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Incidental Mutations
27
incidental mutations are currently displayed, and affect
27
genes.
2
are Possibly Damaging.
15
are Probably Damaging.
6
are Probably Benign.
3
are Probably Null.
0
create premature stop codons.
3
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 27 of 27]
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
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
45847
0610009O20Rik
0.235
R0560
G1
225
Y
18
38254498
L230Q
T
A
missense
Het
probably damaging
1.000
0.647
06/11/2013
2
45823
AI464131
0.000
R0560
G1
225
Y
4
41498167
R488W
G
A
missense
Het
probably damaging
0.991
0.647
06/11/2013
3
45839
Apob
0.902
R0560
G1
223
Y
12
8005101
Y1334H
T
C
missense
Het
probably damaging
1.000
0.355
phenotype
06/11/2013
4
45841
Arsb
0.250
R0560
G1
225
Y
13
93790198
T159A
A
G
missense
Het
possibly damaging
0.659
0.489
phenotype
06/11/2013
5
45814
Asb18
0.000
R0560
G1
225
Y
1
90014528
V17G
A
C
missense
Het
probably damaging
1.000
0.249
phenotype
06/11/2013
6
45828
Bicd1
0.000
R0560
G1
225
Y
6
149511962
K284E
A
G
missense
Het
probably benign
0.345
0.073
phenotype
06/11/2013
7
45824
Bspry
0.082
R0560
G1
225
Y
4
62486449
R161G
A
G
missense
Het
probably damaging
0.998
0.647
06/11/2013
8
45837
Ccdc138
0.111
R0560
G1
225
Y
10
58575717
T636A
A
G
missense
Het
probably damaging
0.999
0.263
06/11/2013
9
45816
Cubn
1.000
R0560
G1
225
Y
2
13428680
W1140R
A
T
missense
Het
probably damaging
1.000
0.655
phenotype
06/11/2013
10
45829
Cyp2t4
0.085
R0560
G1
225
Y
7
27158511
T479A
A
G
missense
Het
probably damaging
0.985
0.647
06/11/2013
11
45845
Dtx3l
0.236
R0560
G1
225
Y
16
35932935
S434P
A
G
missense
Het
probably damaging
1.000
0.165
phenotype
06/11/2013
12
45818
Duox2
0.000
R0560
G1
225
Y
2
122291554
V611A
A
G
missense
Het
probably benign
0.038
0.100
phenotype
06/11/2013
13
45846
Epb41l3
0.000
R0560
G1
225
Y
17
69274897
T
G
critical splice donor site
2 bp
Het
probably null
0.949
phenotype
06/11/2013
14
45840
Fam161b
0.081
R0560
G1
189
Y
12
84357718
D63N
C
T
missense
Het
probably damaging
0.959
0.107
06/11/2013
15
45836
Gm5422
0.787
R0560
G1
225
N
10
31249244
G
A
exon
Het
noncoding transcript
06/11/2013
16
45817
Gpr158
0.000
R0560
G1
225
Y
2
21825274
D710V
A
T
missense
Het
probably damaging
1.000
0.430
06/11/2013
17
45821
Krtcap2
0.248
R0560
G1
225
Y
3
89249142
T
C
critical splice donor site
2 bp
Het
probably null
0.958
06/11/2013
18
45844
Mtrf1
0.097
R0560
G1
225
Y
14
79406850
D199E
T
A
missense
Het
probably damaging
1.000
0.647
phenotype
06/11/2013
19
45842
Naip6
0.124
R0560
G1
121
Y
13
100300600
A472T
C
T
missense
Het
probably benign
0.077
0.407
phenotype
06/11/2013
20
45815
Ncf2
0.096
R0560
G1
189
Y
1
152821522
Y47N
T
A
missense
Het
probably damaging
1.000
0.742
phenotype
06/11/2013
21
45822
Ovgp1
0.000
R0560
G1
225
Y
3
105986410
T
C
unclassified
Het
probably benign
0.090
phenotype
06/11/2013
22
45819
Siglec1
0.076
R0560
G1
170
Y
2
131070346
T1692N
G
T
missense
Het
probably benign
0.016
0.113
phenotype
06/11/2013
23
45833
Slc10a2
0.000
R0560
G1
225
Y
8
5089092
N284S
T
C
missense
Het
probably benign
0.019
0.065
phenotype
06/11/2013
24
45838
Slfn3
0.000
R0560
G1
225
Y
11
83213152
F283S
T
C
missense
Het
probably damaging
0.993
0.647
phenotype
06/11/2013
25
45834
Trank1
0.000
R0560
G1
225
Y
9
111391086
F2297S
T
C
missense
Het
possibly damaging
0.879
0.179
06/11/2013
26
45830
Vmn2r69
0.078
R0560
G1
225
Y
7
85409714
A
G
critical splice donor site
2 bp
Het
probably null
0.976
06/11/2013
27
45825
Vps13d
1.000
R0560
G1
225
Y
4
145054190
E3957G
T
C
missense
Het
probably damaging
0.997
0.118
phenotype
06/11/2013
[records 1 to 27 of 27]