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
33
incidental mutations are currently displayed, and affect
33
genes.
6
are Possibly Damaging.
9
are Probably Damaging.
16
are Probably Benign.
2
are Probably Null.
0
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 33 of 33]
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
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
178672
Agtr1a
0.000
IGL01870
G1
13
30381327 (GRCm38)
D125G
A
G
missense
Het
probably damaging
1.000
phenotype
2014-05-07
2
178690
Arhgap31
0.202
IGL01870
G1
16
38618242 (GRCm38)
K300E
T
C
missense
Het
probably damaging
1.000
phenotype
2014-05-07
3
278959
Cma2
0.066
IGL01870
G1
14
55973737 (GRCm38)
S162Y
C
A
missense
Het
probably benign
0.001
2015-04-16
4
178679
Cntn4
0.347
IGL01870
G1
6
106489715 (GRCm38)
T193A
A
G
missense
Het
possibly damaging
0.953
phenotype
2014-05-07
5
178685
Col22a1
0.000
IGL01870
G1
15
71952528 (GRCm38)
M556L
T
A
missense
Het
probably benign
0.073
phenotype
2014-05-07
6
178680
Dld
0.971
IGL01870
G1
12
31335467 (GRCm38)
S292P
A
G
missense
Het
possibly damaging
0.894
phenotype
2014-05-07
7
178695
Dnah6
0.123
IGL01870
G1
6
73032569 (GRCm38)
D3746E
A
T
missense
Het
probably benign
0.035
phenotype
2014-05-07
8
178683
Eea1
0.261
IGL01870
G1
10
95973986 (GRCm38)
T9A
A
G
missense
Het
probably damaging
0.998
2014-05-07
9
178681
Fam102a
0.236
IGL01870
G1
2
32566282 (GRCm38)
S319P
T
C
missense
Het
probably benign
0.010
2014-05-07
10
178677
Gbf1
1.000
IGL01870
G1
19
46285669 (GRCm38)
K1714R
A
G
missense
Het
probably benign
0.001
phenotype
2014-05-07
11
278958
Gm10718
0.539
IGL01870
G1
9
3025118 (GRCm38)
Y194F
A
T
missense
Het
probably benign
0.001
2015-04-16
12
178682
Gm12794
0.048
IGL01870
G1
4
101940690 (GRCm38)
L95H
T
A
missense
Het
probably benign
0.032
2014-05-07
13
178669
H2-M1
0.054
IGL01870
G1
17
36670063 (GRCm38)
M327K
A
T
missense
Het
probably benign
0.375
2014-05-07
14
178694
Ifnz
IGL01870
G1
4
88783311 (GRCm38)
S176T
T
A
missense
Het
possibly damaging
0.780
2014-05-07
15
178678
Irak4
0.482
IGL01870
G1
15
94547870 (GRCm38)
Y10H
T
C
missense
Het
probably benign
0.276
phenotype
2014-05-07
16
178673
Irx5
0.000
IGL01870
G1
8
92359777 (GRCm38)
F163L
T
C
missense
Het
probably damaging
1.000
phenotype
2014-05-07
17
178670
Jak3
0.689
IGL01870
G1
8
71680790 (GRCm38)
P376S
C
T
missense
Het
probably damaging
1.000
phenotype
2014-05-07
18
178684
Lrrc25
0.080
IGL01870
G1
8
70617787 (GRCm38)
S73P
T
C
missense
Het
possibly damaging
0.827
2014-05-07
19
178676
Macf1
1.000
IGL01870
G1
4
123474113 (GRCm38)
G2285D
C
T
missense
Het
probably damaging
0.991
phenotype
2014-05-07
20
178668
Muc4
0.099
IGL01870
G1
16
32753196 (GRCm38)
T1025S
A
T
missense
Het
probably benign
0.015
phenotype
2014-05-07
21
178693
Mylk2
0.259
IGL01870
G1
2
152915214 (GRCm38)
N303S
A
G
missense
Het
probably benign
0.205
phenotype
2014-05-07
22
178667
Olfr111
0.505
IGL01870
G1
17
37530664 (GRCm38)
R229H
G
A
missense
Het
probably benign
0.004
0.085
phenotype
2014-05-07
23
178675
Pcnx
0.000
IGL01870
G1
12
81975893 (GRCm38)
V1512A
T
C
missense
Het
probably benign
0.007
phenotype
2014-05-07
24
178689
Phlda3
0.073
IGL01870
G1
1
135766638 (GRCm38)
S64G
A
G
missense
Het
probably benign
0.036
phenotype
2014-05-07
25
178691
Pptc7
0.185
IGL01870
G1
5
122313602 (GRCm38)
S40R
C
A
missense
Het
probably damaging
1.000
2014-05-07
26
178696
Ptpn4
0.236
IGL01870
G1
1
119675547 (GRCm38)
A
C
critical splice donor site
2 bp
Het
probably null
phenotype
2014-05-07
27
178674
Slc10a1
0.000
IGL01870
G1
12
80960528 (GRCm38)
M160V
T
C
missense
Het
probably benign
0.001
phenotype
2014-05-07
28
178692
Stac
0.212
IGL01870
G1
9
111572332 (GRCm38)
I349V
T
C
missense
Het
probably benign
0.223
2014-05-07
29
178671
Synm
0.000
IGL01870
G1
7
67736118 (GRCm38)
S157P
A
G
missense
Het
possibly damaging
0.862
phenotype
2014-05-07
30
178687
Tbc1d9b
0.203
IGL01870
G1
11
50162088 (GRCm38)
L924P
T
C
missense
Het
probably damaging
0.997
2014-05-07
31
178686
Tcaf2
0.102
IGL01870
G1
6
42624477 (GRCm38)
V883I
C
T
missense
Het
possibly damaging
0.469
2014-05-07
32
178697
Upp1
0.234
IGL01870
G1
11
9125700 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
0.946
phenotype
2014-05-07
33
178688
Whamm
0.000
IGL01870
G1
7
81595974 (GRCm38)
T726I
C
T
missense
Het
probably damaging
0.960
phenotype
2014-05-07
[records 1 to 33 of 33]