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Incidental Mutations
31
incidental mutations are currently displayed, and affect
31
genes.
6
are Possibly Damaging.
8
are Probably Damaging.
14
are Probably Benign.
2
are Probably Null.
1
create premature stop codons.
1
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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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
97432
Aldh1l2
0.000
R1117
G1
225
N
10
83508623 (GRCm38)
T353I
G
A
missense
Het
probably benign
0.012
phenotype
2014-01-05
2
97408
Arpc1b
0.000
R1117
G1
225
N
5
145125754 (GRCm38)
V226A
T
C
missense
Het
possibly damaging
0.950
phenotype
2014-01-05
3
97400
Casz1
1.000
R1117
G1
225
N
4
148934595 (GRCm38)
T451K
C
A
missense
Het
probably damaging
0.996
phenotype
2014-01-05
4
97430
Ccr4
0.000
R1117
G1
225
N
9
114492017 (GRCm38)
V327M
C
T
missense
Het
probably benign
0.004
phenotype
2014-01-05
5
97386
Cntrl
0.864
R1117
G1
225
N
2
35127973 (GRCm38)
E465G
A
G
missense
Het
probably damaging
1.000
phenotype
2014-01-05
6
97410
Cpa1
0.000
R1117
G1
225
N
6
30645261 (GRCm38)
D412G
A
G
missense
Het
probably benign
0.164
phenotype
2014-01-05
7
97368
Crispld1
0.079
R1117
G1
225
N
1
17749622 (GRCm38)
N281K
T
A
missense
Het
probably benign
0.028
2014-01-05
8
97376
Cul3
1.000
R1117
G1
225
N
1
80280924 (GRCm38)
Q465R
T
C
missense
Het
probably damaging
0.999
phenotype
2014-01-05
9
97468
Cyp2c68
0.000
R1117
G1
225
N
19
39712459 (GRCm38)
T305M
G
A
missense
Het
probably damaging
1.000
2014-01-05
10
97390
Elp4
0.965
R1117
G1
225
N
2
105842311 (GRCm38)
D143G
T
C
missense
Het
probably benign
0.003
phenotype
2014-01-05
11
97394
Etnppl
0.088
R1117
G1
225
N
3
130634563 (GRCm38)
I462M
A
G
missense
Het
probably benign
0.005
2014-01-05
12
97380
Fmo4
0.101
R1117
G1
225
N
1
162803663 (GRCm38)
V245A
A
G
missense
Het
probably benign
0.033
phenotype
2014-01-05
13
97443
Gm4076
0.286
R1117
G1
225
N
13
85127318 (GRCm38)
A
G
exon
Het
noncoding transcript
2014-01-05
14
97460
Gm9573
0.076
R1117
G1
221
N
17
35620028 (GRCm38)
T
C
intron
Het
probably benign
2014-01-05
15
97374
Gtf3c3
0.965
R1117
G1
225
N
1
54417778 (GRCm38)
A488T
C
T
missense
Het
probably damaging
0.998
0.654
phenotype
2014-01-05
16
97456
Kcnj15
0.000
R1117
G1
225
N
16
95295625 (GRCm38)
M8I
G
A
missense
Het
probably benign
0.282
phenotype
2014-01-05
17
97414
Klk1b22
0.052
R1117
G1
225
N
7
44116859 (GRCm38)
M255L
A
T
missense
Het
probably benign
0.004
phenotype
2014-01-05
18
97412
Mmrn1
0.000
R1117
G1
225
N
6
60976325 (GRCm38)
I530K
T
A
missense
Het
possibly damaging
0.513
phenotype
2014-01-05
19
97444
Nid2
0.188
R1117
G1
225
N
14
19763664 (GRCm38)
A
C
critical splice acceptor site
Het
probably null
phenotype
2014-01-05
20
97438
Olfr311
0.088
R1117
G1
225
N
11
58841815 (GRCm38)
K234E
A
G
missense
Het
possibly damaging
0.643
phenotype
2014-01-05
21
97458
Olfr63
0.085
R1117
G1
225
N
17
33268966 (GRCm38)
R81*
C
T
nonsense
Het
probably null
0.976
phenotype
2014-01-05
22
97420
Olfr981
0.132
R1117
G1
225
N
9
40022762 (GRCm38)
F123S
T
C
missense
Het
probably damaging
0.994
phenotype
2014-01-05
23
97422
Peak1
0.336
R1117
G1
225
N
9
56258418 (GRCm38)
T742M
G
A
missense
Het
probably benign
0.045
phenotype
2014-01-05
24
97402
Sel1l3
0.000
R1117
G1
225
N
5
53172607 (GRCm38)
T469S
T
A
missense
Het
probably benign
0.004
2014-01-05
25
97440
Sez6
0.000
R1117
G1
225
N
11
77974514 (GRCm38)
Y659C
A
G
missense
Het
probably damaging
1.000
phenotype
2014-01-05
26
97382
Slc19a2
0.160
R1117
G1
219
N
1
164263456 (GRCm38)
I278F
A
T
missense
Het
possibly damaging
0.858
phenotype
2014-01-05
27
97436
Slc36a3
0.096
R1117
G1
221
N
11
55146180 (GRCm38)
I100V
T
C
missense
Het
possibly damaging
0.778
2014-01-05
28
97464
Tcerg1
1.000
R1117
G1
225
N
18
42574652 (GRCm38)
D1079G
A
G
missense
Het
probably damaging
0.991
phenotype
2014-01-05
29
97426
Trim43c
0.081
R1117
G1
225
N
9
88844977 (GRCm38)
S286P
T
C
missense
Het
probably benign
0.204
0.090
2014-01-05
30
97416
Umod
0.117
R1117
G1
191
N
7
119477306 (GRCm38)
N79S
T
C
missense
Het
possibly damaging
0.707
phenotype
2014-01-05
31
97462
Wdr43
0.964
R1117
G1
148
N
17
71616387 (GRCm38)
T43A
A
G
missense
Het
probably benign
0.353
2014-01-05
[records 1 to 31 of 31]