Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy1 |
A |
G |
11: 7,080,348 (GRCm39) |
T364A |
probably benign |
Het |
Adpgk |
G |
A |
9: 59,221,036 (GRCm39) |
V281I |
probably benign |
Het |
Akap9 |
C |
A |
5: 4,026,235 (GRCm39) |
Q1297K |
possibly damaging |
Het |
Ankrd13d |
T |
C |
19: 4,331,968 (GRCm39) |
E110G |
probably damaging |
Het |
Ankrd53 |
A |
G |
6: 83,740,244 (GRCm39) |
E104G |
possibly damaging |
Het |
Becn2 |
T |
C |
1: 175,748,197 (GRCm39) |
C88R |
possibly damaging |
Het |
Bscl2 |
T |
A |
19: 8,818,514 (GRCm39) |
C40S |
probably benign |
Het |
Btaf1 |
A |
G |
19: 36,958,486 (GRCm39) |
T668A |
probably benign |
Het |
Camk2g |
G |
A |
14: 20,805,775 (GRCm39) |
|
probably benign |
Het |
Cd109 |
A |
T |
9: 78,574,639 (GRCm39) |
D541V |
probably damaging |
Het |
Cep135 |
G |
A |
5: 76,772,586 (GRCm39) |
G657D |
probably benign |
Het |
Coch |
A |
G |
12: 51,649,609 (GRCm39) |
I307V |
probably benign |
Het |
D17H6S53E |
A |
G |
17: 35,346,512 (GRCm39) |
E141G |
probably benign |
Het |
Ddias |
T |
C |
7: 92,508,800 (GRCm39) |
T372A |
probably benign |
Het |
Dffb |
T |
C |
4: 154,049,976 (GRCm39) |
T296A |
probably damaging |
Het |
Dock8 |
A |
G |
19: 25,057,241 (GRCm39) |
Q216R |
probably benign |
Het |
Ephx1 |
A |
G |
1: 180,817,498 (GRCm39) |
I391T |
probably benign |
Het |
Fcgbp |
A |
G |
7: 27,800,701 (GRCm39) |
Y1249C |
probably damaging |
Het |
Gm5592 |
T |
C |
7: 40,807,052 (GRCm39) |
|
probably benign |
Het |
Gm7964 |
A |
G |
7: 83,405,629 (GRCm39) |
N149S |
probably benign |
Het |
Greb1l |
T |
A |
18: 10,542,380 (GRCm39) |
I1325N |
probably damaging |
Het |
H2-T3 |
T |
C |
17: 36,500,957 (GRCm39) |
T20A |
possibly damaging |
Het |
Htr1d |
T |
C |
4: 136,170,815 (GRCm39) |
I348T |
probably damaging |
Het |
Hyal4 |
A |
T |
6: 24,765,737 (GRCm39) |
S364C |
probably damaging |
Het |
Igkv1-133 |
A |
T |
6: 67,701,944 (GRCm39) |
Q16L |
probably benign |
Het |
Irs2 |
C |
T |
8: 11,057,643 (GRCm39) |
G263D |
probably damaging |
Het |
Itga10 |
C |
T |
3: 96,559,054 (GRCm39) |
|
probably benign |
Het |
Kmt2a |
A |
G |
9: 44,760,263 (GRCm39) |
Y529H |
probably damaging |
Het |
Mdfic |
T |
A |
6: 15,770,319 (GRCm39) |
N108K |
probably damaging |
Het |
Met |
A |
T |
6: 17,549,085 (GRCm39) |
D979V |
probably damaging |
Het |
Mettl21e |
T |
A |
1: 44,245,857 (GRCm39) |
I130F |
probably damaging |
Het |
Mlh3 |
C |
T |
12: 85,315,169 (GRCm39) |
C339Y |
probably damaging |
Het |
Mog |
T |
C |
17: 37,323,338 (GRCm39) |
H200R |
possibly damaging |
Het |
Msrb3 |
C |
T |
10: 120,620,103 (GRCm39) |
R72H |
probably damaging |
Het |
Mtmr11 |
A |
G |
3: 96,072,583 (GRCm39) |
H324R |
probably damaging |
Het |
Myh7 |
T |
C |
14: 55,210,838 (GRCm39) |
E1693G |
probably damaging |
Het |
Nadk2 |
T |
A |
15: 9,084,303 (GRCm39) |
W139R |
probably damaging |
Het |
Ndufa9 |
A |
T |
6: 126,821,362 (GRCm39) |
M76K |
possibly damaging |
Het |
Nr1i2 |
A |
G |
16: 38,086,269 (GRCm39) |
|
probably benign |
Het |
Nsd3 |
A |
G |
8: 26,152,835 (GRCm39) |
T392A |
probably damaging |
Het |
Or14a259 |
A |
G |
7: 86,013,308 (GRCm39) |
F79S |
probably benign |
Het |
Or52d3 |
T |
C |
7: 104,229,149 (GRCm39) |
S99P |
probably damaging |
Het |
P2ry2 |
A |
T |
7: 100,647,706 (GRCm39) |
S200T |
probably benign |
Het |
Pcnt |
T |
A |
10: 76,269,584 (GRCm39) |
E228V |
probably benign |
Het |
Phka2 |
T |
A |
X: 159,327,291 (GRCm39) |
Y334* |
probably null |
Het |
Pkhd1l1 |
A |
T |
15: 44,390,265 (GRCm39) |
K1460N |
probably damaging |
Het |
Rpl7a-ps3 |
G |
A |
15: 36,308,429 (GRCm39) |
|
noncoding transcript |
Het |
Rspry1 |
A |
G |
8: 95,376,405 (GRCm39) |
D309G |
probably damaging |
Het |
Scap |
A |
G |
9: 110,209,271 (GRCm39) |
Y648C |
probably damaging |
Het |
Sgcz |
T |
C |
8: 38,420,201 (GRCm39) |
E17G |
probably damaging |
Het |
Slc17a5 |
A |
T |
9: 78,445,556 (GRCm39) |
V433D |
probably damaging |
Het |
Smad9 |
C |
T |
3: 54,696,705 (GRCm39) |
R257W |
probably damaging |
Het |
Srcap |
T |
C |
7: 127,141,319 (GRCm39) |
S1639P |
probably damaging |
Het |
Strn3 |
T |
C |
12: 51,707,999 (GRCm39) |
Y132C |
possibly damaging |
Het |
Tas2r110 |
A |
T |
6: 132,845,433 (GRCm39) |
M155L |
probably benign |
Het |
Tasor2 |
T |
C |
13: 3,645,556 (GRCm39) |
T98A |
probably benign |
Het |
Thbd |
A |
G |
2: 148,248,893 (GRCm39) |
V325A |
probably damaging |
Het |
Trpd52l3 |
T |
A |
19: 29,981,333 (GRCm39) |
C29* |
probably null |
Het |
Trpm1 |
A |
G |
7: 63,894,601 (GRCm39) |
Y951C |
probably damaging |
Het |
Ube3a |
T |
A |
7: 58,921,860 (GRCm39) |
N77K |
probably damaging |
Het |
Upp2 |
G |
A |
2: 58,680,128 (GRCm39) |
R300Q |
possibly damaging |
Het |
Usp35 |
T |
C |
7: 96,961,827 (GRCm39) |
H533R |
probably damaging |
Het |
Veph1 |
C |
T |
3: 66,122,858 (GRCm39) |
V224I |
probably benign |
Het |
Vmn1r30 |
A |
T |
6: 58,412,437 (GRCm39) |
F132I |
probably benign |
Het |
Vmn2r24 |
A |
G |
6: 123,792,997 (GRCm39) |
R775G |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,883,189 (GRCm39) |
|
probably null |
Het |
Vps37c |
T |
A |
19: 10,683,569 (GRCm39) |
|
probably null |
Het |
Zap70 |
C |
T |
1: 36,818,216 (GRCm39) |
T301I |
probably benign |
Het |
Zfp341 |
A |
G |
2: 154,466,801 (GRCm39) |
K57E |
probably damaging |
Het |
Zfp60 |
T |
A |
7: 27,448,753 (GRCm39) |
F474I |
probably benign |
Het |
Zfp786 |
T |
C |
6: 47,798,357 (GRCm39) |
N194D |
probably benign |
Het |
|
Other mutations in Ep400 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Ep400
|
APN |
5 |
110,835,707 (GRCm39) |
missense |
unknown |
|
IGL00585:Ep400
|
APN |
5 |
110,903,771 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL00586:Ep400
|
APN |
5 |
110,887,460 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00816:Ep400
|
APN |
5 |
110,883,356 (GRCm39) |
unclassified |
probably benign |
|
IGL01066:Ep400
|
APN |
5 |
110,816,065 (GRCm39) |
splice site |
probably benign |
|
IGL01302:Ep400
|
APN |
5 |
110,889,914 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01568:Ep400
|
APN |
5 |
110,867,361 (GRCm39) |
missense |
unknown |
|
IGL01833:Ep400
|
APN |
5 |
110,827,874 (GRCm39) |
missense |
unknown |
|
IGL02086:Ep400
|
APN |
5 |
110,824,809 (GRCm39) |
splice site |
probably benign |
|
IGL02266:Ep400
|
APN |
5 |
110,843,163 (GRCm39) |
unclassified |
probably benign |
|
IGL02288:Ep400
|
APN |
5 |
110,831,702 (GRCm39) |
splice site |
probably benign |
|
IGL02301:Ep400
|
APN |
5 |
110,822,826 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02377:Ep400
|
APN |
5 |
110,868,691 (GRCm39) |
missense |
unknown |
|
IGL02382:Ep400
|
APN |
5 |
110,849,594 (GRCm39) |
missense |
unknown |
|
IGL02419:Ep400
|
APN |
5 |
110,845,242 (GRCm39) |
splice site |
probably null |
|
IGL02591:Ep400
|
APN |
5 |
110,881,638 (GRCm39) |
unclassified |
probably benign |
|
IGL02981:Ep400
|
APN |
5 |
110,839,476 (GRCm39) |
splice site |
probably benign |
|
IGL02981:Ep400
|
APN |
5 |
110,903,969 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL03173:Ep400
|
APN |
5 |
110,856,737 (GRCm39) |
unclassified |
probably benign |
|
IGL03244:Ep400
|
APN |
5 |
110,875,429 (GRCm39) |
missense |
unknown |
|
IGL03333:Ep400
|
APN |
5 |
110,851,432 (GRCm39) |
missense |
unknown |
|
santol
|
UTSW |
5 |
110,849,537 (GRCm39) |
missense |
unknown |
|
PIT4243001:Ep400
|
UTSW |
5 |
110,883,446 (GRCm39) |
missense |
unknown |
|
PIT4260001:Ep400
|
UTSW |
5 |
110,841,037 (GRCm39) |
nonsense |
probably null |
|
R0017:Ep400
|
UTSW |
5 |
110,821,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R0179:Ep400
|
UTSW |
5 |
110,816,515 (GRCm39) |
missense |
probably damaging |
0.99 |
R0243:Ep400
|
UTSW |
5 |
110,872,273 (GRCm39) |
splice site |
probably benign |
|
R0366:Ep400
|
UTSW |
5 |
110,849,537 (GRCm39) |
missense |
unknown |
|
R0508:Ep400
|
UTSW |
5 |
110,887,374 (GRCm39) |
missense |
probably benign |
0.00 |
R0541:Ep400
|
UTSW |
5 |
110,852,882 (GRCm39) |
missense |
unknown |
|
R0558:Ep400
|
UTSW |
5 |
110,832,933 (GRCm39) |
splice site |
probably benign |
|
R0576:Ep400
|
UTSW |
5 |
110,858,959 (GRCm39) |
unclassified |
probably benign |
|
R0595:Ep400
|
UTSW |
5 |
110,851,408 (GRCm39) |
missense |
unknown |
|
R0671:Ep400
|
UTSW |
5 |
110,836,062 (GRCm39) |
missense |
unknown |
|
R0763:Ep400
|
UTSW |
5 |
110,813,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Ep400
|
UTSW |
5 |
110,883,388 (GRCm39) |
unclassified |
probably benign |
|
R1300:Ep400
|
UTSW |
5 |
110,821,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R1439:Ep400
|
UTSW |
5 |
110,833,344 (GRCm39) |
missense |
unknown |
|
R1520:Ep400
|
UTSW |
5 |
110,839,644 (GRCm39) |
intron |
probably benign |
|
R1529:Ep400
|
UTSW |
5 |
110,887,311 (GRCm39) |
missense |
probably benign |
0.00 |
R1535:Ep400
|
UTSW |
5 |
110,856,032 (GRCm39) |
unclassified |
probably benign |
|
R1560:Ep400
|
UTSW |
5 |
110,818,972 (GRCm39) |
splice site |
probably null |
|
R1587:Ep400
|
UTSW |
5 |
110,874,768 (GRCm39) |
missense |
probably benign |
0.23 |
R1596:Ep400
|
UTSW |
5 |
110,856,727 (GRCm39) |
unclassified |
probably benign |
|
R1653:Ep400
|
UTSW |
5 |
110,841,040 (GRCm39) |
nonsense |
probably null |
|
R1711:Ep400
|
UTSW |
5 |
110,841,174 (GRCm39) |
unclassified |
probably benign |
|
R1774:Ep400
|
UTSW |
5 |
110,833,357 (GRCm39) |
missense |
unknown |
|
R1836:Ep400
|
UTSW |
5 |
110,852,920 (GRCm39) |
missense |
unknown |
|
R1905:Ep400
|
UTSW |
5 |
110,818,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Ep400
|
UTSW |
5 |
110,851,441 (GRCm39) |
missense |
unknown |
|
R2064:Ep400
|
UTSW |
5 |
110,883,270 (GRCm39) |
unclassified |
probably benign |
|
R2122:Ep400
|
UTSW |
5 |
110,856,716 (GRCm39) |
unclassified |
probably benign |
|
R2144:Ep400
|
UTSW |
5 |
110,851,384 (GRCm39) |
missense |
unknown |
|
R2215:Ep400
|
UTSW |
5 |
110,841,421 (GRCm39) |
unclassified |
probably benign |
|
R2252:Ep400
|
UTSW |
5 |
110,866,957 (GRCm39) |
missense |
unknown |
|
R2253:Ep400
|
UTSW |
5 |
110,866,957 (GRCm39) |
missense |
unknown |
|
R2483:Ep400
|
UTSW |
5 |
110,867,102 (GRCm39) |
missense |
unknown |
|
R2504:Ep400
|
UTSW |
5 |
110,816,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R2512:Ep400
|
UTSW |
5 |
110,856,781 (GRCm39) |
unclassified |
probably benign |
|
R2842:Ep400
|
UTSW |
5 |
110,846,681 (GRCm39) |
nonsense |
probably null |
|
R2920:Ep400
|
UTSW |
5 |
110,903,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R3082:Ep400
|
UTSW |
5 |
110,841,096 (GRCm39) |
unclassified |
probably benign |
|
R3151:Ep400
|
UTSW |
5 |
110,851,435 (GRCm39) |
missense |
unknown |
|
R3552:Ep400
|
UTSW |
5 |
110,877,153 (GRCm39) |
missense |
unknown |
|
R3779:Ep400
|
UTSW |
5 |
110,839,515 (GRCm39) |
missense |
unknown |
|
R3923:Ep400
|
UTSW |
5 |
110,904,389 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4062:Ep400
|
UTSW |
5 |
110,889,847 (GRCm39) |
missense |
probably benign |
0.10 |
R4508:Ep400
|
UTSW |
5 |
110,851,481 (GRCm39) |
missense |
unknown |
|
R4584:Ep400
|
UTSW |
5 |
110,881,763 (GRCm39) |
unclassified |
probably benign |
|
R4585:Ep400
|
UTSW |
5 |
110,901,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R4586:Ep400
|
UTSW |
5 |
110,901,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R4807:Ep400
|
UTSW |
5 |
110,843,444 (GRCm39) |
splice site |
probably null |
|
R4921:Ep400
|
UTSW |
5 |
110,813,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R4976:Ep400
|
UTSW |
5 |
110,868,622 (GRCm39) |
missense |
unknown |
|
R4976:Ep400
|
UTSW |
5 |
110,846,678 (GRCm39) |
missense |
unknown |
|
R5075:Ep400
|
UTSW |
5 |
110,833,351 (GRCm39) |
missense |
unknown |
|
R5120:Ep400
|
UTSW |
5 |
110,904,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R5122:Ep400
|
UTSW |
5 |
110,816,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R5223:Ep400
|
UTSW |
5 |
110,816,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R5284:Ep400
|
UTSW |
5 |
110,815,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R5388:Ep400
|
UTSW |
5 |
110,849,594 (GRCm39) |
missense |
unknown |
|
R5401:Ep400
|
UTSW |
5 |
110,831,037 (GRCm39) |
missense |
unknown |
|
R5431:Ep400
|
UTSW |
5 |
110,824,420 (GRCm39) |
missense |
unknown |
|
R5461:Ep400
|
UTSW |
5 |
110,824,550 (GRCm39) |
nonsense |
probably null |
|
R5568:Ep400
|
UTSW |
5 |
110,904,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R5650:Ep400
|
UTSW |
5 |
110,843,818 (GRCm39) |
critical splice donor site |
probably null |
|
R5778:Ep400
|
UTSW |
5 |
110,867,450 (GRCm39) |
missense |
unknown |
|
R5806:Ep400
|
UTSW |
5 |
110,903,420 (GRCm39) |
nonsense |
probably null |
|
R5814:Ep400
|
UTSW |
5 |
110,843,444 (GRCm39) |
splice site |
probably null |
|
R5830:Ep400
|
UTSW |
5 |
110,831,862 (GRCm39) |
missense |
unknown |
|
R5882:Ep400
|
UTSW |
5 |
110,903,453 (GRCm39) |
missense |
probably benign |
0.00 |
R5931:Ep400
|
UTSW |
5 |
110,883,386 (GRCm39) |
unclassified |
probably benign |
|
R5945:Ep400
|
UTSW |
5 |
110,830,732 (GRCm39) |
missense |
unknown |
|
R5966:Ep400
|
UTSW |
5 |
110,824,766 (GRCm39) |
missense |
unknown |
|
R5973:Ep400
|
UTSW |
5 |
110,877,697 (GRCm39) |
missense |
unknown |
|
R5980:Ep400
|
UTSW |
5 |
110,881,595 (GRCm39) |
unclassified |
probably benign |
|
R6000:Ep400
|
UTSW |
5 |
110,831,067 (GRCm39) |
missense |
unknown |
|
R6006:Ep400
|
UTSW |
5 |
110,852,825 (GRCm39) |
missense |
unknown |
|
R6053:Ep400
|
UTSW |
5 |
110,903,661 (GRCm39) |
missense |
probably benign |
0.22 |
R6145:Ep400
|
UTSW |
5 |
110,904,569 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6154:Ep400
|
UTSW |
5 |
110,903,799 (GRCm39) |
missense |
probably damaging |
0.97 |
R6169:Ep400
|
UTSW |
5 |
110,889,863 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6228:Ep400
|
UTSW |
5 |
110,818,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R6295:Ep400
|
UTSW |
5 |
110,901,675 (GRCm39) |
missense |
probably benign |
0.00 |
R6486:Ep400
|
UTSW |
5 |
110,845,084 (GRCm39) |
unclassified |
probably benign |
|
R6504:Ep400
|
UTSW |
5 |
110,856,703 (GRCm39) |
unclassified |
probably benign |
|
R6607:Ep400
|
UTSW |
5 |
110,831,180 (GRCm39) |
missense |
unknown |
|
R6657:Ep400
|
UTSW |
5 |
110,841,411 (GRCm39) |
unclassified |
probably benign |
|
R6660:Ep400
|
UTSW |
5 |
110,867,313 (GRCm39) |
nonsense |
probably null |
|
R6741:Ep400
|
UTSW |
5 |
110,824,761 (GRCm39) |
missense |
unknown |
|
R6933:Ep400
|
UTSW |
5 |
110,813,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R6937:Ep400
|
UTSW |
5 |
110,859,018 (GRCm39) |
unclassified |
probably benign |
|
R7069:Ep400
|
UTSW |
5 |
110,815,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R7103:Ep400
|
UTSW |
5 |
110,881,651 (GRCm39) |
missense |
unknown |
|
R7156:Ep400
|
UTSW |
5 |
110,833,229 (GRCm39) |
missense |
unknown |
|
R7272:Ep400
|
UTSW |
5 |
110,903,511 (GRCm39) |
nonsense |
probably null |
|
R7365:Ep400
|
UTSW |
5 |
110,867,480 (GRCm39) |
missense |
unknown |
|
R7581:Ep400
|
UTSW |
5 |
110,903,891 (GRCm39) |
missense |
unknown |
|
R7684:Ep400
|
UTSW |
5 |
110,845,218 (GRCm39) |
missense |
unknown |
|
R7699:Ep400
|
UTSW |
5 |
110,843,898 (GRCm39) |
missense |
unknown |
|
R7700:Ep400
|
UTSW |
5 |
110,843,898 (GRCm39) |
missense |
unknown |
|
R7856:Ep400
|
UTSW |
5 |
110,814,450 (GRCm39) |
missense |
probably damaging |
0.99 |
R7954:Ep400
|
UTSW |
5 |
110,816,599 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8098:Ep400
|
UTSW |
5 |
110,841,117 (GRCm39) |
missense |
unknown |
|
R8108:Ep400
|
UTSW |
5 |
110,835,749 (GRCm39) |
missense |
unknown |
|
R8260:Ep400
|
UTSW |
5 |
110,903,478 (GRCm39) |
nonsense |
probably null |
|
R8293:Ep400
|
UTSW |
5 |
110,856,758 (GRCm39) |
missense |
unknown |
|
R8314:Ep400
|
UTSW |
5 |
110,903,619 (GRCm39) |
missense |
unknown |
|
R8351:Ep400
|
UTSW |
5 |
110,887,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R8424:Ep400
|
UTSW |
5 |
110,841,144 (GRCm39) |
missense |
unknown |
|
R8459:Ep400
|
UTSW |
5 |
110,856,757 (GRCm39) |
missense |
unknown |
|
R8529:Ep400
|
UTSW |
5 |
110,867,102 (GRCm39) |
missense |
unknown |
|
R8688:Ep400
|
UTSW |
5 |
110,868,685 (GRCm39) |
missense |
unknown |
|
R8744:Ep400
|
UTSW |
5 |
110,889,925 (GRCm39) |
missense |
unknown |
|
R8923:Ep400
|
UTSW |
5 |
110,831,864 (GRCm39) |
missense |
unknown |
|
R9005:Ep400
|
UTSW |
5 |
110,858,959 (GRCm39) |
missense |
unknown |
|
R9087:Ep400
|
UTSW |
5 |
110,815,430 (GRCm39) |
nonsense |
probably null |
|
R9146:Ep400
|
UTSW |
5 |
110,849,635 (GRCm39) |
nonsense |
probably null |
|
R9383:Ep400
|
UTSW |
5 |
110,833,351 (GRCm39) |
missense |
unknown |
|
R9479:Ep400
|
UTSW |
5 |
110,877,730 (GRCm39) |
missense |
unknown |
|
R9496:Ep400
|
UTSW |
5 |
110,855,853 (GRCm39) |
missense |
unknown |
|
R9582:Ep400
|
UTSW |
5 |
110,824,315 (GRCm39) |
critical splice donor site |
probably null |
|
R9607:Ep400
|
UTSW |
5 |
110,831,805 (GRCm39) |
missense |
unknown |
|
R9712:Ep400
|
UTSW |
5 |
110,904,509 (GRCm39) |
missense |
unknown |
|
R9746:Ep400
|
UTSW |
5 |
110,889,872 (GRCm39) |
missense |
unknown |
|
X0012:Ep400
|
UTSW |
5 |
110,821,062 (GRCm39) |
small deletion |
probably benign |
|
X0021:Ep400
|
UTSW |
5 |
110,830,730 (GRCm39) |
missense |
unknown |
|
Z1176:Ep400
|
UTSW |
5 |
110,904,501 (GRCm39) |
missense |
unknown |
|
Z1177:Ep400
|
UTSW |
5 |
110,881,609 (GRCm39) |
missense |
unknown |
|
Z1177:Ep400
|
UTSW |
5 |
110,831,230 (GRCm39) |
missense |
unknown |
|
Z1188:Ep400
|
UTSW |
5 |
110,903,549 (GRCm39) |
missense |
unknown |
|
|