Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap9 |
T |
C |
5: 4,026,151 (GRCm39) |
S1269P |
probably benign |
Het |
Aqr |
T |
C |
2: 113,943,058 (GRCm39) |
T1172A |
probably benign |
Het |
Art2a |
A |
T |
7: 101,203,956 (GRCm39) |
L194* |
probably null |
Het |
Atrn |
T |
C |
2: 130,823,962 (GRCm39) |
F967S |
probably damaging |
Het |
Btnl1 |
A |
G |
17: 34,601,436 (GRCm39) |
D323G |
probably damaging |
Het |
Cadps |
C |
A |
14: 12,505,808 (GRCm38) |
C754F |
probably damaging |
Het |
Catspere2 |
A |
G |
1: 177,950,351 (GRCm39) |
D734G |
possibly damaging |
Het |
Ccdc7b |
A |
G |
8: 129,837,401 (GRCm39) |
T131A |
probably benign |
Het |
Cfap298 |
A |
T |
16: 90,724,314 (GRCm39) |
V136D |
probably damaging |
Het |
Cic |
A |
T |
7: 24,972,203 (GRCm39) |
I645L |
probably benign |
Het |
Clca3a1 |
C |
A |
3: 144,722,619 (GRCm39) |
C251F |
probably damaging |
Het |
Cldn16 |
A |
T |
16: 26,296,308 (GRCm39) |
T95S |
probably benign |
Het |
Cntnap4 |
C |
T |
8: 113,537,342 (GRCm39) |
H738Y |
probably benign |
Het |
Col8a2 |
A |
T |
4: 126,204,812 (GRCm39) |
|
probably benign |
Het |
Corin |
A |
T |
5: 72,487,042 (GRCm39) |
V706D |
probably damaging |
Het |
Cuzd1 |
G |
A |
7: 130,916,529 (GRCm39) |
P310L |
probably damaging |
Het |
Cyp4a12a |
T |
C |
4: 115,184,509 (GRCm39) |
F295L |
probably benign |
Het |
Cyp4a12b |
T |
G |
4: 115,289,703 (GRCm39) |
M190R |
probably damaging |
Het |
Dagla |
A |
G |
19: 10,248,373 (GRCm39) |
Y96H |
probably damaging |
Het |
Dapp1 |
T |
C |
3: 137,644,932 (GRCm39) |
Q148R |
probably benign |
Het |
Dcaf17 |
T |
A |
2: 70,918,924 (GRCm39) |
S499R |
probably benign |
Het |
Ddx27 |
T |
A |
2: 166,861,904 (GRCm39) |
D135E |
probably benign |
Het |
Defb3 |
A |
T |
8: 19,345,172 (GRCm39) |
I43F |
possibly damaging |
Het |
Dnajc10 |
T |
G |
2: 80,178,122 (GRCm39) |
F710V |
probably damaging |
Het |
Dnhd1 |
T |
C |
7: 105,327,256 (GRCm39) |
L735P |
probably damaging |
Het |
Dnmt1 |
G |
A |
9: 20,837,989 (GRCm39) |
P242S |
probably benign |
Het |
Dync1h1 |
G |
A |
12: 110,615,917 (GRCm39) |
D3022N |
probably benign |
Het |
Epc1 |
T |
C |
18: 6,449,138 (GRCm39) |
N453S |
possibly damaging |
Het |
Eral1 |
A |
T |
11: 77,969,130 (GRCm39) |
N123K |
probably damaging |
Het |
Ercc5 |
G |
A |
1: 44,198,017 (GRCm39) |
V145I |
probably benign |
Het |
Evc |
A |
G |
5: 37,481,057 (GRCm39) |
S263P |
probably damaging |
Het |
Fancc |
A |
T |
13: 63,495,378 (GRCm39) |
M182K |
probably benign |
Het |
Fbxl3 |
G |
T |
14: 103,320,526 (GRCm39) |
A355E |
probably damaging |
Het |
Fig4 |
A |
C |
10: 41,064,628 (GRCm39) |
S872A |
probably damaging |
Het |
Gm14393 |
C |
A |
2: 174,904,497 (GRCm39) |
|
probably benign |
Het |
Gm27013 |
A |
T |
6: 130,498,003 (GRCm39) |
|
noncoding transcript |
Het |
Gprc5a |
T |
A |
6: 135,060,450 (GRCm39) |
M313K |
probably benign |
Het |
H2ac15 |
T |
C |
13: 21,937,882 (GRCm39) |
N39S |
possibly damaging |
Het |
H2-T3 |
T |
C |
17: 36,500,236 (GRCm39) |
|
probably null |
Het |
Hap1 |
G |
A |
11: 100,245,550 (GRCm39) |
T138M |
probably benign |
Het |
Hook3 |
T |
G |
8: 26,522,039 (GRCm39) |
K679T |
probably damaging |
Het |
Ints2 |
G |
T |
11: 86,140,101 (GRCm39) |
R244S |
probably damaging |
Het |
Itgb4 |
T |
C |
11: 115,884,151 (GRCm39) |
V945A |
probably damaging |
Het |
Itih2 |
C |
T |
2: 10,115,211 (GRCm39) |
S387N |
probably benign |
Het |
Jmjd7 |
T |
A |
2: 119,862,649 (GRCm39) |
M306K |
probably benign |
Het |
Klra2 |
T |
A |
6: 131,207,120 (GRCm39) |
D163V |
probably benign |
Het |
Kmo |
T |
A |
1: 175,478,138 (GRCm39) |
M208K |
probably damaging |
Het |
Kmo |
G |
T |
1: 175,478,139 (GRCm39) |
M208I |
possibly damaging |
Het |
Masp2 |
A |
G |
4: 148,698,358 (GRCm39) |
T480A |
probably damaging |
Het |
Mogs |
G |
T |
6: 83,095,619 (GRCm39) |
R812L |
possibly damaging |
Het |
Mrpl43 |
A |
G |
19: 44,994,328 (GRCm39) |
I97T |
possibly damaging |
Het |
Myoz1 |
A |
G |
14: 20,700,663 (GRCm39) |
W185R |
probably damaging |
Het |
Ncam2 |
T |
A |
16: 81,262,457 (GRCm39) |
H303Q |
probably benign |
Het |
Ntaq1 |
A |
T |
15: 58,011,740 (GRCm39) |
I34F |
probably damaging |
Het |
Nufip2 |
T |
C |
11: 77,632,554 (GRCm39) |
V690A |
unknown |
Het |
Obox1 |
A |
T |
7: 15,290,152 (GRCm39) |
N165I |
possibly damaging |
Het |
Or1j1 |
C |
T |
2: 36,702,537 (GRCm39) |
C189Y |
probably damaging |
Het |
Or4b1d |
T |
A |
2: 89,968,558 (GRCm39) |
E308D |
probably benign |
Het |
Or4c113 |
T |
G |
2: 88,885,498 (GRCm39) |
I91L |
possibly damaging |
Het |
Or6c35 |
A |
G |
10: 129,169,142 (GRCm39) |
T131A |
probably benign |
Het |
Pex1 |
A |
G |
5: 3,683,885 (GRCm39) |
Y1127C |
probably damaging |
Het |
Pno1 |
T |
C |
11: 17,161,438 (GRCm39) |
K24E |
probably benign |
Het |
Qdpr |
T |
A |
5: 45,596,669 (GRCm39) |
N165I |
possibly damaging |
Het |
Robo2 |
A |
G |
16: 73,758,761 (GRCm39) |
V674A |
probably damaging |
Het |
Runx1t1 |
A |
T |
4: 13,889,864 (GRCm39) |
T598S |
unknown |
Het |
Samd11 |
A |
G |
4: 156,333,889 (GRCm39) |
L174P |
probably damaging |
Het |
Scn2a |
T |
A |
2: 65,573,395 (GRCm39) |
|
probably null |
Het |
Slc4a1 |
G |
T |
11: 102,252,245 (GRCm39) |
|
probably benign |
Het |
Snx25 |
A |
T |
8: 46,569,474 (GRCm39) |
|
probably benign |
Het |
Sox2 |
A |
G |
3: 34,705,193 (GRCm39) |
N210S |
probably benign |
Het |
Spag6 |
T |
C |
2: 18,736,958 (GRCm39) |
|
probably null |
Het |
Speer4b |
A |
T |
5: 27,703,036 (GRCm39) |
L154Q |
probably null |
Het |
Stt3a |
T |
A |
9: 36,653,089 (GRCm39) |
Q531L |
probably damaging |
Het |
Tcl1 |
A |
C |
12: 105,183,767 (GRCm39) |
|
probably benign |
Het |
Trip11 |
A |
T |
12: 101,849,600 (GRCm39) |
M1488K |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,798,747 (GRCm39) |
H509R |
probably benign |
Het |
Ulk3 |
C |
T |
9: 57,501,593 (GRCm39) |
L425F |
possibly damaging |
Het |
Vmn1r238 |
T |
A |
18: 3,123,294 (GRCm39) |
K40M |
probably damaging |
Het |
Vopp1 |
G |
A |
6: 57,731,533 (GRCm39) |
P153S |
probably damaging |
Het |
Zbtb42 |
C |
T |
12: 112,646,976 (GRCm39) |
R384W |
probably damaging |
Het |
Zfp14 |
G |
T |
7: 29,738,341 (GRCm39) |
Q215K |
probably damaging |
Het |
Zfp473 |
A |
T |
7: 44,382,376 (GRCm39) |
Y651* |
probably null |
Het |
Zfp735 |
G |
T |
11: 73,580,550 (GRCm39) |
E16D |
possibly damaging |
Het |
Zfp846 |
G |
T |
9: 20,504,809 (GRCm39) |
C223F |
probably damaging |
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 |
|
R3623:Ep400
|
UTSW |
5 |
110,867,102 (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 |
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 |
|
|