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Incidental Mutations
38
incidental mutations are currently displayed, and affect
37
genes.
8
are Possibly Damaging.
11
are Probably Damaging.
17
are Probably Benign.
2
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 38 of 38]
10
25
50
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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
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
362874
1810055G02Rik
0.062
IGL02883
19
3716972 (GRCm38)
S186R
C
A
missense
Het
possibly damaging
0.827
2015-12-18
2
362897
Acap2
0.149
IGL02883
16
31096345 (GRCm38)
A
G
unclassified
Het
probably benign
2015-12-18
3
362868
Cacna1h
0.000
IGL02883
17
25380532 (GRCm38)
R1726S
G
T
missense
Het
probably damaging
1.000
phenotype
2015-12-18
4
362890
Cdca2
0.083
IGL02883
14
67707497 (GRCm38)
S133G
T
C
missense
Het
probably damaging
0.999
phenotype
2015-12-18
5
362887
Cep295nl
0.000
IGL02883
11
118333909 (GRCm38)
S36R
A
T
missense
Het
probably benign
0.008
2015-12-18
6
362885
Crispld1
0.079
IGL02883
1
17746789 (GRCm38)
N190S
A
G
missense
Het
possibly damaging
0.870
2015-12-18
7
362870
Crtam
0.062
IGL02883
9
40994501 (GRCm38)
V44A
A
G
missense
Het
probably benign
0.000
phenotype
2015-12-18
8
362867
Crtc1
0.456
IGL02883
8
70406125 (GRCm38)
G112S
C
T
missense
Het
probably benign
0.276
phenotype
2015-12-18
9
362894
Cyp17a1
0.200
IGL02883
19
46669351 (GRCm38)
N254S
T
C
missense
Het
probably benign
0.001
phenotype
2015-12-18
10
362875
Dmrta1
0.000
IGL02883
4
89688774 (GRCm38)
S156P
T
C
missense
Het
probably benign
0.000
phenotype
2015-12-18
11
362877
Eno2
0.219
IGL02883
6
124766209 (GRCm38)
V188G
A
C
missense
Het
probably damaging
0.999
phenotype
2015-12-18
12
362878
Fam20a
0.000
IGL02883
11
109675127 (GRCm38)
I427N
A
T
missense
Het
probably damaging
0.990
phenotype
2015-12-18
13
362888
Fat2
0.000
IGL02883
11
55256618 (GRCm38)
K3933E
T
C
missense
Het
probably benign
0.161
phenotype
2015-12-18
14
362862
Gm15448
0.048
IGL02883
7
3822180 (GRCm38)
S488P
A
G
missense
Het
possibly damaging
0.955
2015-12-18
15
362861
Igkv8-30
0.118
IGL02883
6
70117617 (GRCm38)
M1V
T
C
start codon destroyed
Het
probably null
0.845
2015-12-18
16
362896
Ist1
0.866
IGL02883
8
109683668 (GRCm38)
G
A
splice site
Het
probably benign
phenotype
2015-12-18
17
362892
Kank4
0.071
IGL02883
4
98773453 (GRCm38)
E765G
T
C
missense
Het
possibly damaging
0.865
2015-12-18
18
362889
Kat14
1.000
IGL02883
2
144393529 (GRCm38)
L92S
T
C
missense
Het
probably damaging
1.000
phenotype
2015-12-18
19
362879
Kcnu1
0.000
IGL02883
8
25849827 (GRCm38)
V58I
G
A
missense
Het
probably benign
0.000
phenotype
2015-12-18
20
362886
Lrba
0.000
IGL02883
3
86445413 (GRCm38)
I1956N
T
A
missense
Het
probably damaging
0.993
phenotype
2015-12-18
21
362882
Lrba
0.000
IGL02883
3
86354206 (GRCm38)
V1489E
T
A
missense
Het
probably damaging
0.999
phenotype
2015-12-18
22
362883
Mdn1
1.000
IGL02883
4
32763199 (GRCm38)
V5100I
G
A
missense
Het
probably benign
0.051
2015-12-18
23
362884
Mkrn2os
0.070
IGL02883
6
115586709 (GRCm38)
G122*
C
A
nonsense
Het
probably null
2015-12-18
24
362873
Nme3
0.173
IGL02883
17
24896906 (GRCm38)
Y78H
T
C
missense
Het
probably benign
0.316
phenotype
2015-12-18
25
362864
Pkd1l2
0.000
IGL02883
8
117065745 (GRCm38)
T436I
G
A
missense
Het
probably benign
0.070
0.072
phenotype
2015-12-18
26
362869
Ppp2r5c
0.000
IGL02883
12
110522563 (GRCm38)
V56G
T
G
missense
Het
possibly damaging
0.480
phenotype
2015-12-18
27
362865
Pramef25
0.060
IGL02883
4
143949848 (GRCm38)
T229A
T
C
missense
Het
possibly damaging
0.642
2015-12-18
28
362872
Prdm10
1.000
IGL02883
9
31327348 (GRCm38)
V179M
G
A
missense
Het
probably damaging
0.989
phenotype
2015-12-18
29
362891
Rab11fip2
0.162
IGL02883
19
59906998 (GRCm38)
V344A
A
G
missense
Het
probably damaging
1.000
2015-12-18
30
362866
Selp
0.104
IGL02883
1
164130102 (GRCm38)
A267T
G
A
missense
Het
probably benign
0.004
phenotype
2015-12-18
31
362876
Sf3a1
1.000
IGL02883
11
4179192 (GRCm38)
W718R
T
A
missense
Het
probably damaging
0.998
phenotype
2015-12-18
32
362863
Taar9
0.080
IGL02883
10
24109480 (GRCm38)
N19D
T
C
missense
Het
probably benign
0.084
phenotype
2015-12-18
33
362880
Tas2r113
0.060
IGL02883
6
132893419 (GRCm38)
S137A
T
G
missense
Het
probably damaging
0.999
2015-12-18
34
362871
Traf4
0.914
IGL02883
11
78161621 (GRCm38)
I66N
A
T
missense
Het
possibly damaging
0.716
phenotype
2015-12-18
35
362893
Ucp3
0.060
IGL02883
7
100480642 (GRCm38)
T164S
A
T
missense
Het
probably benign
0.003
phenotype
2015-12-18
36
362881
Uggt1
0.466
IGL02883
1
36177615 (GRCm38)
N96K
A
T
missense
Het
probably benign
0.030
phenotype
2015-12-18
37
362895
Uqcc1
0.926
IGL02883
2
155911829 (GRCm38)
Q42L
T
A
missense
Het
possibly damaging
0.934
phenotype
2015-12-18
38
362860
Vmn1r128
IGL02883
7
21349515 (GRCm38)
K48R
A
G
missense
Het
probably benign
0.001
2015-12-18
[records 1 to 38 of 38]