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Incidental Mutations
168
incidental mutations are currently displayed, and affect
153
genes.
10
are Possibly Damaging.
31
are Probably Damaging.
107
are Probably Benign.
17
are Probably Null.
6
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 100 of 168]
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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
511256
2810004N23Rik
0.562
FR4342
214.46
N
8
124839833 (GRCm38)
TT
TTATGT
frame shift
Homo
probably null
2018-04-05
2
511206
4930402H24Rik
0.000
FR4342
156.47
N
2
130770742 (GRCm38)
TCC
TCCCCC
small insertion
Het
probably benign
phenotype
2018-04-05
3
511245
4930433I11Rik
0.067
FR4342
186.47
N
7
40993055 (GRCm38)
AACC
A
small deletion
Het
probably benign
2018-04-05
4
511231
4930548H24Rik
0.049
FR4342
214.46
N
5
31487373 (GRCm38)
GAGAAG
GAG
small deletion
Homo
probably benign
2018-04-05
5
511293
7530416G11Rik
0.069
FR4342
222
N
15
85494307 (GRCm38)
E45V
T
A
missense
Homo
unknown
2018-04-05
6
324205
Aars2
1.000
R4342
G1
225
Y
17
45516495 (GRCm38)
C488R
T
C
missense
Het
probably benign
0.000
0.090
phenotype
2015-06-24
7
324208
Adamts19
0.000
R4342
G1
225
Y
18
58942500 (GRCm38)
H489L
A
T
missense
Het
probably damaging
1.000
0.850
phenotype
2015-06-24
8
511250
AF366264
0.684
FR4342
87.01
N
8
13837613 (GRCm38)
H159Q
G
C
missense
Het
probably benign
0.002
2018-04-05
9
324210
Ahnak
0.260
R4342
G1
225
Y
19
9012083 (GRCm38)
V3577A
T
C
missense
Het
possibly damaging
0.794
0.073
phenotype
2015-06-24
10
511216
Ankrd35
0.000
FR4342
113.47
N
3
96683515 (GRCm38)
TCCCC
TCCC
frame shift
Het
probably null
2018-04-05
11
511258
Anxa2
0.000
FR4342
130.47
N
9
69480205 (GRCm38)
CCC
CCCACC
small insertion
Het
probably benign
phenotype
2018-04-05
12
511259
Anxa2
0.000
FR4342
154.47
N
9
69480210 (GRCm38)
C
CCCA
small insertion
Het
probably benign
phenotype
2018-04-05
13
511302
Apc
0.970
FR4342
214.47
N
18
34281999 (GRCm38)
CAATAAAGC
CAATAAAGCAAATAAAGC
intron
Homo
probably benign
phenotype
2018-04-05
14
324186
Arhgap44
0.000
R4342
G1
119
Y
11
65012061 (GRCm38)
R401*
G
A
nonsense
Het
probably null
0.971
2015-06-24
15
511272
Arrb2
0.000
FR4342
222
N
11
70438671 (GRCm38)
T269M
C
T
missense
Homo
probably damaging
1.000
phenotype
2018-04-05
16
511275
Bcas3
0.686
FR4342
222
N
11
85509497 (GRCm38)
V431I
G
A
missense
Homo
probably benign
0.115
2018-04-05
17
511283
Begain
0.000
FR4342
123.97
N
12
109033418 (GRCm38)
CCCCGCC
CCCCGCCCCCGCC
unclassified
Homo
probably benign
2018-04-05
18
511205
Catsper2
0.120
FR4342
210.47
N
2
121397793 (GRCm38)
TCA
TCAACA
utr 3 prime
Het
probably benign
phenotype
2018-04-05
19
324195
Cbx3-ps2
R4342
G1
225
Y
13
65559688 (GRCm38)
T
C
intron
Het
noncoding transcript
0.087
2015-06-24
20
324171
Ccdc174
1.000
R4342
G1
225
Y
6
91885356 (GRCm38)
L86*
T
A
nonsense
Het
probably null
0.976
phenotype
2015-06-24
21
511263
Cd164
0.214
FR4342
222
N
10
41521926 (GRCm38)
A59S
G
T
missense
Homo
probably benign
0.003
0.090
phenotype
2018-04-05
22
511244
Cd22
0.000
FR4342
222
N
7
30878082 (GRCm38)
R2H
C
T
missense
Homo
possibly damaging
0.948
0.179
phenotype
2018-04-05
23
324163
Cd38
0.000
R4342
G1
225
Y
5
43869089 (GRCm38)
I72L
A
C
missense
Het
probably benign
0.003
0.090
phenotype
2015-06-24
24
324177
Cers4
0.000
R4342
G1
225
Y
8
4521223 (GRCm38)
L264P
T
C
missense
Het
probably damaging
0.999
0.880
phenotype
2015-06-24
25
324178
Cldn23
0.071
R4342
G1
225
Y
8
35825498 (GRCm38)
S279P
A
G
missense
Het
probably benign
0.002
0.069
phenotype
2015-06-24
26
511273
Cluh
0.233
FR4342
217.47
N
11
74669524 (GRCm38)
GAGCCT
GAGCCTCAGCCT
small insertion
Het
probably benign
phenotype
2018-04-05
27
511274
Cluh
0.233
FR4342
217.47
N
11
74669526 (GRCm38)
GCCTGA
GCCTGAACCTGA
small insertion
Het
probably benign
phenotype
2018-04-05
28
511279
Cntnap1
0.270
FR4342
217.47
N
11
101189575 (GRCm38)
AGCCCC
AGCCCCCGCCCC
unclassified
Het
probably benign
phenotype
2018-04-05
29
511294
Col2a1
1.000
FR4342
225.01
N
15
97988981 (GRCm38)
C
A
splice site
Het
probably null
0.976
phenotype
2018-04-05
30
511261
Col6a5
0.845
FR4342
222
N
9
105934174 (GRCm38)
N715K
A
T
missense
Homo
unknown
phenotype
2018-04-05
31
511268
Cpeb4
0.351
FR4342
108.46
N
11
31927638 (GRCm38)
T
TGA
critical splice acceptor site
Homo
probably benign
phenotype
2018-04-05
32
324162
Cth
0.000
R4342
G1
225
Y
3
157924976 (GRCm38)
T19S
T
A
missense
Het
probably damaging
1.000
0.298
phenotype
2015-06-24
33
511255
D230025D16Rik
0.284
FR4342
222
N
8
105241098 (GRCm38)
G207E
G
A
missense
Homo
probably benign
0.000
2018-04-05
34
511260
Dbr1
1.000
FR4342
217.47
N
9
99583680 (GRCm38)
AGGAGG
AGGAGGGGGAGG
unclassified
Het
probably benign
phenotype
2018-04-05
35
511251
Defa29
0.050
FR4342
140.01
N
8
21326144 (GRCm38)
R69P
C
G
missense
Het
probably benign
0.000
2018-04-05
36
511280
Dhx8
0.969
FR4342
148.47
N
11
101738206 (GRCm38)
CG
CGAGAACGG
frame shift
Het
probably null
phenotype
2018-04-05
37
511289
Dnah12
0.169
FR4342
222
N
14
26849385 (GRCm38)
G2817V
G
T
missense
Homo
probably damaging
1.000
0.299
2018-04-05
38
324201
Dnajc22
0.087
R4342
G1
225
Y
15
99104464 (GRCm38)
L330*
T
A
nonsense
Het
probably null
0.976
2015-06-24
39
511232
Dthd1
0.228
FR4342
214.46
N
5
62843026 (GRCm38)
C
CTTA
small insertion
Homo
probably benign
phenotype
2018-04-05
40
511297
E4f1
1.000
FR4342
102.47
N
17
24455197 (GRCm38)
GC
GCCCC
unclassified
Het
probably benign
phenotype
2018-04-05
41
324206
Epas1
1.000
R4342
G1
225
Y
17
86823800 (GRCm38)
C336Y
G
A
missense
Het
probably damaging
1.000
0.953
phenotype
2015-06-24
42
324176
Evi5l
0.108
R4342
G1
225
Y
8
4183492 (GRCm38)
A
C
utr 5 prime
Het
probably benign
2015-06-24
43
511303
F830016B08Rik
0.054
FR4342
214.46
N
18
60299941 (GRCm38)
A
ACAG
small insertion
Homo
probably benign
2018-04-05
44
511221
Fam166b
0.090
FR4342
214.46
N
4
43427384 (GRCm38)
CAGAG
CAG
frame shift
Homo
probably null
2018-04-05
45
324185
Fam71b
0.000
R4342
G1
225
Y
11
46407216 (GRCm38)
D449G
A
G
missense
Het
possibly damaging
0.672
2015-06-24
46
511233
Fbrsl1
0.078
FR4342
157.47
N
5
110378125 (GRCm38)
GTGTGTGTGCTGGTGCGTGTGCTGGTG
GTGTGTGTGCTGGTGTGTGTGCTGGTGCGTGTGCTGGTG
small insertion
Het
probably benign
2018-04-05
47
324182
Fbxl2
0.000
R4342
G1
225
Y
9
113985306 (GRCm38)
H272Q
A
T
missense
Het
probably benign
0.000
0.071
phenotype
2015-06-24
48
511257
Fbxo22
0.000
FR4342
98.01
N
9
55221070 (GRCm38)
A
C
splice site
231 bp
Het
probably null
phenotype
2018-04-05
49
324194
Fgd3
0.129
R4342
G1
225
Y
13
49273709 (GRCm38)
C
T
critical splice donor site
1 bp
Het
probably null
0.958
2015-06-24
50
324161
Fhdc1
0.431
R4342
G1
222
Y
3
84444826 (GRCm38)
V1031F
C
A
missense
Het
probably benign
0.418
0.064
2015-06-24
51
511213
Flg
0.367
FR4342
81.01
N
3
93290513 (GRCm38)
G
A
unclassified
Het
probably benign
phenotype
2018-04-05
52
511204
Fmn1
0.323
FR4342
214.47
N
2
113525783 (GRCm38)
TCC
TCCTCCACC
small insertion
Homo
probably benign
phenotype
2018-04-05
53
511290
Frmpd2
0.000
FR4342
222
N
14
33511021 (GRCm38)
L399F
G
T
missense
Homo
probably damaging
1.000
phenotype
2018-04-05
54
324167
Fscn1
0.470
R4342
G1
225
Y
5
142972021 (GRCm38)
Y308H
T
C
missense
Het
probably damaging
1.000
0.920
phenotype
2015-06-24
55
511219
Gbp2b
0.000
FR4342
139.01
N
3
142603652 (GRCm38)
I175V
A
G
missense
Het
probably benign
0.002
phenotype
2018-04-05
56
511270
Gjc2
0.000
FR4342
214.46
N
11
59182743 (GRCm38)
T
TCCCG
unclassified
Homo
probably benign
phenotype
2018-04-05
57
511224
Gm13103
0.077
FR4342
165.47
N
4
143851643 (GRCm38)
AA
AATA
frame shift
Homo
probably null
2018-04-05
58
511209
Gm14496
0.000
FR4342
82.01
N
2
181995906 (GRCm38)
K258Q
A
C
missense
Het
probably benign
0.006
2018-04-05
59
511264
Gm4340
FR4342
152.47
N
10
104196066 (GRCm38)
CAGAAG
CAGAAGAAG
small insertion
Het
probably benign
2018-04-05
60
511265
Gm4340
FR4342
143.47
N
10
104196099 (GRCm38)
CAGAAG
CAGAAGAAG
small insertion
Het
probably benign
2018-04-05
61
324170
Gm5878
0.056
R4342
G1
225
Y
6
85125651 (GRCm38)
R31*
G
A
nonsense
Het
probably null
0.976
2015-06-24
62
511222
Gm7534
0.060
FR4342
214.46
N
4
134202631 (GRCm38)
G
GCTC
small insertion
Homo
probably benign
2018-04-05
63
324153
Gm996
0.101
R4342
G1
225
Y
2
25579108 (GRCm38)
Y264H
A
G
missense
Het
possibly damaging
0.915
0.117
2015-06-24
64
511301
Gpatch11
0.116
FR4342
217.47
N
17
78842178 (GRCm38)
AGAGGA
AGAGGATGAGGA
small insertion
Het
probably benign
2018-04-05
65
324191
Gpatch2l
0.000
R4342
G1
225
Y
12
86260679 (GRCm38)
V277A
T
C
missense
Het
probably benign
0.001
0.060
2015-06-24
66
324207
Greb1l
1.000
R4342
G1
225
Y
18
10544561 (GRCm38)
M1385K
T
A
missense
Het
probably benign
0.115
0.118
2015-06-24
67
324203
Grin2a
0.582
R4342
G1
225
Y
16
9653589 (GRCm38)
I605T
A
G
missense
Het
possibly damaging
0.518
0.453
phenotype
2015-06-24
68
511300
H2-Q4
0.056
FR4342
222
N
17
35380405 (GRCm38)
D155N
G
A
missense
Homo
probably damaging
1.000
0.647
phenotype
2018-04-05
69
511285
Hist1h1t
0.000
FR4342
122.46
N
13
23695913 (GRCm38)
TGTGG
TG
unclassified
Homo
probably benign
phenotype
2018-04-05
70
511236
Hoxa3
1.000
FR4342
216.23
N
6
52170130 (GRCm38)
G
GCTT
unclassified
Homo
probably benign
phenotype
2018-04-05
71
324202
Hoxc11
0.852
R4342
G1
225
Y
15
102954671 (GRCm38)
S49F
C
T
missense
Het
probably damaging
1.000
0.257
phenotype
2015-06-24
72
511203
Ifi208
0.000
FR4342
214.46
N
1
173677698 (GRCm38)
ATGGTG
ATG
small deletion
Homo
probably benign
2018-04-05
73
324204
Igf2r
0.918
R4342
G1
225
Y
17
12709511 (GRCm38)
E982K
C
T
missense
Het
possibly damaging
0.955
0.145
phenotype
2015-06-24
74
324193
Ighv10-3
0.199
R4342
G1
225
Y
12
114523504 (GRCm38)
M99K
A
T
missense
Het
possibly damaging
0.737
0.179
2015-06-24
75
511284
Ighv5-9
0.312
FR4342
222
N
12
113661877 (GRCm38)
S82N
C
T
missense
Homo
probably benign
0.017
0.090
2018-04-05
76
324190
Itgb4
1.000
R4342
G1
225
Y
11
115988729 (GRCm38)
T614S
A
T
missense
Het
probably benign
0.007
0.117
phenotype
2015-06-24
77
324199
Kcnv1
0.000
R4342
G1
225
Y
15
45114444 (GRCm38)
T66M
G
A
missense
Het
probably damaging
1.000
0.906
phenotype
2015-06-24
78
511239
Klra10
0.057
FR4342
120.01
N
6
130272747 (GRCm38)
R192C
G
A
missense
Het
probably benign
0.008
2018-04-05
79
511243
Kmt2b
1.000
FR4342
217.47
N
7
30586375 (GRCm38)
TCCTCC
TCCTCCCCCTCC
unclassified
Het
probably benign
phenotype
2018-04-05
80
511277
Krt10
0.364
FR4342
218.11
N
11
99386199 (GRCm38)
CGCC
CGCCGCC
unclassified
Het
probably benign
phenotype
2018-04-05
81
511278
Krt10
0.364
FR4342
214.46
N
11
99386203 (GRCm38)
ACC
ACCCCC
unclassified
Homo
probably benign
phenotype
2018-04-05
82
511212
Lce1m
FR4342
108.47
N
3
93018247 (GRCm38)
CGCTGCTGCTGCCACAGCA
C
unclassified
Het
probably benign
2018-04-05
83
511252
Mak16
0.969
FR4342
149
N
8
31161749 (GRCm38)
E203D
T
G,A
missense
Homo
probably benign
0.003
2018-04-05
84
324196
Mast4
0.335
R4342
G1
225
Y
13
102774248 (GRCm38)
V461A
A
G
missense
Het
probably damaging
1.000
0.267
phenotype
2015-06-24
85
324160
Mcts2
0.932
R4342
G1
225
Y
2
152687664 (GRCm38)
V132M
G
A
missense
Het
probably damaging
1.000
0.647
2015-06-24
86
511210
Med12l
0.271
FR4342
175.47
N
3
59275988 (GRCm38)
AGC
AGCGGC
small insertion
Het
probably benign
phenotype
2018-04-05
87
511211
Med12l
0.271
FR4342
168.47
N
3
59275994 (GRCm38)
AGCGGC
AGCGGCGGC
small insertion
Het
probably benign
phenotype
2018-04-05
88
324173
Mical3
0.173
R4342
G1
225
Y
6
120934838 (GRCm38)
E1083*
C
A
nonsense
Het
probably null
0.976
2015-06-24
89
511234
Mn1
1.000
FR4342
193.47
N
5
111419706 (GRCm38)
AGC
AGCGGC
small insertion
Het
probably benign
phenotype
2018-04-05
90
511267
Nacad
0.000
FR4342
217.47
N
11
6599762 (GRCm38)
TC
TCAGGGGC
small insertion
Het
probably benign
2018-04-05
91
511288
Naip1
0.000
FR4342
83.01
N
13
100425471 (GRCm38)
R1062K
C
T
missense
Het
probably benign
0.005
phenotype
2018-04-05
92
324181
Nbeal2
0.261
R4342
G1
225
Y
9
110631793 (GRCm38)
A
G
intron
Het
probably benign
0.090
phenotype
2015-06-24
93
511271
Ndel1
1.000
FR4342
225.01
N
11
68833409 (GRCm38)
P246L
G
A
missense
Het
probably damaging
0.966
phenotype
2018-04-05
94
324198
Nek4
0.387
R4342
G1
225
Y
14
30953906 (GRCm38)
V66A
T
C
missense
Het
probably damaging
1.000
0.643
phenotype
2015-06-24
95
511299
Nelfe
1.000
FR4342
217.47
N
17
34854089 (GRCm38)
AC
ACAAAGAGCGGGATCGAGACAGAGCC
unclassified
Het
probably benign
phenotype
2018-04-05
96
324151
Nfasc
1.000
R4342
G1
225
Y
1
132631705 (GRCm38)
F229S
A
G
missense
Het
probably damaging
0.999
0.582
phenotype
2015-06-24
97
324183
Nhsl1
0.000
R4342
G1
225
Y
10
18526689 (GRCm38)
F1221S
T
C
missense
Het
probably damaging
1.000
0.062
2015-06-24
98
324187
Nr1d1
0.000
R4342
G1
225
Y
11
98771814 (GRCm38)
K118Q
T
G
missense
Het
probably damaging
0.998
0.156
phenotype
2015-06-24
99
324179
Ntm
0.140
R4342
G1
225
Y
9
29109431 (GRCm38)
E164G
T
C
missense
Het
probably damaging
0.982
0.225
phenotype
2015-06-24
100
511247
Olfr495
0.234
FR4342
150.01
N
7
108395893 (GRCm38)
T258A
A
G
missense
Het
probably benign
0.000
phenotype
2018-04-05
[records 1 to 100 of 168]
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