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Incidental Mutations
38
incidental mutations are currently displayed, and affect
37
genes.
4
are Possibly Damaging.
11
are Probably Damaging.
18
are Probably Benign.
3
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 38 of 38]
10
25
50
100
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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
322059
Anapc5
0.956
R4287
G1
225
Y
5
122800601 (GRCm38)
V362A
A
G
missense
Het
probably benign
0.021
0.134
phenotype
2015-06-20
2
322052
Ash1l
1.000
R4287
G1
225
Y
3
89066415 (GRCm38)
C2594S
T
A
missense
Het
probably damaging
0.993
0.975
phenotype
2015-06-20
3
322068
Ccdc82
0.093
R4287
G1
225
Y
9
13253418 (GRCm38)
Q303K
C
A
missense
Het
probably benign
0.126
0.103
2015-06-20
4
322070
Cog1
0.860
R4287
G1
225
Y
11
113654027 (GRCm38)
Y345C
A
G
missense
Het
probably damaging
0.991
0.121
phenotype
2015-06-20
5
322055
Fpgt
0.130
R4287
G1
225
Y
3
155091360 (GRCm38)
T
C
unclassified
Het
probably benign
0.090
phenotype
2015-06-20
6
322051
Glrb
1.000
R4287
G1
225
Y
3
80845232 (GRCm38)
V408D
A
T
missense
Het
possibly damaging
0.842
0.248
phenotype
2015-06-20
7
322047
Gm7135
0.123
R4287
G1
225
Y
1
97400398 (GRCm38)
A
G
exon
Het
noncoding transcript
0.087
2015-06-20
8
322048
Il1rn
0.076
R4287
G1
225
Y
2
24349545 (GRCm38)
L151P
T
C
missense
Het
probably damaging
0.962
0.647
phenotype
2015-06-20
9
322049
Itgav
1.000
R4287
G1
225
Y
2
83724840 (GRCm38)
E36*
G
T
nonsense
Het
probably null
0.976
phenotype
2015-06-20
10
322071
Kidins220
1.000
R4287
G1
225
Y
12
25056846 (GRCm38)
E1433K
G
A
missense
Het
possibly damaging
0.815
0.122
phenotype
2015-06-20
11
322063
Klk14
0.000
R4287
G1
225
Y
7
43692077 (GRCm38)
C51Y
G
A
missense
Het
probably damaging
1.000
0.793
phenotype
2015-06-20
12
368372
Klra3
0.048
R4287
G1
225
Y
6
130334302 (GRCm38)
C39R
A
G
missense
Het
probably benign
0.076
0.090
2016-02-02
13
322053
Lce1i
0.094
R4287
G1
225
Y
3
92777435 (GRCm38)
S145P
A
G
missense
Het
unknown
0.076
2015-06-20
14
322079
Memo1
1.000
R4287
G1
225
Y
17
74255298 (GRCm38)
T
C
critical splice acceptor site
Het
probably null
0.948
phenotype
2015-06-20
15
368373
Mpp3
0.000
R4287
G1
225
Y
11
102023463 (GRCm38)
A102V
G
A
missense
Het
probably damaging
1.000
0.605
phenotype
2016-02-02
16
322062
Mug2
0.061
R4287
G1
225
Y
6
122063673 (GRCm38)
D727E
T
A
missense
Het
probably benign
0.001
0.090
2015-06-20
17
322081
Ndufb8
1.000
R4287
G1
225
Y
19
44552691 (GRCm38)
I107V
T
C
missense
Het
probably benign
0.124
0.090
2015-06-20
18
322076
Olfr186
0.083
R4287
G1
225
Y
16
59027613 (GRCm38)
M98K
A
T
missense
Het
probably benign
0.005
0.128
phenotype
2015-06-20
19
322072
Pnn
1.000
R4287
G1
225
Y
12
59072170 (GRCm38)
T513I
C
T
missense
Het
possibly damaging
0.861
0.179
phenotype
2015-06-20
20
322066
Ric8a
1.000
R4287
G1
225
Y
7
140861422 (GRCm38)
Y210C
A
G
missense
Het
probably damaging
1.000
0.831
phenotype
2015-06-20
21
322073
Ripor2
0.219
R4287
G1
225
Y
13
24725009 (GRCm38)
V1037M
G
A
missense
Het
probably damaging
0.997
0.130
phenotype
2015-06-20
22
322074
Rreb1
0.962
R4287
G1
225
Y
13
37931931 (GRCm38)
T1089S
A
T
missense
Het
probably benign
0.029
0.092
phenotype
2015-06-20
23
368370
Rrs1
1.000
R4287
G1
20
Y
1
9546215 (GRCm38)
S231L
C
T
missense
Het
probably damaging
1.000
0.647
2016-02-02
24
368371
Rrs1
1.000
R4287
G1
64
Y
1
9546223 (GRCm38)
R234C
C
T
missense
Het
possibly damaging
0.822
0.197
2016-02-02
25
322065
Sec23ip
0.583
R4287
G1
225
Y
7
128777333 (GRCm38)
D838G
A
G
missense
Het
probably benign
0.367
0.205
phenotype
2015-06-20
26
322080
Setbp1
0.573
R4287
G1
225
Y
18
78859061 (GRCm38)
I464V
T
C
missense
Het
probably benign
0.025
0.059
phenotype
2015-06-20
27
322057
Slc25a51
0.171
R4287
G1
225
Y
4
45399768 (GRCm38)
V141M
C
T
missense
Het
probably benign
0.427
0.160
2015-06-20
28
322061
Slc41a3
0.000
R4287
G1
225
Y
6
90640922 (GRCm38)
H310L
A
T
missense
Het
probably benign
0.001
0.090
phenotype
2015-06-20
29
322060
Smurf1
0.000
R4287
G1
225
Y
5
144891458 (GRCm38)
S363P
A
G
missense
Het
probably benign
0.001
0.071
phenotype
2015-06-20
30
322056
Tln1
1.000
R4287
G1
225
Y
4
43543509 (GRCm38)
R1269Q
C
T
missense
Het
probably benign
0.006
0.086
phenotype
2015-06-20
31
322069
Tmed3
0.085
R4287
G1
218
Y
9
89704898 (GRCm38)
S10P
A
G
missense
Het
probably benign
0.228
0.106
2015-06-20
32
322075
Tomm70a
0.969
R4287
G1
225
Y
16
57140622 (GRCm38)
Y313D
T
G
missense
Het
probably damaging
1.000
0.721
phenotype
2015-06-20
33
322078
Umodl1
0.000
R4287
G1
225
Y
17
30988065 (GRCm38)
E810G
A
G
missense
Het
probably benign
0.113
0.097
2015-06-20
34
322054
Unc5c
1.000
R4287
G1
225
Y
3
141714674 (GRCm38)
I52T
T
C
missense
Het
probably damaging
0.996
0.393
phenotype
2015-06-20
35
322067
Unc5d
0.224
R4287
G1
225
Y
8
28719796 (GRCm38)
Y432F
T
A
missense
Het
probably benign
0.003
0.064
phenotype
2015-06-20
36
322077
Vmn2r97
0.060
R4287
G1
225
Y
17
18948075 (GRCm38)
A
T
intron
Het
probably benign
0.090
2015-06-20
37
322064
Zfp629
0.345
R4287
G1
225
Y
7
127611938 (GRCm38)
Y233C
T
C
missense
Het
probably damaging
1.000
0.407
2015-06-20
38
322058
Zfp986
0.186
R4287
G1
117
N
4
145892518 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
2015-06-20
[records 1 to 38 of 38]