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Incidental Mutations
49
incidental mutations are currently displayed, and affect
49
genes.
11
are Possibly Damaging.
23
are Probably Damaging.
11
are Probably Benign.
1
are Probably Null.
0
create premature stop codons.
0
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 49 of 49]
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
487615
4930548H24Rik
0.054
R6183
G1
225.01
N
5
31487976 (GRCm38)
Y358H
T
C
missense
Het
probably damaging
0.985
2017-10-10
2
487625
5830411N06Rik
0.000
R6183
G1
225.01
N
7
140296034 (GRCm38)
T404A
A
G
missense
Het
possibly damaging
0.817
2017-10-10
3
487614
Abcb4
0.000
R6183
G1
225.01
N
5
8918718 (GRCm38)
D352E
T
A
missense
Het
probably benign
0.000
phenotype
2017-10-10
4
487606
Adgrb3
0.552
R6183
G1
225.01
N
1
25094370 (GRCm38)
I972L
T
A
missense
Het
probably damaging
0.980
phenotype
2017-10-10
5
487642
Alg3
0.238
R6183
G1
225.01
N
16
20610641 (GRCm38)
Y33C
T
C
missense
Het
probably benign
0.019
phenotype
2017-10-10
6
487623
Atp1a3
1.000
R6183
G1
225.01
N
7
24981752 (GRCm38)
G816D
C
T
missense
Het
probably damaging
1.000
phenotype
2017-10-10
7
487629
Ces1g
0.063
R6183
G1
225.01
N
8
93331239 (GRCm38)
V145M
C
T
missense
Het
possibly damaging
0.483
phenotype
2017-10-10
8
487618
Clip1
0.000
R6183
G1
203.01
N
5
123642604 (GRCm38)
S339P
A
G
missense
Het
probably damaging
1.000
phenotype
2017-10-10
9
487640
Col2a1
1.000
R6183
G1
225.01
N
15
97988790 (GRCm38)
T378N
G
T
missense
Het
unknown
phenotype
2017-10-10
10
487610
Dennd4b
0.235
R6183
G1
125.47
N
3
90275568 (GRCm38)
ACAGCAGCAGCAGCAGCAGCAGCAGCAGCAG
ACAGCAGCAGCAGCAGCAGCAGCAGCAG
utr 3 prime
Het
probably benign
2017-10-10
11
487637
Dnah12
0.220
R6183
G1
225.01
N
14
26861769 (GRCm38)
L3207Q
T
A
missense
Het
probably damaging
1.000
2017-10-10
12
487631
Efcab5
0.087
R6183
G1
225.01
N
11
77137258 (GRCm38)
T416A
T
C
missense
Het
probably benign
0.042
2017-10-10
13
487630
Ephb1
0.000
R6183
G1
225.01
N
9
102195325 (GRCm38)
I85N
A
T
missense
Het
probably damaging
0.999
phenotype
2017-10-10
14
487611
Etnppl
0.079
R6183
G1
225.01
N
3
130620317 (GRCm38)
C22R
T
C
missense
Het
probably damaging
1.000
2017-10-10
15
487649
F830016B08Rik
0.053
R6183
G1
225.01
N
18
60299877 (GRCm38)
T11A
A
G
missense
Het
probably benign
0.002
2017-10-10
16
487635
Gm5458
R6183
G1
89.01
N
14
19599644 (GRCm38)
V171L
C
A
missense
Het
probably damaging
0.958
2017-10-10
17
501826
Helb
0.142
R6183
G1
97.01
N
10
120112998 (GRCm38)
G
T
splice site
Het
probably null
phenotype
2017-12-04
18
487646
Hnrnpll
0.869
R6183
G1
225.01
N
17
80049876 (GRCm38)
V237A
A
G
missense
Het
possibly damaging
0.455
phenotype
2017-10-10
19
487609
Hps3
0.097
R6183
G1
225.01
N
3
20008868 (GRCm38)
T712A
T
C
missense
Het
probably benign
0.042
phenotype
2017-10-10
20
487617
Ibsp
0.102
R6183
G1
225.01
N
5
104306030 (GRCm38)
E78G
A
G
missense
Het
possibly damaging
0.953
phenotype
2017-10-10
21
487634
Ighv1-62-2
R6183
G1
92.01
N
12
115446436 (GRCm38)
A111V
G
A
missense
Het
probably damaging
0.965
2017-10-10
22
487619
Igkv4-63
R6183
G1
225.01
N
6
69378124 (GRCm38)
Q58K
G
T
missense
Het
probably damaging
1.000
2017-10-10
23
487643
Iqcg
0.000
R6183
G1
225.01
N
16
33030923 (GRCm38)
Y226C
T
C
missense
Het
probably damaging
0.999
phenotype
2017-10-10
24
487605
Khdc1a
0.058
R6183
G1
225.01
N
1
21350108 (GRCm38)
D30V
A
T
missense
Het
possibly damaging
0.804
2017-10-10
25
487626
Krtap5-5
0.486
R6183
G1
225.01
N
7
142229787 (GRCm38)
C42F
C
A
missense
Het
unknown
2017-10-10
26
487622
Lmod3
0.108
R6183
G1
225.01
N
6
97252553 (GRCm38)
N7D
T
C
missense
Het
probably damaging
0.998
phenotype
2017-10-10
27
487648
Lvrn
0.516
R6183
G1
225.01
N
18
46850685 (GRCm38)
N165S
A
G
missense
Het
probably benign
0.139
2017-10-10
28
487650
Ms4a4c
0.053
R6183
G1
225.01
N
19
11426229 (GRCm38)
T192A
A
G
missense
Het
possibly damaging
0.594
2017-10-10
29
487639
Ncald
0.000
R6183
G1
225.01
N
15
37397232 (GRCm38)
V68D
A
T
missense
Het
probably damaging
1.000
phenotype
2017-10-10
30
487638
Olfr1507
0.057
R6183
G1
225.01
N
14
52490731 (GRCm38)
T78S
T
A
missense
Het
probably benign
0.050
phenotype
2017-10-10
31
487647
Pcdhgb7
0.091
R6183
G1
225.01
N
18
37752262 (GRCm38)
I162F
A
T
missense
Het
probably damaging
0.967
phenotype
2017-10-10
32
487620
Prokr1
0.000
R6183
G1
179.01
N
6
87588852 (GRCm38)
T4A
T
C
missense
Het
possibly damaging
0.944
phenotype
2017-10-10
33
487632
Qrich2
0.067
R6183
G1
225.01
N
11
116458129 (GRCm38)
T
A
unclassified
Het
probably benign
2017-10-10
34
487607
Rgl1
0.256
R6183
G1
225.01
N
1
152586570 (GRCm38)
E60K
C
T
missense
Het
possibly damaging
0.944
phenotype
2017-10-10
35
487633
Rtn1
0.000
R6183
G1
225.01
N
12
72408491 (GRCm38)
W21R
A
T
missense
Het
probably benign
0.091
phenotype
2017-10-10
36
487645
Spast
0.000
R6183
G1
225.01
N
17
74373358 (GRCm38)
I438M
A
G
missense
Het
probably damaging
0.986
phenotype
2017-10-10
37
487608
Sptbn5
0.258
R6183
G1
225.01
N
2
120059417 (GRCm38)
C
T
unclassified
Het
probably benign
2017-10-10
38
487652
Sry
0.318
R6183
G1
222
N
Y
2662975 (GRCm38)
Q228H
C
G
missense
Het
unknown
0.087
phenotype
2017-10-10
39
487612
Tas1r1
0.060
R6183
G1
82.01
N
4
152032541 (GRCm38)
I212T
A
G
missense
Het
probably damaging
0.999
phenotype
2017-10-10
40
487616
Tbc1d1
0.000
R6183
G1
225.01
N
5
64275425 (GRCm38)
N439D
A
G
missense
Het
probably damaging
1.000
phenotype
2017-10-10
41
487651
Tjp2
1.000
R6183
G1
158.01
N
19
24100791 (GRCm38)
A913T
C
T
missense
Het
probably damaging
0.992
phenotype
2017-10-10
42
487627
Tnfrsf26
0.070
R6183
G1
225.01
N
7
143611757 (GRCm38)
L47P
A
G
missense
Het
probably damaging
0.985
2017-10-10
43
487628
Unc13a
1.000
R6183
G1
225.01
N
8
71644666 (GRCm38)
S1195T
A
T
missense
Het
probably damaging
0.996
phenotype
2017-10-10
44
487636
Usp54
0.000
R6183
G1
225.01
N
14
20552245 (GRCm38)
R1346G
T
C
missense
Het
probably damaging
0.989
2017-10-10
45
487621
Vmn1r54
0.064
R6183
G1
225.01
N
6
90269290 (GRCm38)
M62K
T
A
missense
Het
possibly damaging
0.605
2017-10-10
46
487613
Vmn2r125
0.058
R6183
G1
225.01
N
4
156350069 (GRCm38)
D50V
A
T
missense
Het
probably damaging
0.968
2017-10-10
47
487624
Vmn2r66
0.092
R6183
G1
225.01
N
7
84995558 (GRCm38)
D548G
T
C
missense
Het
possibly damaging
0.810
0.179
2017-10-10
48
487644
Vmn2r95
0.081
R6183
G1
225.01
N
17
18443930 (GRCm38)
N470K
T
A
missense
Het
probably damaging
0.988
2017-10-10
49
487641
Zc3h7a
0.143
R6183
G1
225.01
N
16
11147370 (GRCm38)
I633N
A
T
missense
Het
possibly damaging
0.807
2017-10-10
[records 1 to 49 of 49]