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Incidental Mutations
30
incidental mutations are currently displayed, and affect
30
genes.
6
are Possibly Damaging.
14
are Probably Damaging.
8
are Probably Benign.
1
are Probably Null.
1
create premature stop codons.
0
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 30 of 30]
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
63480
Acacb
0.000
V1662
164
N
633
5
114238708 (GRCm38)
G1951R
G
C
missense
Het
probably damaging
0.999
phenotype
2013-07-30
2
63498
Adamts12
0.104
V1662
144
N
633
15
11071808 (GRCm38)
L146Q
T
A
missense
Het
probably benign
0.126
0.217
phenotype
2013-07-30
3
63485
Adgra1
0.166
V1662
176
N
633
7
139852579 (GRCm38)
I111T
T
C
missense
Het
probably damaging
0.977
0.701
phenotype
2013-07-30
4
63496
Amph
0.233
V1662
131
N
633
13
19139370 (GRCm38)
V601M
G
A
missense
Het
probably benign
0.358
phenotype
2013-07-30
5
63471
Arfgef1
1.000
V1662
105
N
633
1
10173253 (GRCm38)
K1024E
T
C
missense
Het
probably damaging
1.000
0.405
phenotype
2013-07-30
6
63477
Arhgef2
0.678
V1662
192
N
633
3
88633329 (GRCm38)
R154Q
G
A
missense
Het
probably damaging
0.998
phenotype
2013-07-30
7
63478
Bank1
0.060
V1662
141
N
633
3
136054418 (GRCm38)
D782V
T
A
missense
Het
probably damaging
0.999
0.071
phenotype
2013-07-30
8
63493
Bhlha9
0.000
V1662
178
N
633
11
76673036 (GRCm38)
R163L
G
T
missense
Het
probably benign
0.300
phenotype
2013-07-30
9
63502
Cacna1h
0.000
V1662
131
N
633
17
25377309 (GRCm38)
N1913D
T
C
missense
Het
possibly damaging
0.676
phenotype
2013-07-30
10
63495
Cd7
0.000
V1662
181
N
633
11
121037126 (GRCm38)
I184V
T
C
missense
Het
probably benign
0.007
phenotype
2013-07-30
11
63481
Cdk2ap1
1.000
V1662
106
N
633
5
124348676 (GRCm38)
I68F
T
A
missense
Het
possibly damaging
0.861
phenotype
2013-07-30
12
63500
Cfap44
0.000
V1662
99
N
633
16
44449138 (GRCm38)
Y1168*
C
A
nonsense
Het
probably null
0.976
phenotype
2013-07-30
13
63482
D6Ertd527e
0.188
V1662
120
N
633
6
87111892 (GRCm38)
S346P
T
C
missense
Het
unknown
2013-07-30
14
63504
Daam2
0.000
V1662
160
N
633
17
49464601 (GRCm38)
L839P
A
G
missense
Het
possibly damaging
0.848
Daam1 conditional KO
increases the severity of the heart phenotype (abnormal ventricular morphology and pressure) of the Daam1 single KO. [provided by MGI curators] (source: MGI)">phenotype
2013-07-30
15
63488
Fam198a
0.052
V1662
199
N
633
9
121965025 (GRCm38)
R82G
A
G
missense
Het
probably damaging
0.992
2013-07-30
16
63503
Gm7030
0.178
V1662
114
N
633
17
36128931 (GRCm38)
Y104H
A
G
missense
Het
probably benign
0.006
2013-07-30
17
63499
Golgb1
0.900
V1662
89
N
633
16
36898542 (GRCm38)
H270R
A
G
missense
Het
probably benign
0.001
0.063
phenotype
2013-07-30
18
63473
Itgav
1.000
V1662
106
N
633
2
83783854 (GRCm38)
R519W
C
T
missense
Het
possibly damaging
0.910
phenotype
2013-07-30
19
63472
Lrp1b
0.000
V1662
158
N
633
2
41122932 (GRCm38)
I2001K
A
T
missense
Het
probably damaging
0.992
0.828
phenotype
2013-07-30
20
63479
Lrrc40
0.146
V1662
137
N
633
3
158052789 (GRCm38)
I277K
T
A
missense
Het
probably damaging
1.000
0.647
2013-07-30
21
63474
Olfr1025-ps1
0.061
V1662
172
N
633
2
85918594 (GRCm38)
T223K
C
A
missense
Het
probably benign
0.097
2013-07-30
22
63484
Olfr1350
0.065
V1662
209
N
633
7
6570819 (GRCm38)
Y276F
A
T
missense
Het
probably damaging
1.000
0.647
phenotype
2013-07-30
23
63492
Olfr1373
0.053
V1662
203
N
633
11
52145177 (GRCm38)
M118V
T
C
missense
Het
probably damaging
0.999
phenotype
2013-07-30
24
63486
Olfr524
0.066
V1662
118
N
633
7
140201958 (GRCm38)
D271N
C
T
missense
Het
possibly damaging
0.810
phenotype
2013-07-30
25
63483
Pyroxd1
1.000
V1662
95
N
633
6
142358443 (GRCm38)
G307S
G
A
missense
Het
probably damaging
0.975
2013-07-30
26
63470
Rp1
0.136
V1662
199
N
633
1
4349560 (GRCm38)
Y443F
T
A
missense
Het
probably damaging
0.996
phenotype
2013-07-30
27
63487
Rpusd4
0.922
V1662
200
N
633
9
35272761 (GRCm38)
S237R
C
A
missense
Het
probably benign
0.059
2013-07-30
28
63494
Sdk2
0.087
V1662
119
N
633
11
113834908 (GRCm38)
W1172G
A
C
missense
Het
probably damaging
1.000
phenotype
2013-07-30
29
63489
Utrn
0.000
V1662
89
N
633
10
12421640 (GRCm38)
Y675H
A
G
missense
Het
probably damaging
1.000
0.480
phenotype
2013-07-30
30
63497
Vmn1r193
0.056
V1662
146
N
633
13
22219075 (GRCm38)
I249T
A
G
missense
Het
possibly damaging
0.936
2013-07-30
[records 1 to 30 of 30]