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Incidental Mutations
49
incidental mutations are currently displayed, and affect
49
genes.
7
are Possibly Damaging.
21
are Probably Damaging.
17
are Probably Benign.
4
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 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
501082
Abca12
1.000
R5529
G1
225
N
1
71264881 (GRCm38)
Y2079C
T
C
missense
Het
probably damaging
1.000
phenotype
2017-12-01
2
433565
Alg2
1.000
R5529
G1
225
N
4
47472101 (GRCm38)
R236G
T
C
missense
Het
probably damaging
0.990
phenotype
2016-10-06
3
501083
Alpl
1.000
R5529
G1
225
N
4
137746422 (GRCm38)
N323I
T
A
missense
Het
probably damaging
0.990
phenotype
2017-12-01
4
433571
Anxa3
0.000
R5529
G1
225
N
5
96828379 (GRCm38)
E172G
A
G
missense
Het
probably benign
0.001
phenotype
2016-10-06
5
433597
Atp8a2
0.326
R5529
G1
225
N
14
59793865 (GRCm38)
A
G
critical splice donor site
2 bp
Het
probably null
phenotype
2016-10-06
6
433596
Cadps
1.000
R5529
G1
225
N
14
12454285 (GRCm38)
K1078E
T
C
missense
Het
probably damaging
0.999
phenotype
2016-10-06
7
433584
Ces2e
0.057
R5529
G1
225
N
8
104929911 (GRCm38)
V258L
G
T
missense
Het
probably benign
0.001
2016-10-06
8
433603
Daam2
0.000
R5529
G1
169
N
17
49459057 (GRCm38)
F1041S
A
G
missense
Het
probably benign
0.000
Daam1 conditional KO
increases the severity of the heart phenotype (abnormal ventricular morphology and pressure) of the Daam1 single KO. [provided by MGI curators] (source: MGI)">phenotype
2016-10-06
9
433599
Dcstamp
0.392
R5529
G1
225
N
15
39754536 (GRCm38)
I114V
A
G
missense
Het
probably benign
0.036
phenotype
2016-10-06
10
433581
Ddhd2
0.119
R5529
G1
225
N
8
25739560 (GRCm38)
R496Q
C
T
missense
Het
probably benign
0.001
phenotype
2016-10-06
11
433580
Dnhd1
0.080
R5529
G1
225
N
7
105703209 (GRCm38)
R2523Q
G
A
missense
Het
probably damaging
1.000
0.589
2016-10-06
12
433590
Eml6
0.208
R5529
G1
225
N
11
29764126 (GRCm38)
R1335S
T
A
missense
Het
probably benign
0.043
2016-10-06
13
433595
F12
0.090
R5529
G1
225
N
13
55422059 (GRCm38)
N102S
T
C
missense
Het
probably benign
0.043
phenotype
2016-10-06
14
433561
Fbn1
0.941
R5529
G1
225
N
2
125373950 (GRCm38)
L712F
G
A
missense
Het
probably benign
0.006
phenotype
2016-10-06
15
433606
Fgf1
0.000
R5529
G1
225
N
18
38858604 (GRCm38)
F37L
G
T
missense
Het
probably damaging
0.999
phenotype
2016-10-06
16
433598
Fgf14
0.168
R5529
G1
225
N
14
123980455 (GRCm38)
H212L
T
A
missense
Het
probably damaging
0.998
phenotype
2016-10-06
17
433605
Gm10036
0.722
R5529
G1
225
N
18
15832801 (GRCm38)
Q3L
A
T
missense
Het
probably benign
0.154
2016-10-06
18
433594
Hivep1
0.604
R5529
G1
225
N
13
42156650 (GRCm38)
F789L
T
C
missense
Het
possibly damaging
0.808
phenotype
2016-10-06
19
433567
Hspg2
1.000
R5529
G1
225
N
4
137551828 (GRCm38)
T3074N
C
A
missense
Het
probably damaging
0.998
phenotype
2016-10-06
20
433583
Katnb1
1.000
R5529
G1
225
N
8
95097672 (GRCm38)
R495C
C
T
missense
Het
probably damaging
0.993
phenotype
2016-10-06
21
433559
Kdm5b
0.308
R5529
G1
225
N
1
134588003 (GRCm38)
H122Y
C
T
missense
Het
probably damaging
0.998
phenotype
2016-10-06
22
433586
Ky
0.401
R5529
G1
225
N
9
102542075 (GRCm38)
S427L
C
T
missense
Het
probably benign
0.097
phenotype
2016-10-06
23
433592
Med9
0.649
R5529
G1
225
N
11
59960660 (GRCm38)
V105G
T
G
missense
Het
probably benign
0.273
phenotype
2016-10-06
24
433604
Ndufa11
0.071
R5529
G1
225
N
17
56721059 (GRCm38)
V43D
T
A
missense
Het
probably damaging
0.995
2016-10-06
25
433577
Nlrp4b
0.072
R5529
G1
225
N
7
10714946 (GRCm38)
C359S
T
A
missense
Het
possibly damaging
0.910
2016-10-06
26
433560
Olfr361
0.130
R5529
G1
225
N
2
37084909 (GRCm38)
I280F
T
A
missense
Het
possibly damaging
0.666
phenotype
2016-10-06
27
433579
Olfr558
0.072
R5529
G1
225
N
7
102709693 (GRCm38)
K145*
A
T
nonsense
Het
probably null
phenotype
2016-10-06
28
433600
Paxbp1
0.958
R5529
G1
225
N
16
91030513 (GRCm38)
Y478F
T
A
missense
Het
possibly damaging
0.623
phenotype
2016-10-06
29
433572
Pole
1.000
R5529
G1
225
N
5
110332466 (GRCm38)
E92K
G
A
missense
Het
probably benign
0.202
phenotype
2016-10-06
30
433570
Prom1
0.373
R5529
G1
225
N
5
44026768 (GRCm38)
L449M
G
T
missense
Het
probably damaging
0.999
phenotype
2016-10-06
31
433578
Psg28
0.079
R5529
G1
225
N
7
18430448 (GRCm38)
T113I
G
A
missense
Het
probably benign
0.149
2016-10-06
32
433569
Reln
0.958
R5529
G1
225
N
5
21932715 (GRCm38)
V2493G
A
C
missense
Het
possibly damaging
0.715
phenotype
2016-10-06
33
433557
Rp1
0.093
R5529
G1
225
N
1
4345832 (GRCm38)
V1686I
C
T
missense
Het
probably benign
0.419
phenotype
2016-10-06
34
433607
Setbp1
0.507
R5529
G1
225
N
18
79086652 (GRCm38)
I122V
T
C
missense
Het
probably damaging
0.985
phenotype
2016-10-06
35
501084
Setd5
1.000
R5529
G1
216
N
6
113121568 (GRCm38)
Y721H
T
C
missense
Het
probably damaging
1.000
phenotype
2017-12-01
36
433591
Shroom1
0.095
R5529
G1
225
N
11
53463922 (GRCm38)
F223S
T
C
missense
Het
probably damaging
1.000
phenotype
2016-10-06
37
433601
Son
0.956
R5529
G1
133
N
16
91655466 (GRCm38)
L367Q
T
A
missense
Het
probably damaging
1.000
phenotype
2016-10-06
38
433588
Spred2
0.477
R5529
G1
225
N
11
20021301 (GRCm38)
D363Y
G
T
missense
Het
probably damaging
0.999
phenotype
2016-10-06
39
433558
Tbc1d8
0.000
R5529
G1
225
N
1
39372755 (GRCm38)
Y1000S
T
G
missense
Het
probably benign
0.420
2016-10-06
40
433593
Tdp2
0.758
R5529
G1
225
N
13
24838236 (GRCm38)
K213*
A
T
nonsense
Het
probably null
phenotype
2016-10-06
41
433587
Tmem89
0.082
R5529
G1
225
N
9
108915477 (GRCm38)
I146T
T
C
missense
Het
probably damaging
0.981
2016-10-06
42
433575
Vhl
1.000
R5529
G1
225
N
6
113629463 (GRCm38)
V147A
T
C
missense
Het
probably benign
0.002
phenotype
2016-10-06
43
433576
Vmn2r23
0.068
R5529
G1
225
N
6
123713451 (GRCm38)
L429F
C
T
missense
Het
probably benign
0.001
2016-10-06
44
433589
Vrk2
0.222
R5529
G1
225
N
11
26499036 (GRCm38)
D186G
T
C
missense
Het
probably damaging
1.000
phenotype
2016-10-06
45
433562
Wisp2
0.000
R5529
G1
225
N
2
163825359 (GRCm38)
T
C
critical splice donor site
2 bp
Het
probably null
phenotype
2016-10-06
46
433566
Zbtb40
0.113
R5529
G1
225
N
4
136983163 (GRCm38)
F1222L
A
G
missense
Het
possibly damaging
0.897
2016-10-06
47
433585
Zfp266
0.069
R5529
G1
190
N
9
20506734 (GRCm38)
S7P
A
G
missense
Het
probably damaging
0.989
phenotype
2016-10-06
48
433602
Zfp472
0.000
R5529
G1
225
N
17
32978433 (GRCm38)
I494K
T
A
missense
Het
possibly damaging
0.918
2016-10-06
49
433574
Zfp655
0.270
R5529
G1
225
N
5
145244736 (GRCm38)
E468G
A
G
missense
Het
probably damaging
0.959
phenotype
2016-10-06
[records 1 to 49 of 49]