Home
Phenotypic Mutations
Incidental Mutations
Engineered Mutations
Candidate Explorer
Protocols
Mutation Statistics
About
Contact
Links
Request Mice
Beutler Lab
APN
Strains @ MMRRC
Search Phenotypes
NEW
Candidate Explorer
Staff Login
Download
Incidental Mutations
53
incidental mutations are currently displayed, and affect
52
genes.
7
are Possibly Damaging.
12
are Probably Damaging.
28
are Probably Benign.
5
are Probably Null.
2
create premature stop codons.
4
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 53 of 53]
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
603867
4932438A13Rik
1.000
RF021
G1
217.73
N
3
37050748 (GRCm38)
TTATTATTATTAT
TTATTATTATTATTAATATTATTATTAT
critical splice acceptor site
Het
probably benign
phenotype
2019-12-04
2
603859
A030005L19Rik
RF021
G1
199.72
N
1
82913569 (GRCm38)
GTGGTGGCTG
GTGGTGGCTGTGGTGGCTG
small insertion
Het
probably benign
2019-12-04
3
603910
AI837181
0.000
RF021
G1
128.47
N
19
5425234 (GRCm38)
CGG
CGGTGG
small insertion
Het
probably benign
2019-12-04
4
603855
Ankrd44
0.151
RF021
G1
225.01
Y
1
54778312 (GRCm38)
H79R
T
C
missense
Het
probably damaging
0.999
2019-12-04
5
603857
Atg9a
1.000
RF021
G1
225.01
Y
1
75182629 (GRCm38)
E826V
T
A
missense
Het
probably damaging
0.963
0.076
phenotype
2019-12-04
6
603914
Atrnl1
0.220
RF021
G1
225.01
Y
19
57642473 (GRCm38)
V224A
T
C
missense
Het
probably benign
0.003
0.070
phenotype
2019-12-04
7
603903
Cpn2
0.052
RF021
G1
225.01
Y
16
30259338 (GRCm38)
A515V
G
A
missense
Het
probably benign
0.000
2019-12-04
8
603879
Cyp2a12
0.071
RF021
G1
225.01
Y
7
27035360 (GRCm38)
F402S
T
C
missense
Het
possibly damaging
0.731
2019-12-04
9
603865
Defb22
0.000
RF021
G1
214.46
N
2
152485832 (GRCm38)
TGCGGCA
TGCGGCAGAGCTGGGCGTTGCGGCA
small insertion
Het
probably benign
2019-12-04
10
603860
Diexf
0.970
RF021
G1
225.01
Y
1
193120666 (GRCm38)
F248L
A
G
missense
Het
probably benign
0.000
2019-12-04
11
603877
Dnah10
0.000
RF021
G1
225.01
Y
5
124777907 (GRCm38)
V2016F
G
T
missense
Het
probably damaging
1.000
phenotype
2019-12-04
12
603858
Dock10
0.303
RF021
G1
218.01
Y
1
80564573 (GRCm38)
T
C
critical splice acceptor site
Het
probably null
0.949
phenotype
2019-12-04
13
603874
Efhd2
0.142
RF021
G1
214.46
N
4
141874773 (GRCm38)
GCC
GCCGCCCCC
small insertion
Het
probably benign
phenotype
2019-12-04
14
603902
Fam131a
0.086
RF021
G1
128.01
Y
16
20694940 (GRCm38)
A
C
intron
Het
probably benign
2019-12-04
15
603878
Gm6614
0.056
RF021
G1
225.01
Y
6
142008714 (GRCm38)
V31E
A
T
missense
Het
probably damaging
0.984
2019-12-04
16
603898
Gm7247
0.144
RF021
G1
214.46
N
14
51364324 (GRCm38)
AGACCAGACC
A
small deletion
Het
probably benign
2019-12-04
17
603895
Gna13
1.000
RF021
G1
225.01
Y
11
109392392 (GRCm38)
V186A
T
C
missense
Het
probably benign
0.000
phenotype
2019-12-04
18
603876
Grk3
0.000
RF021
G1
225.01
Y
5
112941688 (GRCm38)
I333L
T
A
missense
Het
probably benign
0.201
phenotype
2019-12-04
19
603909
Gstp1
0.402
RF021
G1
225.01
N
19
4035507 (GRCm38)
V200E
A
T
missense
Het
probably benign
0.006
phenotype
2019-12-04
20
603882
Gtf2h1
0.969
RF021
G1
225.01
Y
7
46803865 (GRCm38)
V74G
T
G
missense
Het
possibly damaging
0.877
2019-12-04
21
603908
Kcnh8
0.000
RF021
G1
225.01
Y
17
52978239 (GRCm38)
R1079H
G
A
missense
Het
probably benign
0.004
phenotype
2019-12-04
22
603863
Kiz
0.000
RF021
G1
225.01
Y
2
146870830 (GRCm38)
D138G
A
G
missense
Het
possibly damaging
0.742
phenotype
2019-12-04
23
603881
Kmt2b
1.000
RF021
G1
217.47
N
7
30586357 (GRCm38)
TTCTCCT
TTCTCCTTCTCCT
unclassified
Het
probably benign
phenotype
2019-12-04
24
603890
Lats1
0.835
RF021
G1
225.01
Y
10
7710608 (GRCm38)
T912A
A
G
missense
Het
probably damaging
1.000
phenotype
2019-12-04
25
603869
Lce1m
RF021
G1
217.47
N
3
93018269 (GRCm38)
GCTGCCACC
GCTGCCACCACTTCTGCCACC
unclassified
Het
probably benign
2019-12-04
26
603870
Lce1m
RF021
G1
187.47
N
3
93018295 (GRCm38)
TGCC
TGCCGCCGCTGCCGCC
unclassified
Het
probably benign
2019-12-04
27
603889
Lrrc2
0.000
RF021
G1
214.46
Y
9
110981676 (GRCm38)
TTGATTCGGTTCACC
T
makesense
Het
probably null
phenotype
2019-12-04
28
603868
Med12l
0.271
RF021
G1
225.01
Y
3
59073290 (GRCm38)
F359S
T
C
missense
Het
probably benign
0.191
phenotype
2019-12-04
29
603907
Mut
1.000
RF021
G1
225.01
Y
17
40951758 (GRCm38)
I444V
A
G
missense
Het
probably benign
0.009
phenotype
2019-12-04
30
603854
Ncoa2
0.959
RF021
G1
118.47
Y
1
13149109 (GRCm38)
CTTAAAA
C
critical splice acceptor site
Het
probably benign
phenotype
2019-12-04
31
603888
Ngp
0.000
RF021
G1
225.01
Y
9
110421756 (GRCm38)
T114A
A
G
missense
Het
possibly damaging
0.545
2019-12-04
32
603883
Nlrc5
0.000
RF021
G1
225.01
Y
8
94476888 (GRCm38)
T539S
A
T
missense
Het
probably benign
0.161
phenotype
2019-12-04
33
603911
Nxf1
1.000
RF021
G1
225.01
N
19
8772309 (GRCm38)
D190G
A
G
missense
Het
probably damaging
1.000
phenotype
2019-12-04
34
603886
Olfr229
0.078
RF021
G1
225.01
Y
9
39910045 (GRCm38)
M81L
A
T
missense
Het
probably benign
0.002
0.090
phenotype
2019-12-04
35
603892
Olfr769
0.068
RF021
G1
225.01
Y
10
129112342 (GRCm38)
F28I
A
T
missense
Het
probably damaging
0.987
phenotype
2019-12-04
36
603875
Pramef25
0.060
RF021
G1
225.01
Y
4
143948908 (GRCm38)
Q449H
C
G
missense
Het
probably damaging
0.963
2019-12-04
37
603905
Prdm15
0.000
RF021
G1
225.01
Y
16
97808756 (GRCm38)
H563Y
G
A
missense
Het
probably damaging
1.000
2019-12-04
38
603866
Rbm12
0.872
RF021
G1
214.59
N
2
156096106 (GRCm38)
CAGG
CAGGGATTGCGGGACCTGGTATTGCGGGACCAGG
intron
Het
probably benign
phenotype
2019-12-04
39
603897
Sema3g
0.000
RF021
G1
225.01
Y
14
31227841 (GRCm38)
H660Y
C
T
missense
Het
probably damaging
1.000
phenotype
2019-12-04
40
603912
Smarca2
0.000
RF021
G1
214.46
N
19
26630997 (GRCm38)
AGCAGCAGCAGCAGCAGCAGCA
AGCAGCAGCAGCAGCAGCAGCAGCAGCA
unclassified
Het
probably benign
phenotype
2019-12-04
41
603871
Stpg2
0.058
RF021
G1
113.01
Y
3
139212250 (GRCm38)
A
T
critical splice acceptor site
Het
probably null
0.948
2019-12-04
42
603891
Taar7f
0.085
RF021
G1
225.01
Y
10
24050423 (GRCm38)
T305M
C
T
missense
Het
possibly damaging
0.889
2019-12-04
43
603880
Tbcb
0.958
RF021
G1
225.01
Y
7
30224346 (GRCm38)
V208M
C
T
missense
Het
probably damaging
1.000
2019-12-04
44
603894
Tenm2
0.448
RF021
G1
225.01
Y
11
36024203 (GRCm38)
Q2169L
T
A
missense
Het
possibly damaging
0.951
phenotype
2019-12-04
45
603872
Tln1
1.000
RF021
G1
225.01
Y
4
43555890 (GRCm38)
V108A
A
G
missense
Het
probably damaging
1.000
phenotype
2019-12-04
46
603896
Tmc8
0.050
RF021
G1
191.01
Y
11
117783234 (GRCm38)
M42T
T
C
missense
Het
probably benign
0.003
phenotype
2019-12-04
47
603899
Trdc
0.087
RF021
G1
225.01
Y
14
54144203 (GRCm38)
V115A
T
C
missense
Het
phenotype
2019-12-04
48
603861
Ttbk2
1.000
RF021
G1
225.01
Y
2
120748634 (GRCm38)
V669A
A
G
missense
Het
probably benign
0.000
phenotype
2019-12-04
49
603873
Tusc1
0.000
RF021
G1
207.59
N
4
93335316 (GRCm38)
GCC
GCCACCACC
small insertion
Het
probably benign
phenotype
2019-12-04
50
603862
Vps16
0.969
RF021
G1
225.01
Y
2
130438209 (GRCm38)
H118R
A
G
missense
Het
probably benign
0.090
phenotype
2019-12-04
51
603893
Wdpcp
0.895
RF021
G1
225.01
Y
11
21711587 (GRCm38)
C286*
T
A
nonsense
Het
probably null
phenotype
2019-12-04
52
603901
Zbed4
0.580
RF021
G1
225.01
N
15
88781236 (GRCm38)
Y502*
C
A
nonsense
Het
probably null
2019-12-04
53
603856
Zdbf2
0.108
RF021
G1
225.01
Y
1
63302652 (GRCm38)
N63K
T
A
missense
Het
possibly damaging
0.816
phenotype
2019-12-04
[records 1 to 53 of 53]