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Incidental Mutations
44
incidental mutations are currently displayed, and affect
44
genes.
8
are Possibly Damaging.
13
are Probably Damaging.
20
are Probably Benign.
3
are Probably Null.
0
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 44 of 44]
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
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
73990
Abhd18
0.074
IGL01319
G1
3
40933642
V307E
T
A
missense
Het
probably benign
0.001
10/07/2013
2
73974
Bub1b
1.000
IGL01319
G1
2
118614994
I265T
T
C
missense
Het
possibly damaging
0.485
phenotype
10/07/2013
3
73973
Cntnap3
0.059
IGL01319
G1
13
64787837
T404I
G
A
missense
Het
probably damaging
1.000
phenotype
10/07/2013
4
73993
Disc1
0.425
IGL01319
G1
8
125087891
S165P
T
C
missense
Het
probably damaging
0.991
phenotype
10/07/2013
5
73991
Dock1
1.000
IGL01319
G1
7
134789278
F756L
T
C
missense
Het
probably benign
0.000
phenotype
10/07/2013
6
73962
Dock2
0.000
IGL01319
G1
11
34698790
V480A
A
G
missense
Het
possibly damaging
0.608
phenotype
10/07/2013
7
73988
Drc3
0.154
IGL01319
G1
11
60364962
D125G
A
G
missense
Het
probably null
0.697
10/07/2013
8
73971
Emid1
0.108
IGL01319
G1
11
5143859
C96Y
C
T
missense
Het
probably damaging
1.000
10/07/2013
9
73977
F13b
0.000
IGL01319
G1
1
139506793
N99S
A
G
missense
Het
probably damaging
0.980
phenotype
10/07/2013
10
74002
Fam20a
0.000
IGL01319
G1
11
109678458
A
G
splice site
Het
probably benign
phenotype
10/07/2013
11
73967
Fancd2
1.000
IGL01319
G1
6
113584899
T1243K
C
A
missense
Het
probably damaging
0.979
phenotype
10/07/2013
12
73992
Fbxw14
0.159
IGL01319
G1
9
109278791
K172E
T
C
missense
Het
probably damaging
1.000
10/07/2013
13
73995
Gm13941
0.079
IGL01319
G1
2
111094805
T
C
critical splice acceptor site
Het
probably null
10/07/2013
14
73961
Gtpbp4
0.969
IGL01319
G1
13
8985260
N354K
A
T
missense
Het
probably benign
0.050
phenotype
10/07/2013
15
73964
Igkv2-116
0.215
IGL01319
G1
6
68152404
L50P
T
C
missense
Het
probably benign
0.102
10/07/2013
16
73969
Klrb1-ps1
0.068
IGL01319
G1
6
129116585
P23L
C
T
missense
Het
possibly damaging
0.913
10/07/2013
17
73989
Kng2
0.000
IGL01319
G1
16
23028834
I26F
T
A
missense
Het
probably damaging
0.988
10/07/2013
18
278271
Krt81
0.088
IGL01319
G1
15
101463388
H104Y
G
A
missense
Het
probably benign
0.001
phenotype
04/16/2015
19
73998
Lrpprc
1.000
IGL01319
G1
17
84705412
T
C
utr 3 prime
Het
probably benign
phenotype
10/07/2013
20
73972
Man2a2
0.184
IGL01319
G1
7
80361132
V704M
C
T
missense
Het
possibly damaging
0.941
phenotype
10/07/2013
21
73981
Mbip
0.927
IGL01319
G1
12
56330242
V303A
A
G
missense
Het
probably benign
0.349
10/07/2013
22
73975
Mipep
0.963
IGL01319
G1
14
60843271
M571L
A
T
missense
Het
probably benign
0.001
phenotype
10/07/2013
23
73983
Ncan
0.000
IGL01319
G1
8
70097562
V1188D
A
T
missense
Het
probably damaging
0.989
phenotype
10/07/2013
24
73963
Pcdhb4
0.058
IGL01319
G1
18
37308513
V292A
T
C
missense
Het
probably benign
0.000
10/07/2013
25
73996
Pkd1
1.000
IGL01319
G1
17
24587919
T
C
unclassified
Het
probably benign
phenotype
10/07/2013
26
73976
Ppp2r2c
0.412
IGL01319
G1
5
36947121
S282T
T
A
missense
Het
possibly damaging
0.818
phenotype
10/07/2013
27
73965
Rad54l2
1.000
IGL01319
G1
9
106719046
G231D
C
T
missense
Het
probably benign
0.183
phenotype
10/07/2013
28
73980
Rnf20
1.000
IGL01319
G1
4
49649326
D443E
T
G
missense
Het
probably damaging
0.993
phenotype
10/07/2013
29
73982
Rptor
1.000
IGL01319
G1
11
119891170
M1108V
A
G
missense
Het
probably benign
0.015
phenotype
10/07/2013
30
73970
Serpine2
0.000
IGL01319
G1
1
79810694
V182A
A
G
missense
Het
probably damaging
0.980
0.805
phenotype
10/07/2013
31
73999
Sesn2
0.216
IGL01319
G1
4
132499967
C
T
splice site
Het
probably benign
phenotype
10/07/2013
32
73986
Shank1
0.336
IGL01319
G1
7
44353123
A1422E
C
A
missense
Het
possibly damaging
0.930
phenotype
10/07/2013
33
74001
Slc13a4
0.832
IGL01319
G1
6
35307353
C
T
splice site
5 bp
Het
probably null
phenotype
10/07/2013
34
73994
Snrnp200
1.000
IGL01319
G1
2
127230127
T
C
splice site
Het
probably benign
phenotype
10/07/2013
35
278270
Src
0.899
IGL01319
G1
2
157469503
G461R
G
A
missense
Het
probably damaging
1.000
phenotype
04/16/2015
36
73978
Tbxas1
0.061
IGL01319
G1
6
39017973
I178V
A
G
missense
Het
probably benign
0.092
phenotype
10/07/2013
37
73987
Tmem2
0.803
IGL01319
G1
19
21844757
P1172L
C
T
missense
Het
possibly damaging
0.774
10/07/2013
38
73997
Triml1
0.135
IGL01319
G1
8
43141397
A
G
utr 5 prime
Het
probably benign
phenotype
10/07/2013
39
73985
Tsen2
0.951
IGL01319
G1
6
115576984
Q441L
A
T
missense
Het
probably damaging
0.999
phenotype
10/07/2013
40
74000
Ttc23l
0.083
IGL01319
G1
15
10509406
A
G
splice site
Het
probably benign
10/07/2013
41
73979
Ttc37
0.415
IGL01319
G1
13
76129379
H491R
A
G
missense
Het
probably benign
0.293
phenotype
10/07/2013
42
73968
Ttn
1.000
IGL01319
G1
2
76881304
T
C
intron
Het
probably benign
phenotype
10/07/2013
43
73966
Vsig10l
0.268
IGL01319
G1
7
43465254
S293L
C
T
missense
Het
probably damaging
0.999
10/07/2013
44
73984
Zcchc13
IGL01319
G1
X
103631000
Q110K
C
A
missense
Het
possibly damaging
0.901
10/07/2013
[records 1 to 44 of 44]