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Incidental Mutations
15
incidental mutations are currently displayed, and affect
15
genes.
1
are Possibly Damaging.
3
are Probably Damaging.
9
are Probably Benign.
2
are Probably Null.
0
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 15 of 15]
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
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
66431
Abca4
0.000
K7894
217
N
468
3
122147868
C
CAA
frame shift
Het
probably null
phenotype
08/19/2013
2
26529
Acsl4
K7894
222
Y
468
X
142328060
V632I
C
T
missense
Het
probably benign
0.001
0.079
phenotype
04/16/2013
3
26527
Adcy8
0.078
K7894
222
Y
468
15
64822234
H398R
T
C
missense
Het
probably benign
0.380
0.066
phenotype
04/16/2013
4
44072
Catsperg1
0.069
K7894
34
Y
468
7
29197154
C
T
intron
Het
probably benign
06/10/2013
5
26524
Ccpg1
0.000
K7894
225
Y
468
9
73001877
T
C
critical splice donor site
2 bp
Het
probably null
0.950
04/16/2013
6
26526
Clk4
0.639
K7894
225
Y
468
11
51275766
G
T
unclassified
Het
probably benign
phenotype
04/16/2013
7
26525
Ehbp1
0.533
K7894
225
Y
468
11
22089683
C
T
splice site
Het
probably benign
phenotype
04/16/2013
8
26523
Eri2
0.199
K7894
225
Y
468
7
119785271
D669G
T
C
missense
Het
probably benign
0.394
0.106
04/16/2013
9
26518
Nlrp9c
0.000
K7894
225
Y
468
7
26384898
S419P
A
G
missense
Het
possibly damaging
0.944
0.326
04/16/2013
10
26521
Olfr652
0.075
K7894
225
Y
468
7
104564532
T104A
A
G
missense
Het
probably benign
0.119
0.191
phenotype
04/16/2013
11
26520
Pde8a
0.000
K7894
225
Y
468
7
81306765
P304H
C
A
missense
Het
probably damaging
1.000
0.961
phenotype
04/16/2013
12
26519
Prmt3
0.694
K7894
222
Y
468
7
49826711
Y356C
A
G
missense
Het
probably damaging
1.000
0.756
phenotype
04/16/2013
13
26516
Rsph10b
0.055
K7894
222
Y
468
5
143944520
D151G
A
G
missense
Het
probably damaging
1.000
0.367
04/16/2013
14
26528
Spryd3
0.000
K7894
225
Y
468
15
102118141
V365A
A
G
missense
Het
probably benign
0.008
0.116
04/16/2013
15
26517
Vmn1r58
0.053
K7894
222
Y
468
7
5410703
N176S
T
C
missense
Het
probably benign
0.006
0.090
04/16/2013
[records 1 to 15 of 15]