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Incidental Mutations
65
incidental mutations are currently displayed, and affect
64
genes.
10
are Possibly Damaging.
24
are Probably Damaging.
25
are Probably Benign.
6
are Probably Null.
4
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 65 of 65]
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
237587
Arap3
0.833
R2172
G1
225
N
18
37990560 (GRCm38)
E441V
T
A
missense
Het
probably damaging
0.999
phenotype
2014-10-02
2
237554
Arfip2
0.000
R2172
G1
225
N
7
105637988 (GRCm38)
D64V
T
A
missense
Het
probably damaging
1.000
2014-10-02
3
237518
Atg9a
1.000
R2172
G1
225
N
1
75185685 (GRCm38)
R527L
C
A
missense
Het
probably damaging
0.993
phenotype
2014-10-02
4
237531
Atp1a1
1.000
R2172
G1
225
N
3
101590548 (GRCm38)
I308L
T
G
missense
Het
probably benign
0.000
phenotype
2014-10-02
5
237529
Bcan
0.000
R2172
G1
225
N
3
87996581 (GRCm38)
Y199F
T
A
missense
Het
probably damaging
0.997
phenotype
2014-10-02
6
237565
Bsn
0.352
R2172
G1
225
N
9
108109992 (GRCm38)
T
C
intron
Het
probably benign
phenotype
2014-10-02
7
237542
Ccdc158
0.157
R2172
G1
225
N
5
92632508 (GRCm38)
L902H
A
T
missense
Het
probably damaging
0.998
2014-10-02
8
237516
Dnah7b
0.104
R2172
G1
225
N
1
46124512 (GRCm38)
Y492C
A
G
missense
Het
probably benign
0.121
2014-10-02
9
237577
Dnah9
0.332
R2172
G1
225
N
11
66072779 (GRCm38)
H1783N
G
T
missense
Het
probably damaging
0.996
phenotype
2014-10-02
10
237558
Dpep2
0.186
R2172
G1
225
N
8
105988998 (GRCm38)
V320A
A
G
missense
Het
possibly damaging
0.877
phenotype
2014-10-02
11
237586
Dsc2
0.000
R2172
G1
225
N
18
20045502 (GRCm38)
Y282H
A
G
missense
Het
probably damaging
1.000
phenotype
2014-10-02
12
237572
Egfr
0.915
R2172
G1
225
N
11
16911562 (GRCm38)
P1114S
C
T
missense
Het
probably benign
0.001
phenotype
2014-10-02
13
237522
Fastkd1
0.069
R2172
G1
225
N
2
69700133 (GRCm38)
S560P
A
G
missense
Het
probably damaging
1.000
2014-10-02
14
237530
Gm10696
0.936
R2172
G1
225
N
3
94176298 (GRCm38)
K69Q
T
G
missense
Het
possibly damaging
0.677
2014-10-02
15
237528
Gm14295
0.158
R2172
G1
174
N
2
176811102 (GRCm38)
R795Q
G
A
missense
Het
possibly damaging
0.479
2014-10-02
16
237523
Gpr155
0.000
R2172
G1
225
N
2
73382127 (GRCm38)
V51I
C
T
missense
Het
probably benign
0.001
2014-10-02
17
237541
Gsap
0.131
R2172
G1
225
N
5
21222440 (GRCm38)
G
A
critical splice donor site
1 bp
Het
probably null
phenotype
2014-10-02
18
237579
Hecw1
0.000
R2172
G1
225
N
13
14377706 (GRCm38)
I103F
T
A
missense
Het
probably damaging
1.000
2014-10-02
19
237548
Herc3
0.000
R2172
G1
225
N
6
58887437 (GRCm38)
N685K
T
A
missense
Het
probably damaging
1.000
phenotype
2014-10-02
20
237574
Hnrnph1
1.000
R2172
G1
225
N
11
50382816 (GRCm38)
D244E
T
A
missense
Het
probably benign
0.108
phenotype
2014-10-02
21
237560
Hydin
0.697
R2172
G1
225
N
8
110582049 (GRCm38)
E3989G
A
G
missense
Het
probably benign
0.421
phenotype
2014-10-02
22
237543
Ibsp
0.151
R2172
G1
225
N
5
104310430 (GRCm38)
Y278H
T
C
missense
Het
probably damaging
0.998
phenotype
2014-10-02
23
237583
Ift57
1.000
R2172
G1
225
N
16
49759340 (GRCm38)
N291K
T
G
missense
Het
probably benign
0.032
phenotype
2014-10-02
24
237519
Il15ra
0.050
R2172
G1
209
N
2
11723571 (GRCm38)
T149A
A
G
missense
Het
possibly damaging
0.944
phenotype
2014-10-02
25
237589
Ints5
0.531
R2172
G1
225
N
19
8896282 (GRCm38)
T535I
C
T
missense
Het
possibly damaging
0.728
phenotype
2014-10-02
26
237580
Jarid2
1.000
R2172
G1
225
N
13
44902539 (GRCm38)
L268P
T
C
missense
Het
probably damaging
0.990
phenotype
2014-10-02
27
237539
Klhdc7a
0.000
R2172
G1
182
N
4
139965810 (GRCm38)
T609S
T
A
missense
Het
probably benign
0.250
2014-10-02
28
237563
Lrrc49
0.183
R2172
G1
225
N
9
60602682 (GRCm38)
V429A
A
G
missense
Het
probably benign
0.252
2014-10-02
29
237549
Lsm3
0.827
R2172
G1
184
N
6
91522272 (GRCm38)
V87A
T
C
missense
Het
possibly damaging
0.515
phenotype
2014-10-02
30
237537
Man1c1
0.260
R2172
G1
225
N
4
134703438 (GRCm38)
P11R
G
C
missense
Het
probably damaging
0.998
0.304
2014-10-02
31
237526
Map1a
0.367
R2172
G1
225
N
2
121307932 (GRCm38)
V2726L
G
T
missense
Het
probably damaging
0.999
phenotype
2014-10-02
32
237559
Marveld3
0.065
R2172
G1
225
N
8
109961846 (GRCm38)
S88A
A
C
missense
Het
probably benign
0.225
2014-10-02
33
237568
Mcm9
0.000
R2172
G1
225
N
10
53548574 (GRCm38)
D640G
T
C
missense
Het
probably damaging
1.000
phenotype
2014-10-02
34
237585
Mettl4
0.226
R2172
G1
225
N
17
94733163 (GRCm38)
I399T
A
G
missense
Het
probably benign
0.000
2014-10-02
35
237562
Mmp27
0.066
R2172
G1
225
N
9
7577378 (GRCm38)
L274*
T
A
nonsense
Het
probably null
phenotype
2014-10-02
36
237520
Nacc2
0.000
R2172
G1
225
N
2
26060223 (GRCm38)
D500E
A
C
missense
Het
probably benign
0.002
2014-10-02
37
237573
Nprl3
0.273
R2172
G1
225
N
11
32234894 (GRCm38)
M372L
T
A
missense
Het
probably benign
0.001
Hba
th-J
mutation. [provided by MGI curators] (source: MGI)">phenotype
2014-10-02
38
237555
Olfr478
0.123
R2172
G1
225
N
7
108031467 (GRCm38)
I292N
A
T
missense
Het
probably damaging
1.000
phenotype
2014-10-02
39
266097
Otud7b
1.000
R2172
G1
214
N
3
96153520 (GRCm38)
T
G
splice site
28 bp
Het
probably null
phenotype
2015-02-05
40
237588
Pcx
1.000
R2172
G1
225
N
19
4620881 (GRCm38)
R1070H
G
A
missense
Het
probably benign
0.169
phenotype
2014-10-02
41
237571
Ptprq
0.252
R2172
G1
225
N
10
107590994 (GRCm38)
W1560*
C
T
nonsense
Het
probably null
phenotype
2014-10-02
42
237581
Puf60
0.958
R2172
G1
225
N
15
76070464 (GRCm38)
I520N
A
T
missense
Het
probably damaging
1.000
phenotype
2014-10-02
43
237566
Qars
0.965
R2172
G1
225
N
9
108509200 (GRCm38)
R143C
C
T
missense
Het
probably damaging
0.997
2014-10-02
44
237590
Rfx3
1.000
R2172
G1
225
N
19
27815494 (GRCm38)
Q322*
G
A
nonsense
Het
probably null
phenotype
2014-10-02
45
237578
Samd14
0.062
R2172
G1
215
N
11
95014391 (GRCm38)
V10L
G
T
missense
Het
probably benign
0.000
2014-10-02
46
237567
Setd2
0.936
R2172
G1
225
N
9
110549844 (GRCm38)
R909Q
G
A
missense
Het
probably benign
0.101
phenotype
2014-10-02
47
237557
Sh2d4a
0.000
R2172
G1
225
N
8
68296664 (GRCm38)
S117P
T
C
missense
Het
probably benign
0.001
phenotype
2014-10-02
48
237582
Sharpin
0.259
R2172
G1
183
N
15
76350666 (GRCm38)
C
A
unclassified
Het
probably benign
0.075
phenotype
2014-10-02
49
237564
Skor1
0.441
R2172
G1
123
N
9
63145122 (GRCm38)
A494S
C
A
missense
Het
possibly damaging
0.839
2014-10-02
50
237570
Slc41a2
0.217
R2172
G1
205
N
10
83283774 (GRCm38)
T375A
T
C
missense
Het
probably benign
0.003
2014-10-02
51
237575
Sparc
0.000
R2172
G1
225
N
11
55395801 (GRCm38)
Q324*
G
A
nonsense
Het
probably null
phenotype
2014-10-02
52
237576
Srebf1
1.000
R2172
G1
225
N
11
60206502 (GRCm38)
T171A
T
C
missense
Het
probably benign
0.000
phenotype
2014-10-02
53
237544
Srrd
0.827
R2172
G1
225
N
5
112341122 (GRCm38)
I54T
A
G
missense
Het
possibly damaging
0.948
2014-10-02
54
237546
Tecpr1
0.000
R2172
G1
225
N
5
144196417 (GRCm38)
Q1072K
G
T
missense
Het
probably damaging
0.997
phenotype
2014-10-02
55
237547
Tecpr1
0.000
R2172
G1
196
N
5
144211456 (GRCm38)
V377E
A
T
missense
Het
probably benign
0.100
phenotype
2014-10-02
56
237533
Tln1
1.000
R2172
G1
225
N
4
43545721 (GRCm38)
H919L
T
A
missense
Het
probably benign
0.000
phenotype
2014-10-02
57
237591
Tm9sf3
1.000
R2172
G1
225
N
19
41217420 (GRCm38)
S516N
C
T
missense
Het
probably damaging
0.999
2014-10-02
58
237515
Trpa1
0.138
R2172
G1
225
N
1
14881656 (GRCm38)
T940S
T
A
missense
Het
probably benign
0.010
phenotype
2014-10-02
59
237545
Trpv4
0.239
R2172
G1
225
N
5
114644710 (GRCm38)
R64C
G
A
missense
Het
probably damaging
0.999
phenotype
2014-10-02
60
237556
Tufm
0.954
R2172
G1
225
N
7
126488847 (GRCm38)
E174G
A
G
missense
Het
probably benign
0.007
phenotype
2014-10-02
61
237561
Urb2
0.946
R2172
G1
225
N
8
124031102 (GRCm38)
T1183A
A
G
missense
Het
probably damaging
0.999
2014-10-02
62
237532
Virma
1.000
R2172
G1
225
N
4
11527843 (GRCm38)
M1245L
A
T
missense
Het
possibly damaging
0.817
2014-10-02
63
237551
Vmn2r32
0.215
R2172
G1
169
N
7
7474615 (GRCm38)
Y259C
T
C
missense
Het
probably damaging
0.992
2014-10-02
64
237552
Zfp329
0.000
R2172
G1
225
N
7
12810767 (GRCm38)
F277L
A
G
missense
Het
probably damaging
1.000
2014-10-02
65
237536
Zfp683
0.109
R2172
G1
225
N
4
134055795 (GRCm38)
T190I
C
T
missense
Het
possibly damaging
0.908
phenotype
2014-10-02
[records 1 to 65 of 65]