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Incidental Mutations
83
incidental mutations are currently displayed, and affect
81
genes.
11
are Possibly Damaging.
36
are Probably Damaging.
30
are Probably Benign.
6
are Probably Null.
4
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 83 of 83]
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
542224
1700017D01Rik
0.064
R6970
G1
225.01
N
19
11112314 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
2018-11-28
2
542213
2410089E03Rik
1.000
R6970
G1
225.01
N
15
8187548 (GRCm38)
V750A
T
C
missense
Het
probably benign
0.008
phenotype
2018-11-28
3
542184
Acadsb
0.000
R6970
G1
225.01
N
7
131434315 (GRCm38)
Y285H
T
C
missense
Het
possibly damaging
0.845
phenotype
2018-11-28
4
542206
Adam17
0.935
R6970
G1
225.01
N
12
21345668 (GRCm38)
S285P
A
G
missense
Het
probably benign
0.059
phenotype
2018-11-28
5
542152
Adcy10
0.242
R6970
G1
225.01
N
1
165556916 (GRCm38)
N1082S
A
G
missense
Het
probably benign
0.017
phenotype
2018-11-28
6
542169
Ahdc1
0.389
R6970
G1
225.01
N
4
133062345 (GRCm38)
L299Q
T
A
missense
Het
possibly damaging
0.956
phenotype
2018-11-28
7
542157
Ambra1
0.918
R6970
G1
225.01
N
2
91772600 (GRCm38)
T
A
intron
Het
probably benign
phenotype
2018-11-28
8
542146
Arfgef1
1.000
R6970
G1
225.01
N
1
10153678 (GRCm38)
Q1465R
T
C
missense
Het
probably damaging
0.997
0.309
phenotype
2018-11-28
9
542147
Arfgef1
1.000
R6970
G1
225.01
N
1
10153679 (GRCm38)
Q1465K
G
T
missense
Het
probably damaging
0.988
0.139
phenotype
2018-11-28
10
542172
Atp8a1
0.000
R6970
G1
225.01
N
5
67738462 (GRCm38)
V543A
A
G
missense
Het
probably damaging
0.997
phenotype
2018-11-28
11
542151
BC034090
0.060
R6970
G1
225.01
N
1
155241439 (GRCm38)
D311V
T
A
missense
Het
probably damaging
0.998
2018-11-28
12
542227
Blnk
0.148
R6970
G1
216.01
N
19
40962377 (GRCm38)
P110Q
G
T
missense
Het
probably damaging
0.991
phenotype
2018-11-28
13
542171
Cc2d2a
0.867
R6970
G1
225.01
N
5
43718585 (GRCm38)
E968G
A
G
missense
Het
probably damaging
1.000
phenotype
2018-11-28
14
542218
Ccdc14
0.491
R6970
G1
225.01
N
16
34709533 (GRCm38)
E394V
A
T
missense
Het
probably damaging
1.000
2018-11-28
15
542196
Ccdc162
0.062
R6970
G1
225.01
N
10
41615958 (GRCm38)
H1086Q
A
T
missense
Het
probably benign
0.026
2018-11-28
16
542222
Ccdc85b
R6970
G1
208.01
N
19
5457220 (GRCm38)
I60F
T
A
missense
Het
probably damaging
0.998
phenotype
2018-11-28
17
542181
Ceacam20
0.202
R6970
G1
225.01
N
7
19989977 (GRCm38)
L562Q
T
A
missense
Het
probably damaging
1.000
2018-11-28
18
542155
Cntrl
0.766
R6970
G1
225.01
N
2
35118137 (GRCm38)
F188L
T
C
missense
Het
probably benign
0.000
phenotype
2018-11-28
19
542165
Dclk1
0.552
R6970
G1
225.01
N
3
55466601 (GRCm38)
A
T
intron
Het
probably benign
phenotype
2018-11-28
20
542167
Ddx20
1.000
R6970
G1
225.01
N
3
105680358 (GRCm38)
L434H
A
T
missense
Het
probably damaging
1.000
phenotype
2018-11-28
21
542175
Ddx51
1.000
R6970
G1
225.01
N
5
110656862 (GRCm38)
V547M
G
A
missense
Het
probably damaging
1.000
2018-11-28
22
542208
Dnah11
0.671
R6970
G1
192.01
N
12
118108944 (GRCm38)
Q1472L
T
A
missense
Het
probably benign
0.001
phenotype
2018-11-28
23
542183
Dnajb13
0.213
R6970
G1
225.01
N
7
100507422 (GRCm38)
E149G
T
C
missense
Het
probably damaging
0.968
phenotype
2018-11-28
24
542163
Fat4
1.000
R6970
G1
225.01
N
3
38981775 (GRCm38)
N3192S
A
G
missense
Het
probably damaging
0.998
phenotype
2018-11-28
25
542164
Fat4
1.000
R6970
G1
225.01
N
3
38995971 (GRCm38)
D3994V
A
T
missense
Het
probably damaging
0.999
phenotype
2018-11-28
26
542166
Fcgr1
0.253
R6970
G1
225.01
N
3
96284620 (GRCm38)
C
A
critical splice acceptor site
Het
probably null
phenotype
2018-11-28
27
542203
Gm11639
0.084
R6970
G1
225.01
N
11
104776356 (GRCm38)
E1422G
A
G
missense
Het
probably benign
0.026
2018-11-28
28
542202
Gm12185
0.079
R6970
G1
225.01
N
11
48907912 (GRCm38)
R585*
G
A
nonsense
Het
probably null
2018-11-28
29
542199
Gm32687
R6970
G1
136.01
N
10
81879470 (GRCm38)
H232R
A
G
missense
Het
probably benign
0.448
2018-11-28
30
542201
Gm5431
0.059
R6970
G1
225.01
N
11
48888490 (GRCm38)
A535D
G
T
missense
Het
probably damaging
1.000
2018-11-28
31
542207
Gm8300
R6970
G1
159.01
N
12
87516618 (GRCm38)
G
T
start gained
Het
probably benign
2018-11-28
32
542210
Gm906
0.054
R6970
G1
225.01
N
13
50246971 (GRCm38)
Y440N
A
T
missense
Het
possibly damaging
0.861
2018-11-28
33
542209
Jarid2
1.000
R6970
G1
225.01
N
13
44902985 (GRCm38)
P556S
C
T
missense
Het
probably damaging
1.000
phenotype
2018-11-28
34
542219
Map3k4
0.927
R6970
G1
225.01
N
17
12248916 (GRCm38)
G1077V
C
A
missense
Het
probably damaging
1.000
phenotype
2018-11-28
35
542211
Mast4
0.248
R6970
G1
225.01
N
13
102804647 (GRCm38)
V301I
C
T
missense
Het
probably damaging
1.000
0.152
phenotype
2018-11-28
36
542176
Mlxip
0.340
R6970
G1
225.01
N
5
123445672 (GRCm38)
T433A
A
G
missense
Het
possibly damaging
0.517
phenotype
2018-11-28
37
542223
Mus81
0.425
R6970
G1
225.01
N
19
5485526 (GRCm38)
H199Q
G
T
missense
Het
probably benign
0.447
phenotype
2018-11-28
38
542189
Mylk3
0.302
R6970
G1
225.01
N
8
85359263 (GRCm38)
T54M
G
A
missense
Het
probably damaging
0.974
phenotype
2018-11-28
39
542212
Nalcn
1.000
R6970
G1
225.01
N
14
123314094 (GRCm38)
F1034L
A
G
missense
Het
possibly damaging
0.461
phenotype
2018-11-28
40
542221
Nfatc1
1.000
R6970
G1
225.01
N
18
80667013 (GRCm38)
S513A
A
C
missense
Het
probably benign
0.337
phenotype
2018-11-28
41
542179
Ninj2
0.000
R6970
G1
225.01
N
6
120198131 (GRCm38)
I88V
A
G
missense
Het
possibly damaging
0.911
phenotype
2018-11-28
42
542182
Nomo1
0.645
R6970
G1
225.01
N
7
46045967 (GRCm38)
P277L
C
T
missense
Het
probably damaging
0.966
2018-11-28
43
542154
Nup214
1.000
R6970
G1
225.01
N
2
32051798 (GRCm38)
S571L
C
T
missense
Het
probably damaging
0.999
phenotype
2018-11-28
44
542225
Olfr1469
0.093
R6970
G1
225.01
N
19
13411428 (GRCm38)
N286K
T
A
missense
Het
probably damaging
0.987
phenotype
2018-11-28
45
542178
Olfr461
0.062
R6970
G1
225.01
N
6
40544656 (GRCm38)
S108G
T
C
missense
Het
probably benign
0.311
phenotype
2018-11-28
46
542192
Olfr980
0.081
R6970
G1
225.01
N
9
40006713 (GRCm38)
M79L
T
A
missense
Het
probably benign
0.002
phenotype
2018-11-28
47
542197
Pcdh15
0.000
R6970
G1
225.01
N
10
74502687 (GRCm38)
P1005S
C
T
missense
Het
probably damaging
0.975
phenotype
2018-11-28
48
542214
Pkhd1l1
0.000
R6970
G1
225.01
N
15
44511674 (GRCm38)
A942T
G
A
missense
Het
possibly damaging
0.609
2018-11-28
49
542195
Plagl1
0.410
R6970
G1
225.01
N
10
13125116 (GRCm38)
C34R
T
C
missense
Het
probably damaging
1.000
phenotype
2018-11-28
50
542186
Plekha2
0.000
R6970
G1
225.01
N
8
25059264 (GRCm38)
Q168R
T
C
missense
Het
probably benign
0.001
phenotype
2018-11-28
51
542149
Plekha6
0.186
R6970
G1
225.01
N
1
133263818 (GRCm38)
A146T
G
A
missense
Het
probably benign
0.427
2018-11-28
52
542148
Plekhm3
0.136
R6970
G1
225.01
N
1
64892753 (GRCm38)
K564T
T
G
missense
Het
possibly damaging
0.798
2018-11-28
53
542198
Plpp2
0.000
R6970
G1
225.01
N
10
79530546 (GRCm38)
V26A
A
G
missense
Het
possibly damaging
0.901
phenotype
2018-11-28
54
542191
Prdm10
1.000
R6970
G1
225.01
N
9
31329823 (GRCm38)
Y302*
T
G
nonsense
Het
probably null
phenotype
2018-11-28
55
542174
Prdm8
0.675
R6970
G1
225.01
N
5
98184612 (GRCm38)
E124G
A
G
missense
Het
probably damaging
0.993
phenotype
2018-11-28
56
542150
Prg4
0.134
R6970
G1
225.01
N
1
150455906 (GRCm38)
T
G
intron
Het
probably benign
phenotype
2018-11-28
57
542158
Qser1
0.541
R6970
G1
225.01
N
2
104788130 (GRCm38)
V779A
A
G
missense
Het
probably benign
0.253
2018-11-28
58
542160
Rbm39
1.000
R6970
G1
225.01
N
2
156167584 (GRCm38)
R123C
G
A
missense
Het
probably damaging
0.997
phenotype
2018-11-28
59
542226
Ric1
0.405
R6970
G1
225.01
N
19
29587772 (GRCm38)
P640S
C
T
missense
Het
probably damaging
0.998
2018-11-28
60
542194
Rpl14
0.940
R6970
G1
225.01
N
9
120574227 (GRCm38)
G
A
utr 3 prime
Het
probably benign
phenotype
2018-11-28
61
542216
Rsl1d1
0.930
R6970
G1
225.01
N
16
11193694 (GRCm38)
D382V
T
A
missense
Het
probably benign
0.062
2018-11-28
62
542217
Rubcn
0.906
R6970
G1
163.01
N
16
32868144 (GRCm38)
G
T
intron
Het
probably benign
phenotype
2018-11-28
63
542153
Sec16a
0.954
R6970
G1
225.01
N
2
26430486 (GRCm38)
R1361C
G
A
missense
Het
probably damaging
1.000
phenotype
2018-11-28
64
542204
Slc26a11
0.067
R6970
G1
225.01
N
11
119356972 (GRCm38)
V41G
T
G
missense
Het
probably damaging
1.000
phenotype
2018-11-28
65
542200
Slc41a2
0.217
R6970
G1
225.01
N
10
83316096 (GRCm38)
F172L
A
G
missense
Het
possibly damaging
0.533
2018-11-28
66
542173
Slc4a4
1.000
R6970
G1
225.01
N
5
89179831 (GRCm38)
Y674S
A
C
missense
Het
probably damaging
0.982
phenotype
2018-11-28
67
542159
Strc
0.143
R6970
G1
225.01
N
2
121378014 (GRCm38)
M292R
A
C
missense
Het
probably benign
0.405
phenotype
2018-11-28
68
542168
Syde2
0.103
R6970
G1
188.01
N
3
145988626 (GRCm38)
T210A
A
G
missense
Het
probably benign
0.146
2018-11-28
69
542228
Tcf7l2
1.000
R6970
G1
225.01
N
19
55755048 (GRCm38)
A97E
C
A
missense
Het
probably benign
0.435
phenotype
2018-11-28
70
542188
Tenm3
0.398
R6970
G1
225.01
N
8
48236439 (GRCm38)
D2038N
C
T
missense
Het
probably damaging
1.000
phenotype
2018-11-28
71
542205
Tepsin
0.000
R6970
G1
225.01
N
11
120095364 (GRCm38)
T168M
G
A
missense
Het
probably damaging
0.985
2018-11-28
72
542187
Tex15
0.348
R6970
G1
225.01
N
8
33557428 (GRCm38)
M178L
A
T
missense
Het
probably benign
0.032
phenotype
2018-11-28
73
542193
Tgfbr2
1.000
R6970
G1
225.01
N
9
116110051 (GRCm38)
N236S
T
C
missense
Het
probably damaging
0.969
phenotype
2018-11-28
74
542177
Tnrc18
0.751
R6970
G1
225.01
N
5
142727989 (GRCm38)
V2531A
A
G
missense
Het
probably damaging
0.989
2018-11-28
75
542156
Ttn
1.000
R6970
G1
225.01
N
2
76895423 (GRCm38)
T
G
intron
Het
probably benign
phenotype
2018-11-28
76
542185
Tubgcp3
0.963
R6970
G1
225.01
N
8
12637000 (GRCm38)
D630E
G
T
missense
Het
probably damaging
0.976
2018-11-28
77
542170
Ubr4
1.000
R6970
G1
225.01
N
4
139406528 (GRCm38)
W745*
G
A
nonsense
Het
probably null
phenotype
2018-11-28
78
542220
Vmn2r115
0.086
R6970
G1
225.01
N
17
23346015 (GRCm38)
G292D
G
A
missense
Het
probably benign
0.232
2018-11-28
79
542180
Vmn2r38
R6970
G1
145.01
N
7
9075341 (GRCm38)
K681*
T
A
nonsense
Het
probably null
2018-11-28
80
542215
Xrcc6
0.000
R6970
G1
225.01
N
15
82031174 (GRCm38)
K98E
A
G
missense
Het
probably benign
0.034
phenotype
2018-11-28
81
542190
Zfp423
0.805
R6970
G1
225.01
N
8
87803779 (GRCm38)
V13A
A
G
missense
Het
probably benign
0.003
phenotype
2018-11-28
82
542162
Zfp512b
0.000
R6970
G1
225.01
N
2
181586348 (GRCm38)
I5T
A
G
missense
Het
possibly damaging
0.922
2018-11-28
83
542161
Zmynd8
1.000
R6970
G1
131.01
N
2
165875750 (GRCm38)
E14K
C
T
missense
Het
probably damaging
0.998
phenotype
2018-11-28
[records 1 to 83 of 83]