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Incidental Mutations
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Incidental Mutations
78
incidental mutations are currently displayed, and affect
77
genes.
13
are Possibly Damaging.
28
are Probably Damaging.
28
are Probably Benign.
9
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 78 of 78]
10
25
50
100
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1000
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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
358032
2610507B11Rik
0.960
R4756
G1
225
N
11
78264028
L122H
T
A
missense
Het
probably damaging
0.975
11/11/2015
2
358022
4930550C14Rik
0.107
R4756
G1
225
N
9
53425530
M45L
A
T
missense
Het
probably benign
0.000
11/11/2015
3
357987
Acss2
0.357
R4756
G1
218
N
2
155561143
F627L
T
C
missense
Het
probably damaging
1.000
phenotype
11/11/2015
4
358050
Akap8
0.000
R4756
G1
225
N
17
32316210
S277P
A
G
missense
Het
probably damaging
0.980
phenotype
11/11/2015
5
358003
Akap9
0.406
R4756
G1
225
N
5
4001418
M1395K
T
A
missense
Het
probably damaging
0.994
phenotype
11/11/2015
6
358017
Ank1
0.353
R4756
G1
225
N
8
23122877
D1468G
A
G
missense
Het
probably benign
0.000
phenotype
11/11/2015
7
358011
Apoe
0.377
R4756
G1
225
N
7
19696921
V121A
A
G
missense
Het
probably benign
0.202
phenotype
11/11/2015
8
358024
Aqp9
0.110
R4756
G1
225
N
9
71163049
L12H
A
T
missense
Het
probably damaging
0.999
phenotype
11/11/2015
9
357979
Atp2b4
0.459
R4756
G1
225
N
1
133711791
A1115V
G
A
missense
Het
probably benign
0.005
phenotype
11/11/2015
10
357980
Atp2b4
0.459
R4756
G1
225
N
1
133739396
P139L
G
A
missense
Het
probably benign
0.406
phenotype
11/11/2015
11
358039
B430218F22Rik
0.132
R4756
G1
225
N
13
118387444
T
C
unclassified
Het
probably benign
11/11/2015
12
358009
Brsk1
0.000
R4756
G1
225
N
7
4708867
E572G
A
G
missense
Het
possibly damaging
0.719
phenotype
11/11/2015
13
358007
C130060K24Rik
0.061
R4756
G1
225
N
6
65452914
I198T
T
C
missense
Het
probably benign
0.018
11/11/2015
14
358044
C6
0.119
R4756
G1
225
N
15
4781912
I414T
T
C
missense
Het
probably benign
0.000
phenotype
11/11/2015
15
358000
C8b
0.000
R4756
G1
225
N
4
104786886
M250K
T
A
missense
Het
probably benign
0.000
phenotype
11/11/2015
16
357981
Camk1g
0.220
R4756
G1
225
N
1
193362085
E7V
T
A
missense
Het
probably benign
0.026
phenotype
11/11/2015
17
357993
Clcc1
1.000
R4756
G1
225
N
3
108672920
A
G
splice site
3 bp
Het
probably null
phenotype
11/11/2015
18
357978
Col4a3
0.000
R4756
G1
225
N
1
82716297
G
T
critical splice acceptor site
Het
probably null
phenotype
11/11/2015
19
357975
Cox5b
1.000
R4756
G1
225
N
1
36693229
W104R
T
A
missense
Het
probably damaging
1.000
11/11/2015
20
358055
Cyp2c55
0.105
R4756
G1
225
N
19
39031371
H251P
A
C
missense
Het
probably damaging
0.999
phenotype
11/11/2015
21
358056
Cyp2c67
0.083
R4756
G1
225
N
19
39643744
T60I
G
A
missense
Het
probably benign
0.028
11/11/2015
22
358042
Defb42
0.178
R4756
G1
225
N
14
63048375
V68E
T
A
missense
Het
probably benign
0.008
11/11/2015
23
358046
Ercc4
0.969
R4756
G1
225
N
16
13123423
I225N
T
A
missense
Het
probably damaging
0.997
phenotype
11/11/2015
24
358048
Fam120b
0.000
R4756
G1
225
N
17
15402396
C212F
G
T
missense
Het
probably damaging
1.000
11/11/2015
25
358040
Fgf10
1.000
R4756
G1
225
N
13
118781509
V111A
T
C
missense
Het
probably benign
0.027
phenotype
11/11/2015
26
357977
Fn1
1.000
R4756
G1
225
N
1
71590808
T2186K
G
T
missense
Het
probably damaging
1.000
phenotype
11/11/2015
27
358005
Fras1
0.000
R4756
G1
225
N
5
96781659
V3974A
T
C
missense
Het
probably benign
0.002
phenotype
11/11/2015
28
358029
Galnt4
0.000
R4756
G1
225
N
10
99108500
V29A
T
C
missense
Het
probably benign
0.000
phenotype
11/11/2015
29
358016
Gpr26
0.066
R4756
G1
214
N
7
131967501
Y192H
T
C
missense
Het
probably damaging
1.000
phenotype
11/11/2015
30
358033
Heatr9
0.182
R4756
G1
225
N
11
83516649
L236Q
A
T
missense
Het
probably damaging
1.000
11/11/2015
31
358002
Hivep3
0.000
R4756
G1
225
N
4
120097823
P1112H
C
A
missense
Het
probably damaging
0.976
phenotype
11/11/2015
32
357988
Hnf4g
0.223
R4756
G1
225
N
3
3643009
Y106C
A
G
missense
Het
possibly damaging
0.693
phenotype
11/11/2015
33
358006
Hnrnpdl
0.308
R4756
G1
225
N
5
100037924
Y69*
A
T
nonsense
Het
probably null
phenotype
11/11/2015
34
358020
Itgb1
1.000
R4756
G1
225
N
8
128717222
A320T
G
A
missense
Het
probably damaging
0.978
phenotype
11/11/2015
35
357992
Kcna2
1.000
R4756
G1
225
N
3
107105417
I438T
T
C
missense
Het
probably benign
0.000
phenotype
11/11/2015
36
357998
Kif24
0.000
R4756
G1
225
N
4
41397545
A
G
critical splice donor site
2 bp
Het
probably null
phenotype
11/11/2015
37
358043
Klhl1
0.171
R4756
G1
225
N
14
96151966
T584I
G
A
missense
Het
probably benign
0.386
phenotype
11/11/2015
38
358052
Ltbp1
1.000
R4756
G1
225
N
17
75225204
D91G
A
G
missense
Het
probably damaging
1.000
phenotype
11/11/2015
39
358037
Mdga2
0.000
R4756
G1
225
N
12
66797653
I190M
T
C
missense
Het
probably damaging
0.995
phenotype
11/11/2015
40
357985
Meis2
0.870
R4756
G1
225
N
2
116000205
R276C
G
A
missense
Het
probably damaging
0.999
phenotype
11/11/2015
41
357976
Mob4
0.955
R4756
G1
225
N
1
55152696
R190W
C
T
missense
Het
probably damaging
0.984
phenotype
11/11/2015
42
358013
Mrgpra2a
0.105
R4756
G1
113
N
7
47427366
I48T
A
G
missense
Het
possibly damaging
0.855
11/11/2015
43
358026
Mst1
0.000
R4756
G1
225
N
9
108083627
V481A
T
C
missense
Het
probably benign
0.281
phenotype
11/11/2015
44
357994
Mttp
0.850
R4756
G1
225
N
3
138116071
V245E
A
T
missense
Het
possibly damaging
0.775
phenotype
11/11/2015
45
357996
Nbn
1.000
R4756
G1
225
N
4
15981470
S521T
T
A
missense
Het
probably benign
0.064
phenotype
11/11/2015
46
357982
Neb
0.838
R4756
G1
225
N
2
52193231
T5654N
G
T
missense
Het
probably damaging
0.962
phenotype
11/11/2015
47
358012
Nlrp9a
0.065
R4756
G1
225
N
7
26557441
K161N
A
T
missense
Het
probably damaging
1.000
11/11/2015
48
358019
Nod2
0.221
R4756
G1
225
N
8
88664274
F388C
T
G
missense
Het
possibly damaging
0.593
phenotype
11/11/2015
49
357983
Olfr1248
0.224
R4756
G1
225
N
2
89617470
H241N
G
T
missense
Het
possibly damaging
0.862
phenotype
11/11/2015
50
357984
Olfr1311
0.173
R4756
G1
225
N
2
112020987
F289S
A
G
missense
Het
possibly damaging
0.516
phenotype
11/11/2015
51
358028
Olfr1354
0.258
R4756
G1
225
N
10
78917527
I229N
T
A
missense
Het
probably damaging
0.993
phenotype
11/11/2015
52
358031
Olfr410
0.140
R4756
G1
225
N
11
74334576
F218L
G
T
missense
Het
probably benign
0.000
phenotype
11/11/2015
53
358014
Olfr589
0.155
R4756
G1
225
N
7
103155125
N207K
A
T
missense
Het
probably benign
0.243
phenotype
11/11/2015
54
358021
Olfr843
0.175
R4756
G1
225
N
9
19248857
L181F
G
A
missense
Het
possibly damaging
0.562
phenotype
11/11/2015
55
357990
P2ry1
0.284
R4756
G1
225
N
3
61004477
S346G
A
G
missense
Het
probably benign
0.001
phenotype
11/11/2015
56
358041
Prkcd
0.393
R4756
G1
225
N
14
30599666
F524L
A
G
missense
Het
probably benign
0.001
phenotype
11/11/2015
57
358030
Ramp3
0.080
R4756
G1
225
N
11
6674843
M46L
A
T
missense
Het
probably benign
0.164
phenotype
11/11/2015
58
358004
Rint1
1.000
R4756
G1
225
N
5
23809793
Y278H
T
C
missense
Het
probably damaging
1.000
phenotype
11/11/2015
59
358001
Skint11
0.060
R4756
G1
225
N
4
114194677
T74I
C
T
missense
Het
probably benign
0.299
11/11/2015
60
358018
Slc10a7
0.781
R4756
G1
225
N
8
78706950
T
C
critical splice donor site
2 bp
Het
probably null
11/11/2015
61
358045
Slc45a2
0.102
R4756
G1
225
N
15
11027930
Y528*
T
A
nonsense
Het
probably null
phenotype
11/11/2015
62
358057
Slit1
0.000
R4756
G1
225
N
19
41649013
F329L
A
G
missense
Het
probably damaging
1.000
phenotype
11/11/2015
63
358023
Sltm
0.966
R4756
G1
225
N
9
70591610
M989L
A
T
missense
Het
possibly damaging
0.572
11/11/2015
64
357989
Smad9
0.000
R4756
G1
225
N
3
54794453
T372S
A
T
missense
Het
possibly damaging
0.503
phenotype
11/11/2015
65
358049
Snrpc
R4756
G1
225
N
17
27842332
Y38*
T
A
nonsense
Het
probably null
11/11/2015
66
357991
Spag17
0.000
R4756
G1
225
N
3
100103385
K2065R
A
G
missense
Het
possibly damaging
0.682
phenotype
11/11/2015
67
358034
Stxbp4
0.000
R4756
G1
225
N
11
90607371
K87N
T
A
missense
Het
probably damaging
1.000
11/11/2015
68
358047
Tbc1d23
0.771
R4756
G1
200
N
16
57198895
AT
ATT
frame shift
Het
probably null
phenotype
11/11/2015
69
358015
Tgfb1i1
0.440
R4756
G1
225
N
7
128249399
M96L
A
T
missense
Het
probably damaging
1.000
phenotype
11/11/2015
70
357999
Tnc
0.000
R4756
G1
225
N
4
63967343
I1841F
T
A
missense
Het
probably damaging
0.992
phenotype
11/11/2015
71
358036
Twistnb
0.835
R4756
G1
218
N
12
33437680
T
A
splice site
Het
probably null
11/11/2015
72
357997
Ubap2
0.248
R4756
G1
225
N
4
41211771
H63Q
G
T
missense
Het
probably damaging
1.000
phenotype
11/11/2015
73
358054
Vps13a
0.000
R4756
G1
225
N
19
16655216
N2592S
T
C
missense
Het
probably benign
0.015
phenotype
11/11/2015
74
358051
Xdh
0.529
R4756
G1
225
N
17
73886386
P1305L
G
A
missense
Het
probably benign
0.242
phenotype
11/11/2015
75
358025
Xrn1
0.881
R4756
G1
225
N
9
96039809
R1425K
G
A
missense
Het
probably benign
0.003
phenotype
11/11/2015
76
358010
Zfp418
0.071
R4756
G1
225
N
7
7182763
R575Q
G
A
missense
Het
possibly damaging
0.888
11/11/2015
77
358053
Zfp608
0.863
R4756
G1
225
N
18
54894472
Q1424H
T
A
missense
Het
probably damaging
1.000
11/11/2015
78
358038
Zfp839
0.063
R4756
G1
225
N
12
110855201
L150I
C
A
missense
Het
possibly damaging
0.922
11/11/2015
[records 1 to 78 of 78]