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Incidental Mutations
38
incidental mutations are currently displayed, and affect
38
genes.
5
are Possibly Damaging.
16
are Probably Damaging.
15
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 38 of 38]
10
25
50
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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
186067
5330417C22Rik
0.077
IGL02079
G1
3
108481359 (GRCm38)
N236I
T
A
missense
Het
possibly damaging
0.914
phenotype
2014-05-07
2
186077
Abl1
0.931
IGL02079
G1
2
31689948 (GRCm38)
T
C
splice site
Het
probably benign
phenotype
2014-05-07
3
186063
Ago4
0.906
IGL02079
G1
4
126517084 (GRCm38)
M204K
A
T
missense
Het
probably damaging
0.988
phenotype
2014-05-07
4
186066
Alms1
0.000
IGL02079
G1
6
85628634 (GRCm38)
V2422A
T
C
missense
Het
probably damaging
0.979
phenotype
2014-05-07
5
283375
Ap5z1
0.192
IGL02079
G1
5
142477113 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
phenotype
2015-04-16
6
186073
Arsa
0.289
IGL02079
G1
15
89473351 (GRCm38)
T470A
T
C
missense
Het
probably benign
0.042
phenotype
2014-05-07
7
186061
Bri3bp
0.076
IGL02079
G1
5
125454689 (GRCm38)
V233A
T
C
missense
Het
probably damaging
0.965
2014-05-07
8
186049
Cdc45
1.000
IGL02079
G1
16
18798729 (GRCm38)
M200I
C
T
missense
Het
probably benign
0.059
0.115
phenotype
2014-05-07
9
186074
Csgalnact1
0.095
IGL02079
G1
8
68401492 (GRCm38)
G219V
C
A
missense
Het
probably damaging
1.000
phenotype
2014-05-07
10
186046
Ephb6
0.517
IGL02079
G1
6
41616014 (GRCm38)
D395E
T
A
missense
Het
possibly damaging
0.573
phenotype
2014-05-07
11
186076
Flt1
1.000
IGL02079
G1
5
147568831 (GRCm38)
T
A
splice site
Het
probably benign
phenotype
2014-05-07
12
186065
Fry
0.764
IGL02079
G1
5
150399624 (GRCm38)
N1080I
A
T
missense
Het
probably damaging
0.966
2014-05-07
13
186059
Gdpgp1
0.099
IGL02079
G1
7
80239020 (GRCm38)
D266E
T
A
missense
Het
probably benign
0.013
2014-05-07
14
186069
Gspt1
0.963
IGL02079
G1
16
11240829 (GRCm38)
S123P
A
G
missense
Het
probably benign
0.172
2014-05-07
15
186078
Kctd17
0.000
IGL02079
G1
15
78430156 (GRCm38)
T
C
splice site
Het
probably benign
phenotype
2014-05-07
16
186062
Lamb2
0.851
IGL02079
G1
9
108482113 (GRCm38)
C313S
T
A
missense
Het
probably damaging
1.000
phenotype
2014-05-07
17
186055
Lcor
0.858
IGL02079
G1
19
41555687 (GRCm38)
S106R
T
A
missense
Het
probably benign
0.399
phenotype
2014-05-07
18
186060
Lgr5
1.000
IGL02079
G1
10
115452194 (GRCm38)
S776R
A
C
missense
Het
probably damaging
1.000
phenotype
2014-05-07
19
186054
Mettl16
1.000
IGL02079
G1
11
74817624 (GRCm38)
C510G
T
G
missense
Het
probably damaging
1.000
2014-05-07
20
186047
Mlip
0.130
IGL02079
G1
9
77239529 (GRCm38)
T101A
T
C
missense
Het
possibly damaging
0.707
phenotype
2014-05-07
21
283373
Myh6
1.000
IGL02079
G1
14
54950541 (GRCm38)
L1152Q
A
T
missense
Het
probably damaging
1.000
phenotype
2015-04-16
22
283374
Mylk
0.000
IGL02079
G1
16
34860631 (GRCm38)
R87H
G
A
missense
Het
possibly damaging
0.870
phenotype
2015-04-16
23
186075
Npepl1
0.200
IGL02079
G1
2
174119390 (GRCm38)
C
T
intron
Het
probably benign
2014-05-07
24
186053
Nrxn1
0.000
IGL02079
G1
17
90643083 (GRCm38)
M548K
A
T
missense
Het
probably damaging
0.987
phenotype
2014-05-07
25
186050
Olfr1205
0.051
IGL02079
G1
2
88831647 (GRCm38)
C177S
T
A
missense
Het
probably damaging
1.000
phenotype
2014-05-07
26
186064
Olfr514
0.195
IGL02079
G1
7
108825936 (GRCm38)
E21V
T
A
missense
Het
probably damaging
0.991
phenotype
2014-05-07
27
186072
Pate3
0.160
IGL02079
G1
9
35646153 (GRCm38)
Q69L
T
A
missense
Het
probably damaging
0.999
2014-05-07
28
186071
Piwil1
0.000
IGL02079
G1
5
128742003 (GRCm38)
V192A
T
C
missense
Het
possibly damaging
0.888
phenotype
2014-05-07
29
186070
Plcxd2
0.265
IGL02079
G1
16
45972343 (GRCm38)
I211N
A
T
missense
Het
probably benign
0.434
2014-05-07
30
283371
Plekhg3
0.000
IGL02079
G1
12
76560429 (GRCm38)
Y88N
T
A
missense
Het
probably benign
0.015
2015-04-16
31
186058
Rabgap1l
0.000
IGL02079
G1
1
160738970 (GRCm38)
C58Y
C
T
missense
Het
probably benign
0.001
phenotype
2014-05-07
32
186056
Rnf123
0.239
IGL02079
G1
9
108068302 (GRCm38)
R390*
G
A
nonsense
Het
probably null
phenotype
2014-05-07
33
186068
Rusc2
0.208
IGL02079
G1
4
43425668 (GRCm38)
S1258G
A
G
missense
Het
probably benign
0.000
phenotype
2014-05-07
34
186051
Scn1a
1.000
IGL02079
G1
2
66323360 (GRCm38)
R710G
T
C
missense
Het
probably benign
0.144
phenotype
2014-05-07
35
186057
Wwc1
0.000
IGL02079
G1
11
35876058 (GRCm38)
S457P
A
G
missense
Het
probably damaging
0.999
phenotype
2014-05-07
36
283372
Xdh
0.320
IGL02079
G1
17
73891277 (GRCm38)
G1205D
C
T
missense
Het
probably damaging
1.000
phenotype
2015-04-16
37
186048
Zfp518a
0.912
IGL02079
G1
19
40914617 (GRCm38)
G997R
G
A
missense
Het
probably damaging
1.000
phenotype
2014-05-07
38
186052
Zfp592
0.927
IGL02079
G1
7
81039230 (GRCm38)
S1080P
T
C
missense
Het
probably benign
0.205
phenotype
2014-05-07
[records 1 to 38 of 38]