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Incidental Mutations
44
incidental mutations are currently displayed, and affect
44
genes.
9
are Possibly Damaging.
17
are Probably Damaging.
12
are Probably Benign.
6
are Probably Null.
2
create premature stop codons.
1
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 44 of 44]
10
25
50
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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
259804
9930111J21Rik1
0.062
R3714
G1
174
N
11
48947976 (GRCm38)
T595A
T
C
missense
Het
possibly damaging
0.953
0.538
2015-01-23
2
259809
Abcd4
0.189
R3714
G1
149
N
12
84611759 (GRCm38)
M223I
C
T
missense
Het
probably benign
0.426
0.542
phenotype
2015-01-23
3
259816
Adck5
0.000
R3714
G1
225
N
15
76593938 (GRCm38)
V229I
G
A
missense
Het
probably damaging
0.998
2015-01-23
4
259794
AF366264
0.471
R3714
G1
225
N
8
13836736 (GRCm38)
I452L
T
G
missense
Het
probably benign
0.042
2015-01-23
5
259801
Ankk1
0.063
R3714
G1
225
N
9
49421713 (GRCm38)
D157A
T
G
missense
Het
possibly damaging
0.923
phenotype
2015-01-23
6
259781
Atp1a2
1.000
R3714
G1
225
N
1
172278984 (GRCm38)
I817T
A
G
missense
Het
probably damaging
0.965
phenotype
2015-01-23
7
259825
Ccdc87
0.051
R3714
G1
225
N
19
4840259 (GRCm38)
S260G
A
G
missense
Het
probably benign
0.001
2015-01-23
8
259791
Cers3
0.322
R3714
G1
225
N
7
66786075 (GRCm38)
A261S
G
T
missense
Het
probably benign
0.253
0.105
phenotype
2015-01-23
9
259820
Cntnap5c
0.071
R3714
G1
225
N
17
57892067 (GRCm38)
Q119*
C
T
nonsense
Het
probably null
2015-01-23
10
259813
Cpb2
0.117
R3714
G1
225
N
14
75283217 (GRCm38)
T
A
splice site
Het
probably null
phenotype
2015-01-23
11
259789
Ddx47
0.965
R3714
G1
225
N
6
135019062 (GRCm38)
I329K
T
A
missense
Het
probably damaging
1.000
phenotype
2015-01-23
12
259800
Elavl3
0.400
R3714
G1
225
N
9
22018599 (GRCm38)
D336E
G
T
missense
Het
probably benign
0.111
0.096
phenotype
2015-01-23
13
259797
Fam92b
0.729
R3714
G1
225
N
8
120174837 (GRCm38)
R43H
C
T
missense
Het
probably damaging
1.000
2015-01-23
14
259788
Fras1
0.000
R3714
G1
225
N
5
96645970 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
0.949
phenotype
2015-01-23
15
259796
Fuk
0.183
R3714
G1
183
N
8
110887259 (GRCm38)
D723E
G
T
missense
Het
probably damaging
1.000
phenotype
2015-01-23
16
259821
Garem1
0.187
R3714
G1
225
N
18
21148890 (GRCm38)
E136D
T
A
missense
Het
probably damaging
0.996
phenotype
2015-01-23
17
259787
Haus6
0.738
R3714
G1
225
N
4
86602867 (GRCm38)
I178T
A
G
missense
Het
probably benign
0.008
phenotype
2015-01-23
18
476147
Igkv3-2
0.147
R3714
G1
225
N
6
70698496 (GRCm38)
V10G
T
G
missense
Het
possibly damaging
0.662
2017-05-11
19
259798
Jrkl
0.179
R3714
G1
225
N
9
13244231 (GRCm38)
I475R
A
C
missense
Het
possibly damaging
0.774
phenotype
2015-01-23
20
259793
Lcmt1
1.000
R3714
G1
225
N
7
123404460 (GRCm38)
H146Y
C
T
missense
Het
probably damaging
0.979
phenotype
2015-01-23
21
259828
Lipk
0.058
R3714
G1
90
N
19
34040429 (GRCm38)
N289S
A
G
missense
Het
probably damaging
0.990
0.170
2015-01-23
22
259817
Mb
0.752
R3714
G1
225
N
15
77017589 (GRCm38)
V102A
A
G
missense
Het
probably benign
0.258
phenotype
2015-01-23
23
259823
Mc4r
0.084
R3714
G1
225
N
18
66859821 (GRCm38)
N74Y
T
A
missense
Het
probably damaging
0.999
0.933
phenotype
2015-01-23
24
259806
Mink1
0.000
R3714
G1
225
N
11
70608950 (GRCm38)
R773L
G
T
missense
Het
possibly damaging
0.930
0.080
phenotype
2015-01-23
25
259814
Mroh2b
0.109
R3714
G1
225
N
15
4943649 (GRCm38)
I1045V
A
G
missense
Het
probably benign
0.014
0.083
2015-01-23
26
259805
Myo15
0.000
R3714
G1
225
N
11
60479231 (GRCm38)
E939V
A
T
missense
Het
possibly damaging
0.546
0.179
phenotype
2015-01-23
27
259803
Ndufs7
1.000
R3714
G1
225
N
10
80252421 (GRCm38)
I14T
T
C
missense
Het
probably benign
0.001
phenotype
2015-01-23
28
259790
Nlrp4b
0.084
R3714
G1
225
N
7
10714881 (GRCm38)
V337A
T
C
missense
Het
probably benign
0.039
2015-01-23
29
259812
Npm2
0.000
R3714
G1
225
N
14
70652620 (GRCm38)
T
C
splice site
Het
probably null
phenotype
2015-01-23
30
259783
Olfr1240
0.125
R3714
G1
225
N
2
89439383 (GRCm38)
L299F
G
A
missense
Het
probably damaging
1.000
phenotype
2015-01-23
31
259792
Olfr479
0.063
R3714
G1
225
N
7
108055435 (GRCm38)
F151S
T
C
missense
Het
probably damaging
0.992
phenotype
2015-01-23
32
259819
Olfr92
0.065
R3714
G1
225
N
17
37111335 (GRCm38)
Y216H
A
G
missense
Het
probably damaging
1.000
phenotype
2015-01-23
33
259818
Prdm9
0.490
R3714
G1
225
N
17
15557361 (GRCm38)
K154*
T
A
nonsense
Het
probably null
phenotype
2015-01-23
34
259808
Prkch
0.000
R3714
G1
225
N
12
73775516 (GRCm38)
P630S
C
T
missense
Het
probably damaging
1.000
phenotype
2015-01-23
35
259780
Ptprn
0.473
R3714
G1
225
N
1
75252767 (GRCm38)
T
C
splice site
4 bp
Het
probably null
phenotype
2015-01-23
36
259811
Rnf31
1.000
R3714
G1
225
N
14
55603394 (GRCm38)
D884E
T
A
missense
Het
probably damaging
0.999
phenotype
2015-01-23
37
259826
Slc22a27
0.070
R3714
G1
225
N
19
7926450 (GRCm38)
N107K
A
T
missense
Het
possibly damaging
0.753
2015-01-23
38
259784
Spata5
1.000
R3714
G1
225
N
3
37433209 (GRCm38)
V407I
G
A
missense
Het
probably benign
0.000
phenotype
2015-01-23
39
259786
Tln1
1.000
R3714
G1
225
N
4
43540597 (GRCm38)
A1468D
G
T
missense
Het
probably damaging
0.997
phenotype
2015-01-23
40
476145
Tmem185b
0.243
R3714
G1
225
N
1
119527051 (GRCm38)
F181I
T
A
missense
Het
possibly damaging
0.461
2017-05-11
41
259782
Tmem63a
0.130
R3714
G1
225
N
1
180963114 (GRCm38)
D446N
G
A
missense
Het
possibly damaging
0.483
0.625
2015-01-23
42
476149
Trappc11
0.000
R3714
G1
225
N
8
47505316 (GRCm38)
T
C
intron
Het
probably benign
phenotype
2017-05-11
43
259810
Vmn1r218
0.235
R3714
G1
225
N
13
23136911 (GRCm38)
N63Y
A
T
missense
Het
probably damaging
1.000
0.647
2015-01-23
44
259827
Vps37c
0.078
R3714
G1
225
N
19
10706268 (GRCm38)
D18G
A
G
missense
Het
probably damaging
0.997
0.353
phenotype
2015-01-23
[records 1 to 44 of 44]