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Incidental Mutations
62
incidental mutations are currently displayed, and affect
55
genes.
7
are Possibly Damaging.
14
are Probably Damaging.
30
are Probably Benign.
7
are Probably Null.
0
create premature stop codons.
3
are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 62 of 62]
10
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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
602593
AI837181
0.000
RF002
G1
154.47
N
19
5425234 (GRCm38)
CGG
CGGTGG
small insertion
Het
probably benign
2019-12-04
2
602594
AI837181
0.000
RF002
G1
156.47
N
19
5425235 (GRCm38)
GGC
GGCTGC
small insertion
Het
probably benign
2019-12-04
3
602539
Angptl1
0.085
RF002
G1
225.01
N
1
156857224 (GRCm38)
Q321L
A
T
missense
Het
possibly damaging
0.790
phenotype
2019-12-04
4
602582
AY358078
0.070
RF002
G1
214.46
N
14
51805593 (GRCm38)
T
TAGGATAATGC
nonsense
Het
probably null
2019-12-04
5
602560
Blm
1.000
RF002
G1
217.47
N
7
80512905 (GRCm38)
CCTCCTCCTCCTCCTCCTCCTCCT
CCTCCTCCTCCTGCTCCTCCTCCTCCTCCTCCTCCT
small insertion
Het
probably benign
phenotype
2019-12-04
6
602561
Blm
1.000
RF002
G1
217.47
N
7
80512927 (GRCm38)
CTC
CTCATCCTCCTCATC
small insertion
Het
probably benign
phenotype
2019-12-04
7
602546
Car13
0.000
RF002
G1
225.01
N
3
14654914 (GRCm38)
Y129H
T
C
missense
Het
probably damaging
0.989
phenotype
2019-12-04
8
602568
Cd109
0.000
RF002
G1
217.47
N
9
78712523 (GRCm38)
TTATTTATTTAT
TTATTTATTTATGTATTTATTTAT
critical splice acceptor site
Het
probably benign
phenotype
2019-12-04
9
602569
Cd109
0.000
RF002
G1
217.47
N
9
78712528 (GRCm38)
TATTTAT
TATTTATTTATTCATTTAT
critical splice acceptor site
Het
probably benign
phenotype
2019-12-04
10
602545
Cdh26
0.000
RF002
G1
225.01
N
2
178466631 (GRCm38)
C341R
T
C
missense
Het
probably damaging
1.000
phenotype
2019-12-04
11
602576
Chga
0.063
RF002
G1
189.47
N
12
102561421 (GRCm38)
GCA
GCACCA
small insertion
Het
probably benign
phenotype
2019-12-04
12
602549
Col11a1
0.897
RF002
G1
225.01
N
3
114217001 (GRCm38)
I1689L
A
T
missense
Het
unknown
phenotype
2019-12-04
13
602555
Dnah6
0.123
RF002
G1
225.01
N
6
73101889 (GRCm38)
S2364R
T
G
missense
Het
probably benign
0.000
phenotype
2019-12-04
14
602588
E4f1
1.000
RF002
G1
169.47
N
17
24455186 (GRCm38)
CCG
CCGACG
unclassified
Het
probably benign
phenotype
2019-12-04
15
602562
Fah
1.000
RF002
G1
225.01
N
7
84589628 (GRCm38)
N336K
A
C
missense
Het
probably damaging
0.997
phenotype
2019-12-04
16
602559
Fam71e1
0.122
RF002
G1
217.47
N
7
44500520 (GRCm38)
CCTGGGTCTGAGGGAGGA
CCTGGGTCTGAGGGAGGAAGGCTGGATCCTGGATAACTGGGTCTGAGGGAGGA
nonsense
Het
probably null
2019-12-04
17
602592
Fbxo11
1.000
RF002
G1
225.01
N
17
87996053 (GRCm38)
I664K
A
T
missense
Het
phenotype
2019-12-04
18
602558
Fcgbp
0.000
RF002
G1
225.01
N
7
28089755 (GRCm38)
D582G
A
G
missense
Het
probably benign
0.000
2019-12-04
19
602597
Gabre
RF002
G1
211.46
N
X
72270057 (GRCm38)
C
CCGGCTA
nonsense
Het
probably null
2019-12-04
20
602567
Gm1110
0.072
RF002
G1
225.01
N
9
26920640 (GRCm38)
Y72H
A
G
missense
Het
probably damaging
1.000
2019-12-04
21
602543
Gm14025
0.062
RF002
G1
225.01
N
2
129038794 (GRCm38)
F404S
A
G
missense
Het
2019-12-04
22
602541
Inpp5e
1.000
RF002
G1
225.01
N
2
26408377 (GRCm38)
A71T
C
T
missense
Het
possibly damaging
0.951
phenotype
2019-12-04
23
602565
Iqcm
0.059
RF002
G1
225.01
N
8
75577899 (GRCm38)
T96I
C
T
missense
Het
probably benign
0.006
2019-12-04
24
602547
Lce1m
RF002
G1
217.47
N
3
93018283 (GRCm38)
TGCCACCGCTGC
TGCCACCGCTGCCGCCACCGCTGC
unclassified
Het
probably benign
2019-12-04
25
602548
Lce1m
RF002
G1
217.47
N
3
93018299 (GRCm38)
AC
ACCGCCGCTGCCCC
unclassified
Het
probably benign
2019-12-04
26
602584
Lrch1
0.000
RF002
G1
214.46
N
14
74947574 (GRCm38)
TTGGTGGTGCTGGTGG
TTGGTGG
small deletion
Het
probably benign
phenotype
2019-12-04
27
602577
Lyst
0.300
RF002
G1
225.01
N
13
13634363 (GRCm38)
D206G
A
G
missense
Het
probably benign
0.055
phenotype
2019-12-04
28
602575
Map4k5
0.000
RF002
G1
225.01
N
12
69856856 (GRCm38)
D58E
A
T
missense
Het
probably damaging
0.957
phenotype
2019-12-04
29
602538
Mapkapk2
0.000
RF002
G1
225.01
N
1
131056513 (GRCm38)
S251P
A
G
missense
Het
probably damaging
1.000
phenotype
2019-12-04
30
602563
Mcph1
0.000
RF002
G1
139.47
N
8
18652529 (GRCm38)
CCTG
CCTGCTG
small insertion
Het
probably benign
phenotype
2019-12-04
31
602595
Men1
1.000
RF002
G1
225.01
N
19
6340116 (GRCm38)
S600P
T
C
missense
Het
probably damaging
0.966
phenotype
2019-12-04
32
602590
Mllt1
1.000
RF002
G1
225.01
N
17
56896300 (GRCm38)
V394M
C
T
missense
Het
probably benign
0.088
phenotype
2019-12-04
33
602591
Mllt1
1.000
RF002
G1
225.01
N
17
56896301 (GRCm38)
M393I
C
A
missense
Het
possibly damaging
0.656
phenotype
2019-12-04
34
602566
Nacc1
0.000
RF002
G1
225.01
N
8
84676219 (GRCm38)
E315G
T
C
missense
Het
possibly damaging
0.504
phenotype
2019-12-04
35
602570
Nefh
0.000
RF002
G1
217.47
N
11
4941047 (GRCm38)
GGGGACTTGGCCTC
GGGGACTTGGCCTCACCTAGGGACTTGGCCTC
small insertion
Het
probably benign
phenotype
2019-12-04
36
602571
Nefh
0.000
RF002
G1
214.46
N
11
4941050 (GRCm38)
GACTTGGCCTC
GACTTGGCCTCACCTGGGGACTTGGCCTC
small insertion
Het
probably benign
phenotype
2019-12-04
37
602579
Nid2
0.188
RF002
G1
214.46
N
14
19751366 (GRCm38)
TAACACCGCCA
TA
small deletion
Het
probably benign
phenotype
2019-12-04
38
602596
Olfr1484
0.085
RF002
G1
225.01
N
19
13586051 (GRCm38)
I206N
T
A
missense
Het
probably damaging
0.997
phenotype
2019-12-04
39
602581
Parp2
0.345
RF002
G1
225.01
N
14
50817386 (GRCm38)
E262G
A
G
missense
Het
probably damaging
0.998
phenotype
2019-12-04
40
602551
Pdik1l
0.000
RF002
G1
214.46
N
4
134279375 (GRCm38)
TTT
TTTGTTTTTGTGTT
frame shift
Het
probably null
2019-12-04
41
602585
Pop1
0.958
RF002
G1
225.01
N
15
34502437 (GRCm38)
G90D
G
A
missense
Het
probably damaging
0.999
phenotype
2019-12-04
42
602583
Ppp3cc
0.000
RF002
G1
225.01
N
14
70267339 (GRCm38)
T73A
T
C
missense
Het
possibly damaging
0.516
phenotype
2019-12-04
43
602587
Prdm15
0.000
RF002
G1
225.01
N
16
97799629 (GRCm38)
D810N
C
T
missense
Het
probably damaging
1.000
2019-12-04
44
602578
Prpf4b
1.000
RF002
G1
225.01
N
13
34884236 (GRCm38)
S349R
T
A
missense
Het
unknown
phenotype
2019-12-04
45
602553
Rassf6
0.083
RF002
G1
140.47
N
5
90608921 (GRCm38)
TCCTGTAGAGCAATGGGGATTC
TCCTGTAGAGCAATGGGGATTCTGCCTCACTCATGGGCCTGTAGAGCAATGGGGATTC
utr 3 prime
Het
probably benign
phenotype
2019-12-04
46
602554
Rassf6
0.083
RF002
G1
138.47
N
5
90608925 (GRCm38)
GTAGAGCAATGGGGATTC
GTAGAGCAATGGGGATTCTGCCTCACTCATGGTCCTTTAGAGCAATGGGGATTC
nonsense
Het
probably null
phenotype
2019-12-04
47
602574
Sdk2
0.102
RF002
G1
225.01
N
11
113885252 (GRCm38)
E208G
T
C
missense
Het
probably benign
0.004
phenotype
2019-12-04
48
602573
Smurf2
0.000
RF002
G1
225.01
N
11
106852587 (GRCm38)
P211Q
G
T
missense
Het
probably benign
0.220
phenotype
2019-12-04
49
602564
Snx25
1.000
RF002
G1
225.01
N
8
46116181 (GRCm38)
C
A
critical splice donor site
1 bp
Het
probably null
2019-12-04
50
602550
Spata6
0.000
RF002
G1
225.01
N
4
111828305 (GRCm38)
M469K
T
A
missense
Het
probably benign
0.000
phenotype
2019-12-04
51
602540
Spta1
0.826
RF002
G1
225.01
N
1
174231360 (GRCm38)
A1954S
G
T
missense
Het
possibly damaging
0.623
phenotype
2019-12-04
52
602599
Sry
0.318
RF002
G1
217.47
N
Y
2662564 (GRCm38)
CTGGTCGTGGAACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGGTGGTGGTCATGGAACTGCTG
CTGGTCATGGAACTGCTG
small deletion
Het
probably benign
phenotype
2019-12-04
53
602598
Stard8
0.000
RF002
G1
161.47
N
X
99066515 (GRCm38)
GAG
GAGTAG
nonsense
Het
probably null
phenotype
2019-12-04
54
602589
Tfeb
1.000
RF002
G1
161.47
N
17
47786102 (GRCm38)
AGC
AGCGGC
small insertion
Het
probably benign
phenotype
2019-12-04
55
602572
Tlcd1
0.117
RF002
G1
225.01
N
11
78180194 (GRCm38)
L203Q
T
A
missense
Het
probably benign
0.006
2019-12-04
56
602580
Tlr11
0.000
RF002
G1
225.01
N
14
50361225 (GRCm38)
F223L
T
C
missense
Het
possibly damaging
0.625
2019-12-04
57
602552
Usp48
0.961
RF002
G1
225.01
N
4
137605795 (GRCm38)
V100D
T
A
missense
Het
probably damaging
1.000
phenotype
2019-12-04
58
602557
Vmn2r56
0.064
RF002
G1
91.01
N
7
12694830 (GRCm38)
T503I
G
A
missense
Het
probably benign
0.018
2019-12-04
59
602542
Vps18
1.000
RF002
G1
225.01
N
2
119297390 (GRCm38)
L898P
T
C
missense
Het
probably damaging
1.000
phenotype
2019-12-04
60
602556
Zfp384
0.172
RF002
G1
217.47
N
6
125036471 (GRCm38)
GCCCAGGCCCAGGCCCAGGCCCAG
GCCCAGGCCCAGTCCCAGGCCCAGGCCCAGGCCCAG
unclassified
Het
probably benign
phenotype
2019-12-04
61
602586
Zfp706
0.393
RF002
G1
225.01
N
15
37003705 (GRCm38)
Y39F
T
A
missense
Het
probably benign
0.148
2019-12-04
62
602544
Zhx3
1.000
RF002
G1
225.01
N
2
160781806 (GRCm38)
N147I
T
A
missense
Het
probably damaging
0.983
phenotype
2019-12-04
[records 1 to 62 of 62]