Home
Phenotypic Mutations
Incidental Mutations
Engineered Mutations
Candidate Explorer
Protocols
Mutation Statistics
About
Contact
Links
Request Mice
Beutler Lab
APN
Strains @ MMRRC
Search Phenotypes
NEW
Candidate Explorer
Staff Login
Download
Incidental Mutations
27
incidental mutations are currently displayed, and affect
27
genes.
5
are Possibly Damaging.
10
are Probably Damaging.
10
are Probably Benign.
1
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 27 of 27]
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
264338
4933436I01Rik
0.072
R3148
G1
222
N
X
67921378
D12G
T
C
missense
Het
probably benign
0.059
02/05/2015
2
264329
Adamts18
0.134
R3148
G1
225
N
8
113738858
V701L
C
A
missense
Het
probably damaging
1.000
phenotype
02/05/2015
3
264317
Alg2
1.000
R3148
G1
225
N
4
47472259
V183D
A
T
missense
Het
probably damaging
0.987
phenotype
02/05/2015
4
264315
Ank2
1.000
R3148
G1
225
N
3
126933075
I857V
T
C
missense
Het
probably benign
0.002
phenotype
02/05/2015
5
264321
Asb15
0.000
R3148
G1
225
N
6
24566259
A404S
G
T
missense
Het
probably damaging
1.000
phenotype
02/05/2015
6
264334
Baalc
0.112
R3148
G1
225
N
15
38949173
E106V
A
T
missense
Het
possibly damaging
0.924
phenotype
02/05/2015
7
264337
Catsperd
0.054
R3148
G1
197
N
17
56664039
C701F
G
T
missense
Het
possibly damaging
0.856
phenotype
02/05/2015
8
264320
Cc2d2a
0.887
R3148
G1
225
N
5
43709155
I769N
T
A
missense
Het
probably damaging
0.999
phenotype
02/05/2015
9
264328
Cntnap4
0.094
R3148
G1
225
N
8
112757439
T375A
A
G
missense
Het
probably damaging
1.000
phenotype
02/05/2015
10
264330
Col7a1
1.000
R3148
G1
225
N
9
108961405
T974A
A
G
missense
Het
unknown
phenotype
02/05/2015
11
264331
Ehbp1
0.542
R3148
G1
225
N
11
22100465
Y502C
T
C
missense
Het
probably damaging
0.999
phenotype
02/05/2015
12
264318
Gm13083
0.093
R3148
G1
225
N
4
143617477
D449V
A
T
missense
Het
probably benign
0.299
02/05/2015
13
264324
Kcnj11
0.000
R3148
G1
225
N
7
46099120
V260I
C
T
missense
Het
probably benign
0.001
0.080
phenotype
02/05/2015
14
264323
Klk14
0.000
R3148
G1
225
N
7
43692077
C51Y
G
A
missense
Het
probably damaging
1.000
0.793
phenotype
02/05/2015
15
264335
Marf1
0.186
R3148
G1
225
N
16
14125979
V1380A
A
G
missense
Het
possibly damaging
0.640
phenotype
02/05/2015
16
264313
Olfr1280
0.217
R3148
G1
225
N
2
111316288
F270L
T
C
missense
Het
possibly damaging
0.928
phenotype
02/05/2015
17
264325
Otog
0.742
R3148
G1
225
N
7
46290169
L2124P
T
C
missense
Het
probably damaging
1.000
phenotype
02/05/2015
18
264310
Pam
1.000
R3148
G1
225
N
1
97895678
N256I
T
A
missense
Het
possibly damaging
0.838
phenotype
02/05/2015
19
264322
Pcbp1
0.924
R3148
G1
118
N
6
86525489
E143K
C
T
missense
Het
probably damaging
0.996
phenotype
02/05/2015
20
264312
Prrx1
1.000
R3148
G1
225
N
1
163257848
D171G
T
C
missense
Het
probably benign
0.383
phenotype
02/05/2015
21
477983
Rasal2
0.000
R3148
G1
225
N
1
157243764
A
T
intron
Het
probably benign
phenotype
05/15/2017
22
264311
Serpinb5
0.799
R3148
G1
225
N
1
106881825
H320Q
T
A
missense
Het
probably damaging
0.999
phenotype
02/05/2015
23
264336
Snx4
0.130
R3148
G1
225
N
16
33287724
D296A
A
C
missense
Het
probably benign
0.080
phenotype
02/05/2015
24
264319
Sorcs2
0.000
R3148
G1
190
N
5
36035788
Q778R
T
C
missense
Het
probably benign
0.095
phenotype
02/05/2015
25
264314
Spata16
0.142
R3148
G1
225
N
3
26878712
T
C
critical splice donor site
2 bp
Het
probably null
phenotype
02/05/2015
26
264327
Tcerg1l
0.000
R3148
G1
225
N
7
138259867
Q378K
G
T
missense
Het
probably benign
0.000
02/05/2015
27
264326
Trpm1
0.000
R3148
G1
225
N
7
64235012
Y814H
T
C
missense
Het
probably benign
0.001
phenotype
02/05/2015
[records 1 to 27 of 27]