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Incidental Mutations
29
incidental mutations are currently displayed, and affect
29
genes.
6
are Possibly Damaging.
10
are Probably Damaging.
7
are Probably Benign.
6
are Probably Null.
3
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 29 of 29]
10
25
50
100
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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
312092
9930111J21Rik1
0.062
R3961
G1
163
N
11
48947976
T595A
T
C
missense
Het
possibly damaging
0.953
0.538
04/29/2015
2
312088
AF529169
0.000
R3961
G1
225
N
9
89601910
T478I
G
A
missense
Het
probably damaging
1.000
0.142
04/29/2015
3
312098
Bicral
1.000
R3961
G1
225
N
17
46824825
I486M
T
C
missense
Het
probably damaging
0.965
phenotype
04/29/2015
4
312084
Btbd1
0.299
R3961
G1
225
N
7
81818335
E146*
C
A
nonsense
Het
probably null
phenotype
04/29/2015
5
312090
Cdcp1
0.000
R3961
G1
225
N
9
123182381
T344A
T
C
missense
Het
possibly damaging
0.725
0.179
phenotype
04/29/2015
6
312094
Cenpm
R3961
G1
225
N
15
82234373
L180Q
A
T
missense
Het
possibly damaging
0.936
phenotype
04/29/2015
7
312083
Cers3
0.328
R3961
G1
225
N
7
66786075
A261S
G
T
missense
Het
probably benign
0.253
0.105
phenotype
04/29/2015
8
312099
Dazl
0.000
R3961
G1
225
N
17
50288133
V91A
A
G
missense
Het
probably damaging
0.990
phenotype
04/29/2015
9
312100
Dsc2
0.000
R3961
G1
225
N
18
20051227
V35I
C
T
missense
Het
probably damaging
0.978
0.647
phenotype
04/29/2015
10
312080
Fras1
0.000
R3961
G1
225
N
5
96677385
T
C
critical splice donor site
2 bp
Het
probably null
phenotype
04/29/2015
11
312102
Ltbp3
0.269
R3961
G1
225
N
19
5754022
R854Q
G
A
missense
Het
probably benign
0.023
0.073
phenotype
04/29/2015
12
312076
Mme
0.000
R3961
G1
225
N
3
63345192
M419K
T
A
missense
Het
probably damaging
0.995
phenotype
04/29/2015
13
312086
Ncan
0.000
R3961
G1
225
N
8
70110300
T436M
G
A
missense
Het
probably benign
0.052
phenotype
04/29/2015
14
312089
Nphp3
1.000
R3961
G1
225
N
9
104003042
E88*
G
T
nonsense
Het
probably null
phenotype
04/29/2015
15
312075
Olfr993
0.209
R3961
G1
225
N
2
85414872
I2M
T
C
missense
Het
possibly damaging
0.689
phenotype
04/29/2015
16
312074
Pdcl
0.938
R3961
G1
225
N
2
37352187
M184V
T
C
missense
Het
probably benign
0.005
phenotype
04/29/2015
17
312091
Polr3b
1.000
R3961
G1
225
N
10
84684302
M694T
T
C
missense
Het
possibly damaging
0.893
phenotype
04/29/2015
18
312079
Pramef8
0.066
R3961
G1
225
N
4
143419318
N452K
T
A
missense
Het
probably benign
0.001
04/29/2015
19
312095
Prkdc
0.956
R3961
G1
225
N
16
15829611
T
G
splice site
Het
probably null
phenotype
04/29/2015
20
312087
Prss35
0.100
R3961
G1
225
N
9
86755749
M191V
A
G
missense
Het
probably benign
0.017
04/29/2015
21
312103
Rtn3
0.147
R3961
G1
225
N
19
7458145
S142G
T
C
missense
Het
probably damaging
0.994
0.109
phenotype
04/29/2015
22
312072
Slc19a3
0.163
R3961
G1
225
N
1
83022957
F113Y
A
T
missense
Het
probably damaging
0.995
0.433
phenotype
04/29/2015
23
312101
Taf7
1.000
R3961
G1
225
N
18
37643121
V131A
A
G
missense
Het
probably benign
0.292
phenotype
04/29/2015
24
312077
Tesk1
0.294
R3961
G1
225
N
4
43445133
A
G
splice site
10 bp
Het
probably null
phenotype
04/29/2015
25
312071
Tmem131
0.831
R3961
G1
225
N
1
36818950
D741N
C
T
missense
Het
probably damaging
1.000
04/29/2015
26
312073
Tmem63a
0.142
R3961
G1
225
N
1
180963114
D446N
G
A
missense
Het
possibly damaging
0.483
0.625
04/29/2015
27
312085
Tpte
0.077
R3961
G1
225
N
8
22359415
S553G
A
G
missense
Het
probably damaging
0.989
phenotype
04/29/2015
28
312093
Trpv3
0.092
R3961
G1
225
N
11
73287420
K438*
A
T
nonsense
Het
probably null
phenotype
04/29/2015
29
312097
Vmn2r107
0.127
R3961
G1
225
N
17
20375455
G757R
G
A
missense
Het
probably damaging
0.997
04/29/2015
[records 1 to 29 of 29]