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Incidental Mutations
51
incidental mutations are currently displayed, and affect
50
genes.
4
are Possibly Damaging.
25
are Probably Damaging.
17
are Probably Benign.
5
are Probably Null.
1
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 51 of 51]
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
326069
0610010F05Rik
0.122
R4373
G1
225
Y
11
23615265 (GRCm38)
A
T
splice site
Het
probably null
0.976
2015-07-06
2
326073
3632451O06Rik
0.000
R4373
G1
225
Y
14
49770436 (GRCm38)
T527S
T
A
missense
Het
probably damaging
0.999
0.319
2015-07-06
3
326082
Adck5
0.000
R4373
G1
225
Y
15
76594335 (GRCm38)
A
G
unclassified
Het
probably benign
2015-07-06
4
326060
Akr1b3
0.350
R4373
G1
225
Y
6
34304267 (GRCm38)
A
C
utr 3 prime
Het
probably benign
0.090
phenotype
2015-07-06
5
326059
Asns
0.326
R4373
G1
225
Y
6
7677978 (GRCm38)
S367T
A
T
missense
Het
probably damaging
0.981
0.894
phenotype
2015-07-06
6
326043
BC034090
0.054
R4373
G1
225
Y
1
155226158 (GRCm38)
N120S
T
C
missense
Het
probably benign
0.223
0.073
2015-07-06
7
326046
Bub1
1.000
R4373
G1
225
Y
2
127805236 (GRCm38)
A
T
intron
Het
probably benign
phenotype
2015-07-06
8
386380
Csf1
0.715
R4373
G1
225
Y
3
107756739 (GRCm38)
T38S
T
A
missense
Het
probably damaging
0.998
0.327
phenotype
2016-05-20
9
326048
Ctsz
0.109
R4373
G1
225
Y
2
174428585 (GRCm38)
E268G
T
C
missense
Het
possibly damaging
0.942
0.566
phenotype
2015-07-06
10
326076
Dach1
1.000
R4373
G1
225
Y
14
97827750 (GRCm38)
T685I
G
A
missense
Het
possibly damaging
0.935
0.162
phenotype
2015-07-06
11
326089
Dclre1a
0.000
R4373
G1
225
Y
19
56545442 (GRCm38)
L240S
A
G
missense
Het
probably benign
0.040
0.090
phenotype
2015-07-06
12
326062
Ercc1
1.000
R4373
G1
142
Y
7
19347132 (GRCm38)
G
A
unclassified
Het
probably benign
0.090
phenotype
2015-07-06
13
326066
Esam
0.119
R4373
G1
225
Y
9
37534196 (GRCm38)
T71I
C
T
missense
Het
probably benign
0.000
0.090
phenotype
2015-07-06
14
326083
Espl1
1.000
R4373
G1
225
Y
15
102312989 (GRCm38)
I944V
A
G
missense
Het
probably damaging
0.990
0.143
phenotype
2015-07-06
15
326065
Gde1
0.366
R4373
G1
225
Y
7
118698558 (GRCm38)
L35P
A
G
missense
Het
possibly damaging
0.907
0.362
phenotype
2015-07-06
16
326058
Gm10382
0.064
R4373
G1
201
Y
5
125389583 (GRCm38)
A
G
intron
Het
probably benign
0.090
2015-07-06
17
326086
H2-M10.6
0.051
R4373
G1
225
Y
17
36813066 (GRCm38)
Y141H
T
C
missense
Het
probably damaging
1.000
0.647
2015-07-06
18
326068
Hk1
0.323
R4373
G1
225
Y
10
62315540 (GRCm38)
K10N
C
A
missense
Het
probably damaging
0.978
0.149
phenotype
2015-07-06
19
386379
Lamc3
0.000
R4373
G1
223
Y
2
31898232 (GRCm38)
K135E
A
G
missense
Het
probably damaging
1.000
0.303
phenotype
2016-05-20
20
326061
Lrtm2
0.068
R4373
G1
225
Y
6
119320528 (GRCm38)
F184S
A
G
missense
Het
probably damaging
1.000
0.775
2015-07-06
21
326079
March11
0.345
R4373
G1
139
Y
15
26309446 (GRCm38)
E62G
A
G
missense
Het
probably damaging
0.959
0.136
phenotype
2015-07-06
22
326087
Mtcl1
0.220
R4373
G1
225
Y
17
66380079 (GRCm38)
T611S
T
A
missense
Het
probably benign
0.047
0.090
phenotype
2015-07-06
23
326080
Myc
1.000
R4373
G1
225
Y
15
61989664 (GRCm38)
H373L
A
T
missense
Het
probably damaging
0.992
0.845
phenotype
2015-07-06
24
326074
Myh6
1.000
R4373
G1
187
Y
14
54962108 (GRCm38)
I249F
T
A
missense
Het
probably damaging
0.966
0.378
phenotype
2015-07-06
25
326054
Naaa
0.000
R4373
G1
136
Y
5
92278143 (GRCm38)
T
C
utr 5 prime
Het
probably benign
phenotype
2015-07-06
26
326051
Nfib
1.000
R4373
G1
225
Y
4
82323658 (GRCm38)
V432A
A
G
missense
Het
probably damaging
0.972
0.125
phenotype
2015-07-06
27
326070
Nmt1
1.000
R4373
G1
225
Y
11
103043200 (GRCm38)
K55R
A
G
missense
Het
probably damaging
0.994
0.070
phenotype
2015-07-06
28
326045
Olfr1228
0.066
R4373
G1
225
Y
2
89249245 (GRCm38)
R150G
T
C
missense
Het
possibly damaging
0.899
0.356
phenotype
2015-07-06
29
386381
Opa3
0.059
R4373
G1
69
Y
7
19244774 (GRCm38)
R55W
C
T
missense
Het
probably damaging
0.999
0.672
phenotype
2016-05-20
30
326071
Pfn4
0.000
R4373
G1
225
Y
12
4770182 (GRCm38)
D10E
T
A
missense
Het
probably damaging
0.994
0.647
2015-07-06
31
326044
Pld5
0.000
R4373
G1
225
Y
1
176140017 (GRCm38)
I91F
T
A
missense
Het
probably damaging
1.000
0.085
phenotype
2015-07-06
32
326081
Plec
0.807
R4373
G1
224
Y
15
76183117 (GRCm38)
S1350A
A
C
missense
Het
probably damaging
0.986
0.068
phenotype
2015-07-06
33
326084
Polq
0.415
R4373
G1
225
Y
16
37013181 (GRCm38)
V79F
G
T
missense
Het
probably damaging
0.997
0.182
phenotype
2015-07-06
34
326047
Ppp1r16b
0.000
R4373
G1
225
Y
2
158761765 (GRCm38)
Y537H
T
C
missense
Het
probably damaging
1.000
0.225
phenotype
2015-07-06
35
326055
Prdm8
0.637
R4373
G1
225
Y
5
98186508 (GRCm38)
S645P
T
C
missense
Het
probably damaging
0.996
0.230
phenotype
2015-07-06
36
326042
Rgs1
0.129
R4373
G1
225
Y
1
144247906 (GRCm38)
T94A
T
C
missense
Het
probably benign
0.001
0.064
phenotype
2015-07-06
37
326053
Rpl11
0.931
R4373
G1
225
Y
4
136051143 (GRCm38)
G
A
intron
Het
probably benign
0.090
phenotype
2015-07-06
38
326050
Scamp3
0.906
R4373
G1
161
Y
3
89181927 (GRCm38)
G
A
splice site
Het
probably null
0.910
phenotype
2015-07-06
39
326057
Sgsm1
0.000
R4373
G1
217
Y
5
113258123 (GRCm38)
TTTTATATT
TTT
intron
Het
probably benign
2015-07-06
40
326049
Sirpb1b
0.058
R4373
G1
225
Y
3
15548761 (GRCm38)
I87K
A
T
missense
Het
probably damaging
0.995
0.647
2015-07-06
41
326088
Slc14a2
0.000
R4373
G1
225
Y
18
78207068 (GRCm38)
R62C
G
A
missense
Het
probably damaging
0.998
0.647
phenotype
2015-07-06
42
326041
Stat4
0.398
R4373
G1
225
Y
1
52071941 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
0.949
phenotype
2015-07-06
43
326067
Tex9
0.061
R4373
G1
225
Y
9
72480595 (GRCm38)
A
T
critical splice donor site
2 bp
Het
probably null
0.950
2015-07-06
44
326064
Tsku
0.064
R4373
G1
225
Y
7
98352831 (GRCm38)
T98A
T
C
missense
Het
probably benign
0.006
0.063
phenotype
2015-07-06
45
326077
Ttc23l
0.070
R4373
G1
217
Y
15
10537562 (GRCm38)
CT
CTTGGATT
small insertion
Het
probably benign
0.090
2015-07-06
46
326078
Ttc23l
0.070
R4373
G1
225
Y
15
10537566 (GRCm38)
S206L
G
A
missense
Het
probably benign
0.056
0.090
2015-07-06
47
326085
Vmn2r116
0.065
R4373
G1
225
Y
17
23401421 (GRCm38)
I710L
A
C
missense
Het
probably benign
0.014
0.090
phenotype
2015-07-06
48
326056
Vmn2r16
0.183
R4373
G1
225
Y
5
109363801 (GRCm38)
I625F
A
T
missense
Het
probably damaging
1.000
0.647
2015-07-06
49
326075
Xpo4
0.766
R4373
G1
225
Y
14
57591022 (GRCm38)
Q794*
G
A
nonsense
Het
probably null
0.976
phenotype
2015-07-06
50
326063
Zfp112
0.131
R4373
G1
225
Y
7
24125048 (GRCm38)
I147N
T
A
missense
Het
probably damaging
0.989
0.108
2015-07-06
51
326072
Zmiz1
1.000
R4373
G1
164
Y
14
25636010 (GRCm38)
S140P
T
C
missense
Het
probably damaging
0.974
0.073
phenotype
2015-07-06
[records 1 to 51 of 51]