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Incidental Mutations
39
incidental mutations are currently displayed, and affect
38
genes.
8
are Possibly Damaging.
16
are Probably Damaging.
11
are Probably Benign.
4
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 39 of 39]
10
25
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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
ABI
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
84375
0610010F05Rik
0.191
IGL01444
G1
11
23620225 (GRCm38)
T
G
splice site
Het
probably benign
2013-11-11
2
84348
Adad1
0.311
IGL01444
G1
3
37092034 (GRCm38)
N517I
A
T
missense
Het
probably damaging
1.000
phenotype
2013-11-11
3
84347
Adam25
0.079
IGL01444
G1
8
40754921 (GRCm38)
R408H
G
A
missense
Het
probably benign
0.000
phenotype
2013-11-11
4
84344
Ang
0.133
IGL01444
G1
14
51101667 (GRCm38)
Y88*
C
A
nonsense
Het
probably null
phenotype
2013-11-11
5
84353
Ankrd42
0.062
IGL01444
G1
7
92610585 (GRCm38)
T327A
T
C
missense
Het
probably damaging
0.957
2013-11-11
6
84354
Birc6
1.000
IGL01444
G1
17
74631687 (GRCm38)
D2696G
A
G
missense
Het
probably damaging
0.998
phenotype
2013-11-11
7
84339
Chd3
0.000
IGL01444
G1
11
69348742 (GRCm38)
T1717M
G
A
missense
Het
probably benign
0.285
phenotype
2013-11-11
8
84362
Csmd1
0.000
IGL01444
G1
8
16200055 (GRCm38)
M970L
T
A
missense
Het
probably benign
0.001
phenotype
2013-11-11
9
84351
Dhx32
0.159
IGL01444
G1
7
133748977 (GRCm38)
I121M
T
C
missense
Het
possibly damaging
0.759
phenotype
2013-11-11
10
84356
Dnah11
0.671
IGL01444
G1
12
118020232 (GRCm38)
S2506F
G
A
missense
Het
possibly damaging
0.907
phenotype
2013-11-11
11
84361
Dscam
1.000
IGL01444
G1
16
96673709 (GRCm38)
I1218F
T
A
missense
Het
possibly damaging
0.951
phenotype
2013-11-11
12
84343
Duox1
0.000
IGL01444
G1
2
122340090 (GRCm38)
L1197P
T
C
missense
Het
probably damaging
0.980
phenotype
2013-11-11
13
84376
Eps8l2
0.000
IGL01444
G1
7
141361375 (GRCm38)
T
C
splice site
Het
probably benign
phenotype
2013-11-11
14
84340
Exoc3
0.963
IGL01444
G1
13
74206935 (GRCm38)
K49R
T
C
missense
Het
probably damaging
1.000
phenotype
2013-11-11
15
84349
Exoc8
1.000
IGL01444
G1
8
124895841 (GRCm38)
T596S
T
A
missense
Het
possibly damaging
0.842
phenotype
2013-11-11
16
84355
F13a1
0.000
IGL01444
G1
13
36918577 (GRCm38)
G391R
C
T
missense
Het
probably null
1.000
phenotype
2013-11-11
17
84371
Fam35a
0.082
IGL01444
G1
14
34237557 (GRCm38)
V823F
C
A
missense
Het
probably damaging
1.000
2013-11-11
18
84365
Fat3
0.519
IGL01444
G1
9
15998848 (GRCm38)
S1953T
A
T
missense
Het
probably damaging
0.997
phenotype
2013-11-11
19
84366
Gls2
0.000
IGL01444
G1
10
128201347 (GRCm38)
N252K
C
A
missense
Het
probably damaging
0.999
phenotype
2013-11-11
20
84345
Gm5346
0.061
IGL01444
G1
8
43626433 (GRCm38)
D251E
A
T
missense
Het
probably benign
0.058
2013-11-11
21
84373
Haus2
0.937
IGL01444
G1
2
120615942 (GRCm38)
R115K
G
A
missense
Het
probably benign
0.002
phenotype
2013-11-11
22
84369
Ift122
1.000
IGL01444
G1
6
115884379 (GRCm38)
K262E
A
G
missense
Het
probably benign
0.083
phenotype
2013-11-11
23
84358
Islr2
1.000
IGL01444
G1
9
58198378 (GRCm38)
C533Y
C
T
missense
Het
probably damaging
1.000
phenotype
2013-11-11
24
84367
Lrp2
1.000
IGL01444
G1
2
69443716 (GRCm38)
F3997I
A
T
missense
Het
possibly damaging
0.936
phenotype
2013-11-11
25
84357
Nt5c1a
0.153
IGL01444
G1
4
123216169 (GRCm38)
R354W
C
T
missense
Het
probably damaging
0.997
phenotype
2013-11-11
26
84341
Olfr776
0.062
IGL01444
G1
10
129261335 (GRCm38)
C125S
T
A
missense
Het
probably damaging
1.000
phenotype
2013-11-11
27
84364
Pcolce
0.105
IGL01444
G1
5
137607476 (GRCm38)
S200R
A
T
missense
Het
probably damaging
0.980
phenotype
2013-11-11
28
84346
Plec
0.738
IGL01444
G1
15
76179297 (GRCm38)
V2213A
A
G
missense
Het
possibly damaging
0.455
phenotype
2013-11-11
29
84350
Prmt3
0.390
IGL01444
G1
7
49780372 (GRCm38)
D74E
T
A
missense
Het
probably benign
0.001
phenotype
2013-11-11
30
84372
Ptk7
1.000
IGL01444
G1
17
46565387 (GRCm38)
F1046S
A
G
missense
Het
probably damaging
1.000
phenotype
2013-11-11
31
84342
Ranbp2
1.000
IGL01444
G1
10
58475300 (GRCm38)
Y887H
T
C
missense
Het
possibly damaging
0.790
phenotype
2013-11-11
32
84360
Sez6l2
0.000
IGL01444
G1
7
126961883 (GRCm38)
E447K
G
A
missense
Het
possibly damaging
0.912
phenotype
2013-11-11
33
84374
Snrnp70
0.962
IGL01444
G1
7
45387236 (GRCm38)
C
T
splice site
154 bp
Het
probably null
phenotype
2013-11-11
34
84368
Timm10
0.973
IGL01444
G1
2
84829864 (GRCm38)
V49E
T
A
missense
Het
probably damaging
1.000
phenotype
2013-11-11
35
84377
Tox2
0.000
IGL01444
G1
2
163225466 (GRCm38)
T
C
utr 5 prime
Het
probably benign
2013-11-11
36
84363
Usp20
0.000
IGL01444
G1
2
30998789 (GRCm38)
M1K
T
A
start codon destroyed
Het
probably null
1.000
phenotype
2013-11-11
37
84370
Usp32
1.000
IGL01444
G1
11
85059164 (GRCm38)
L223V
A
C
missense
Het
probably damaging
0.966
2013-11-11
38
84359
Zeb1
0.929
IGL01444
G1
18
5767138 (GRCm38)
S550P
T
C
missense
Het
probably benign
0.000
0.061
phenotype
2013-11-11
39
84352
Zeb1
0.929
IGL01444
G1
18
5767906 (GRCm38)
A806S
G
T
missense
Het
probably damaging
0.997
phenotype
2013-11-11
[records 1 to 39 of 39]