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Incidental Mutations
45
incidental mutations are currently displayed, and affect
45
genes.
6
are Possibly Damaging.
17
are Probably Damaging.
14
are Probably Benign.
8
are Probably Null.
2
create premature stop codons.
3
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 45 of 45]
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
522205
1700029P11Rik
0.345
R6556
G1
225.01
N
15
81980738 (GRCm38)
D60G
A
G
missense
Het
probably damaging
0.989
2018-06-06
2
522132
2310035C23Rik
0.355
R6556
G1
225.01
N
1
105726440 (GRCm38)
F845I
T
A
missense
Het
probably damaging
1.000
2018-06-06
3
522208
4930539E08Rik
0.000
R6556
G1
225.01
N
17
28904611 (GRCm38)
D114V
T
A
missense
Het
probably damaging
0.988
2018-06-06
4
522168
AF366264
0.684
R6556
G1
225.01
N
8
13837690 (GRCm38)
Q134*
G
A
nonsense
Het
probably null
2018-06-06
5
522166
Atp2a1
1.000
R6556
G1
225.01
N
7
126450262 (GRCm38)
P536Q
G
T
missense
Het
probably benign
0.372
phenotype
2018-06-06
6
522210
Cabyr
0.087
R6556
G1
225.01
N
18
12751016 (GRCm38)
S187T
T
A
missense
Het
probably benign
0.074
0.064
phenotype
2018-06-06
7
522187
Camkk1
0.000
R6556
G1
225.01
N
11
73033870 (GRCm38)
N303I
A
T
missense
Het
probably benign
0.319
phenotype
2018-06-06
8
522170
Cdh13
0.000
R6556
G1
225.01
N
8
118968187 (GRCm38)
P259S
C
T
missense
Het
probably damaging
0.990
phenotype
2018-06-06
9
522212
Csnk1g3
0.000
R6556
G1
225.01
N
18
53930282 (GRCm38)
D255G
A
G
missense
Het
possibly damaging
0.821
phenotype
2018-06-06
10
522160
Dennd5b
0.156
R6556
G1
225.01
N
6
149014251 (GRCm38)
A
C
splice site
Het
probably null
phenotype
2018-06-06
11
522185
Dnajc14
0.000
R6556
G1
225.01
N
10
128814631 (GRCm38)
D528G
A
G
missense
Het
probably benign
0.417
2018-06-06
12
522156
Edem1
0.515
R6556
G1
225.01
N
6
108854357 (GRCm38)
F593S
T
C
missense
Het
probably benign
0.001
2018-06-06
13
522191
Erbb2
1.000
R6556
G1
225.01
N
11
98436082 (GRCm38)
D1106N
G
A
missense
Het
possibly damaging
0.917
phenotype
2018-06-06
14
522218
Ermp1
0.000
R6556
G1
225.01
N
19
29612921 (GRCm38)
M794V
T
C
missense
Het
possibly damaging
0.910
phenotype
2018-06-06
15
522200
Fam208a
1.000
R6556
G1
187.01
N
14
27429258 (GRCm38)
Y64D
T
G
missense
Het
probably benign
0.000
phenotype
2018-06-06
16
522144
Fam214b
0.224
R6556
G1
225.01
N
4
43033896 (GRCm38)
R460H
C
T
missense
Het
probably damaging
0.960
2018-06-06
17
522148
Fip1l1
0.942
R6556
G1
225.01
N
5
74547177 (GRCm38)
T
A
critical splice donor site
2 bp
Het
probably null
2018-06-06
18
522193
Gm11639
0.107
R6556
G1
225.01
N
11
105008251 (GRCm38)
N4343S
A
G
missense
Het
probably null
0.026
2018-06-06
19
522154
Gm20730
0.074
R6556
G1
225.01
N
6
43081542 (GRCm38)
C112Y
C
T
missense
Het
probably damaging
0.999
2018-06-06
20
522164
Gtf2h1
0.969
R6556
G1
225.01
N
7
46808665 (GRCm38)
C245S
T
A
missense
Het
probably damaging
1.000
2018-06-06
21
522158
Hdhd5
0.277
R6556
G1
225.01
N
6
120523554 (GRCm38)
H61R
T
C
missense
Het
probably benign
0.001
2018-06-06
22
522197
Ighv1-71
R6556
G1
139.01
N
12
115742472 (GRCm38)
V31E
A
T
missense
Het
probably damaging
0.990
2018-06-06
23
522174
Igsf9b
0.487
R6556
G1
225.01
N
9
27329555 (GRCm38)
F688S
T
C
missense
Het
probably damaging
1.000
2018-06-06
24
522152
Iqcd
0.058
R6556
G1
225.01
N
5
120602378 (GRCm38)
V258A
T
C
missense
Het
probably damaging
0.987
2018-06-06
25
522183
Kcnc2
0.000
R6556
G1
198.01
N
10
112271856 (GRCm38)
G51R
G
C
missense
Het
probably benign
0.037
0.103
phenotype
2018-06-06
26
522189
Lpo
0.000
R6556
G1
225.01
N
11
87817763 (GRCm38)
Y136*
G
T
nonsense
Het
probably null
phenotype
2018-06-06
27
522203
Med30
R6556
G1
86.01
N
15
52730383 (GRCm38)
A
G
utr 3 prime
Het
probably benign
phenotype
2018-06-06
28
522140
Mertk
0.145
R6556
G1
225.01
N
2
128776421 (GRCm38)
V524D
T
A
missense
Het
probably benign
0.229
phenotype
2018-06-06
29
522134
Olfr1156
0.115
R6556
G1
225.01
N
2
87949976 (GRCm38)
I86V
T
C
missense
Het
probably benign
0.005
phenotype
2018-06-06
30
522136
Olfr1261
0.060
R6556
G1
225.01
N
2
89994173 (GRCm38)
F260Y
T
A
missense
Het
probably benign
0.394
phenotype
2018-06-06
31
522138
Olfr1263
0.098
R6556
G1
225.01
N
2
90015094 (GRCm38)
Y55H
T
C
missense
Het
probably damaging
1.000
phenotype
2018-06-06
32
522149
Pde6b
0.000
R6556
G1
225.01
N
5
108421501 (GRCm38)
M358K
T
A
missense
Het
possibly damaging
0.564
phenotype
2018-06-06
33
522179
Prep
1.000
R6556
G1
217.47
N
10
45158314 (GRCm38)
GA
G
frame shift
Het
probably null
phenotype
2018-06-06
34
522199
Prpf4b
1.000
R6556
G1
225.01
N
13
34896032 (GRCm38)
R793Q
G
A
missense
Het
probably damaging
0.983
phenotype
2018-06-06
35
522216
Rela
1.000
R6556
G1
225.01
N
19
5647338 (GRCm38)
N524K
T
A
missense
Het
probably damaging
1.000
phenotype
2018-06-06
36
522207
Rnaset2a
0.310
R6556
G1
145.01
N
17
8141648 (GRCm38)
D74G
T
C
missense
Het
probably damaging
0.999
2018-06-06
37
522146
Serinc2
0.090
R6556
G1
225.01
N
4
130258271 (GRCm38)
I267F
T
A
missense
Het
probably damaging
0.999
2018-06-06
38
522172
Sesn3
0.000
R6556
G1
225.01
N
9
14321253 (GRCm38)
F274S
T
C
missense
Het
possibly damaging
0.950
phenotype
2018-06-06
39
522202
Spag1
0.781
R6556
G1
225.01
N
15
36195407 (GRCm38)
Y249H
T
C
missense
Het
probably damaging
1.000
phenotype
2018-06-06
40
522195
Sstr1
1.000
R6556
G1
225.01
N
12
58213692 (GRCm38)
D367V
A
T
missense
Het
possibly damaging
0.936
phenotype
2018-06-06
41
522162
Tnnt1
0.161
R6556
G1
225.01
N
7
4509577 (GRCm38)
E110G
T
C
missense
Het
probably damaging
0.999
phenotype
2018-06-06
42
522177
Tpm1
1.000
R6556
G1
225.01
N
9
67028169 (GRCm38)
T
A
critical splice acceptor site
Het
probably null
phenotype
2018-06-06
43
522214
Unc93b1
0.000
R6556
G1
225.01
N
19
3944105 (GRCm38)
V412A
T
C
missense
Het
probably benign
0.000
phenotype
2018-06-06
44
522142
Uox
0.407
R6556
G1
225.01
N
3
146624648 (GRCm38)
G
C
critical splice donor site
1 bp
Het
probably null
phenotype
2018-06-06
45
522181
Usp44
0.000
R6556
G1
225.01
N
10
93846008 (GRCm38)
Y107H
T
C
missense
Het
probably benign
0.196
phenotype
2018-06-06
[records 1 to 45 of 45]