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Incidental Mutations
96
incidental mutations are currently displayed, and affect
96
genes.
16
are Possibly Damaging.
31
are Probably Damaging.
37
are Probably Benign.
6
are Probably Null.
4
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 96 of 96]
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
591399
1110025L11Rik
0.098
R7658
G1
225.01
N
16
89063730 (GRCm38)
S72Y
G
T
missense
Het
unknown
2019-11-12
2
591358
6430531B16Rik
0.050
R7658
G1
225.01
N
7
139976618 (GRCm38)
N152S
T
C
missense
Het
probably benign
0.000
2019-11-12
3
591378
Abca8b
0.000
R7658
G1
225.01
N
11
109935717 (GRCm38)
K1568N
T
A
missense
Het
probably benign
0.002
phenotype
2019-11-12
4
591393
Adcy6
0.000
R7658
G1
225.01
N
15
98596067 (GRCm38)
Y865F
T
A
missense
Het
probably benign
0.002
phenotype
2019-11-12
5
591334
Adgrf3
0.000
R7658
G1
225.01
N
5
30197206 (GRCm38)
V608D
A
T
missense
Het
probably benign
0.415
2019-11-12
6
591353
Agbl1
0.000
R7658
G1
225.01
N
7
76766369 (GRCm38)
A965S
G
T
missense
Het
unknown
phenotype
2019-11-12
7
591340
Agbl3
0.000
R7658
G1
225.01
N
6
34832508 (GRCm38)
P690L
C
T
missense
Het
probably benign
0.112
phenotype
2019-11-12
8
591331
Akap9
0.563
R7658
G1
225.01
N
5
3968745 (GRCm38)
H1109D
C
G
missense
Het
probably benign
0.038
0.090
phenotype
2019-11-12
9
591369
Amt
1.000
R7658
G1
225.01
N
9
108297231 (GRCm38)
H65P
A
C
missense
Het
probably damaging
0.984
phenotype
2019-11-12
10
591362
Ankrd11
1.000
R7658
G1
225.01
N
8
122893664 (GRCm38)
T1150S
T
A
missense
Het
probably benign
0.000
phenotype
2019-11-12
11
591316
Arhgap15
0.528
R7658
G1
225.01
N
2
44142268 (GRCm38)
H288P
A
C
missense
Het
probably benign
0.177
phenotype
2019-11-12
12
591391
Arhgap39
0.146
R7658
G1
225.01
N
15
76737417 (GRCm38)
M328K
A
T
missense
Het
probably benign
0.026
2019-11-12
13
591366
Arhgef12
0.953
R7658
G1
225.01
N
9
42992536 (GRCm38)
K743R
T
C
missense
Het
probably damaging
0.999
phenotype
2019-11-12
14
591405
Atg2a
0.289
R7658
G1
225.01
N
19
6251263 (GRCm38)
V789G
T
G
missense
Het
probably damaging
1.000
2019-11-12
15
591398
Ccdc54
0.063
R7658
G1
225.01
N
16
50590481 (GRCm38)
T141A
T
C
missense
Het
probably benign
0.092
2019-11-12
16
591335
Ccng2
0.000
R7658
G1
225.01
N
5
93273343 (GRCm38)
S237R
C
G
missense
Het
probably benign
0.003
0.090
phenotype
2019-11-12
17
591361
Cdh5
1.000
R7658
G1
225.01
N
8
104129401 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
phenotype
2019-11-12
18
591372
Cdkl3
0.818
R7658
G1
225.01
N
11
52027182 (GRCm38)
V404A
T
C
missense
Het
not run
phenotype
2019-11-12
19
591341
Chrm2
0.094
R7658
G1
225.01
N
6
36523249 (GRCm38)
I14F
A
T
missense
Het
probably benign
0.002
phenotype
2019-11-12
20
591343
Cnbp
1.000
R7658
G1
225.01
N
6
87845276 (GRCm38)
K89E
T
C
missense
Het
possibly damaging
0.496
phenotype
2019-11-12
21
591345
Cntn6
0.156
R7658
G1
225.01
N
6
104650483 (GRCm38)
D92E
T
A
missense
Het
probably benign
0.292
phenotype
2019-11-12
22
591324
Col15a1
0.081
R7658
G1
225.01
N
4
47245591 (GRCm38)
F114S
T
C
missense
Het
possibly damaging
0.460
phenotype
2019-11-12
23
591370
Csrnp1
1.000
R7658
G1
225.01
N
9
119972403 (GRCm38)
F530S
A
G
missense
Het
probably benign
0.000
phenotype
2019-11-12
24
591357
Dcun1d3
0.323
R7658
G1
225.01
N
7
119857668 (GRCm38)
V274M
C
T
missense
Het
probably damaging
1.000
2019-11-12
25
591326
Dph2
1.000
R7658
G1
225.01
N
4
117890281 (GRCm38)
H302L
T
A
missense
Het
possibly damaging
0.633
phenotype
2019-11-12
26
591397
Fam162a
0.000
R7658
G1
225.01
N
16
36046400 (GRCm38)
Y118*
A
T
nonsense
Het
probably null
2019-11-12
27
591394
Fam186a
0.067
R7658
G1
225.01
N
15
99939844 (GRCm38)
Y2840H
A
G
missense
Het
unknown
2019-11-12
28
591360
Fto
0.000
R7658
G1
225.01
N
8
91666322 (GRCm38)
K466E
A
G
missense
Het
probably benign
0.345
phenotype
2019-11-12
29
591404
Gal
0.000
R7658
G1
225.01
N
19
3413309 (GRCm38)
Y41F
T
A
missense
Het
probably damaging
0.999
phenotype
2019-11-12
30
591313
Gigyf2
0.934
R7658
G1
225.01
N
1
87419138 (GRCm38)
L620F
A
T
missense
Het
unknown
phenotype
2019-11-12
31
591337
Git2
0.231
R7658
G1
225.01
N
5
114766489 (GRCm38)
R123H
C
T
missense
Het
probably damaging
1.000
phenotype
2019-11-12
32
591386
Glud1
0.937
R7658
G1
225.01
N
14
34311157 (GRCm38)
E87V
A
T
missense
Het
probably benign
0.251
phenotype
2019-11-12
33
591332
Gm21190
0.139
R7658
G1
225.01
N
5
15527925 (GRCm38)
E94A
T
G
missense
Het
possibly damaging
0.481
2019-11-12
34
591349
Gm5592
0.066
R7658
G1
225.01
N
7
41288710 (GRCm38)
V472A
T
C
missense
Het
probably benign
0.025
2019-11-12
35
591388
Gpc5
0.000
R7658
G1
225.01
N
14
115428208 (GRCm38)
N481K
T
A
missense
Het
possibly damaging
0.908
0.121
phenotype
2019-11-12
36
591327
Gpn2
0.968
R7658
G1
225.01
N
4
133591376 (GRCm38)
E304G
A
G
missense
Het
probably benign
0.006
2019-11-12
37
591390
Gsdmc2
0.064
R7658
G1
225.01
N
15
63825054 (GRCm38)
T423A
T
C
missense
Het
probably damaging
1.000
2019-11-12
38
591374
Gucy2e
0.272
R7658
G1
225.01
N
11
69226229 (GRCm38)
Q789*
G
A
nonsense
Het
probably null
phenotype
2019-11-12
39
591344
Gxylt2
0.000
R7658
G1
225.01
N
6
100783143 (GRCm38)
V213E
T
A
missense
Het
probably damaging
1.000
phenotype
2019-11-12
40
591382
Ighv1-75
0.233
R7658
G1
225.01
N
12
115834111 (GRCm38)
L64F
G
A
missense
Het
possibly damaging
0.841
2019-11-12
41
591346
Il17re
0.000
R7658
G1
225.01
N
6
113458982 (GRCm38)
C30R
T
C
missense
Het
probably benign
0.226
phenotype
2019-11-12
42
591319
Il7
0.177
R7658
G1
225.01
N
3
7604082 (GRCm38)
D31E
G
T
missense
Het
probably benign
0.371
phenotype
2019-11-12
43
591354
Ints4
0.962
R7658
G1
225.01
N
7
97529253 (GRCm38)
Y687H
T
C
missense
Het
possibly damaging
0.902
phenotype
2019-11-12
44
591352
Kdelr1
0.000
R7658
G1
225.01
N
7
45882977 (GRCm38)
V202G
T
G
missense
Het
probably benign
0.063
phenotype
2019-11-12
45
591387
Khnyn
0.077
R7658
G1
225.01
N
14
55887139 (GRCm38)
Y283*
C
A
nonsense
Het
probably null
phenotype
2019-11-12
46
591380
Klf11
0.000
R7658
G1
225.01
N
12
24653671 (GRCm38)
V52A
T
C
missense
Het
probably damaging
0.998
phenotype
2019-11-12
47
591333
Klhl7
0.580
R7658
G1
225.01
N
5
24141286 (GRCm38)
N310S
A
G
missense
Het
probably benign
0.111
phenotype
2019-11-12
48
591377
Krt27
0.079
R7658
G1
225.01
N
11
99349486 (GRCm38)
L202Q
A
T
missense
Het
possibly damaging
0.690
phenotype
2019-11-12
49
591321
Lce1d
0.091
R7658
G1
225.01
N
3
92686047 (GRCm38)
C20R
A
G
missense
Het
unknown
2019-11-12
50
591351
Lim2
0.309
R7658
G1
225.01
N
7
43433630 (GRCm38)
I80F
A
T
missense
Het
possibly damaging
0.655
phenotype
2019-11-12
51
591392
Lrrk2
0.335
R7658
G1
225.01
N
15
91700358 (GRCm38)
F326Y
T
A
missense
Het
possibly damaging
0.914
phenotype
2019-11-12
52
591384
Lyst
0.300
R7658
G1
225.01
N
13
13730476 (GRCm38)
Y3246F
A
T
missense
Het
possibly damaging
0.626
phenotype
2019-11-12
53
591318
Mafb
0.615
R7658
G1
225.01
N
2
160366435 (GRCm38)
H81L
T
A
missense
Het
possibly damaging
0.675
phenotype
2019-11-12
54
591395
Mfsd5
0.527
R7658
G1
225.01
N
15
102280877 (GRCm38)
R228H
G
A
missense
Het
probably benign
0.003
2019-11-12
55
591364
Mmp1b
0.064
R7658
G1
225.01
N
9
7386675 (GRCm38)
F150I
A
T
missense
Het
possibly damaging
0.586
phenotype
2019-11-12
56
591381
Mthfd1
1.000
R7658
G1
225.01
N
12
76270435 (GRCm38)
L20Q
T
A
missense
Het
probably damaging
1.000
phenotype
2019-11-12
57
591329
Mxra8
0.000
R7658
G1
225.01
N
4
155842963 (GRCm38)
T402A
A
G
missense
Het
probably benign
0.038
phenotype
2019-11-12
58
591401
Ndc80
0.963
R7658
G1
225.01
N
17
71508663 (GRCm38)
L376M
A
T
missense
Het
probably damaging
0.957
phenotype
2019-11-12
59
591385
Nsd1
1.000
R7658
G1
225.01
N
13
55277639 (GRCm38)
R1536S
A
T
missense
Het
probably damaging
0.996
phenotype
2019-11-12
60
591320
Nup210l
0.469
R7658
G1
225.01
N
3
90211993 (GRCm38)
H1874Q
C
A
missense
Het
probably benign
0.430
phenotype
2019-11-12
61
591339
Nyap1
0.125
R7658
G1
225.01
N
5
137732974 (GRCm38)
H776R
T
C
missense
Het
probably benign
0.000
phenotype
2019-11-12
62
591325
Patj
0.000
R7658
G1
225.01
N
4
98688179 (GRCm38)
H1773Q
C
A
missense
Het
probably damaging
1.000
phenotype
2019-11-12
63
591315
Pax8
1.000
R7658
G1
225.01
N
2
24436511 (GRCm38)
T280S
T
A
missense
Het
probably benign
0.004
phenotype
2019-11-12
64
591402
Pcdhb19
0.059
R7658
G1
225.01
N
18
37498981 (GRCm38)
T610A
A
G
missense
Het
probably damaging
0.992
phenotype
2019-11-12
65
591356
Pde2a
0.763
R7658
G1
225.01
N
7
101511581 (GRCm38)
D919G
A
G
missense
Het
possibly damaging
0.791
phenotype
2019-11-12
66
591376
Pdk2
0.000
R7658
G1
225.01
N
11
95028965 (GRCm38)
Y240F
T
A
missense
Het
probably damaging
1.000
phenotype
2019-11-12
67
591348
Peg3
0.000
R7658
G1
225.01
N
7
6709610 (GRCm38)
I871N
A
T
missense
Het
probably damaging
1.000
phenotype
2019-11-12
68
591330
Pex1
0.645
R7658
G1
225.01
N
5
3596244 (GRCm38)
A
T
unclassified
Het
probably benign
phenotype
2019-11-12
69
591355
Pgm2l1
0.269
R7658
G1
225.01
N
7
100250328 (GRCm38)
R50W
C
T
missense
Het
probably damaging
0.975
2019-11-12
70
591338
Phkg1
0.064
R7658
G1
225.01
N
5
129865923 (GRCm38)
K262N
T
A
missense
Het
probably damaging
1.000
phenotype
2019-11-12
71
591368
Pik3r4
1.000
R7658
G1
225.01
N
9
105644511 (GRCm38)
E92G
A
G
missense
Het
probably damaging
0.981
phenotype
2019-11-12
72
591323
Prmt6
0.000
R7658
G1
225.01
N
3
110250385 (GRCm38)
V196E
A
T
missense
Het
possibly damaging
0.513
phenotype
2019-11-12
73
591383
Ptprn2
0.233
R7658
G1
225.01
N
12
116722119 (GRCm38)
M66R
T
G
missense
Het
probably benign
0.013
phenotype
2019-11-12
74
591389
Rai14
0.444
R7658
G1
225.01
N
15
10593103 (GRCm38)
G152R
C
T
missense
Het
probably damaging
1.000
0.757
2019-11-12
75
591379
Recql5
0.343
R7658
G1
225.01
N
11
115923276 (GRCm38)
S348T
A
T
missense
Het
probably damaging
0.999
phenotype
2019-11-12
76
591406
Rfk
1.000
R7658
G1
225.01
N
19
17398682 (GRCm38)
T
G
critical splice donor site
2 bp
Het
probably null
phenotype
2019-11-12
77
591322
Selenbp1
0.000
R7658
G1
225.01
N
3
94944102 (GRCm38)
M389L
A
T
missense
Het
probably benign
0.027
phenotype
2019-11-12
78
591363
Sipa1l2
0.356
R7658
G1
225.01
N
8
125492290 (GRCm38)
R103C
G
A
missense
Het
probably benign
0.004
phenotype
2019-11-12
79
591336
Slc10a6
0.075
R7658
G1
225.01
N
5
103629190 (GRCm38)
S15C
T
A
missense
Het
probably damaging
0.987
2019-11-12
80
591403
Slc12a2
0.000
R7658
G1
225.01
N
18
57932524 (GRCm38)
V944L
G
T
missense
Het
probably benign
0.016
phenotype
2019-11-12
81
591375
Slc16a11
0.000
R7658
G1
225.01
N
11
70215317 (GRCm38)
L127Q
T
A
missense
Het
possibly damaging
0.956
2019-11-12
82
591396
St6gal1
0.069
R7658
G1
225.01
N
16
23356228 (GRCm38)
Y272C
A
G
missense
Het
probably damaging
1.000
phenotype
2019-11-12
83
591371
Stab2
0.000
R7658
G1
225.01
N
10
86981135 (GRCm38)
V133F
C
A
missense
Het
probably benign
0.119
phenotype
2019-11-12
84
591312
Stradb
0.000
R7658
G1
225.01
N
1
58992726 (GRCm38)
V266I
G
A
missense
Het
probably damaging
0.961
phenotype
2019-11-12
85
591347
Tmem150b
0.210
R7658
G1
225.01
N
7
4720759 (GRCm38)
W140R
A
G
missense
Het
probably benign
0.001
phenotype
2019-11-12
86
591359
Tnnt3
1.000
R7658
G1
225.01
N
7
142512096 (GRCm38)
K157*
A
T
nonsense
Het
probably null
phenotype
2019-11-12
87
591314
Trove2
0.168
R7658
G1
225.01
N
1
143770873 (GRCm38)
T45A
T
C
missense
Het
probably damaging
0.996
phenotype
2019-11-12
88
591317
Ttn
1.000
R7658
G1
225.01
N
2
76723769 (GRCm38)
K30863N
T
G
missense
Het
probably damaging
0.999
phenotype
2019-11-12
89
591407
Vldlr
0.389
R7658
G1
225.01
N
19
27243136 (GRCm38)
R592H
G
A
missense
Het
probably benign
0.331
phenotype
2019-11-12
90
591342
Vmn1r12
0.083
R7658
G1
225.01
N
6
57158898 (GRCm38)
A
T
intron
Het
probably benign
2019-11-12
91
591350
Vmn2r63
0.070
R7658
G1
225.01
N
7
42925269 (GRCm38)
S519R
A
C
missense
Het
probably damaging
1.000
2019-11-12
92
591400
Zbtb22
0.232
R7658
G1
225.01
N
17
33918497 (GRCm38)
E539Q
G
C
missense
Het
probably damaging
0.992
2019-11-12
93
591365
Zbtb44
0.732
R7658
G1
225.01
N
9
31054079 (GRCm38)
A262T
G
A
missense
Het
probably benign
0.001
2019-11-12
94
591367
Zfp280d
0.345
R7658
G1
225.01
N
9
72324072 (GRCm38)
N455I
A
T
missense
Het
probably damaging
0.999
2019-11-12
95
591373
Zfp287
0.000
R7658
G1
225.01
N
11
62725263 (GRCm38)
N201D
T
C
missense
Het
probably damaging
0.995
phenotype
2019-11-12
96
591328
Zfp988
0.224
R7658
G1
111.01
N
4
147332294 (GRCm38)
L395P
T
C
missense
Het
probably damaging
1.000
2019-11-12
[records 1 to 96 of 96]