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Incidental Mutations
30
incidental mutations are currently displayed, and affect
30
genes.
2
are Possibly Damaging.
8
are Probably Damaging.
16
are Probably Benign.
4
are Probably Null.
1
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 30 of 30]
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
15423
1700028P14Rik
0.147
R0036
G1
Y
19
23616568 (GRCm38)
A
T
unclassified
Het
probably benign
0.252
2012-12-21
2
15458
Cfap44
0.000
R0036
G1
Y
16
44439069 (GRCm38)
E1098G
A
G
missense
Het
possibly damaging
0.834
0.091
phenotype
2012-12-21
3
201480
Ctsq
0.069
R0036
G1
77
Y
13
61037671 (GRCm38)
C
T
critical splice donor site
1 bp
Het
probably null
0.975
2014-06-13
4
18600
Dock9
0.000
R0036
G1
Y
14
121622853 (GRCm38)
V886M
C
T
missense
Het
probably damaging
0.995
0.130
2013-03-25
5
15459
Eaf2
0.631
R0036
G1
Y
16
36800658 (GRCm38)
Y224C
T
C
missense
Het
probably benign
0.009
0.060
phenotype
2012-12-21
6
64616
Egln3
0.000
R0036
G1
93
Y
12
54185592 (GRCm38)
D142E
A
T
missense
Het
possibly damaging
0.955
0.184
phenotype
2013-08-06
7
15771
Eif5b
1.000
R0036
G1
Y
1
38019111 (GRCm38)
S165T
T
A
missense
Het
probably benign
0.226
0.083
phenotype
2012-12-21
8
15645
Eln
1.000
R0036
G1
Y
5
134711060 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
0.976
phenotype
2012-12-21
9
201479
Fam120a
0.000
R0036
G1
46
Y
13
48889264 (GRCm38)
G
A
splice site
Het
probably benign
0.090
2014-06-13
10
201475
Hspg2
1.000
R0036
G1
32
Y
4
137542849 (GRCm38)
T2373A
A
G
missense
Het
probably damaging
0.999
0.162
phenotype
2014-06-13
11
15654
Jakmip1
0.263
R0036
G1
Y
5
37134304 (GRCm38)
K514R
A
G
missense
Het
probably null
0.383
0.100
phenotype
2012-12-21
12
15577
Myo1e
0.000
R0036
G1
Y
9
70341308 (GRCm38)
W435R
T
A
missense
Het
probably damaging
1.000
0.975
phenotype
2012-12-21
13
18602
Nadsyn1
0.000
R0036
G1
Y
7
143811291 (GRCm38)
I226V
T
C
missense
Het
probably benign
0.227
0.112
phenotype
2013-03-25
14
18599
Nedd4l
0.268
R0036
G1
Y
18
65051123 (GRCm38)
T
C
intron
Het
probably benign
0.090
phenotype
2013-03-25
15
64619
Pcyox1l
0.000
R0036
G1
93
Y
18
61697421 (GRCm38)
T460K
G
T
missense
Het
probably benign
0.129
0.090
2013-08-06
16
64613
Phrf1
0.000
R0036
G1
115
Y
7
141261780 (GRCm38)
M1435T
T
C
missense
Het
probably damaging
0.996
0.100
2013-08-06
17
15433
Ppic
0.118
R0036
G1
Y
18
53409192 (GRCm38)
I148N
A
T
missense
Het
probably damaging
1.000
0.957
phenotype
2012-12-21
18
64614
Rnf157
0.000
R0036
G1
86
Y
11
116396302 (GRCm38)
Y32H
A
G
missense
Het
probably damaging
1.000
0.484
phenotype
2013-08-06
19
201473
Rnf224
0.104
R0036
G1
57
Y
2
25236131 (GRCm38)
R70Q
C
T
missense
Het
probably damaging
1.000
0.647
2014-06-13
20
201474
Rusc2
0.208
R0036
G1
78
Y
4
43424009 (GRCm38)
D1054E
C
A
missense
Het
probably damaging
1.000
0.647
phenotype
2014-06-13
21
64612
S100a16
0.122
R0036
G1
117
Y
3
90542456 (GRCm38)
M82K
T
A
missense
Het
probably benign
0.003
0.090
2013-08-06
22
15680
Sdr16c6
0.057
R0036
G1
Y
4
4063335 (GRCm38)
C
A
splice site
Het
probably benign
2012-12-21
23
201478
Serpina3j
0.055
R0036
G1
52
Y
12
104317347 (GRCm38)
T235A
A
G
missense
Het
probably benign
0.075
0.090
2014-06-13
24
201472
Sgo2a
0.000
R0036
G1
50
Y
1
58015628 (GRCm38)
S324P
T
C
missense
Het
probably benign
0.142
0.091
phenotype
2014-06-13
25
64618
Slf1
0.000
R0036
G1
96
Y
13
77100951 (GRCm38)
Q373K
G
T
missense
Het
probably benign
0.017
0.090
phenotype
2013-08-06
26
201481
Son
0.958
R0036
G1
37
Y
16
91660166 (GRCm38)
T
A
intron
Het
probably benign
0.071
phenotype
2014-06-13
27
15456
Tfg
0.922
R0036
G1
Y
16
56690995 (GRCm38)
Q324K
G
T
missense
Het
probably benign
0.177
0.082
phenotype
2012-12-21
28
201476
Tril
0.174
R0036
G1
24
Y
6
53818633 (GRCm38)
A535T
C
T
missense
Het
probably benign
0.000
0.090
phenotype
2014-06-13
29
201477
Vipr1
1.000
R0036
G1
29
Y
9
121660983 (GRCm38)
D141N
G
A
missense
Het
probably benign
0.000
0.090
phenotype
2014-06-13
30
15745
Wdr64
0.057
R0036
G1
Y
1
175728930 (GRCm38)
G248*
G
T
nonsense
Het
probably null
0.976
2012-12-21
[records 1 to 30 of 30]