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Incidental Mutations
45
incidental mutations are currently displayed, and affect
45
genes.
3
are Possibly Damaging.
18
are Probably Damaging.
17
are Probably Benign.
6
are Probably Null.
1
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
73227
1600012H06Rik
0.125
IGL01301
G1
17
14943919 (GRCm38)
C
T
splice site
1090 bp
Het
probably null
phenotype
2013-10-07
2
73243
Acacb
0.000
IGL01301
G1
5
114246498 (GRCm38)
I2238L
A
T
missense
Het
probably benign
0.000
phenotype
2013-10-07
3
73247
Aldh1l2
0.000
IGL01301
G1
10
83522846 (GRCm38)
Y95C
T
C
missense
Het
probably damaging
0.999
phenotype
2013-10-07
4
73244
Asxl2
0.920
IGL01301
G1
12
3501425 (GRCm38)
T1056A
A
G
missense
Het
probably damaging
1.000
phenotype
2013-10-07
5
73231
B4galnt1
0.000
IGL01301
G1
10
127169779 (GRCm38)
T250A
A
G
missense
Het
possibly damaging
0.555
phenotype
2013-10-07
6
73253
Cela3b
0.063
IGL01301
G1
4
137423843 (GRCm38)
A
T
critical splice donor site
2 bp
Het
probably null
phenotype
2013-10-07
7
73226
Chst3
0.197
IGL01301
G1
10
60185832 (GRCm38)
T398A
T
C
missense
Het
probably damaging
0.999
phenotype
2013-10-07
8
73225
Cngb3
0.083
IGL01301
G1
4
19425625 (GRCm38)
T478A
A
G
missense
Het
probably damaging
1.000
phenotype
2013-10-07
9
73223
Cyp4a10
0.060
IGL01301
G1
4
115518455 (GRCm38)
L45P
T
C
missense
Het
probably damaging
1.000
phenotype
2013-10-07
10
73238
Defb21
0.065
IGL01301
G1
2
152574751 (GRCm38)
E49G
A
G
missense
Het
possibly damaging
0.847
2013-10-07
11
73237
Dnajc1
0.130
IGL01301
G1
2
18308834 (GRCm38)
T159A
T
C
missense
Het
probably damaging
0.989
phenotype
2013-10-07
12
73234
Dnmbp
0.000
IGL01301
G1
19
43902354 (GRCm38)
S325P
A
G
missense
Het
probably benign
0.036
phenotype
2013-10-07
13
73233
Fam91a1
0.000
IGL01301
G1
15
58442871 (GRCm38)
F534L
T
C
missense
Het
probably damaging
0.993
phenotype
2013-10-07
14
73236
Fermt2
1.000
IGL01301
G1
14
45464863 (GRCm38)
E488G
T
C
missense
Het
probably damaging
0.997
phenotype
2013-10-07
15
73219
Filip1
0.522
IGL01301
G1
9
79819180 (GRCm38)
D719G
T
C
missense
Het
possibly damaging
0.928
phenotype
2013-10-07
16
73245
Gad1-ps
0.186
IGL01301
G1
10
99445151 (GRCm38)
A
G
exon
Het
noncoding transcript
2013-10-07
17
73224
Glra3
0.000
IGL01301
G1
8
55940962 (GRCm38)
A36E
C
A
missense
Het
probably benign
0.001
phenotype
2013-10-07
18
73261
Gm9884
IGL01301
G1
1
25830648 (GRCm38)
T
A
unclassified
Het
probably benign
2013-10-07
19
73255
Hectd2
0.000
IGL01301
G1
19
36569370 (GRCm38)
T
C
splice site
Het
probably benign
2013-10-07
20
73257
Hnrnpm
1.000
IGL01301
G1
17
33669168 (GRCm38)
C
T
critical splice donor site
1 bp
Het
probably null
phenotype
2013-10-07
21
73218
Lrrk2
0.405
IGL01301
G1
15
91767339 (GRCm38)
Y1733N
T
A
missense
Het
probably damaging
1.000
phenotype
2013-10-07
22
73248
Mindy1
0.000
IGL01301
G1
3
95288390 (GRCm38)
L148P
T
C
missense
Het
probably damaging
1.000
2013-10-07
23
73242
Mkrn2
0.000
IGL01301
G1
6
115611789 (GRCm38)
Y164*
C
A
nonsense
Het
probably null
phenotype
2013-10-07
24
73240
Msra
0.119
IGL01301
G1
14
64210435 (GRCm38)
Y135C
T
C
missense
Het
probably damaging
1.000
phenotype
2013-10-07
25
73241
Ndst3
0.248
IGL01301
G1
3
123548916 (GRCm38)
A749T
C
T
missense
Het
probably damaging
0.970
phenotype
2013-10-07
26
73235
Ngdn
1.000
IGL01301
G1
14
55017114 (GRCm38)
A41S
G
T
missense
Het
probably benign
0.148
phenotype
2013-10-07
27
73249
Nlrp12
0.145
IGL01301
G1
7
3240092 (GRCm38)
S597T
A
T
missense
Het
probably damaging
0.999
phenotype
2013-10-07
28
73220
Olfr1451
0.194
IGL01301
G1
19
12999417 (GRCm38)
I144F
A
T
missense
Het
probably damaging
0.988
phenotype
2013-10-07
29
73251
Pabpc6
0.098
IGL01301
G1
17
9667970 (GRCm38)
S551P
A
G
missense
Het
probably benign
0.000
2013-10-07
30
73232
Plekhg5
0.138
IGL01301
G1
4
152112553 (GRCm38)
A752V
C
T
missense
Het
probably benign
0.000
phenotype
2013-10-07
31
73246
Prpf4b
1.000
IGL01301
G1
13
34884291 (GRCm38)
S368P
T
C
missense
Het
probably benign
0.226
phenotype
2013-10-07
32
73254
Pus7
0.638
IGL01301
G1
5
23746424 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
2013-10-07
33
73259
Rad23b
1.000
IGL01301
G1
4
55366774 (GRCm38)
T
C
splice site
Het
probably benign
phenotype
2013-10-07
34
73260
Rgs13
0.000
IGL01301
G1
1
144171414 (GRCm38)
T
C
splice site
Het
probably benign
phenotype
2013-10-07
35
73262
Sfpq
1.000
IGL01301
G1
4
127026760 (GRCm38)
T
C
splice site
Het
probably benign
phenotype
2013-10-07
36
73221
Slc9a9
0.000
IGL01301
G1
9
95055459 (GRCm38)
S455T
T
A
missense
Het
probably benign
0.025
phenotype
2013-10-07
37
73256
Slco1a1
0.210
IGL01301
G1
6
141932530 (GRCm38)
A
G
splice site
Het
probably benign
phenotype
2013-10-07
38
73229
Tmem26
0.068
IGL01301
G1
10
68778606 (GRCm38)
N284Y
A
T
missense
Het
probably damaging
1.000
phenotype
2013-10-07
39
73239
Tmem87a
0.133
IGL01301
G1
2
120380769 (GRCm38)
I232V
T
C
missense
Het
probably benign
0.011
2013-10-07
40
73250
Trpm2
0.141
IGL01301
G1
10
77923984 (GRCm38)
L1106P
A
G
missense
Het
probably damaging
0.997
phenotype
2013-10-07
41
73258
Vmn1r18
0.055
IGL01301
G1
6
57389667 (GRCm38)
T
C
utr 3 prime
Het
probably benign
2013-10-07
42
73230
Zfp213
0.056
IGL01301
G1
17
23561417 (GRCm38)
A43D
G
T
missense
Het
probably benign
0.176
phenotype
2013-10-07
43
73228
Zfp365
0.000
IGL01301
G1
10
67909354 (GRCm38)
V198A
A
G
missense
Het
probably damaging
0.997
phenotype
2013-10-07
44
73252
Zfp395
0.000
IGL01301
G1
14
65394751 (GRCm38)
T
A
splice site
Het
probably null
2013-10-07
45
73222
Zfp618
0.156
IGL01301
G1
4
63132826 (GRCm38)
V615M
G
A
missense
Het
probably damaging
0.998
2013-10-07
[records 1 to 45 of 45]