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Incidental Mutations
68
incidental mutations are currently displayed, and affect
68
genes.
14
are Possibly Damaging.
22
are Probably Damaging.
26
are Probably Benign.
3
are Probably Null.
1
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 68 of 68]
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
437130
1700129C05Rik
0.063
R5574
G1
225
Y
14
59142756 (GRCm38)
N31I
T
A
missense
Het
possibly damaging
0.593
0.179
2016-10-26
2
437139
3110002H16Rik
0.762
R5574
G1
217
Y
18
12185006 (GRCm38)
CTGTGTGTT
CTGTGTGTTGTGTGTT
frame shift
Het
probably null
phenotype
2016-10-26
3
437134
Acvr1b
1.000
R5574
G1
225
Y
15
101202077 (GRCm38)
M304K
T
A
missense
Het
probably benign
0.033
0.813
phenotype
2016-10-26
4
437136
Adamts1
0.000
R5574
G1
225
Y
16
85799642 (GRCm38)
D106E
G
T
missense
Het
probably damaging
0.995
0.647
phenotype
2016-10-26
5
437108
Blm
1.000
R5574
G1
225
Y
7
80499773 (GRCm38)
C696F
C
A
missense
Het
probably damaging
1.000
0.709
phenotype
2016-10-26
6
437128
Bnip3l-ps
0.160
R5574
G1
225
Y
12
18217118 (GRCm38)
T
A
unclassified
Het
noncoding transcript
0.683
2016-10-26
7
437096
C87499
0.412
R5574
G1
225
Y
4
88628043 (GRCm38)
E354A
T
G
missense
Het
probably benign
0.104
0.301
2016-10-26
8
437095
Ccdc171
0.166
R5574
G1
225
Y
4
83693753 (GRCm38)
N895I
A
T
missense
Het
probably damaging
1.000
0.096
phenotype
2016-10-26
9
437123
Cdhr4
0.287
R5574
G1
225
Y
9
107993328 (GRCm38)
A
T
unclassified
Het
probably benign
2016-10-26
10
437114
Cfap97
0.067
R5574
G1
225
Y
8
46170142 (GRCm38)
S190P
T
C
missense
Het
probably damaging
1.000
0.183
2016-10-26
11
437125
Chrnb1
0.901
R5574
G1
225
Y
11
69793683 (GRCm38)
A
C
unclassified
Het
probably benign
phenotype
2016-10-26
12
437111
Clns1a
1.000
R5574
G1
225
Y
7
97720958 (GRCm38)
A
G
unclassified
Het
probably benign
0.090
phenotype
2016-10-26
13
437097
Col8a2
0.324
R5574
G1
225
Y
4
126311268 (GRCm38)
G
A
unclassified
Het
probably benign
0.929
phenotype
2016-10-26
14
437082
Cr2
0.125
R5574
G1
225
Y
1
195141236 (GRCm38)
E721V
T
A
missense
Het
probably damaging
1.000
0.349
phenotype
2016-10-26
15
437119
Csk
1.000
R5574
G1
225
Y
9
57629301 (GRCm38)
V172A
A
G
missense
Het
probably benign
0.002
0.058
phenotype
2016-10-26
16
437103
Cyp2g1
0.000
R5574
G1
225
Y
7
26820740 (GRCm38)
V466M
G
A
missense
Het
possibly damaging
0.810
0.179
phenotype
2016-10-26
17
437137
Cyp4f13
0.106
R5574
G1
225
Y
17
32929205 (GRCm38)
Y349H
A
G
missense
Het
probably benign
0.390
0.186
phenotype
2016-10-26
18
437135
Dnm1l
1.000
R5574
G1
225
Y
16
16329821 (GRCm38)
Y205C
T
C
missense
Het
probably damaging
0.998
0.369
phenotype
2016-10-26
19
484564
Dync1i2
0.970
R5574
G1
225
Y
2
71233650 (GRCm38)
T113S
A
T
missense
Het
probably benign
0.150
0.098
phenotype
2017-08-14
20
437093
Edem2
0.918
R5574
G1
225
Y
2
155716155 (GRCm38)
E186G
T
C
missense
Het
probably damaging
1.000
0.681
phenotype
2016-10-26
21
437094
Eya2
0.789
R5574
G1
225
Y
2
165763816 (GRCm38)
R380H
G
A
missense
Het
probably damaging
0.999
0.647
phenotype
2016-10-26
22
437122
Fam214a
0.356
R5574
G1
225
Y
9
75010390 (GRCm38)
D757V
A
T
missense
Het
probably damaging
0.998
0.096
2016-10-26
23
437102
Fam60a
0.935
R5574
G1
165
Y
6
148944880 (GRCm38)
C
T
unclassified
Het
probably benign
0.090
2016-10-26
24
437118
Gldn
0.338
R5574
G1
225
Y
9
54312922 (GRCm38)
T132A
A
G
missense
Het
probably damaging
0.996
0.174
phenotype
2016-10-26
25
437090
Gm13941
0.068
R5574
G1
225
Y
2
111100606 (GRCm38)
I74K
A
T
missense
Het
unknown
0.087
2016-10-26
26
437117
Gm3898
0.080
R5574
G1
141
Y
9
43830042 (GRCm38)
C
T
intron
Het
noncoding transcript
0.116
2016-10-26
27
437141
Ighmbp2
1.000
R5574
G1
225
Y
19
3271536 (GRCm38)
V408I
C
T
missense
Het
probably benign
0.000
0.062
phenotype
2016-10-26
28
484566
Klhdc10
0.218
R5574
G1
225
Y
6
30439865 (GRCm38)
L127F
C
T
missense
Het
possibly damaging
0.915
0.093
2017-08-14
29
437100
Letm1
0.965
R5574
G1
199
Y
5
33769386 (GRCm38)
T189M
G
A
missense
Het
possibly damaging
0.458
0.179
phenotype
2016-10-26
30
437098
Lrrc17
0.000
R5574
G1
225
Y
5
21570357 (GRCm38)
I306F
A
T
missense
Het
possibly damaging
0.902
0.281
phenotype
2016-10-26
31
437133
Lrrk2
0.335
R5574
G1
225
Y
15
91787016 (GRCm38)
V2000E
T
A
missense
Het
probably damaging
1.000
0.952
phenotype
2016-10-26
32
437113
Mettl9
0.117
R5574
G1
225
Y
7
121047870 (GRCm38)
E66D
A
T
missense
Het
probably benign
0.034
0.070
2016-10-26
33
437132
Mroh1
0.071
R5574
G1
158
Y
15
76433931 (GRCm38)
V877D
T
A
missense
Het
probably benign
0.000
0.090
2016-10-26
34
437131
Mycbp2
1.000
R5574
G1
225
Y
14
103142767 (GRCm38)
V3760M
C
T
missense
Het
possibly damaging
0.940
0.097
phenotype
2016-10-26
35
437099
Nos3
0.000
R5574
G1
225
Y
5
24368861 (GRCm38)
T208A
A
G
missense
Het
possibly damaging
0.801
0.072
phenotype
2016-10-26
36
437084
Npdc1
0.000
R5574
G1
225
Y
2
25408945 (GRCm38)
D284N
G
A
missense
Het
probably damaging
1.000
0.551
phenotype
2016-10-26
37
437085
Obp2a
0.000
R5574
G1
225
Y
2
25700830 (GRCm38)
T70S
A
T
missense
Het
possibly damaging
0.491
0.314
2016-10-26
38
437087
Olfr1040
0.108
R5574
G1
225
Y
2
86146191 (GRCm38)
D181G
T
C
missense
Het
probably damaging
1.000
0.647
phenotype
2016-10-26
39
437088
Olfr1100
0.090
R5574
G1
225
Y
2
86978523 (GRCm38)
V91A
A
G
missense
Het
probably benign
0.001
0.090
phenotype
2016-10-26
40
437089
Olfr1245
0.201
R5574
G1
225
Y
2
89574977 (GRCm38)
V250I
C
T
missense
Het
possibly damaging
0.938
0.179
phenotype
2016-10-26
41
437116
Olfr145
0.105
R5574
G1
225
Y
9
37897581 (GRCm38)
Y59F
A
T
missense
Het
probably damaging
0.997
0.229
phenotype
2016-10-26
42
437112
Olfr69
0.062
R5574
G1
225
Y
7
103768116 (GRCm38)
I94L
T
G
missense
Het
possibly damaging
0.956
0.158
phenotype
2016-10-26
43
437115
Pate2
0.000
R5574
G1
225
Y
9
35686115 (GRCm38)
A
G
intron
Het
probably benign
0.090
2016-10-26
44
437138
Pdzph1
0.138
R5574
G1
225
Y
17
58973947 (GRCm38)
F447L
A
G
missense
Het
probably benign
0.003
0.090
2016-10-26
45
437121
Pias1
0.949
R5574
G1
225
Y
9
62920493 (GRCm38)
C211R
A
G
missense
Het
probably damaging
0.991
0.385
phenotype
2016-10-26
46
484565
Plb1
0.059
R5574
G1
225
Y
5
32329947 (GRCm38)
S929G
A
G
missense
Het
probably benign
0.127
0.278
phenotype
2017-08-14
47
437106
Prc1
1.000
R5574
G1
202
N
7
80294542 (GRCm38)
G
A
unclassified
Het
probably benign
phenotype
2016-10-26
48
437080
Prex2
0.135
R5574
G1
225
Y
1
11140058 (GRCm38)
D574G
A
G
missense
Het
probably damaging
0.999
0.172
phenotype
2016-10-26
49
437086
Rapgef4
0.573
R5574
G1
225
Y
2
72034120 (GRCm38)
G
A
critical splice donor site
1 bp
Het
probably null
0.949
phenotype
2016-10-26
50
437127
Rock2
0.847
R5574
G1
225
Y
12
16961641 (GRCm38)
M690T
T
C
missense
Het
possibly damaging
0.549
0.072
phenotype
2016-10-26
51
437143
Slc18a2
1.000
R5574
G1
166
Y
19
59261405 (GRCm38)
I25V
A
G
missense
Het
probably benign
0.089
0.076
phenotype
2016-10-26
52
457954
Slc9a5
0.110
R5574
G1
225
N
8
105364691 (GRCm38)
I701K
T
A
missense
Het
probably benign
0.116
2017-02-16
53
437142
Sorcs1
0.140
R5574
G1
225
Y
19
50222133 (GRCm38)
N765Y
T
A
missense
Het
probably damaging
1.000
0.171
phenotype
2016-10-26
54
437126
Ssh2
0.175
R5574
G1
225
Y
11
77450115 (GRCm38)
I698L
A
T
missense
Het
probably benign
0.000
0.090
phenotype
2016-10-26
55
437083
Stam
0.381
R5574
G1
225
Y
2
14115864 (GRCm38)
D58G
A
G
missense
Het
probably damaging
1.000
0.645
phenotype
2016-10-26
56
437120
Thsd4
0.100
R5574
G1
225
Y
9
59972400 (GRCm38)
R1018L
C
A
missense
Het
probably damaging
1.000
0.647
2016-10-26
57
484567
Tnxb
0.000
R5574
G1
225
Y
17
34711024 (GRCm38)
T2911A
A
G
missense
Het
probably benign
0.000
0.090
phenotype
2017-08-14
58
437091
Trpm7
1.000
R5574
G1
225
Y
2
126813030 (GRCm38)
F1329L
A
C
missense
Het
probably benign
0.000
0.069
phenotype
2016-10-26
59
437092
Ttll9
0.062
R5574
G1
225
Y
2
152984248 (GRCm38)
E126G
A
G
missense
Het
possibly damaging
0.901
0.098
2016-10-26
60
437105
Tubgcp5
0.964
R5574
G1
225
Y
7
55805329 (GRCm38)
V258M
G
A
missense
Het
probably benign
0.008
0.090
2016-10-26
61
437107
Unc45a
1.000
R5574
G1
225
Y
7
80334856 (GRCm38)
A232V
G
A
missense
Het
probably damaging
0.977
0.157
phenotype
2016-10-26
62
437081
Utp14b
0.000
R5574
G1
225
Y
1
78666409 (GRCm38)
V675M
G
A
missense
Het
probably damaging
1.000
0.815
phenotype
2016-10-26
63
437109
Vmn2r67
0.110
R5574
G1
225
Y
7
85151891 (GRCm38)
H279L
T
A
missense
Het
probably benign
0.002
0.090
2016-10-26
64
437110
Vmn2r75
0.076
R5574
G1
225
Y
7
86166302 (GRCm38)
A118E
G
T
missense
Het
probably benign
0.217
0.090
2016-10-26
65
437140
Wdr36
1.000
R5574
G1
225
Y
18
32865959 (GRCm38)
Q886L
A
T
missense
Het
probably damaging
1.000
0.169
phenotype
2016-10-26
66
437124
Zfp433
0.236
R5574
G1
180
N
10
81719291 (GRCm38)
Y27*
T
A
nonsense
Het
probably null
2016-10-26
67
437104
Zfp715
0.090
R5574
G1
225
Y
7
43311039 (GRCm38)
S43T
A
T
missense
Het
possibly damaging
0.942
0.087
2016-10-26
68
437129
Zfyve26
0.000
R5574
G1
225
Y
12
79239924 (GRCm38)
S2297P
A
G
missense
Het
possibly damaging
0.630
0.074
phenotype
2016-10-26
[records 1 to 68 of 68]