotype
2016-12-20
53
449113
Trappc1
1.000
R5817
G1
225
Y
11
69324234 (GRCm38)
Q26L
A
T
missense
Het
possibly damaging
0.540
0.150
phenotype
2016-12-20
54
501575
Trpm2
0.141
R5817
G1
225
Y
10
77965980 (GRCm38)
G84W
C
A
missense
Het
probably damaging
1.000
0.165
phenotype
2017-12-01
55
449075
Ttn
1.000
R5817
G1
225
Y
2
76742666 (GRCm38)
T24215M
G
A
missense
Het
probably damaging
0.999
0.647
phenotype
2016-12-20
56
449091
Ubn2
0.891
R5817
G1
225
Y
6
38479153 (GRCm38)
T337K
C
A
missense
Het
probably damaging
1.000
0.169
2016-12-20
57
449084
Ubr4
1.000
R5817
G1
225
Y
4
139468847 (GRCm38)
K1265E
A
G
missense
Het
probably damaging
1.000
0.430
phenotype
2016-12-20
58
449121
Vmn1r214
0.053
R5817
G1
225
Y
13
23035321 (GRCm38)
I328M
T
G
missense
Het
probably damaging
0.983
0.647
2016-12-20
59
449111
Xcr1
0.087
R5817
G1
225
Y
9
123855857 (GRCm38)
C280Y
C
T
missense
Het
possibly damaging
0.945
0.363
phenotype
2016-12-20
60
449125
Zc3h13
0.960
R5817
G1
225
Y
14
75328132 (GRCm38)
E895G
A
G
missense
Het
probably damaging
0.959
0.154
2016-12-20
[records 1 to 60 of 60]