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Incidental Mutations
19
incidental mutations are currently displayed, and affect
19
genes.
1
are Possibly Damaging.
9
are Probably Damaging.
7
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 19 of 19]
10
25
50
100
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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
97791
Abca6
0.000
R0992
G1
225
N
11
110211684
T905A
T
C
missense
Het
probably damaging
0.999
phenotype
01/05/2014
2
97775
Arhgap20
0.296
R0992
G1
225
N
9
51816786
R100G
A
G
missense
Het
probably damaging
0.957
phenotype
01/05/2014
3
97783
Bsn
0.294
R0992
G1
225
N
9
108114354
R1400*
G
A
nonsense
Het
probably null
phenotype
01/05/2014
4
97779
Clstn2
0.000
R0992
G1
225
N
9
97445712
S948P
A
G
missense
Het
probably benign
0.002
phenotype
01/05/2014
5
97757
Col15a1
0.087
R0992
G1
225
N
4
47300491
V1029M
G
A
missense
Het
probably damaging
0.959
phenotype
01/05/2014
6
97765
D6Ertd527e
0.118
R0992
G1
225
N
6
87111524
T223S
C
G
missense
Het
unknown
0.087
01/05/2014
7
97771
Disc1
0.425
R0992
G1
225
N
8
125088042
I215T
T
C
missense
Het
probably damaging
0.998
phenotype
01/05/2014
8
97785
Dna2
1.000
R0992
G1
225
N
10
62949187
R28W
C
T
missense
Het
probably benign
0.077
0.090
phenotype
01/05/2014
9
97747
Dst
0.257
R0992
G1
225
N
1
34199536
N3773S
A
G
missense
Het
probably damaging
0.966
phenotype
01/05/2014
10
97745
Gdap1
0.000
R0992
G1
225
N
1
17147105
Y96C
A
G
missense
Het
probably damaging
1.000
phenotype
01/05/2014
11
97787
Glipr1l1
0.055
R0992
G1
225
N
10
112062325
R112G
A
G
missense
Het
probably benign
0.000
01/05/2014
12
97773
Gria4
0.602
R0992
G1
225
N
9
4795238
S13P
A
G
missense
Het
probably benign
0.000
phenotype
01/05/2014
13
97793
Noxred1
0.064
R0992
G1
225
N
12
87224226
N207S
T
C
missense
Het
probably benign
0.153
01/05/2014
14
97799
Pom121l2
0.064
R0992
G1
225
N
13
21982759
Q400L
A
T
missense
Het
probably benign
0.008
01/05/2014
15
97753
Sla2
0.000
R0992
G1
96
N
2
156874472
E243G
T
C
missense
Het
probably damaging
0.989
phenotype
01/05/2014
16
97761
Srpk2
0.000
R0992
G1
225
N
5
23545543
I54T
A
G
missense
Het
probably damaging
0.993
phenotype
01/05/2014
17
97789
Tenm2
0.501
R0992
G1
225
N
11
36063177
G1236R
C
T
missense
Het
possibly damaging
0.945
0.777
phenotype
01/05/2014
18
97809
Trim15
0.147
R0992
G1
225
N
17
36865011
V215M
C
T
missense
Het
probably damaging
0.980
phenotype
01/05/2014
19
97803
Uchl3
0.134
R0992
G1
225
N
14
101668533
I144T
T
C
missense
Het
probably benign
0.081
phenotype
01/05/2014
[records 1 to 19 of 19]