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Incidental Mutations
31
incidental mutations are currently displayed, and affect
31
genes.
9
are Possibly Damaging.
8
are Probably Damaging.
12
are Probably Benign.
2
are Probably Null.
0
create premature stop codons.
2
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 31 of 31]
10
25
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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
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
527870
Atxn1
0.000
R6688
G1
225.01
Y
13
45567671
H249Q
A
T
missense
Het
probably damaging
0.986
0.647
phenotype
07/23/2018
2
527858
Cd22
0.000
R6688
G1
225.01
Y
7
30872964
S362A
A
C
missense
Het
possibly damaging
0.908
phenotype
07/23/2018
3
527878
Cep120
0.809
R6688
G1
225.01
Y
18
53724536
P286S
G
A
missense
Het
probably benign
0.123
0.074
phenotype
07/23/2018
4
527863
Ces1g
0.061
R6688
G1
225.01
Y
8
93306972
P441S
G
A
missense
Het
possibly damaging
0.919
0.179
phenotype
07/23/2018
5
527864
Ces2h
0.071
R6688
G1
225.01
Y
8
105017840
I316V
A
G
missense
Het
probably benign
0.000
0.090
phenotype
07/23/2018
6
527877
Cntnap5c
0.064
R6688
G1
225.01
Y
17
58293904
D747E
T
A
missense
Het
possibly damaging
0.715
0.075
07/23/2018
7
527865
Cwf19l2
0.906
R6688
G1
225.01
Y
9
3450015
V572A
T
C
missense
Het
probably benign
0.002
0.059
07/23/2018
8
527853
Cyb5rl
0.139
R6688
G1
225.01
Y
4
107073905
A128V
C
T
missense
Het
probably damaging
0.993
0.453
07/23/2018
9
527849
Dnttip1
1.000
R6688
G1
225.01
Y
2
164765161
Y241H
T
C
missense
Het
probably damaging
1.000
0.812
phenotype
07/23/2018
10
527859
Gm2381
0.135
R6688
G1
225.01
Y
7
42820586
A38V
G
A
missense
Het
probably benign
0.004
0.090
07/23/2018
11
527868
Golga4
0.000
R6688
G1
225.01
Y
9
118514210
T11A
A
G
missense
Het
possibly damaging
0.659
0.179
phenotype
07/23/2018
12
527867
Ip6k2
0.000
R6688
G1
225.01
Y
9
108806011
T440K
C
A
missense
Het
probably benign
0.001
phenotype
07/23/2018
13
527848
Kif5c
0.000
R6688
G1
225.01
Y
2
49688737
N126D
A
G
missense
Het
probably benign
0.065
0.098
phenotype
07/23/2018
14
527852
Mdn1
1.000
R6688
G1
225.01
Y
4
32774041
F5551I
T
A
missense
Het
possibly damaging
0.740
0.179
07/23/2018
15
527874
Myh11
1.000
R6688
G1
195.01
Y
16
14205553
L1587P
A
G
missense
Het
probably damaging
1.000
0.931
phenotype
07/23/2018
16
527857
Nop53
0.964
R6688
G1
143.01
Y
7
15945854
V67A
A
G
missense
Het
possibly damaging
0.908
0.437
phenotype
07/23/2018
17
527876
Olfr107
0.060
R6688
G1
225.01
Y
17
37405905
R119H
G
A
missense
Het
probably benign
0.300
0.090
phenotype
07/23/2018
18
527854
Paxip1
1.000
R6688
G1
225.01
Y
5
27744137
T1045A
T
C
missense
Het
probably benign
0.176
0.132
phenotype
07/23/2018
19
527866
Pdzd3
0.000
R6688
G1
225.01
Y
9
44248230
C
T
critical splice donor site
1 bp
Het
probably null
0.949
phenotype
07/23/2018
20
527875
Plg
0.278
R6688
G1
225.01
Y
17
12391845
H215L
A
T
missense
Het
probably damaging
1.000
phenotype
07/23/2018
21
527872
Psmb5
0.958
R6688
G1
225.01
Y
14
54616673
R116L
C
A
missense
Het
probably damaging
0.984
0.677
phenotype
07/23/2018
22
527851
Rapgef2
1.000
R6688
G1
225.01
Y
3
79069128
Q1307L
T
A
missense
Het
probably benign
0.027
0.070
phenotype
07/23/2018
23
527850
Serpini2
0.074
R6688
G1
225.01
Y
3
75259563
E129G
T
C
missense
Het
possibly damaging
0.879
0.165
phenotype
07/23/2018
24
527861
Stx1b
0.270
R6688
G1
225.01
Y
7
127807896
R209Q
C
T
missense
Het
probably damaging
0.997
phenotype
07/23/2018
25
527873
Tcf20
0.745
R6688
G1
225.01
Y
15
82854535
I905T
A
G
missense
Het
possibly damaging
0.676
0.071
phenotype
07/23/2018
26
527879
Tmem252
0.067
R6688
G1
126.01
Y
19
24674099
A11T
G
A
missense
Het
probably benign
0.319
0.165
07/23/2018
27
527855
Tpst2
0.662
R6688
G1
169.01
Y
5
112307757
N54S
A
G
missense
Het
probably benign
0.000
0.090
phenotype
07/23/2018
28
527860
Usp31
0.168
R6688
G1
225.01
Y
7
121678330
S269G
T
C
missense
Het
probably benign
0.010
07/23/2018
29
527869
Wasf1
0.522
R6688
G1
225.01
Y
10
40926620
T
C
critical splice donor site
2 bp
Het
probably null
0.948
phenotype
07/23/2018
30
527871
Zfp429
0.081
R6688
G1
225.01
Y
13
67396130
V58D
A
T
missense
Het
probably damaging
0.977
0.647
07/23/2018
31
527862
Zfp958
0.084
R6688
G1
225.01
Y
8
4628940
T322A
A
G
missense
Het
possibly damaging
0.909
07/23/2018
[records 1 to 31 of 31]