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Incidental Mutations
33
incidental mutations are currently displayed, and affect
33
genes.
4
are Possibly Damaging.
16
are Probably Damaging.
8
are Probably Benign.
4
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 33 of 33]
10
25
50
100
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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
151266
4932438A13Rik
1.000
R1270
G1
225
Y
3
36952184 (GRCm38)
H1662Q
T
A
missense
Het
probably damaging
0.999
0.740
phenotype
2014-01-29
2
151285
Abcc3
0.000
R1270
G1
225
Y
11
94357384 (GRCm38)
R1129Q
C
T
missense
Het
probably damaging
0.996
0.156
phenotype
2014-01-29
3
151289
Adam7
0.056
R1270
G1
225
Y
14
68527669 (GRCm38)
K93M
T
A
missense
Het
probably damaging
0.980
0.647
phenotype
2014-01-29
4
151281
Aldh1a2
1.000
R1270
G1
225
Y
9
71281706 (GRCm38)
L301V
T
G
missense
Het
probably benign
0.032
0.190
phenotype
2014-01-29
5
229963
Alg9
1.000
R1270
G1
39
Y
9
50787572 (GRCm38)
A
G
intron
Het
probably benign
0.090
phenotype
2014-09-18
6
151286
Aspg
0.220
R1270
G1
225
Y
12
112116447 (GRCm38)
T187I
C
T
missense
Het
probably damaging
1.000
0.147
2014-01-29
7
151292
C4a
0.133
R1270
G1
193
Y
17
34814528 (GRCm38)
A
G
unclassified
Het
noncoding transcript
0.087
2014-01-29
8
151293
Cdh2
1.000
R1270
G1
225
Y
18
16627557 (GRCm38)
T
G
splice site
Het
probably benign
0.090
phenotype
2014-01-29
9
151272
Ceacam1
0.116
R1270
G1
225
Y
7
25466314 (GRCm38)
T
C
splice site
3 bp
Het
probably null
0.976
phenotype
2014-01-29
10
151265
Cep250
0.000
R1270
G1
195
Y
2
155990681 (GRCm38)
V1509I
G
A
missense
Het
probably benign
0.012
0.078
phenotype
2014-01-29
11
151288
D130043K22Rik
0.000
R1270
G1
225
Y
13
24857338 (GRCm38)
S248P
T
C
missense
Het
probably benign
0.001
0.090
phenotype
2014-01-29
12
151261
Dgkd
0.781
R1270
G1
131
Y
1
87934125 (GRCm38)
M801L
A
T
missense
Het
probably damaging
0.963
0.415
phenotype
2014-01-29
13
151271
E330021D16Rik
0.257
R1270
G1
225
Y
6
136401787 (GRCm38)
I15N
A
T
missense
Het
probably damaging
0.970
0.408
2014-01-29
14
151278
Edc4
1.000
R1270
G1
225
Y
8
105891264 (GRCm38)
E1152G
A
G
missense
Het
possibly damaging
0.904
0.208
phenotype
2014-01-29
15
151277
Enkd1
0.000
R1270
G1
225
Y
8
105703901 (GRCm38)
I334T
A
G
missense
Het
probably damaging
1.000
0.312
2014-01-29
16
151287
Gli3
1.000
R1270
G1
225
Y
13
15723744 (GRCm38)
A803V
C
T
missense
Het
probably benign
0.021
0.069
phenotype
2014-01-29
17
151276
Glrx3
1.000
R1270
G1
225
Y
7
137453414 (GRCm38)
N95S
A
G
missense
Het
probably benign
0.016
0.064
phenotype
2014-01-29
18
151284
Ints2
1.000
R1270
G1
225
Y
11
86233085 (GRCm38)
G626R
C
T
missense
Het
probably damaging
0.999
0.333
phenotype
2014-01-29
19
151279
Kank2
0.156
R1270
G1
225
Y
9
21772760 (GRCm38)
N724K
A
T
missense
Het
probably damaging
1.000
0.374
phenotype
2014-01-29
20
151290
Kctd20
0.240
R1270
G1
225
Y
17
28966931 (GRCm38)
D416G
A
G
missense
Het
possibly damaging
0.871
0.061
2014-01-29
21
151274
Lmtk3
0.416
R1270
G1
126
Y
7
45793828 (GRCm38)
E645G
A
G
missense
Het
probably damaging
0.959
0.074
phenotype
2014-01-29
22
151275
Mrgpra9
0.050
R1270
G1
225
Y
7
47252783 (GRCm38)
A
T
critical splice donor site
2 bp
Het
probably null
0.976
2014-01-29
23
151268
Muc1
0.338
R1270
G1
225
Y
3
89232107 (GRCm38)
Y605N
T
A
missense
Het
probably damaging
1.000
0.103
phenotype
2014-01-29
24
151263
Olfr1256
0.103
R1270
G1
225
Y
2
89835322 (GRCm38)
V208M
C
T
missense
Het
possibly damaging
0.896
0.227
phenotype
2014-01-29
25
151280
Olfr146
0.056
R1270
G1
225
Y
9
39019247 (GRCm38)
I98R
A
C
missense
Het
possibly damaging
0.899
0.179
phenotype
2014-01-29
26
151273
Prx
0.000
R1270
G1
225
Y
7
27518930 (GRCm38)
I952N
T
A
missense
Het
probably damaging
0.965
0.260
phenotype
2014-01-29
27
151264
Shf
0.000
R1270
G1
96
Y
2
122368682 (GRCm38)
P51S
G
A
missense
Het
probably damaging
0.958
0.152
2014-01-29
28
151270
Skint5
0.055
R1270
G1
225
Y
4
113942659 (GRCm38)
Y90*
A
T
nonsense
Het
probably null
0.976
2014-01-29
29
151262
Swt1
0.173
R1270
G1
225
Y
1
151384391 (GRCm38)
N752K
A
T
missense
Het
probably benign
0.001
0.090
2014-01-29
30
151282
Taar1
0.115
R1270
G1
225
Y
10
23920533 (GRCm38)
V43A
T
C
missense
Het
probably damaging
0.999
0.728
phenotype
2014-01-29
31
151283
Tenm2
0.448
R1270
G1
225
Y
11
36041659 (GRCm38)
N1702D
T
C
missense
Het
probably damaging
0.999
0.131
phenotype
2014-01-29
32
151291
Tff2
0.067
R1270
G1
155
Y
17
31144169 (GRCm38)
C
T
critical splice donor site
1 bp
Het
probably null
0.976
phenotype
2014-01-29
33
151267
Trim2
0.309
R1270
G1
185
Y
3
84167677 (GRCm38)
A686V
G
A
missense
Het
probably damaging
0.998
0.603
phenotype
2014-01-29
[records 1 to 33 of 33]