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Incidental Mutations
21
incidental mutations are currently displayed, and affect
21
genes.
4
are Possibly Damaging.
8
are Probably Damaging.
7
are Probably Benign.
2
are Probably Null.
2
create premature stop codons.
0
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 21 of 21]
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
27826
Acsm2
0.000
IGL00930
G1
7
119592310
S534P
T
C
missense
Het
possibly damaging
0.907
04/17/2013
2
28175
Adamts15
0.000
IGL00930
G1
9
30902053
P939S
G
A
missense
Het
probably damaging
1.000
phenotype
04/17/2013
3
27632
Alms1
0.000
IGL00930
G1
6
85601310
S207P
T
C
missense
Het
probably damaging
0.976
phenotype
04/17/2013
4
27256
Chd7
0.953
IGL00930
G1
4
8805181
K747E
A
G
missense
Het
probably damaging
0.998
phenotype
04/17/2013
5
28952
Dock5
0.611
IGL00930
G1
14
67771077
N1457K
G
T
missense
Het
probably damaging
1.000
phenotype
04/17/2013
6
29149
Donson
0.966
IGL00930
G1
16
91682591
E323G
T
C
missense
Het
possibly damaging
0.785
phenotype
04/17/2013
7
29420
Epc1
1.000
IGL00930
G1
18
6449196
M434L
T
A
missense
Het
probably benign
0.000
phenotype
04/17/2013
8
26656
Fcer1a
0.052
IGL00930
G1
1
173222533
A
G
unclassified
Het
probably benign
phenotype
04/17/2013
9
27255
Hemgn
0.000
IGL00930
G1
4
46396383
C284*
A
T
nonsense
Het
probably null
04/17/2013
10
278084
Hnrnpm
1.000
IGL00930
G1
17
33649902
R517L
C
A
missense
Het
probably damaging
0.988
phenotype
04/16/2015
11
28174
Olfr854
0.279
IGL00930
G1
9
19567175
S67P
A
G
missense
Het
probably damaging
1.000
phenotype
04/17/2013
12
28340
Pcdh15
0.000
IGL00930
G1
10
74630698
E1450K
G
A
missense
Het
probably benign
0.084
phenotype
04/17/2013
13
29511
Pfpl
0.107
IGL00930
G1
19
12429645
H420L
A
T
missense
Het
probably benign
0.001
04/17/2013
14
27440
Pitpnm2
0.000
IGL00930
G1
5
124121663
A
G
unclassified
Het
probably benign
phenotype
04/17/2013
15
28739
Pole2
1.000
IGL00930
G1
12
69226445
A
G
splice site
Het
probably benign
phenotype
04/17/2013
16
27824
Prmt3
0.668
IGL00930
G1
7
49792009
Y245N
T
A
missense
Het
probably damaging
0.999
phenotype
04/17/2013
17
29280
Rpl10a
0.923
IGL00930
G1
17
28329007
Y41H
T
C
missense
Het
probably damaging
0.999
phenotype
04/17/2013
18
27439
Tpst1
0.118
IGL00930
G1
5
130102134
K148N
A
T
missense
Het
probably benign
0.189
phenotype
04/17/2013
19
28855
Vmn1r199
0.099
IGL00930
G1
13
22382859
T108A
A
G
missense
Het
possibly damaging
0.636
04/17/2013
20
29421
Wdr7
0.891
IGL00930
G1
18
63740244
C525*
T
A
nonsense
Het
probably null
phenotype
04/17/2013
21
27825
Zfp646
0.234
IGL00930
G1
7
127879130
T160A
A
G
missense
Het
possibly damaging
0.907
04/17/2013
[records 1 to 21 of 21]