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Incidental Mutations
36
incidental mutations are currently displayed, and affect
36
genes.
5
are Possibly Damaging.
17
are Probably Damaging.
11
are Probably Benign.
2
are Probably Null.
1
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 36 of 36]
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
285435
0610040J01Rik
0.089
IGL02229
5
63898353 (GRCm38)
D144G
A
G
missense
Het
probably damaging
0.993
2015-04-16
2
285436
Adgrg1
0.151
IGL02229
8
95003511 (GRCm38)
D114Y
G
T
missense
Het
probably damaging
1.000
phenotype
2015-04-16
3
285432
Ago4
0.910
IGL02229
4
126511532 (GRCm38)
N416I
T
A
missense
Het
probably benign
0.336
phenotype
2015-04-16
4
285431
Aoc1
0.000
IGL02229
6
48905909 (GRCm38)
Q240*
C
T
nonsense
Het
probably null
phenotype
2015-04-16
5
285420
Atl1
0.333
IGL02229
12
69926025 (GRCm38)
V40I
G
A
missense
Het
probably benign
0.011
phenotype
2015-04-16
6
285429
Cdh2
1.000
IGL02229
18
16624753 (GRCm38)
I591V
T
C
missense
Het
probably benign
0.000
phenotype
2015-04-16
7
285410
Cic
0.951
IGL02229
7
25290950 (GRCm38)
Q1959K
C
A
missense
Het
probably damaging
0.959
phenotype
2015-04-16
8
285419
Cmya5
0.324
IGL02229
13
93092686 (GRCm38)
E1965K
C
T
missense
Het
possibly damaging
0.543
2015-04-16
9
285422
Csgalnact1
0.069
IGL02229
8
68401492 (GRCm38)
G219V
C
A
missense
Het
probably damaging
1.000
phenotype
2015-04-16
10
285427
Cspp1
0.146
IGL02229
1
10083556 (GRCm38)
S397P
T
C
missense
Het
probably damaging
0.999
phenotype
2015-04-16
11
285437
D130043K22Rik
0.000
IGL02229
13
24875924 (GRCm38)
Y593H
T
C
missense
Het
probably damaging
1.000
phenotype
2015-04-16
12
285415
Dck
0.000
IGL02229
5
88774105 (GRCm38)
Y142C
A
G
missense
Het
probably damaging
1.000
phenotype
2015-04-16
13
285433
Eea1
0.178
IGL02229
10
96018184 (GRCm38)
E568V
A
T
missense
Het
probably damaging
1.000
2015-04-16
14
285441
Gabra3
IGL02229
X
72501077 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
phenotype
2015-04-16
15
285408
Gucy2f
IGL02229
X
142179988 (GRCm38)
S342P
A
G
missense
Het
probably benign
0.000
phenotype
2015-04-16
16
285412
Hbb-bh1
0.000
IGL02229
7
103842825 (GRCm38)
I61F
T
A
missense
Het
possibly damaging
0.774
phenotype
2015-04-16
17
285430
Hook1
0.000
IGL02229
4
96001251 (GRCm38)
S235P
T
C
missense
Het
possibly damaging
0.928
phenotype
2015-04-16
18
285413
Hoxd12
0.290
IGL02229
2
74675934 (GRCm38)
R230H
G
A
missense
Het
probably damaging
1.000
phenotype
2015-04-16
19
285426
Iglc2
0.066
IGL02229
16
19198733 (GRCm38)
A41T
C
T
missense
Het
probably benign
0.039
2015-04-16
20
285414
Il1r1
0.080
IGL02229
1
40313358 (GRCm38)
K566E
A
G
missense
Het
probably damaging
0.989
phenotype
2015-04-16
21
285425
Kcns3
0.120
IGL02229
12
11092092 (GRCm38)
M202K
A
T
missense
Het
probably damaging
1.000
phenotype
2015-04-16
22
285423
Krt7
0.000
IGL02229
15
101427616 (GRCm38)
A442D
C
A
missense
Het
probably benign
0.091
phenotype
2015-04-16
23
285418
Ltk
0.000
IGL02229
2
119758573 (GRCm38)
R200H
C
T
missense
Het
probably benign
0.007
phenotype
2015-04-16
24
285411
Macf1
1.000
IGL02229
4
123509826 (GRCm38)
D582E
G
T
missense
Het
probably damaging
0.998
phenotype
2015-04-16
25
285428
Mbnl3
IGL02229
X
51139341 (GRCm38)
Y69N
A
T
missense
Het
probably damaging
1.000
phenotype
2015-04-16
26
285438
Mpp1
0.000
IGL02229
X
75121428 (GRCm38)
T
C
unclassified
Het
probably benign
phenotype
2015-04-16
27
285417
Myo18b
1.000
IGL02229
5
112878110 (GRCm38)
S25P
A
G
missense
Het
unknown
phenotype
2015-04-16
28
285434
Nsd3
0.259
IGL02229
8
25710748 (GRCm38)
N1289S
A
G
missense
Het
probably damaging
0.978
phenotype
2015-04-16
29
285406
Olfr26
0.062
IGL02229
9
38855416 (GRCm38)
M118K
T
A
missense
Het
possibly damaging
0.617
phenotype
2015-04-16
30
285439
Pacs2
0.000
IGL02229
12
113056800 (GRCm38)
A
G
splice site
Het
probably benign
phenotype
2015-04-16
31
285424
Rab3gap2
0.000
IGL02229
1
185259383 (GRCm38)
K689E
A
G
missense
Het
possibly damaging
0.714
phenotype
2015-04-16
32
285409
Sva
0.070
IGL02229
6
42042222 (GRCm38)
C109S
T
A
missense
Het
probably damaging
0.981
2015-04-16
33
285416
Taf3
0.963
IGL02229
2
9952834 (GRCm38)
N174S
T
C
missense
Het
probably damaging
0.999
phenotype
2015-04-16
34
285407
Tbc1d5
0.000
IGL02229
17
50852600 (GRCm38)
M393K
A
T
missense
Het
probably damaging
0.999
2015-04-16
35
285421
Tmem242
0.111
IGL02229
17
5411407 (GRCm38)
S129T
A
T
missense
Het
probably benign
0.049
2015-04-16
36
285440
Ttn
1.000
IGL02229
2
76871169 (GRCm38)
A
T
unclassified
Het
probably benign
phenotype
2015-04-16
[records 1 to 36 of 36]