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Incidental Mutations
56
incidental mutations are currently displayed, and affect
56
genes.
8
are Possibly Damaging.
27
are Probably Damaging.
13
are Probably Benign.
7
are Probably Null.
2
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 56 of 56]
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
507534
Ank3
0.833
R6274
G1
225.01
Y
10
70002565 (GRCm38)
R1566K
G
A
missense
Het
possibly damaging
0.913
0.065
phenotype
2018-03-15
2
507525
Ano1
1.000
R6274
G1
211.01
Y
7
144618863 (GRCm38)
S528T
A
T
missense
Het
probably benign
0.008
phenotype
2018-03-15
3
507557
Araf
0.487
R6274
G1
222
Y
X
20860100 (GRCm38)
R601L
G
T
missense
Homo
probably damaging
0.979
0.114
phenotype
2018-03-15
4
507530
Bcl2l10
0.000
R6274
G1
225.01
Y
9
75351072 (GRCm38)
I172T
T
C
missense
Het
possibly damaging
0.842
phenotype
2018-03-15
5
507507
Bpifb3
0.000
R6274
G1
225.01
Y
2
153929323 (GRCm38)
N385I
A
T
missense
Het
possibly damaging
0.870
phenotype
2018-03-15
6
507512
Bsnd
0.050
R6274
G1
225.01
Y
4
106486635 (GRCm38)
V158A
A
G
missense
Het
probably damaging
0.963
0.647
phenotype
2018-03-15
7
507505
Cacna1s
1.000
R6274
G1
225.01
Y
1
136089045 (GRCm38)
N481S
A
G
missense
Het
probably benign
0.019
0.078
phenotype
2018-03-15
8
507508
Cdk5rap1
0.356
R6274
G1
225.01
Y
2
154368241 (GRCm38)
V138A
A
G
missense
Het
probably damaging
0.992
phenotype
2018-03-15
9
507535
Cep290
0.921
R6274
G1
225.01
Y
10
100530207 (GRCm38)
E1099G
A
G
missense
Het
probably damaging
0.999
0.254
phenotype
2018-03-15
10
507526
Cers1
0.329
R6274
G1
109.01
Y
8
70331077 (GRCm38)
L225Q
T
A
missense
Het
probably damaging
0.998
phenotype
2018-03-15
11
507552
Cfb
0.000
R6274
G1
153.01
Y
17
34862093 (GRCm38)
Q7R
T
C
missense
Het
probably benign
0.177
0.078
phenotype
2018-03-15
12
507538
Clk4
0.561
R6274
G1
225.01
Y
11
51271921 (GRCm38)
S98G
A
G
missense
Het
possibly damaging
0.691
0.059
phenotype
2018-03-15
13
507517
Clock
0.824
R6274
G1
225.01
Y
5
76237153 (GRCm38)
S406P
A
G
missense
Het
probably benign
0.450
0.073
phenotype
2018-03-15
14
507546
Csmd3
0.000
R6274
G1
225.01
Y
15
47621437 (GRCm38)
I3178V
T
C
missense
Het
probably benign
0.000
2018-03-15
15
507504
Dock10
0.303
R6274
G1
225.01
Y
1
80538823 (GRCm38)
S1397P
A
G
missense
Het
probably damaging
0.996
phenotype
2018-03-15
16
507509
Fer1l4
0.000
R6274
G1
225.01
Y
2
156029268 (GRCm38)
L1421P
A
G
missense
Het
probably damaging
0.998
2018-03-15
17
507549
Fetub
0.059
R6274
G1
225.01
Y
16
22932331 (GRCm38)
R143C
C
T
missense
Het
probably damaging
1.000
0.261
phenotype
2018-03-15
18
529380
Greb1
0.000
R6274
G1
58.01
Y
12
16735151 (GRCm38)
T91K
G
T
missense
Het
probably damaging
0.967
phenotype
2018-08-01
19
507521
Grid2ip
0.130
R6274
G1
225.01
Y
5
143380429 (GRCm38)
S379N
G
A
missense
Het
probably damaging
0.997
phenotype
2018-03-15
20
507545
Gucy1b2
0.189
R6274
G1
225.01
Y
14
62415939 (GRCm38)
C336S
A
T
missense
Het
probably damaging
1.000
phenotype
2018-03-15
21
507514
Hdac1
1.000
R6274
G1
225.01
Y
4
129519109 (GRCm38)
C261R
A
G
missense
Het
probably damaging
1.000
phenotype
2018-03-15
22
507554
Hrasls5
0.000
R6274
G1
225.01
Y
19
7637466 (GRCm38)
T231I
C
T
missense
Het
probably damaging
1.000
0.514
2018-03-15
23
507516
Htt
1.000
R6274
G1
225.01
Y
5
34852087 (GRCm38)
S1471P
T
C
missense
Het
possibly damaging
0.805
phenotype
2018-03-15
24
507542
Ice1
0.952
R6274
G1
225.01
Y
13
70594839 (GRCm38)
V2134A
A
G
missense
Het
probably damaging
0.968
0.633
2018-03-15
25
507537
Ikzf1
0.000
R6274
G1
225.01
Y
11
11768961 (GRCm38)
Q310*
C
T
nonsense
Het
probably null
0.976
phenotype
2018-03-15
26
507543
Il3ra
0.076
R6274
G1
225.01
Y
14
14350180 (GRCm38)
V112I
G
A
missense
Het
probably benign
0.191
0.090
phenotype
2018-03-15
27
507506
Kif21b
0.128
R6274
G1
225.01
Y
1
136149418 (GRCm38)
I393V
A
G
missense
Het
possibly damaging
0.570
0.101
phenotype
2018-03-15
28
507547
Krt74
0.000
R6274
G1
224.01
Y
15
101763437 (GRCm38)
T
C
exon
Het
noncoding transcript
0.087
2018-03-15
29
507539
Krtap29-1
0.122
R6274
G1
225.01
Y
11
99978983 (GRCm38)
N24S
T
C
missense
Het
probably null
0.003
2018-03-15
30
507553
Mut
1.000
R6274
G1
225.01
Y
17
40956245 (GRCm38)
V570A
T
C
missense
Het
probably benign
0.005
0.202
phenotype
2018-03-15
31
507544
Myh7
0.868
R6274
G1
225.01
Y
14
54979486 (GRCm38)
D1138G
T
C
missense
Het
probably damaging
0.974
0.908
phenotype
2018-03-15
32
507533
Nktr
0.698
R6274
G1
225.01
Y
9
121731565 (GRCm38)
I125T
T
C
missense
Het
probably damaging
0.999
0.915
phenotype
2018-03-15
33
507523
Nlrp2
0.000
R6274
G1
225.01
Y
7
5317555 (GRCm38)
L861Q
A
T
missense
Het
probably damaging
1.000
phenotype
2018-03-15
34
507551
Notch3
0.000
R6274
G1
225.01
Y
17
32147290 (GRCm38)
R990L
C
A
missense
Het
probably benign
0.000
0.090
phenotype
2018-03-15
35
507556
Nrap
0.000
R6274
G1
225.01
Y
19
56361721 (GRCm38)
D655G
T
C
missense
Het
probably benign
0.210
2018-03-15
36
507513
Olfr1329
0.101
R6274
G1
225.01
Y
4
118917230 (GRCm38)
V79E
A
T
missense
Het
probably benign
0.007
phenotype
2018-03-15
37
507555
Olfr1451
0.148
R6274
G1
225.01
Y
19
12999870 (GRCm38)
V295I
G
A
missense
Het
probably damaging
0.969
phenotype
2018-03-15
38
507550
Osbpl11
1.000
R6274
G1
225.01
Y
16
33227056 (GRCm38)
I463N
T
A
missense
Het
probably damaging
1.000
0.936
phenotype
2018-03-15
39
507524
Pcsk6
0.293
R6274
G1
225.01
Y
7
66033844 (GRCm38)
R749W
A
T
missense
Het
probably damaging
0.999
0.647
phenotype
2018-03-15
40
507532
Plxnb1
0.000
R6274
G1
225.01
Y
9
109112141 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
phenotype
2018-03-15
41
507522
Polr1a
1.000
R6274
G1
225.01
Y
6
71954890 (GRCm38)
T
A
splice site
45 bp
Het
probably null
0.976
phenotype
2018-03-15
42
507515
Ppm1g
1.000
R6274
G1
225.01
Y
5
31206406 (GRCm38)
I153V
T
C
missense
Het
probably damaging
0.989
phenotype
2018-03-15
43
507536
Ppp1r12a
1.000
R6274
G1
225.01
Y
10
108260890 (GRCm38)
S191P
T
C
missense
Het
probably benign
0.002
0.057
phenotype
2018-03-15
44
507548
Prodh
0.000
R6274
G1
225.01
Y
16
18081058 (GRCm38)
K178E
T
C
missense
Het
possibly damaging
0.907
0.090
phenotype
2018-03-15
45
507520
Rilpl2
0.000
R6274
G1
225.01
Y
5
124469848 (GRCm38)
V103A
A
G
missense
Het
possibly damaging
0.752
phenotype
2018-03-15
46
507527
Sap18b
0.945
R6274
G1
225.01
Y
8
95825541 (GRCm38)
H60Y
C
T
missense
Het
probably benign
0.065
phenotype
2018-03-15
47
507510
Sclt1
0.216
R6274
G1
225.01
Y
3
41629516 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
0.949
phenotype
2018-03-15
48
507541
Serpinb1a
0.136
R6274
G1
225.01
Y
13
32842866 (GRCm38)
H364Q
G
T
missense
Het
probably damaging
0.998
phenotype
2018-03-15
49
507519
Sez6l
0.000
R6274
G1
192.01
Y
5
112475365 (GRCm38)
Q107*
G
A
nonsense
Het
probably null
phenotype
2018-03-15
50
507528
Sipa1l2
0.356
R6274
G1
225.01
Y
8
125469872 (GRCm38)
V708I
C
T
missense
Het
probably damaging
0.999
phenotype
2018-03-15
51
507511
Tbc1d2
0.097
R6274
G1
200.01
Y
4
46629912 (GRCm38)
G252R
C
T
missense
Het
probably benign
0.007
0.090
2018-03-15
52
507529
Uaca
0.119
R6274
G1
225.01
Y
9
60850291 (GRCm38)
T
A
splice site
Het
probably null
0.976
phenotype
2018-03-15
53
507531
Uqcrc1
0.961
R6274
G1
225.01
Y
9
108942156 (GRCm38)
H95N
C
A
missense
Het
probably damaging
1.000
2018-03-15
54
507558
Usp9y
0.064
R6274
G1
222
Y
Y
1316735 (GRCm38)
R1938H
C
T
missense
Homo
probably damaging
0.990
0.647
phenotype
2018-03-15
55
507540
Wnk4
0.416
R6274
G1
225.01
Y
11
101265431 (GRCm38)
R42W
C
T
missense
Het
probably damaging
1.000
0.255
phenotype
2018-03-15
56
507518
Zfp326
0.390
R6274
G1
225.01
Y
5
105905980 (GRCm38)
L242Q
T
A
missense
Het
probably damaging
0.996
0.493
2018-03-15
[records 1 to 56 of 56]