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
38
incidental mutations are currently displayed, and affect
38
genes.
6
are Possibly Damaging.
15
are Probably Damaging.
13
are Probably Benign.
2
are Probably Null.
2
create premature stop codons.
0
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
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
104437
Abca12
1.000
IGL01700
G1
1
71280390 (GRCm38)
M1778L
T
A
missense
Het
probably benign
0.000
phenotype
2014-01-21
2
104446
Aldh6a1
0.248
IGL01700
G1
12
84439538 (GRCm38)
C202Y
C
T
missense
Het
probably damaging
0.995
phenotype
2014-01-21
3
104439
Ankrd36
0.052
IGL01700
G1
11
5632198 (GRCm38)
T276A
A
G
missense
Het
probably benign
0.048
2014-01-21
4
104421
Ankrd55
0.000
IGL01700
G1
13
112381168 (GRCm38)
I556T
T
C
missense
Het
probably benign
0.158
2014-01-21
5
104436
Aqp4
0.139
IGL01700
G1
18
15399865 (GRCm38)
I57T
A
G
missense
Het
probably benign
0.443
phenotype
2014-01-21
6
104425
Atp1a1
1.000
IGL01700
G1
3
101594258 (GRCm38)
D43G
T
C
missense
Het
possibly damaging
0.952
phenotype
2014-01-21
7
104435
Cyld
0.000
IGL01700
G1
8
88707099 (GRCm38)
R172H
G
A
missense
Het
probably damaging
0.990
phenotype
2014-01-21
8
104442
Diexf
0.970
IGL01700
G1
1
193118265 (GRCm38)
P416S
G
A
missense
Het
probably damaging
1.000
2014-01-21
9
104419
Ear2
0.057
IGL01700
G1
14
44103259 (GRCm38)
R125*
A
T
nonsense
Het
probably null
2014-01-21
10
104451
Efcab9
0.056
IGL01700
G1
11
32527451 (GRCm38)
R24G
T
C
missense
Het
probably damaging
1.000
2014-01-21
11
104450
F7
0.075
IGL01700
G1
8
13028685 (GRCm38)
Q39K
C
A
missense
Het
probably benign
0.023
phenotype
2014-01-21
12
104456
Galntl6
0.106
IGL01700
G1
8
57958460 (GRCm38)
A
T
splice site
Het
probably benign
2014-01-21
13
104432
Kcnj5
0.000
IGL01700
G1
9
32322629 (GRCm38)
V130A
A
G
missense
Het
probably damaging
1.000
phenotype
2014-01-21
14
104424
Magee2
IGL01700
G1
X
104855968 (GRCm38)
I359T
A
G
missense
Het
possibly damaging
0.491
phenotype
2014-01-21
15
104423
Myh1
0.000
IGL01700
G1
11
67211412 (GRCm38)
I843S
T
G
missense
Het
probably damaging
0.998
phenotype
2014-01-21
16
104443
Nfat5
0.914
IGL01700
G1
8
107339130 (GRCm38)
M98K
T
A
missense
Het
probably damaging
0.992
phenotype
2014-01-21
17
104433
Nrip3
0.052
IGL01700
G1
7
109761867 (GRCm38)
N200I
T
A
missense
Het
possibly damaging
0.947
2014-01-21
18
104422
Olfr818
0.050
IGL01700
G1
10
129945941 (GRCm38)
N40K
A
T
missense
Het
probably damaging
1.000
phenotype
2014-01-21
19
104430
Phkb
0.832
IGL01700
G1
8
86017465 (GRCm38)
Q581L
A
T
missense
Het
probably benign
0.062
phenotype
2014-01-21
20
104452
Plxdc2
0.000
IGL01700
G1
2
16512115 (GRCm38)
V69A
T
C
missense
Het
probably benign
0.005
phenotype
2014-01-21
21
104449
Pou3f1
1.000
IGL01700
G1
4
124658857 (GRCm38)
W384L
G
T
missense
Het
probably damaging
1.000
phenotype
2014-01-21
22
104448
Prrc2a
0.855
IGL01700
G1
17
35150667 (GRCm38)
S1890L
G
A
missense
Het
possibly damaging
0.930
phenotype
2014-01-21
23
104447
Psmc1
1.000
IGL01700
G1
12
100113078 (GRCm38)
P27H
C
A
missense
Het
probably damaging
0.999
phenotype
2014-01-21
24
104429
Pvr
0.100
IGL01700
G1
7
19909232 (GRCm38)
A359S
C
A
missense
Het
probably benign
0.108
phenotype
2014-01-21
25
104440
Rasal1
0.000
IGL01700
G1
5
120676817 (GRCm38)
I711F
A
T
missense
Het
probably benign
0.061
phenotype
2014-01-21
26
104426
Ror1
1.000
IGL01700
G1
4
100409771 (GRCm38)
A223V
C
T
missense
Het
probably damaging
1.000
phenotype
2014-01-21
27
104445
Slc22a16
0.083
IGL01700
G1
10
40603908 (GRCm38)
I638L
A
T
missense
Het
unknown
phenotype
2014-01-21
28
104427
Slfn10-ps
0.057
IGL01700
G1
11
83029112 (GRCm38)
C
T
unclassified
Het
noncoding transcript
2014-01-21
29
104434
Sptbn4
0.379
IGL01700
G1
7
27404268 (GRCm38)
L1176P
A
G
missense
Het
probably damaging
1.000
phenotype
2014-01-21
30
104444
Usp21
0.000
IGL01700
G1
1
171283402 (GRCm38)
F421I
A
T
missense
Het
probably damaging
0.964
phenotype
2014-01-21
31
104420
Vmn1r61
0.072
IGL01700
G1
7
5611203 (GRCm38)
R37S
T
A
missense
Het
possibly damaging
0.817
2014-01-21
32
104438
Vps13a
0.000
IGL01700
G1
19
16744857 (GRCm38)
R364*
G
A
nonsense
Het
probably null
phenotype
2014-01-21
33
104431
Vps29
0.962
IGL01700
G1
5
122362867 (GRCm38)
Y165C
A
G
missense
Het
probably damaging
1.000
phenotype
2014-01-21
34
104454
Wdfy4
0.000
IGL01700
G1
14
33020238 (GRCm38)
T
C
splice site
Het
probably benign
2014-01-21
35
104441
Wdr24
1.000
IGL01700
G1
17
25825828 (GRCm38)
D219G
A
G
missense
Het
probably damaging
0.999
2014-01-21
36
104455
Xpo1
1.000
IGL01700
G1
11
23276422 (GRCm38)
T
C
splice site
Het
probably benign
phenotype
2014-01-21
37
104428
Zfp831
0.000
IGL01700
G1
2
174644918 (GRCm38)
T462K
C
A
missense
Het
possibly damaging
0.861
2014-01-21
38
104453
Zswim5
0.000
IGL01700
G1
4
116986461 (GRCm38)
T
C
unclassified
Het
probably benign
2014-01-21
[records 1 to 38 of 38]