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Incidental Mutations
35
incidental mutations are currently displayed, and affect
33
genes.
5
are Possibly Damaging.
17
are Probably Damaging.
9
are Probably Benign.
2
are Probably Null.
1
create premature stop codons.
0
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 35 of 35]
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
318516
Acmsd
0.000
R4195
G1
225
Y
1
127749194 (GRCm38)
L152R
T
G
missense
Het
probably damaging
1.000
0.920
phenotype
2015-06-10
2
318533
Actg2
0.000
R4195
G1
225
Y
6
83523173 (GRCm38)
T39P
T
G
missense
Het
probably damaging
0.998
0.821
phenotype
2015-06-10
3
318515
Agap1
0.209
R4195
G1
225
Y
1
89834539 (GRCm38)
E531G
A
G
missense
Het
probably damaging
0.986
0.436
phenotype
2015-06-10
4
318540
Alox12b
1.000
R4195
G1
225
Y
11
69169600 (GRCm38)
S661G
A
G
missense
Het
probably benign
0.023
0.220
phenotype
2015-06-10
5
318542
Apod
0.300
R4195
G1
225
Y
16
31297574 (GRCm38)
M113V
T
C
missense
Het
probably benign
0.389
0.159
phenotype
2015-06-10
6
368353
Atl3
0.000
R4195
G1
225
Y
19
7518546 (GRCm38)
I171V
A
G
missense
Het
possibly damaging
0.587
0.146
phenotype
2016-01-29
7
318522
Atrn
0.000
R4195
G1
225
Y
2
130933412 (GRCm38)
T145K
C
A
missense
Het
probably damaging
0.996
0.354
phenotype
2015-06-10
8
318545
Cacna1f
0.000
R4195
G1
222
Y
X
7608930 (GRCm38)
H57R
A
G
missense
Het
probably damaging
0.996
0.090
phenotype
2015-06-10
9
318544
Cldn9
0.181
R4195
G1
108
Y
17
23683174 (GRCm38)
E159G
T
C
missense
Het
probably damaging
1.000
0.890
phenotype
2015-06-10
10
318513
Cnnm4
0.343
R4195
G1
225
Y
1
36499508 (GRCm38)
H590Q
C
A
missense
Het
probably benign
0.056
0.104
phenotype
2015-06-10
11
318511
Col19a1
1.000
R4195
G1
225
Y
1
24534052 (GRCm38)
S213L
G
A
missense
Het
unknown
0.100
phenotype
2015-06-10
12
318523
Cse1l
1.000
R4195
G1
225
Y
2
166929979 (GRCm38)
T387A
A
G
missense
Het
probably damaging
1.000
0.276
phenotype
2015-06-10
13
318535
Eif4enif1
0.402
R4195
G1
225
Y
11
3243186 (GRCm38)
V675A
T
C
missense
Het
possibly damaging
0.890
0.061
phenotype
2015-06-10
14
318537
Fbll1
0.293
R4195
G1
225
Y
11
35797666 (GRCm38)
S257P
A
G
missense
Het
possibly damaging
0.928
0.077
2015-06-10
15
318538
Fbll1
0.293
R4195
G1
222
Y
11
35797872 (GRCm38)
H188L
T
A
missense
Het
possibly damaging
0.749
0.086
2015-06-10
16
318524
Frem2
1.000
R4195
G1
225
Y
3
53539268 (GRCm38)
F2360L
A
G
missense
Het
possibly damaging
0.896
0.184
phenotype
2015-06-10
17
318532
G3bp2
1.000
R4195
G1
225
Y
5
92055416 (GRCm38)
S349P
A
G
missense
Het
probably damaging
0.985
0.213
2015-06-10
18
318534
Gm2396
0.323
R4195
G1
84
Y
9
88917662 (GRCm38)
A
G
intron
Het
noncoding transcript
2015-06-10
19
318541
Gm281
0.081
R4195
G1
225
Y
14
13829772 (GRCm38)
V657L
C
A
missense
Het
probably benign
0.049
0.090
2015-06-10
20
368352
Gm6569
0.091
R4195
G1
188
Y
15
73836243 (GRCm38)
P22L
C
T
missense
Het
probably damaging
0.958
0.109
2016-01-29
21
318517
Itih2
0.106
R4195
G1
225
Y
2
10115285 (GRCm38)
N314D
T
C
missense
Het
probably damaging
1.000
0.465
phenotype
2015-06-10
22
318512
Lman2l
0.821
R4195
G1
225
Y
1
36424941 (GRCm38)
I266M
A
C
missense
Het
probably damaging
0.983
0.192
phenotype
2015-06-10
23
318514
Mrps9
0.930
R4195
G1
221
Y
1
42901094 (GRCm38)
T
G
intron
Het
probably benign
0.090
phenotype
2015-06-10
24
318525
Mtmr11
0.149
R4195
G1
225
Y
3
96167891 (GRCm38)
T
C
splice site
Het
probably benign
0.090
2015-06-10
25
318519
Neb
0.831
R4195
G1
225
Y
2
52271559 (GRCm38)
R2074S
G
T
missense
Het
probably damaging
1.000
0.156
phenotype
2015-06-10
26
318520
Neb
0.831
R4195
G1
225
Y
2
52290835 (GRCm38)
H1226Q
A
T
missense
Het
probably damaging
1.000
0.227
phenotype
2015-06-10
27
318518
Nmi
0.109
R4195
G1
225
Y
2
51948620 (GRCm38)
S301A
A
C
missense
Het
probably benign
0.001
0.090
phenotype
2015-06-10
28
318526
Olfr266
0.082
R4195
G1
225
Y
3
106822012 (GRCm38)
C182*
A
T
nonsense
Het
probably null
0.976
phenotype
2015-06-10
29
318531
Pclo
0.000
R4195
G1
225
Y
5
14677563 (GRCm38)
A
G
unclassified
Het
probably benign
0.105
phenotype
2015-06-10
30
318536
Pkd1l1
1.000
R4195
G1
225
Y
11
8909929 (GRCm38)
I560F
T
A
missense
Het
probably damaging
0.995
0.259
phenotype
2015-06-10
31
318528
Polr1e
1.000
R4195
G1
225
Y
4
45019327 (GRCm38)
Y59H
T
C
missense
Het
probably damaging
0.999
0.523
2015-06-10
32
318521
Slc30a4
0.000
R4195
G1
225
Y
2
122685270 (GRCm38)
T401M
G
A
missense
Het
probably damaging
1.000
0.647
phenotype
2015-06-10
33
318530
Tas1r3
0.068
R4195
G1
225
Y
4
155862985 (GRCm38)
E81G
T
C
missense
Het
probably damaging
0.999
0.705
phenotype
2015-06-10
34
318529
Zfp990
0.064
R4195
G1
225
Y
4
145536977 (GRCm38)
A
T
splice site
2058 bp
Het
probably null
0.976
2015-06-10
35
318527
Zzz3
1.000
R4195
G1
225
Y
3
152428465 (GRCm38)
T387A
A
G
missense
Het
probably benign
0.024
0.101
2015-06-10
[records 1 to 35 of 35]