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Incidental Mutations
71
incidental mutations are currently displayed, and affect
71
genes.
12
are Possibly Damaging.
23
are Probably Damaging.
23
are Probably Benign.
10
are Probably Null.
3
create premature stop codons.
3
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 71 of 71]
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
224357
2810408A11Rik
0.053
R2034
G1
225
Y
11
69900559 (GRCm38)
I65V
T
C
missense
Het
probably benign
0.003
0.090
2014-08-25
2
224351
Abca13
0.000
R2034
G1
225
Y
11
9292628 (GRCm38)
N1497S
A
G
missense
Het
possibly damaging
0.831
0.090
phenotype
2014-08-25
3
224365
Afmid
0.000
R2034
G1
98
Y
11
117835235 (GRCm38)
N184K
C
A
missense
Het
probably benign
0.072
0.119
phenotype
2014-08-25
4
224297
Ampd2
0.167
R2034
G1
225
Y
3
108077363 (GRCm38)
I459N
A
T
missense
Het
possibly damaging
0.907
0.179
phenotype
2014-08-25
5
224285
Anapc1
1.000
R2034
G1
225
Y
2
128648458 (GRCm38)
D1018G
T
C
missense
Het
possibly damaging
0.918
0.146
phenotype
2014-08-25
6
224329
Ano9
0.064
R2034
G1
225
Y
7
141108135 (GRCm38)
I223F
T
A
missense
Het
probably damaging
0.989
0.323
phenotype
2014-08-25
7
224325
B3gnt6
0.119
R2034
G1
185
Y
7
98194018 (GRCm38)
L245P
A
G
missense
Het
possibly damaging
0.922
0.535
phenotype
2014-08-25
8
224389
Bag6
1.000
R2034
G1
225
Y
17
35144692 (GRCm38)
R784Q
G
A
missense
Het
probably damaging
0.989
0.099
phenotype
2014-08-25
9
224361
Brca1
1.000
R2034
G1
225
Y
11
101489849 (GRCm38)
S1786T
C
G
missense
Het
probably benign
0.000
0.090
phenotype
2014-08-25
10
224287
Btbd3
0.361
R2034
G1
225
Y
2
138278983 (GRCm38)
S26A
T
G
missense
Het
probably benign
0.148
0.100
2014-08-25
11
224371
Cacna1d
0.836
R2034
G1
224
Y
14
30089863 (GRCm38)
V1277L
C
A
missense
Het
probably damaging
1.000
0.252
phenotype
2014-08-25
12
224337
Casp12
0.000
R2034
G1
225
Y
9
5346491 (GRCm38)
T6I
C
T
missense
Het
probably damaging
0.971
0.647
phenotype
2014-08-25
13
224341
Col7a1
1.000
R2034
G1
225
Y
9
108963007 (GRCm38)
V1262A
T
C
missense
Het
unknown
0.087
phenotype
2014-08-25
14
224291
Crh
0.464
R2034
G1
170
Y
3
19694098 (GRCm38)
G127C
C
A
missense
Het
probably damaging
0.999
0.149
phenotype
2014-08-25
15
224311
D5Ertd579e
0.243
R2034
G1
225
Y
5
36613538 (GRCm38)
L64*
A
T
nonsense
Het
probably null
0.976
2014-08-25
16
224301
Dab1
0.818
R2034
G1
217
Y
4
104731751 (GRCm38)
A524V
C
T
missense
Het
probably benign
0.289
0.223
phenotype
2014-08-25
17
224353
Ddc
1.000
R2034
G1
225
Y
11
11880456 (GRCm38)
I63L
T
A
missense
Het
probably benign
0.400
0.068
phenotype
2014-08-25
18
224405
Eif3a
0.970
R2034
G1
225
Y
19
60762130 (GRCm38)
C
T
unclassified
Het
probably benign
0.118
2014-08-25
19
224279
Fsip2
0.076
R2034
G1
225
Y
2
82989494 (GRCm38)
N5190K
T
A
missense
Het
probably benign
0.429
0.090
phenotype
2014-08-25
20
224343
Gm5420
0.127
R2034
G1
225
Y
10
21691613 (GRCm38)
A
G
exon
Het
noncoding transcript
0.087
2014-08-25
21
224277
Grb14
0.217
R2034
G1
225
Y
2
64923529 (GRCm38)
A
G
splice site
Het
probably benign
0.090
phenotype
2014-08-25
22
224309
Gsap
0.130
R2034
G1
225
Y
5
21270595 (GRCm38)
I545F
A
T
missense
Het
probably damaging
0.999
0.095
phenotype
2014-08-25
23
224367
Hectd1
1.000
R2034
G1
225
Y
12
51757116 (GRCm38)
A
T
splice site
Het
probably null
0.976
phenotype
2014-08-25
24
224289
Helz2
0.000
R2034
G1
225
Y
2
181232578 (GRCm38)
P2041L
G
A
missense
Het
probably damaging
1.000
0.151
phenotype
2014-08-25
25
224339
Herc1
0.000
R2034
G1
225
Y
9
66441972 (GRCm38)
A2038T
G
A
missense
Het
probably benign
0.013
0.078
phenotype
2014-08-25
26
224265
Il10
0.764
R2034
G1
225
Y
1
131024185 (GRCm38)
Q152K
C
A
missense
Het
probably benign
0.000
0.090
phenotype
2014-08-25
27
224319
Klrg1
0.000
R2034
G1
225
Y
6
122279637 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
0.948
phenotype
2014-08-25
28
224295
Lrig2
1.000
R2034
G1
225
Y
3
104494092 (GRCm38)
T160A
T
C
missense
Het
probably benign
0.000
0.057
phenotype
2014-08-25
29
224315
Mmd2
0.000
R2034
G1
213
Y
5
142575184 (GRCm38)
A
T
critical splice donor site
2 bp
Het
probably null
0.949
phenotype
2014-08-25
30
224333
Mmp2
0.646
R2034
G1
225
Y
8
92836912 (GRCm38)
S338F
C
T
missense
Het
probably damaging
1.000
0.270
phenotype
2014-08-25
31
224377
Nalcn
1.000
R2034
G1
225
Y
14
123283603 (GRCm38)
D1630A
T
G
missense
Het
probably benign
0.007
0.059
phenotype
2014-08-25
32
224255
Ncoa2
0.959
R2034
G1
225
Y
1
13164983 (GRCm38)
S909G
T
C
missense
Het
probably benign
0.005
0.071
phenotype
2014-08-25
33
224275
Neb
0.847
R2034
G1
225
Y
2
52280611 (GRCm38)
M1683K
A
T
missense
Het
possibly damaging
0.778
0.338
phenotype
2014-08-25
34
224317
Nfe2l3
0.000
R2034
G1
225
Y
6
51458370 (GRCm38)
I637V
A
G
missense
Het
possibly damaging
0.501
0.072
phenotype
2014-08-25
35
224387
Npw
0.052
R2034
G1
155
Y
17
24658268 (GRCm38)
S53F
G
A
missense
Het
probably damaging
0.996
0.647
phenotype
2014-08-25
36
224345
Nrbf2
0.498
R2034
G1
225
Y
10
67275564 (GRCm38)
A
T
splice site
Het
probably benign
2014-08-25
37
224383
Nrros
0.000
R2034
G1
225
Y
16
32144157 (GRCm38)
W311*
C
T
nonsense
Het
probably null
0.976
phenotype
2014-08-25
38
224273
Nup188
0.959
R2034
G1
225
Y
2
30310085 (GRCm38)
T
A
unclassified
Het
probably benign
0.090
phenotype
2014-08-25
39
224403
Olfr1444
0.177
R2034
G1
225
Y
19
12861787 (GRCm38)
M4K
T
A
missense
Het
possibly damaging
0.824
0.816
phenotype
2014-08-25
40
224373
Olfr726
0.067
R2034
G1
225
Y
14
50083983 (GRCm38)
M233V
T
C
missense
Het
probably benign
0.337
0.090
phenotype
2014-08-25
41
224375
Parp4
0.171
R2034
G1
225
Y
14
56634263 (GRCm38)
I1133F
A
T
missense
Het
probably damaging
0.995
0.143
phenotype
2014-08-25
42
224395
Pcdhb11
0.069
R2034
G1
225
Y
18
37422493 (GRCm38)
V292A
T
C
missense
Het
probably benign
0.001
0.090
2014-08-25
43
224335
Pcnx2
0.000
R2034
G1
225
Y
8
125818667 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
0.949
phenotype
2014-08-25
44
224369
Phf2
0.334
R2034
G1
225
Y
13
48817730 (GRCm38)
S489P
A
G
missense
Het
unknown
0.066
phenotype
2014-08-25
45
224355
Pik3r5
0.193
R2034
G1
225
Y
11
68493577 (GRCm38)
N598K
T
A
missense
Het
probably damaging
0.987
0.588
phenotype
2014-08-25
46
224261
Pikfyve
1.000
R2034
G1
225
Y
1
65222357 (GRCm38)
E432D
A
T
missense
Het
probably damaging
0.999
0.647
phenotype
2014-08-25
47
224307
Pink1
0.000
R2034
G1
225
Y
4
138318032 (GRCm38)
I274V
T
C
missense
Het
possibly damaging
0.877
0.074
phenotype
2014-08-25
48
224257
Pkhd1
0.094
R2034
G1
225
Y
1
20200669 (GRCm38)
T3220I
G
A
missense
Het
probably damaging
1.000
0.240
phenotype
2014-08-25
49
224269
Plxna2
0.000
R2034
G1
225
Y
1
194780594 (GRCm38)
I890V
A
G
missense
Het
probably benign
0.004
0.143
phenotype
2014-08-25
50
224305
Pomgnt1
0.000
R2034
G1
225
Y
4
116157927 (GRCm38)
V492A
T
C
missense
Het
possibly damaging
0.870
0.212
phenotype
2014-08-25
51
266046
Prp2
R2034
G1
225
N
6
132595984 (GRCm38)
G
T
splice site
Het
probably null
phenotype
2015-02-05
52
224271
Rabl6
0.000
R2034
G1
225
Y
2
25585432 (GRCm38)
E543G
T
C
missense
Het
possibly damaging
0.586
0.179
phenotype
2014-08-25
53
224299
Rgp1
1.000
R2034
G1
225
Y
4
43581605 (GRCm38)
T
A
splice site
Het
probably null
0.812
2014-08-25
54
224401
Rps6kb2
0.166
R2034
G1
225
Y
19
4161107 (GRCm38)
T140A
T
C
missense
Het
probably damaging
0.999
0.623
phenotype
2014-08-25
55
224293
S100a11
0.143
R2034
G1
225
Y
3
93526122 (GRCm38)
I91T
T
C
missense
Het
probably benign
0.000
0.090
phenotype
2014-08-25
56
224263
Serpine2
0.000
R2034
G1
225
Y
1
79796852 (GRCm38)
L230P
A
G
missense
Het
probably damaging
0.998
0.966
phenotype
2014-08-25
57
224397
Sh3tc2
0.000
R2034
G1
225
Y
18
61987666 (GRCm38)
D370G
A
G
missense
Het
probably damaging
1.000
0.325
phenotype
2014-08-25
58
224385
Sim2
1.000
R2034
G1
163
Y
16
94085942 (GRCm38)
I43L
A
C
missense
Het
probably damaging
0.957
0.454
phenotype
2014-08-25
59
224379
Skp2
0.000
R2034
G1
225
Y
15
9113698 (GRCm38)
G376C
C
A
missense
Het
probably damaging
1.000
0.514
phenotype
2014-08-25
60
224399
Slc14a2
0.000
R2034
G1
225
Y
18
78183583 (GRCm38)
L419P
A
G
missense
Het
probably damaging
0.990
0.768
phenotype
2014-08-25
61
224347
Srgap1
0.261
R2034
G1
225
Y
10
121792746 (GRCm38)
E817K
C
T
missense
Het
probably damaging
0.977
0.118
phenotype
2014-08-25
62
224313
Stag3
0.000
R2034
G1
225
Y
5
138298001 (GRCm38)
E442G
A
G
missense
Het
possibly damaging
0.819
0.225
phenotype
2014-08-25
63
224253
Sulf1
0.440
R2034
G1
225
Y
1
12820421 (GRCm38)
N361S
A
G
missense
Het
probably damaging
1.000
0.575
phenotype
2014-08-25
64
224393
Tmco6
0.061
R2034
G1
225
Y
18
36737856 (GRCm38)
A
G
splice site
4 bp
Het
probably null
0.976
2014-08-25
65
224363
Tmem104
0.000
R2034
G1
225
Y
11
115243547 (GRCm38)
I303N
T
A
missense
Het
probably benign
0.421
0.090
2014-08-25
66
224359
Ttll6
0.000
R2034
G1
225
Y
11
96135526 (GRCm38)
D86Y
G
T
missense
Het
probably damaging
0.988
0.647
2014-08-25
67
224323
Vmn1r120
0.072
R2034
G1
225
Y
7
21052958 (GRCm38)
E276A
T
G
missense
Het
possibly damaging
0.564
0.179
2014-08-25
68
224321
Vmn1r64
0.050
R2034
G1
225
Y
7
5883989 (GRCm38)
M185T
A
G
missense
Het
probably benign
0.092
0.090
2014-08-25
69
224349
Vmn2r85
0.095
R2034
G1
225
Y
10
130426373 (GRCm38)
A
T
splice site
Het
probably benign
0.090
2014-08-25
70
224327
Vwa3a
0.000
R2034
G1
225
Y
7
120782645 (GRCm38)
K568*
A
T
nonsense
Het
probably null
0.976
2014-08-25
71
224303
Zcchc11
0.000
R2034
G1
225
Y
4
108512195 (GRCm38)
R651W
C
T
missense
Het
probably damaging
1.000
0.647
phenotype
2014-08-25
[records 1 to 71 of 71]