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
55
incidental mutations are currently displayed, and affect
54
genes.
10
are Possibly Damaging.
17
are Probably Damaging.
24
are Probably Benign.
1
are Probably Null.
1
create premature stop codons.
0
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 55 of 55]
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
540835
5430403G16Rik
0.111
R6945
G1
225.01
Y
5
109676845 (GRCm38)
N246K
A
C
missense
Het
probably benign
0.247
0.090
2018-11-28
2
540834
AA792892
R6945
G1
131.01
N
5
94383631 (GRCm38)
H125Y
C
T
missense
Het
possibly damaging
0.570
2018-11-28
3
540860
Abcc5
0.000
R6945
G1
225.01
Y
16
20400009 (GRCm38)
T208S
T
A
missense
Het
probably benign
0.000
phenotype
2018-11-28
4
540869
Acaa2
0.845
R6945
G1
225.01
Y
18
74793309 (GRCm38)
E112G
A
G
missense
Het
probably benign
0.004
phenotype
2018-11-28
5
540859
Adgrb1
0.000
R6945
G1
225.01
Y
15
74550024 (GRCm38)
N881S
A
G
missense
Het
probably damaging
0.994
0.233
phenotype
2018-11-28
6
540863
Adgre1
0.229
R6945
G1
225.01
Y
17
57410844 (GRCm38)
E314G
A
G
missense
Het
probably benign
0.014
0.090
phenotype
2018-11-28
7
540864
Adgre1
0.229
R6945
G1
225.01
Y
17
57420399 (GRCm38)
E443G
A
G
missense
Het
probably benign
0.394
0.090
phenotype
2018-11-28
8
540820
Akp3
0.311
R6945
G1
225.01
Y
1
87125631 (GRCm38)
Y102C
A
G
missense
Het
probably damaging
1.000
0.962
phenotype
2018-11-28
9
540866
Birc6
1.000
R6945
G1
225.01
Y
17
74579531 (GRCm38)
N618S
A
G
missense
Het
probably benign
0.035
0.058
phenotype
2018-11-28
10
540846
Bpifc
0.088
R6945
G1
225.01
Y
10
85979214 (GRCm38)
V296A
A
G
missense
Het
probably benign
0.002
2018-11-28
11
540854
Cacna2d3
0.000
R6945
G1
143.01
Y
14
28969318 (GRCm38)
G
A
intron
Het
probably benign
phenotype
2018-11-28
12
540824
Cacnb4
0.260
R6945
G1
225.01
Y
2
52474954 (GRCm38)
N99S
T
C
missense
Het
probably damaging
0.999
0.588
phenotype
2018-11-28
13
540833
Cd38
0.000
R6945
G1
225.01
Y
5
43908006 (GRCm38)
Y283C
A
G
missense
Het
probably damaging
1.000
phenotype
2018-11-28
14
540867
Celf4
1.000
R6945
G1
222.01
Y
18
25496236 (GRCm38)
Q411L
T
A
missense
Het
probably damaging
0.996
phenotype
2018-11-28
15
540843
Cemip
0.074
R6945
G1
225.01
Y
7
83998547 (GRCm38)
H108Q
A
T
missense
Het
probably damaging
0.999
phenotype
2018-11-28
16
540848
Col23a1
0.059
R6945
G1
225.01
Y
11
51561893 (GRCm38)
E225G
A
G
missense
Het
unknown
phenotype
2018-11-28
17
540853
Dnah11
0.554
R6945
G1
225.01
Y
12
118060310 (GRCm38)
E1902G
T
C
missense
Het
probably damaging
1.000
0.349
phenotype
2018-11-28
18
540817
Dst
0.197
R6945
G1
225.01
Y
1
34190490 (GRCm38)
D2063G
A
G
missense
Het
probably damaging
1.000
0.115
phenotype
2018-11-28
19
540825
Fsip2
0.076
R6945
G1
225.01
Y
2
82992840 (GRCm38)
I6306L
A
T
missense
Het
probably benign
0.163
0.082
phenotype
2018-11-28
20
540842
Furin
1.000
R6945
G1
155.01
N
7
80391090 (GRCm38)
S667P
A
G
missense
Het
possibly damaging
0.816
phenotype
2018-11-28
21
540829
Glmp
0.000
R6945
G1
225.01
Y
3
88325832 (GRCm38)
S92R
T
A
missense
Het
probably benign
0.024
phenotype
2018-11-28
22
540851
Gm11563
0.061
R6945
G1
225.01
Y
11
99658472 (GRCm38)
C152S
C
G
missense
Het
unknown
0.161
2018-11-28
23
540857
Gm3486
0.410
R6945
G1
225.01
Y
14
41484561 (GRCm38)
V185A
A
G
missense
Het
probably benign
0.026
2018-11-28
24
540844
Gm4070
R6945
G1
162.01
N
7
105901980 (GRCm38)
Q622*
G
A
nonsense
Het
probably null
2018-11-28
25
540845
Hyal1
0.151
R6945
G1
225.01
Y
9
107579170 (GRCm38)
A102E
C
A
missense
Het
probably damaging
0.972
phenotype
2018-11-28
26
540831
Invs
0.685
R6945
G1
194.01
Y
4
48421785 (GRCm38)
C806R
T
C
missense
Het
probably benign
0.005
0.066
phenotype
2018-11-28
27
540832
L1td1
0.099
R6945
G1
225.01
Y
4
98733696 (GRCm38)
V165A
T
C
missense
Het
probably benign
0.326
0.090
phenotype
2018-11-28
28
540865
Lama1
1.000
R6945
G1
225.01
Y
17
67813866 (GRCm38)
T2666A
A
G
missense
Het
0.087
phenotype
2018-11-28
29
540855
Lrit1
0.072
R6945
G1
225.01
Y
14
37060095 (GRCm38)
V242L
G
C
missense
Het
probably damaging
0.992
0.186
phenotype
2018-11-28
30
540823
Lrrc8a
1.000
R6945
G1
225.01
Y
2
30256227 (GRCm38)
Y351C
A
G
missense
Het
probably damaging
1.000
0.616
phenotype
2018-11-28
31
540828
Myh7b
0.000
R6945
G1
225.01
Y
2
155622232 (GRCm38)
F551S
T
C
missense
Het
possibly damaging
0.949
phenotype
2018-11-28
32
540850
Myo19
0.150
R6945
G1
225.01
Y
11
84897560 (GRCm38)
T333A
A
G
missense
Het
probably benign
0.058
0.223
2018-11-28
33
540819
Nrp2
0.956
R6945
G1
225.01
Y
1
62760788 (GRCm38)
N387I
A
T
missense
Het
probably damaging
1.000
0.974
phenotype
2018-11-28
34
540837
Oas2
0.092
R6945
G1
225.01
Y
5
120736139 (GRCm38)
D543G
T
C
missense
Het
probably benign
0.002
phenotype
2018-11-28
35
540826
Olfr1040
0.108
R6945
G1
225.01
Y
2
86146084 (GRCm38)
S217P
A
G
missense
Het
probably damaging
1.000
0.647
phenotype
2018-11-28
36
540862
Olfr117
0.071
R6945
G1
225.01
Y
17
37659514 (GRCm38)
I273T
A
G
missense
Het
possibly damaging
0.952
0.179
phenotype
2018-11-28
37
540827
Pak7
0.000
R6945
G1
225.01
Y
2
136100939 (GRCm38)
V427A
A
G
missense
Het
probably benign
0.148
0.121
phenotype
2018-11-28
38
540849
Pfas
1.000
R6945
G1
225.01
Y
11
69000530 (GRCm38)
A247V
G
A
missense
Het
probably benign
0.000
0.090
phenotype
2018-11-28
39
540870
Psat1
1.000
R6945
G1
225.01
Y
19
15917181 (GRCm38)
T115S
T
A
missense
Het
probably benign
0.297
phenotype
2018-11-28
40
540847
Psme4
0.000
R6945
G1
225.01
Y
11
30837437 (GRCm38)
D1077E
T
A
missense
Het
probably benign
0.064
phenotype
2018-11-28
41
540821
Rabgap1l
0.000
R6945
G1
225.01
Y
1
160682182 (GRCm38)
S442P
A
G
missense
Het
probably benign
0.286
0.089
phenotype
2018-11-28
42
540852
Ralgapa1
0.745
R6945
G1
225.01
Y
12
55776191 (GRCm38)
M280T
A
G
missense
Het
possibly damaging
0.637
phenotype
2018-11-28
43
540816
Rb1cc1
1.000
R6945
G1
225.01
Y
1
6261032 (GRCm38)
E394D
A
T
missense
Het
probably damaging
1.000
0.647
phenotype
2018-11-28
44
540868
Seh1l
1.000
R6945
G1
225.01
Y
18
67789390 (GRCm38)
V271A
T
C
missense
Het
probably benign
0.003
phenotype
2018-11-28
45
540818
Sf3b1
1.000
R6945
G1
225.01
Y
1
54997156 (GRCm38)
N919K
A
T
missense
Het
probably benign
0.450
0.078
phenotype
2018-11-28
46
540856
Sftpd
0.225
R6945
G1
225.01
Y
14
41174492 (GRCm38)
S245P
A
G
missense
Het
possibly damaging
0.882
phenotype
2018-11-28
47
540830
Slc22a15
0.073
R6945
G1
225.01
N
3
101924114 (GRCm38)
E2G
T
C
missense
Het
probably damaging
0.992
phenotype
2018-11-28
48
540822
Spta1
0.826
R6945
G1
225.01
Y
1
174209325 (GRCm38)
D1134G
A
G
missense
Het
possibly damaging
0.895
phenotype
2018-11-28
49
540838
Syna
1.000
R6945
G1
225.01
Y
5
134558961 (GRCm38)
V378A
A
G
missense
Het
probably damaging
0.968
phenotype
2018-11-28
50
540836
Tchp
0.000
R6945
G1
225.01
Y
5
114709350 (GRCm38)
K77E
A
G
missense
Het
possibly damaging
0.759
2018-11-28
51
540841
Tescl
0.058
R6945
G1
225.01
Y
7
24333531 (GRCm38)
N123S
T
C
missense
Het
probably benign
0.002
2018-11-28
52
540858
Trio
1.000
R6945
G1
225.01
Y
15
27824090 (GRCm38)
R1443Q
C
T
missense
Het
probably damaging
1.000
0.493
phenotype
2018-11-28
53
540839
Trrap
1.000
R6945
G1
225.01
Y
5
144790855 (GRCm38)
Y462F
A
T
missense
Het
possibly damaging
0.659
0.095
phenotype
2018-11-28
54
540840
Vmn1r78
0.058
R6945
G1
225.01
Y
7
12152905 (GRCm38)
T148A
A
G
missense
Het
probably benign
0.011
2018-11-28
55
540861
Vmn2r111
0.087
R6945
G1
225.01
Y
17
22559051 (GRCm38)
N549S
T
C
missense
Het
possibly damaging
0.502
0.179
2018-11-28
[records 1 to 55 of 55]