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Incidental Mutations
64
incidental mutations are currently displayed, and affect
64
genes.
9
are Possibly Damaging.
26
are Probably Damaging.
21
are Probably Benign.
5
are Probably Null.
2
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 64 of 64]
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
93065
Actn4
0.841
IGL01637
G1
7
28904684 (GRCm38)
I384N
A
T
missense
Het
probably damaging
1.000
phenotype
2013-12-09
2
93060
Adsl
1.000
IGL01637
G1
15
80948700 (GRCm38)
Q51H
G
T
missense
Het
probably null
0.240
phenotype
2013-12-09
3
93072
Apcdd1
0.165
IGL01637
G1
18
62937286 (GRCm38)
E208G
A
G
missense
Het
probably damaging
1.000
phenotype
2013-12-09
4
93082
Arrdc4
0.169
IGL01637
G1
7
68744832 (GRCm38)
R155*
G
A
nonsense
Het
probably null
phenotype
2013-12-09
5
93032
Atp9b
0.095
IGL01637
G1
18
80756455 (GRCm38)
E823G
T
C
missense
Het
probably benign
0.058
2013-12-09
6
93083
Bmp1
1.000
IGL01637
G1
14
70492461 (GRCm38)
W468R
A
G
missense
Het
probably damaging
1.000
phenotype
2013-12-09
7
93081
C6
0.120
IGL01637
G1
15
4759917 (GRCm38)
I281M
A
G
missense
Het
possibly damaging
0.691
phenotype
2013-12-09
8
93067
Ccdc88b
0.000
IGL01637
G1
19
6846710 (GRCm38)
T1392A
T
C
missense
Het
probably benign
0.134
phenotype
2013-12-09
9
93071
Dhx34
0.444
IGL01637
G1
7
16205473 (GRCm38)
S665Y
G
T
missense
Het
probably damaging
1.000
phenotype
2013-12-09
10
93087
Dock1
1.000
IGL01637
G1
7
135137813 (GRCm38)
A
T
critical splice acceptor site
Het
probably null
phenotype
2013-12-09
11
93075
Dpp7
0.094
IGL01637
G1
2
25354613 (GRCm38)
N252S
T
C
missense
Het
probably benign
0.006
phenotype
2013-12-09
12
93037
Dyrk2
0.550
IGL01637
G1
10
118860507 (GRCm38)
V282A
A
G
missense
Het
probably damaging
0.995
phenotype
2013-12-09
13
93035
Edrf1
0.603
IGL01637
G1
7
133650525 (GRCm38)
L401P
T
C
missense
Het
probably damaging
1.000
phenotype
2013-12-09
14
93054
Epc1
1.000
IGL01637
G1
18
6439724 (GRCm38)
V150A
A
G
missense
Het
probably benign
0.224
phenotype
2013-12-09
15
93064
Fam170a
0.000
IGL01637
G1
18
50281667 (GRCm38)
M127L
A
T
missense
Het
possibly damaging
0.881
0.104
2013-12-09
16
93055
Fam19a3
0.032
IGL01637
G1
3
104773079 (GRCm38)
V75M
C
T
missense
Het
probably damaging
1.000
phenotype
2013-12-09
17
93070
Gabrg1
0.055
IGL01637
G1
5
70777205 (GRCm38)
T277S
T
A
missense
Het
probably damaging
0.995
phenotype
2013-12-09
18
93088
Galntl5
0.000
IGL01637
G1
5
25189825 (GRCm38)
T
C
splice site
Het
probably benign
phenotype
2013-12-09
19
93058
Gbp2b
0.000
IGL01637
G1
3
142598312 (GRCm38)
N56S
A
G
missense
Het
probably damaging
0.999
phenotype
2013-12-09
20
93073
Gfm2
0.660
IGL01637
G1
13
97150409 (GRCm38)
V172E
T
A
missense
Het
probably damaging
1.000
phenotype
2013-12-09
21
93051
Gm10419
IGL01637
G1
5
108372358 (GRCm38)
T
C
unclassified
Het
probably benign
2013-12-09
22
93027
Gm7293
0.805
IGL01637
G1
9
51623606 (GRCm38)
A
G
exon
Het
noncoding transcript
2013-12-09
23
93028
Gstm3
0.090
IGL01637
G1
3
107967633 (GRCm38)
E101G
T
C
missense
Het
probably damaging
1.000
2013-12-09
24
93079
Ifnlr1
0.000
IGL01637
G1
4
135686545 (GRCm38)
W2R
T
C
missense
Het
possibly damaging
0.630
phenotype
2013-12-09
25
93044
Ighv13-1
0.186
IGL01637
G1
12
114267733 (GRCm38)
A
T
unclassified
Het
probably benign
2013-12-09
26
93041
Ighv7-1
0.083
IGL01637
G1
12
113896503 (GRCm38)
I90F
T
A
missense
Het
possibly damaging
0.780
2013-12-09
27
93068
Itga2b
0.287
IGL01637
G1
11
102455583 (GRCm38)
L1009P
A
G
missense
Het
probably damaging
1.000
phenotype
2013-12-09
28
93077
Kif1a
0.867
IGL01637
G1
1
93039853 (GRCm38)
V1112A
A
G
missense
Het
possibly damaging
0.952
phenotype
2013-12-09
29
93030
Kif5a
1.000
IGL01637
G1
10
127245368 (GRCm38)
D232E
A
T
missense
Het
possibly damaging
0.940
phenotype
2013-12-09
30
93085
Klb
0.889
IGL01637
G1
5
65375679 (GRCm38)
G
A
critical splice acceptor site
Het
probably null
phenotype
2013-12-09
31
93033
Lrriq1
0.069
IGL01637
G1
10
103215628 (GRCm38)
A421V
G
A
missense
Het
probably benign
0.000
2013-12-09
32
93074
Mdga1
0.262
IGL01637
G1
17
29839871 (GRCm38)
R721C
G
A
missense
Het
probably damaging
1.000
phenotype
2013-12-09
33
93089
Mrpl48
0.901
IGL01637
G1
7
100550532 (GRCm38)
G
T
splice site
Het
probably benign
phenotype
2013-12-09
34
93080
Myo18b
1.000
IGL01637
G1
5
112840629 (GRCm38)
R1030S
T
A
missense
Het
possibly damaging
0.817
phenotype
2013-12-09
35
93031
Nf1
1.000
IGL01637
G1
11
79547120 (GRCm38)
H2101Q
T
A
missense
Het
probably damaging
0.999
phenotype
2013-12-09
36
93047
Nlrp3
0.063
IGL01637
G1
11
59549378 (GRCm38)
L594I
C
A
missense
Het
probably damaging
0.992
phenotype
2013-12-09
37
93066
Notch2
1.000
IGL01637
G1
3
98146060 (GRCm38)
T2013I
C
T
missense
Het
probably damaging
1.000
phenotype
2013-12-09
38
93034
Olfr1018
0.076
IGL01637
G1
2
85822988 (GRCm38)
T6S
A
T
missense
Het
probably benign
0.003
phenotype
2013-12-09
39
93049
Olfr131
0.085
IGL01637
G1
17
38082103 (GRCm38)
L292F
G
A
missense
Het
possibly damaging
0.896
phenotype
2013-12-09
40
278721
Olfr593
0.051
IGL01637
G1
7
103212177 (GRCm38)
R95S
C
A
missense
Het
probably benign
0.000
phenotype
2015-04-16
41
93029
Olfr812
0.051
IGL01637
G1
10
129842610 (GRCm38)
L144P
A
G
missense
Het
probably benign
0.140
phenotype
2013-12-09
42
93040
Olfr845
0.114
IGL01637
G1
9
19338964 (GRCm38)
F168S
T
C
missense
Het
probably damaging
1.000
phenotype
2013-12-09
43
93053
Panx3
0.000
IGL01637
G1
9
37664056 (GRCm38)
D170G
T
C
missense
Het
probably damaging
0.976
phenotype
2013-12-09
44
93078
Pclo
0.000
IGL01637
G1
5
14540034 (GRCm38)
S783G
A
G
missense
Het
unknown
phenotype
2013-12-09
45
93039
Pde3b
0.000
IGL01637
G1
7
114526901 (GRCm38)
L790*
T
A
nonsense
Het
probably null
phenotype
2013-12-09
46
93086
Pik3r2
0.000
IGL01637
G1
8
70772348 (GRCm38)
T
C
unclassified
Het
probably benign
phenotype
2013-12-09
47
93063
Rassf4
0.069
IGL01637
G1
6
116641690 (GRCm38)
F211L
A
G
missense
Het
probably damaging
0.999
phenotype
2013-12-09
48
93056
Rbl2
1.000
IGL01637
G1
8
91106438 (GRCm38)
P666S
C
T
missense
Het
probably benign
0.000
phenotype
2013-12-09
49
93061
Rnf123
0.144
IGL01637
G1
9
108058238 (GRCm38)
F979L
A
G
missense
Het
probably damaging
0.997
phenotype
2013-12-09
50
93057
Rock2
0.847
IGL01637
G1
12
16965171 (GRCm38)
D788E
T
A
missense
Het
probably benign
0.000
phenotype
2013-12-09
51
93048
Serpina3b
0.065
IGL01637
G1
12
104132957 (GRCm38)
T244A
A
G
missense
Het
probably benign
0.003
2013-12-09
52
93059
Setd1b
1.000
IGL01637
G1
5
123148513 (GRCm38)
S541P
T
C
missense
Het
unknown
phenotype
2013-12-09
53
93052
Slc12a4
0.311
IGL01637
G1
8
105960707 (GRCm38)
D60G
T
C
missense
Het
possibly damaging
0.718
phenotype
2013-12-09
54
93036
Stac2
0.164
IGL01637
G1
11
98041354 (GRCm38)
E241G
T
C
missense
Het
probably benign
0.004
2013-12-09
55
93076
Tas2r115
0.050
IGL01637
G1
6
132737629 (GRCm38)
Y120H
A
G
missense
Het
probably damaging
0.993
2013-12-09
56
93043
Tmtc2
0.108
IGL01637
G1
10
105370085 (GRCm38)
F450I
A
T
missense
Het
probably benign
0.003
phenotype
2013-12-09
57
93084
Txnl1
0.469
IGL01637
G1
18
63674191 (GRCm38)
I198N
A
T
missense
Het
probably damaging
0.978
2013-12-09
58
93046
Ubr2
0.859
IGL01637
G1
17
46956654 (GRCm38)
M1049K
A
T
missense
Het
probably damaging
0.998
phenotype
2013-12-09
59
93038
Ugt2b5
0.060
IGL01637
G1
5
87139900 (GRCm38)
E136G
T
C
missense
Het
probably benign
0.044
2013-12-09
60
93045
Unc13b
0.350
IGL01637
G1
4
43241066 (GRCm38)
T3623I
C
T
missense
Het
probably damaging
1.000
phenotype
2013-12-09
61
93062
Usp13
0.000
IGL01637
G1
3
32919064 (GRCm38)
S797T
T
A
missense
Het
probably benign
0.023
2013-12-09
62
93050
Vmn1r173
0.536
IGL01637
G1
7
23702948 (GRCm38)
T203S
A
T
missense
Het
probably damaging
0.959
2013-12-09
63
93042
Vwf
0.238
IGL01637
G1
6
125645736 (GRCm38)
I1718N
T
A
missense
Het
probably damaging
1.000
phenotype
2013-12-09
64
93069
Zfr
1.000
IGL01637
G1
15
12159646 (GRCm38)
H676R
A
G
missense
Het
probably benign
0.260
phenotype
2013-12-09
[records 1 to 64 of 64]