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Incidental Mutations
59
incidental mutations are currently displayed, and affect
59
genes.
7
are Possibly Damaging.
27
are Probably Damaging.
19
are Probably Benign.
5
are Probably Null.
3
create premature stop codons.
0
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 59 of 59]
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
656156
Aasdhppt
1.000
R8516
G1
225.01
N
9
4309373 (GRCm38)
S22T
A
T
missense
Het
probably benign
0.034
phenotype
2020-10-20
2
656170
Actr8
1.000
R8516
G1
225.01
N
14
29990899 (GRCm38)
A500S
G
T
missense
Het
probably benign
0.168
2020-10-20
3
656132
Adamtsl1
0.247
R8516
G1
225.01
N
4
86342543 (GRCm38)
Y1005C
A
G
missense
Het
probably damaging
1.000
phenotype
2020-10-20
4
656161
Ank3
0.841
R8516
G1
225.01
N
10
69927729 (GRCm38)
Y884*
T
A
nonsense
Het
probably null
phenotype
2020-10-20
5
656178
Arhgap28
0.000
R8516
G1
225.01
N
17
67873073 (GRCm38)
R306G
T
C
missense
Het
probably benign
0.075
phenotype
2020-10-20
6
656172
Atp8a2
0.507
R8516
G1
225.01
N
14
59691472 (GRCm38)
I1044M
A
C
missense
Het
probably benign
0.005
phenotype
2020-10-20
7
656125
Bahd1
0.000
R8516
G1
225.01
N
2
118916971 (GRCm38)
Y357C
A
G
missense
Het
probably benign
0.025
phenotype
2020-10-20
8
656171
Btd
0.228
R8516
G1
225.01
N
14
31666867 (GRCm38)
T182S
A
T
missense
Het
probably damaging
1.000
phenotype
2020-10-20
9
656165
Casc3
0.945
R8516
G1
225.01
N
11
98822781 (GRCm38)
R280C
C
T
missense
Het
probably damaging
0.999
phenotype
2020-10-20
10
656129
Cisd2
0.152
R8516
G1
225.01
N
3
135411013 (GRCm38)
T106A
T
C
missense
Het
probably damaging
0.998
phenotype
2020-10-20
11
656142
Cldn15
0.000
R8516
G1
225.01
N
5
136974696 (GRCm38)
C184F
G
T
missense
Het
probably damaging
0.985
phenotype
2020-10-20
12
656162
Clk4
0.694
R8516
G1
225.01
N
11
51275261 (GRCm38)
R198Q
G
A
missense
Het
probably damaging
0.973
phenotype
2020-10-20
13
656154
Coprs
0.170
R8516
G1
225.01
N
8
13885065 (GRCm38)
F163L
G
T
missense
Het
probably damaging
1.000
phenotype
2020-10-20
14
656175
Csmd3
0.000
R8516
G1
225.01
N
15
47629365 (GRCm38)
R2216*
G
A
nonsense
Het
probably null
2020-10-20
15
656155
Defb7
0.094
R8516
G1
225.01
N
8
19497607 (GRCm38)
I43F
A
T
missense
Het
possibly damaging
0.868
2020-10-20
16
656158
Dpp8
0.202
R8516
G1
225.01
N
9
65078009 (GRCm38)
T783K
C
A
missense
Het
probably damaging
1.000
phenotype
2020-10-20
17
656167
Eif2s1
1.000
R8516
G1
221.01
N
12
78881162 (GRCm38)
G204D
G
A
missense
Het
probably damaging
1.000
phenotype
2020-10-20
18
656133
Elavl4
0.429
R8516
G1
225.01
N
4
110251379 (GRCm38)
N56S
T
C
missense
Het
probably damaging
1.000
phenotype
2020-10-20
19
656138
Emilin1
0.114
R8516
G1
225.01
N
5
30917171 (GRCm38)
R252H
G
A
missense
Het
probably damaging
1.000
phenotype
2020-10-20
20
656126
Exd1
0.000
R8516
G1
225.01
N
2
119520073 (GRCm38)
L569Q
A
T
missense
Het
probably damaging
0.974
phenotype
2020-10-20
21
656153
Gm498
0.078
R8516
G1
225.01
N
7
143897274 (GRCm38)
I342N
T
A
missense
Het
probably damaging
0.979
2020-10-20
22
656135
Gpn2
0.964
R8516
G1
225.01
N
4
133584831 (GRCm38)
R125C
C
T
missense
Het
probably damaging
0.993
2020-10-20
23
656127
Gria2
0.573
R8516
G1
225.01
N
3
80706987 (GRCm38)
E582G
T
C
missense
Het
probably benign
0.274
phenotype
2020-10-20
24
656137
Hadha
1.000
R8516
G1
225.01
N
5
30126584 (GRCm38)
V458E
A
T
missense
Het
probably damaging
1.000
phenotype
2020-10-20
25
656166
Hap1
0.668
R8516
G1
225.01
N
11
100356067 (GRCm38)
K4R
T
C
missense
Het
possibly damaging
0.659
phenotype
2020-10-20
26
656141
Hectd4
0.393
R8516
G1
225.01
N
5
121349010 (GRCm38)
H3356L
A
T
missense
Het
possibly damaging
0.533
2020-10-20
27
656147
Herc2
0.932
R8516
G1
225.01
N
7
56206570 (GRCm38)
V3919I
G
A
missense
Het
probably benign
0.051
phenotype
2020-10-20
28
656122
Lgr6
0.000
R8516
G1
225.01
N
1
135075283 (GRCm38)
N76K
G
T
missense
Het
probably damaging
1.000
phenotype
2020-10-20
29
656151
Olfr692
0.185
R8516
G1
225.01
N
7
105368769 (GRCm38)
I148V
A
G
missense
Het
probably benign
0.001
phenotype
2020-10-20
30
656149
P4ha3
0.060
R8516
G1
225.01
N
7
100314662 (GRCm38)
M462V
A
G
missense
Het
probably damaging
0.974
phenotype
2020-10-20
31
656152
Pde3b
0.000
R8516
G1
225.01
N
7
114526849 (GRCm38)
M773L
A
T
missense
Het
probably benign
0.011
phenotype
2020-10-20
32
656157
Peak1
0.189
R8516
G1
225.01
N
9
56260000 (GRCm38)
S215G
T
C
missense
Het
probably damaging
0.999
phenotype
2020-10-20
33
656179
Pgm5
0.208
R8516
G1
225.01
N
19
24815710 (GRCm38)
M331L
T
A
missense
Het
probably benign
0.000
phenotype
2020-10-20
34
656173
Piwil2
0.000
R8516
G1
225.01
N
14
70420739 (GRCm38)
V213A
A
G
missense
Het
probably benign
0.185
phenotype
2020-10-20
35
656136
Plch2
0.000
R8516
G1
225.01
N
4
154986307 (GRCm38)
H1205R
T
C
missense
Het
probably benign
0.000
phenotype
2020-10-20
36
656146
Pop4
1.000
R8516
G1
225.01
N
7
38267402 (GRCm38)
M85K
A
T
missense
Het
probably benign
0.005
phenotype
2020-10-20
37
656130
Ppp3ca
0.000
R8516
G1
225.01
N
3
136877768 (GRCm38)
I212N
T
A
missense
Het
probably damaging
1.000
phenotype
2020-10-20
38
656139
Prom1
0.381
R8516
G1
225.01
N
5
44007099 (GRCm38)
K714R
T
C
missense
Het
probably benign
0.052
phenotype
2020-10-20
39
656131
Psip1
0.500
R8516
G1
225.01
N
4
83466715 (GRCm38)
G207S
C
T
missense
Het
probably benign
0.000
phenotype
2020-10-20
40
656174
Rgs22
0.000
R8516
G1
225.01
N
15
36010335 (GRCm38)
*1259Q
A
G
makesense
Het
probably null
2020-10-20
41
656124
Scn1a
1.000
R8516
G1
225.01
N
2
66326134 (GRCm38)
G477D
C
T
missense
Het
possibly damaging
0.787
phenotype
2020-10-20
42
656121
Sf3b1
1.000
R8516
G1
225.01
N
1
55012103 (GRCm38)
E222G
T
C
missense
Het
probably null
0.007
phenotype
2020-10-20
43
656148
Snrpa1
0.965
R8516
G1
225.01
N
7
66070633 (GRCm38)
G195R
G
A
missense
Het
probably benign
0.446
2020-10-20
44
656163
Spem2
0.055
R8516
G1
225.01
N
11
69816895 (GRCm38)
R415G
T
C
missense
Het
possibly damaging
0.533
2020-10-20
45
656169
Tmem167
0.456
R8516
G1
173.01
N
13
90098396 (GRCm38)
V13E
T
A
missense
Het
probably damaging
0.998
2020-10-20
46
656128
Trim2
0.287
R8516
G1
225.01
N
3
84208320 (GRCm38)
A102T
C
T
missense
Het
probably damaging
1.000
phenotype
2020-10-20
47
656150
Trim30b
0.000
R8516
G1
225.01
N
7
104357404 (GRCm38)
S82P
A
G
missense
Het
probably benign
0.002
2020-10-20
48
656140
Uba6
1.000
R8516
G1
225.01
N
5
86127748 (GRCm38)
S760R
A
C
missense
Het
possibly damaging
0.780
phenotype
2020-10-20
49
656123
Upf2
1.000
R8516
G1
225.01
N
2
6018971 (GRCm38)
F711L
T
C
missense
Het
unknown
phenotype
2020-10-20
50
656160
Utrn
0.000
R8516
G1
225.01
N
10
12486510 (GRCm38)
D2693V
T
A
missense
Het
probably damaging
0.993
phenotype
2020-10-20
51
656144
Vmn1r30
0.122
R8516
G1
225.01
N
6
58435124 (GRCm38)
Y241S
T
G
missense
Het
probably damaging
0.957
2020-10-20
52
656177
Vmn2r110
0.177
R8516
G1
225.01
N
17
20574613 (GRCm38)
L598P
A
G
missense
Het
probably damaging
1.000
2020-10-20
53
656164
Wfdc18
0.109
R8516
G1
225.01
N
11
83709158 (GRCm38)
F14Y
T
A
missense
Het
probably benign
0.008
2020-10-20
54
656176
Wnt10b
0.000
R8516
G1
225.01
N
15
98772880 (GRCm38)
C256S
A
T
missense
Het
probably damaging
0.993
phenotype
2020-10-20
55
656159
Xrn1
0.906
R8516
G1
225.01
N
9
96048391 (GRCm38)
Y1554*
T
A
nonsense
Het
probably null
phenotype
2020-10-20
56
656134
Zc3h12a
0.798
R8516
G1
225.01
N
4
125119839 (GRCm38)
S411C
T
A
missense
Het
probably damaging
0.993
phenotype
2020-10-20
57
656145
Zfp112
0.194
R8516
G1
225.01
N
7
24123964 (GRCm38)
G63E
G
A
missense
Het
probably benign
0.000
2020-10-20
58
656143
Zfp786
0.079
R8516
G1
225.01
N
6
47820543 (GRCm38)
L487Q
A
T
missense
Het
probably damaging
0.999
2020-10-20
59
656168
Zfp953
0.061
R8516
G1
225.01
N
13
67345355 (GRCm38)
Y75F
T
A
missense
Het
possibly damaging
0.549
2020-10-20
[records 1 to 59 of 59]