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Incidental Mutations
36
incidental mutations are currently displayed, and affect
35
genes.
6
are Possibly Damaging.
10
are Probably Damaging.
16
are Probably Benign.
4
are Probably Null.
3
create premature stop codons.
0
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 36 of 36]
10
25
50
100
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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
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
306639
0610009L18Rik
IGL00978
G1
11
120350947 (GRCm38)
T
C
unclassified
Het
probably benign
2015-04-16
2
29465
Alpk2
0.000
IGL00978
G1
18
65291534 (GRCm38)
A
T
splice site
Het
probably benign
2013-04-17
3
28260
Angptl8
0.000
IGL00978
G1
9
21837053 (GRCm38)
T
C
intron
Het
probably benign
phenotype
2013-04-17
4
27344
AU040320
0.000
IGL00978
G1
4
126828839 (GRCm38)
D383E
T
A
missense
Het
probably benign
0.003
phenotype
2013-04-17
5
29201
Cep97
1.000
IGL00978
G1
16
55924960 (GRCm38)
C
T
splice site
Het
probably benign
2013-04-17
6
27936
Clcn4
0.000
IGL00978
G1
7
7287673 (GRCm38)
L649H
A
T
missense
Het
probably damaging
0.992
phenotype
2013-04-17
7
26762
Col5a2
1.000
IGL00978
G1
1
45376739 (GRCm38)
N1416S
T
C
missense
Het
probably benign
0.013
phenotype
2013-04-17
8
28656
Erbb2
1.000
IGL00978
G1
11
98435630 (GRCm38)
P1027S
C
T
missense
Het
probably damaging
1.000
phenotype
2013-04-17
9
306640
Eya1
0.859
IGL00978
G1
1
14270701 (GRCm38)
A
G
splice site
Het
probably benign
phenotype
2015-04-16
10
28900
Gfm2
0.660
IGL00978
G1
13
97162977 (GRCm38)
I402T
T
C
missense
Het
probably benign
0.201
phenotype
2013-04-17
11
27021
Gmeb2
0.168
IGL00978
G1
2
181259043 (GRCm38)
V187E
A
T
missense
Het
probably benign
0.184
phenotype
2013-04-17
12
28788
Hectd1
1.000
IGL00978
G1
12
51791390 (GRCm38)
H662R
T
C
missense
Het
possibly damaging
0.948
phenotype
2013-04-17
13
27346
Ifne
0.000
IGL00978
G1
4
88880031 (GRCm38)
Q50R
T
C
missense
Het
probably benign
0.170
phenotype
2013-04-17
14
28790
Kidins220
1.000
IGL00978
G1
12
25057474 (GRCm38)
D1642G
A
G
missense
Het
probably damaging
1.000
phenotype
2013-04-17
15
27345
Klhl32
0.075
IGL00978
G1
4
24682245 (GRCm38)
D146V
T
A
missense
Het
probably damaging
0.999
2013-04-17
16
28655
Krt36
0.058
IGL00978
G1
11
100102948 (GRCm38)
I355V
T
C
missense
Het
probably damaging
0.975
phenotype
2013-04-17
17
27160
Lrrcc1
0.000
IGL00978
G1
3
14536128 (GRCm38)
S73R
T
A
missense
Het
possibly damaging
0.910
2013-04-17
18
29550
Ltbp3
0.212
IGL00978
G1
19
5754019 (GRCm38)
H853L
A
T
missense
Het
probably benign
0.262
phenotype
2013-04-17
19
28427
Map3k5
0.000
IGL00978
G1
10
20141567 (GRCm38)
R1369Q
G
A
missense
Het
probably damaging
1.000
phenotype
2013-04-17
20
27020
Mcm8
0.639
IGL00978
G1
2
132821406 (GRCm38)
N148S
A
G
missense
Het
probably benign
0.000
phenotype
2013-04-17
21
28084
Mylk3
0.238
IGL00978
G1
8
85355526 (GRCm38)
L211*
A
T
nonsense
Het
probably null
phenotype
2013-04-17
22
27161
Nras
0.472
IGL00978
G1
3
103058916 (GRCm38)
T
C
utr 5 prime
Het
probably benign
phenotype
2013-04-17
23
29353
Olfr135
0.059
IGL00978
G1
17
38208982 (GRCm38)
I246F
A
T
missense
Het
probably damaging
0.991
phenotype
2013-04-17
24
27935
Olfr670
0.089
IGL00978
G1
7
104960716 (GRCm38)
N5K
A
T
missense
Het
probably damaging
0.957
0.647
phenotype
2013-04-17
25
28426
Os9
0.000
IGL00978
G1
10
127120509 (GRCm38)
Y66N
A
T
missense
Het
probably damaging
0.997
phenotype
2013-04-17
26
29549
Pitpnm1
0.000
IGL00978
G1
19
4101228 (GRCm38)
D15G
A
G
missense
Het
possibly damaging
0.606
phenotype
2013-04-17
27
27709
Reg3a
0.049
IGL00978
G1
6
78382301 (GRCm38)
R95*
A
T
nonsense
Het
probably null
2013-04-17
28
28999
Rnf17
0.540
IGL00978
G1
14
56512271 (GRCm38)
P1425S
C
T
missense
Het
probably damaging
1.000
phenotype
2013-04-17
29
29464
Smad2
1.000
IGL00978
G1
18
76299775 (GRCm38)
T
C
splice site
Het
probably benign
phenotype
2013-04-17
30
28789
Ttll5
0.458
IGL00978
G1
12
85933482 (GRCm38)
Q76*
C
T
nonsense
Het
probably null
phenotype
2013-04-17
31
27937
Uri1
0.000
IGL00978
G1
7
37996731 (GRCm38)
A
T
splice site
Het
probably benign
phenotype
2013-04-17
32
29355
Vmn2r102
0.000
IGL00978
G1
17
19678923 (GRCm38)
G
T
splice site
5 bp
Het
probably null
2013-04-17
33
27934
Vmn2r70
0.160
IGL00978
G1
7
85563799 (GRCm38)
M467L
T
G
missense
Het
probably benign
0.001
2013-04-17
34
29354
Zfp318
0.000
IGL00978
G1
17
46413726 (GRCm38)
D2218E
T
A
missense
Het
possibly damaging
0.638
phenotype
2013-04-17
35
28653
Zfp692
0.000
IGL00978
G1
11
58314029 (GRCm38)
I405T
T
C
missense
Het
possibly damaging
0.945
2013-04-17
36
28654
Zfp692
0.000
IGL00978
G1
11
58309998 (GRCm38)
H235R
A
G
missense
Het
possibly damaging
0.917
2013-04-17
[records 1 to 36 of 36]