Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts7 |
G |
A |
9: 90,060,331 (GRCm39) |
|
probably null |
Het |
Adora2a |
T |
A |
10: 75,169,238 (GRCm39) |
V234E |
probably damaging |
Het |
Alpk1 |
T |
C |
3: 127,479,965 (GRCm39) |
D188G |
probably damaging |
Het |
Ankdd1a |
C |
T |
9: 65,415,343 (GRCm39) |
A227T |
possibly damaging |
Het |
Ankrd17 |
A |
G |
5: 90,392,013 (GRCm39) |
F1886L |
probably benign |
Het |
Anks1 |
T |
G |
17: 28,269,613 (GRCm39) |
L769R |
probably damaging |
Het |
Apol10a |
A |
G |
15: 77,373,161 (GRCm39) |
I266V |
probably benign |
Het |
Arhgef28 |
T |
C |
13: 98,121,896 (GRCm39) |
Y556C |
probably damaging |
Het |
Brd8 |
T |
A |
18: 34,744,304 (GRCm39) |
T175S |
probably damaging |
Het |
Camsap2 |
C |
T |
1: 136,208,937 (GRCm39) |
V852I |
probably benign |
Het |
Cd55b |
G |
T |
1: 130,341,803 (GRCm39) |
P278Q |
probably damaging |
Het |
Cep290 |
T |
A |
10: 100,367,028 (GRCm39) |
S1126R |
possibly damaging |
Het |
Cfh |
C |
T |
1: 140,030,155 (GRCm39) |
C906Y |
probably damaging |
Het |
Chst13 |
C |
A |
6: 90,286,260 (GRCm39) |
R234L |
probably damaging |
Het |
Clcn7 |
T |
C |
17: 25,376,502 (GRCm39) |
F611L |
probably benign |
Het |
Cntnap1 |
A |
G |
11: 101,075,441 (GRCm39) |
D873G |
probably damaging |
Het |
Cntnap5b |
T |
C |
1: 100,091,871 (GRCm39) |
I518T |
probably damaging |
Het |
Col28a1 |
T |
C |
6: 8,014,969 (GRCm39) |
E812G |
probably damaging |
Het |
Cpa1 |
T |
C |
6: 30,640,953 (GRCm39) |
I148T |
probably damaging |
Het |
Cyp11a1 |
A |
G |
9: 57,932,383 (GRCm39) |
N232S |
probably benign |
Het |
Dhrs13 |
A |
G |
11: 77,923,519 (GRCm39) |
D79G |
probably damaging |
Het |
Disp1 |
T |
C |
1: 182,868,712 (GRCm39) |
E1236G |
possibly damaging |
Het |
Dnah1 |
A |
C |
14: 31,026,544 (GRCm39) |
L778R |
probably damaging |
Het |
Dnah14 |
CTGTG |
CTG |
1: 181,412,589 (GRCm39) |
|
probably null |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Dock9 |
A |
T |
14: 121,799,492 (GRCm39) |
I1729N |
probably damaging |
Het |
Dysf |
T |
C |
6: 84,114,248 (GRCm39) |
V1192A |
possibly damaging |
Het |
Enpp2 |
A |
G |
15: 54,762,742 (GRCm39) |
S169P |
probably damaging |
Het |
Fam114a2 |
T |
G |
11: 57,404,972 (GRCm39) |
R43S |
probably damaging |
Het |
Fam13a |
T |
C |
6: 58,917,239 (GRCm39) |
T546A |
probably benign |
Het |
Fos |
A |
T |
12: 85,522,460 (GRCm39) |
D163V |
probably damaging |
Het |
Fras1 |
T |
C |
5: 96,912,805 (GRCm39) |
Y3370H |
probably damaging |
Het |
Fshr |
T |
C |
17: 89,507,961 (GRCm39) |
N27S |
probably null |
Het |
Galnt6 |
A |
G |
15: 100,591,305 (GRCm39) |
S600P |
possibly damaging |
Het |
Gars1 |
T |
A |
6: 55,032,809 (GRCm39) |
N260K |
probably damaging |
Het |
Gpr158 |
C |
G |
2: 21,820,422 (GRCm39) |
P640A |
possibly damaging |
Het |
Grep1 |
T |
C |
17: 23,925,124 (GRCm39) |
N495S |
possibly damaging |
Het |
Grik3 |
A |
G |
4: 125,526,205 (GRCm39) |
D146G |
probably benign |
Het |
Hdac4 |
T |
C |
1: 91,923,896 (GRCm39) |
T205A |
probably benign |
Het |
Kcnq3 |
T |
C |
15: 65,876,643 (GRCm39) |
D500G |
probably benign |
Het |
Kmt5c |
A |
G |
7: 4,749,480 (GRCm39) |
K333E |
probably benign |
Het |
Krt81 |
A |
G |
15: 101,357,404 (GRCm39) |
S443P |
probably benign |
Het |
M6pr |
T |
C |
6: 122,292,121 (GRCm39) |
|
probably null |
Het |
Mccc2 |
T |
A |
13: 100,130,085 (GRCm39) |
I91L |
probably benign |
Het |
Nip7 |
A |
G |
8: 107,785,055 (GRCm39) |
D110G |
probably damaging |
Het |
Nol8 |
T |
A |
13: 49,829,829 (GRCm39) |
F1093I |
probably damaging |
Het |
Nrxn1 |
T |
C |
17: 90,872,874 (GRCm39) |
T1027A |
possibly damaging |
Het |
Ofcc1 |
T |
A |
13: 40,302,052 (GRCm39) |
M495L |
probably benign |
Het |
Or13p10 |
A |
T |
4: 118,523,490 (GRCm39) |
M259L |
probably benign |
Het |
Or7e178 |
A |
G |
9: 20,225,742 (GRCm39) |
M158T |
probably benign |
Het |
Pafah1b2 |
A |
T |
9: 45,886,425 (GRCm39) |
V81D |
probably damaging |
Het |
Pcdhga4 |
A |
T |
18: 37,818,966 (GRCm39) |
S172C |
probably damaging |
Het |
Pds5a |
A |
G |
5: 65,813,639 (GRCm39) |
V282A |
probably damaging |
Het |
Plat |
A |
G |
8: 23,262,282 (GRCm39) |
D102G |
possibly damaging |
Het |
Plce1 |
C |
A |
19: 38,757,909 (GRCm39) |
Q1961K |
probably damaging |
Het |
Plppr3 |
T |
A |
10: 79,697,566 (GRCm39) |
K444* |
probably null |
Het |
Plscr3 |
A |
G |
11: 69,738,472 (GRCm39) |
|
probably null |
Het |
Prtg |
A |
T |
9: 72,813,468 (GRCm39) |
T943S |
probably benign |
Het |
Racgap1 |
A |
G |
15: 99,521,834 (GRCm39) |
F519L |
probably benign |
Het |
Rbms2 |
A |
T |
10: 127,987,050 (GRCm39) |
|
probably null |
Het |
Rfx7 |
A |
G |
9: 72,524,237 (GRCm39) |
T476A |
possibly damaging |
Het |
Rnf150 |
T |
A |
8: 83,810,131 (GRCm39) |
L421Q |
possibly damaging |
Het |
Sema3b |
A |
G |
9: 107,478,119 (GRCm39) |
L422P |
possibly damaging |
Het |
Shank2 |
G |
A |
7: 143,963,417 (GRCm39) |
A921T |
probably benign |
Het |
Skint3 |
A |
T |
4: 112,113,072 (GRCm39) |
E227D |
probably damaging |
Het |
Slc25a19 |
G |
A |
11: 115,508,386 (GRCm39) |
R201C |
possibly damaging |
Het |
Slc38a10 |
G |
T |
11: 120,038,645 (GRCm39) |
A40D |
probably damaging |
Het |
Slc5a4b |
T |
C |
10: 75,917,185 (GRCm39) |
T284A |
probably benign |
Het |
Smc1b |
A |
T |
15: 85,011,824 (GRCm39) |
F154I |
probably benign |
Het |
Spry2 |
A |
T |
14: 106,130,418 (GRCm39) |
M256K |
possibly damaging |
Het |
Stkld1 |
C |
T |
2: 26,833,899 (GRCm39) |
P129S |
probably damaging |
Het |
Syce2 |
T |
C |
8: 85,599,371 (GRCm39) |
L13S |
possibly damaging |
Het |
Tbc1d15 |
C |
A |
10: 115,069,148 (GRCm39) |
V74L |
possibly damaging |
Het |
Tecpr2 |
T |
A |
12: 110,911,185 (GRCm39) |
V1074D |
probably damaging |
Het |
Tex36 |
G |
A |
7: 133,197,054 (GRCm39) |
T21I |
probably benign |
Het |
Ttn |
T |
G |
2: 76,554,454 (GRCm39) |
D30787A |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,622,264 (GRCm39) |
Q13710L |
probably benign |
Het |
Vat1l |
C |
T |
8: 115,098,391 (GRCm39) |
A387V |
probably damaging |
Het |
Vil1 |
G |
A |
1: 74,460,470 (GRCm39) |
G209D |
possibly damaging |
Het |
Vmn1r113 |
G |
T |
7: 20,521,792 (GRCm39) |
D195Y |
probably damaging |
Het |
Vmn2r69 |
A |
C |
7: 85,064,799 (GRCm39) |
I29R |
probably benign |
Het |
Vti1b |
G |
A |
12: 79,207,323 (GRCm39) |
Q76* |
probably null |
Het |
Zfp423 |
C |
A |
8: 88,508,662 (GRCm39) |
V540F |
possibly damaging |
Het |
Zfp644 |
T |
C |
5: 106,785,990 (GRCm39) |
N186D |
probably damaging |
Het |
Zfp647 |
G |
A |
15: 76,796,285 (GRCm39) |
P125L |
probably damaging |
Het |
Zfp787 |
G |
A |
7: 6,135,360 (GRCm39) |
A297V |
probably damaging |
Het |
Zfp827 |
G |
T |
8: 79,787,324 (GRCm39) |
Q163H |
probably damaging |
Het |
Zfp955b |
T |
A |
17: 33,522,160 (GRCm39) |
V543E |
probably benign |
Het |
|
Other mutations in Usp34 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00477:Usp34
|
APN |
11 |
23,418,879 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01307:Usp34
|
APN |
11 |
23,367,676 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01313:Usp34
|
APN |
11 |
23,423,206 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01794:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01826:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01827:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01830:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01867:Usp34
|
APN |
11 |
23,334,411 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01939:Usp34
|
APN |
11 |
23,295,141 (GRCm39) |
splice site |
probably benign |
|
IGL01977:Usp34
|
APN |
11 |
23,402,661 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01985:Usp34
|
APN |
11 |
23,402,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02011:Usp34
|
APN |
11 |
23,421,554 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02302:Usp34
|
APN |
11 |
23,417,243 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02423:Usp34
|
APN |
11 |
23,304,900 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02491:Usp34
|
APN |
11 |
23,382,630 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02532:Usp34
|
APN |
11 |
23,320,291 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02561:Usp34
|
APN |
11 |
23,301,652 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02706:Usp34
|
APN |
11 |
23,338,659 (GRCm39) |
splice site |
probably benign |
|
IGL02891:Usp34
|
APN |
11 |
23,437,166 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03079:Usp34
|
APN |
11 |
23,382,247 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL03089:Usp34
|
APN |
11 |
23,396,958 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03175:Usp34
|
APN |
11 |
23,438,686 (GRCm39) |
missense |
probably benign |
|
IGL03256:Usp34
|
APN |
11 |
23,370,090 (GRCm39) |
nonsense |
probably null |
|
IGL03280:Usp34
|
APN |
11 |
23,304,897 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03289:Usp34
|
APN |
11 |
23,343,818 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03408:Usp34
|
APN |
11 |
23,396,957 (GRCm39) |
missense |
possibly damaging |
0.92 |
Chub
|
UTSW |
11 |
23,414,686 (GRCm39) |
missense |
probably damaging |
0.99 |
Cicione
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5571_Usp34_680
|
UTSW |
11 |
23,407,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R5713_Usp34_003
|
UTSW |
11 |
23,293,515 (GRCm39) |
missense |
possibly damaging |
0.94 |
Roebuck
|
UTSW |
11 |
23,436,810 (GRCm39) |
splice site |
probably benign |
|
stoat
|
UTSW |
11 |
23,437,203 (GRCm39) |
missense |
|
|
tunnelvision
|
UTSW |
11 |
23,396,968 (GRCm39) |
missense |
|
|
I2288:Usp34
|
UTSW |
11 |
23,382,473 (GRCm39) |
splice site |
probably benign |
|
R0047:Usp34
|
UTSW |
11 |
23,414,403 (GRCm39) |
missense |
probably benign |
0.34 |
R0047:Usp34
|
UTSW |
11 |
23,414,403 (GRCm39) |
missense |
probably benign |
0.34 |
R0099:Usp34
|
UTSW |
11 |
23,313,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Usp34
|
UTSW |
11 |
23,383,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R0240:Usp34
|
UTSW |
11 |
23,383,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R0403:Usp34
|
UTSW |
11 |
23,283,838 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0432:Usp34
|
UTSW |
11 |
23,351,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R0446:Usp34
|
UTSW |
11 |
23,417,207 (GRCm39) |
missense |
probably damaging |
0.97 |
R0455:Usp34
|
UTSW |
11 |
23,396,741 (GRCm39) |
splice site |
probably benign |
|
R0470:Usp34
|
UTSW |
11 |
23,386,001 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0472:Usp34
|
UTSW |
11 |
23,334,509 (GRCm39) |
splice site |
probably benign |
|
R0512:Usp34
|
UTSW |
11 |
23,401,997 (GRCm39) |
missense |
probably benign |
0.04 |
R0557:Usp34
|
UTSW |
11 |
23,353,848 (GRCm39) |
missense |
probably damaging |
0.98 |
R0562:Usp34
|
UTSW |
11 |
23,382,406 (GRCm39) |
splice site |
probably benign |
|
R0656:Usp34
|
UTSW |
11 |
23,422,967 (GRCm39) |
missense |
probably damaging |
0.99 |
R0693:Usp34
|
UTSW |
11 |
23,402,637 (GRCm39) |
missense |
probably damaging |
0.97 |
R0739:Usp34
|
UTSW |
11 |
23,417,243 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1061:Usp34
|
UTSW |
11 |
23,334,420 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1078:Usp34
|
UTSW |
11 |
23,383,175 (GRCm39) |
splice site |
probably benign |
|
R1223:Usp34
|
UTSW |
11 |
23,396,464 (GRCm39) |
splice site |
probably null |
|
R1295:Usp34
|
UTSW |
11 |
23,334,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R1430:Usp34
|
UTSW |
11 |
23,409,151 (GRCm39) |
missense |
probably damaging |
0.97 |
R1445:Usp34
|
UTSW |
11 |
23,301,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R1468:Usp34
|
UTSW |
11 |
23,391,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Usp34
|
UTSW |
11 |
23,391,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Usp34
|
UTSW |
11 |
23,438,862 (GRCm39) |
missense |
probably benign |
0.20 |
R1475:Usp34
|
UTSW |
11 |
23,423,253 (GRCm39) |
missense |
probably damaging |
0.99 |
R1628:Usp34
|
UTSW |
11 |
23,438,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R1631:Usp34
|
UTSW |
11 |
23,410,651 (GRCm39) |
missense |
probably damaging |
0.99 |
R1655:Usp34
|
UTSW |
11 |
23,325,051 (GRCm39) |
missense |
probably benign |
0.05 |
R1741:Usp34
|
UTSW |
11 |
23,314,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1854:Usp34
|
UTSW |
11 |
23,376,153 (GRCm39) |
missense |
probably benign |
0.24 |
R1867:Usp34
|
UTSW |
11 |
23,311,593 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1869:Usp34
|
UTSW |
11 |
23,314,479 (GRCm39) |
missense |
probably benign |
0.37 |
R1870:Usp34
|
UTSW |
11 |
23,314,479 (GRCm39) |
missense |
probably benign |
0.37 |
R1871:Usp34
|
UTSW |
11 |
23,314,479 (GRCm39) |
missense |
probably benign |
0.37 |
R1967:Usp34
|
UTSW |
11 |
23,314,503 (GRCm39) |
missense |
probably benign |
0.01 |
R2051:Usp34
|
UTSW |
11 |
23,414,468 (GRCm39) |
missense |
probably damaging |
0.97 |
R2132:Usp34
|
UTSW |
11 |
23,414,556 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2156:Usp34
|
UTSW |
11 |
23,332,602 (GRCm39) |
missense |
probably damaging |
0.98 |
R2205:Usp34
|
UTSW |
11 |
23,335,147 (GRCm39) |
missense |
probably damaging |
0.97 |
R2342:Usp34
|
UTSW |
11 |
23,353,599 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3431:Usp34
|
UTSW |
11 |
23,320,466 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3812:Usp34
|
UTSW |
11 |
23,414,517 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3872:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3873:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3874:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3875:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3925:Usp34
|
UTSW |
11 |
23,293,640 (GRCm39) |
missense |
probably benign |
0.28 |
R3972:Usp34
|
UTSW |
11 |
23,407,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R4018:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4042:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4155:Usp34
|
UTSW |
11 |
23,367,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R4197:Usp34
|
UTSW |
11 |
23,394,189 (GRCm39) |
missense |
probably damaging |
0.98 |
R4352:Usp34
|
UTSW |
11 |
23,270,727 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4379:Usp34
|
UTSW |
11 |
23,334,499 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4444:Usp34
|
UTSW |
11 |
23,385,998 (GRCm39) |
missense |
probably damaging |
0.98 |
R4475:Usp34
|
UTSW |
11 |
23,407,975 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4501:Usp34
|
UTSW |
11 |
23,351,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R4527:Usp34
|
UTSW |
11 |
23,371,257 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4603:Usp34
|
UTSW |
11 |
23,414,633 (GRCm39) |
missense |
probably damaging |
0.97 |
R4612:Usp34
|
UTSW |
11 |
23,382,268 (GRCm39) |
missense |
probably damaging |
0.99 |
R4673:Usp34
|
UTSW |
11 |
23,314,480 (GRCm39) |
small deletion |
probably benign |
|
R4707:Usp34
|
UTSW |
11 |
23,437,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R4736:Usp34
|
UTSW |
11 |
23,343,749 (GRCm39) |
splice site |
probably null |
|
R4867:Usp34
|
UTSW |
11 |
23,401,999 (GRCm39) |
missense |
probably benign |
0.28 |
R4879:Usp34
|
UTSW |
11 |
23,323,410 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4977:Usp34
|
UTSW |
11 |
23,438,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Usp34
|
UTSW |
11 |
23,414,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Usp34
|
UTSW |
11 |
23,408,086 (GRCm39) |
intron |
probably benign |
|
R5068:Usp34
|
UTSW |
11 |
23,410,665 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5304:Usp34
|
UTSW |
11 |
23,293,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R5320:Usp34
|
UTSW |
11 |
23,283,739 (GRCm39) |
missense |
probably benign |
|
R5327:Usp34
|
UTSW |
11 |
23,418,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Usp34
|
UTSW |
11 |
23,438,659 (GRCm39) |
missense |
probably benign |
0.04 |
R5328:Usp34
|
UTSW |
11 |
23,414,616 (GRCm39) |
missense |
probably benign |
0.01 |
R5390:Usp34
|
UTSW |
11 |
23,394,202 (GRCm39) |
critical splice donor site |
probably null |
|
R5434:Usp34
|
UTSW |
11 |
23,362,271 (GRCm39) |
missense |
probably damaging |
0.99 |
R5523:Usp34
|
UTSW |
11 |
23,299,198 (GRCm39) |
missense |
probably benign |
0.39 |
R5567:Usp34
|
UTSW |
11 |
23,438,336 (GRCm39) |
missense |
probably damaging |
0.97 |
R5571:Usp34
|
UTSW |
11 |
23,407,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R5645:Usp34
|
UTSW |
11 |
23,325,024 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5713:Usp34
|
UTSW |
11 |
23,293,515 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5719:Usp34
|
UTSW |
11 |
23,304,846 (GRCm39) |
missense |
probably benign |
0.00 |
R5813:Usp34
|
UTSW |
11 |
23,371,340 (GRCm39) |
missense |
probably benign |
0.38 |
R5921:Usp34
|
UTSW |
11 |
23,414,686 (GRCm39) |
missense |
probably damaging |
0.99 |
R5928:Usp34
|
UTSW |
11 |
23,386,040 (GRCm39) |
missense |
probably damaging |
0.98 |
R5944:Usp34
|
UTSW |
11 |
23,313,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R6198:Usp34
|
UTSW |
11 |
23,434,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R6229:Usp34
|
UTSW |
11 |
23,396,778 (GRCm39) |
missense |
probably damaging |
0.99 |
R6320:Usp34
|
UTSW |
11 |
23,402,520 (GRCm39) |
missense |
probably damaging |
0.98 |
R6341:Usp34
|
UTSW |
11 |
23,331,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R6374:Usp34
|
UTSW |
11 |
23,388,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R6398:Usp34
|
UTSW |
11 |
23,438,666 (GRCm39) |
missense |
probably benign |
|
R6438:Usp34
|
UTSW |
11 |
23,314,266 (GRCm39) |
missense |
probably benign |
0.02 |
R6668:Usp34
|
UTSW |
11 |
23,410,659 (GRCm39) |
missense |
probably damaging |
0.97 |
R6700:Usp34
|
UTSW |
11 |
23,389,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R6783:Usp34
|
UTSW |
11 |
23,362,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R6821:Usp34
|
UTSW |
11 |
23,317,491 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6855:Usp34
|
UTSW |
11 |
23,402,569 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6916:Usp34
|
UTSW |
11 |
23,408,023 (GRCm39) |
missense |
probably damaging |
0.98 |
R7020:Usp34
|
UTSW |
11 |
23,343,954 (GRCm39) |
missense |
probably benign |
0.05 |
R7026:Usp34
|
UTSW |
11 |
23,311,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R7085:Usp34
|
UTSW |
11 |
23,313,097 (GRCm39) |
missense |
|
|
R7101:Usp34
|
UTSW |
11 |
23,376,183 (GRCm39) |
missense |
|
|
R7168:Usp34
|
UTSW |
11 |
23,414,585 (GRCm39) |
missense |
|
|
R7192:Usp34
|
UTSW |
11 |
23,410,571 (GRCm39) |
missense |
|
|
R7264:Usp34
|
UTSW |
11 |
23,283,566 (GRCm39) |
missense |
probably benign |
0.00 |
R7325:Usp34
|
UTSW |
11 |
23,369,052 (GRCm39) |
missense |
|
|
R7343:Usp34
|
UTSW |
11 |
23,438,868 (GRCm39) |
missense |
|
|
R7358:Usp34
|
UTSW |
11 |
23,311,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R7369:Usp34
|
UTSW |
11 |
23,382,361 (GRCm39) |
missense |
|
|
R7389:Usp34
|
UTSW |
11 |
23,295,200 (GRCm39) |
missense |
|
|
R7459:Usp34
|
UTSW |
11 |
23,314,458 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7517:Usp34
|
UTSW |
11 |
23,396,968 (GRCm39) |
missense |
|
|
R7729:Usp34
|
UTSW |
11 |
23,399,268 (GRCm39) |
missense |
|
|
R7777:Usp34
|
UTSW |
11 |
23,332,638 (GRCm39) |
missense |
|
|
R7810:Usp34
|
UTSW |
11 |
23,362,314 (GRCm39) |
missense |
|
|
R7836:Usp34
|
UTSW |
11 |
23,396,614 (GRCm39) |
missense |
|
|
R7862:Usp34
|
UTSW |
11 |
23,414,718 (GRCm39) |
missense |
|
|
R7993:Usp34
|
UTSW |
11 |
23,327,622 (GRCm39) |
missense |
|
|
R8050:Usp34
|
UTSW |
11 |
23,396,787 (GRCm39) |
missense |
|
|
R8054:Usp34
|
UTSW |
11 |
23,311,295 (GRCm39) |
missense |
|
|
R8239:Usp34
|
UTSW |
11 |
23,396,750 (GRCm39) |
missense |
|
|
R8266:Usp34
|
UTSW |
11 |
23,436,810 (GRCm39) |
splice site |
probably benign |
|
R8347:Usp34
|
UTSW |
11 |
23,362,345 (GRCm39) |
missense |
|
|
R8409:Usp34
|
UTSW |
11 |
23,407,811 (GRCm39) |
missense |
|
|
R8692:Usp34
|
UTSW |
11 |
23,379,325 (GRCm39) |
missense |
|
|
R8694:Usp34
|
UTSW |
11 |
23,434,161 (GRCm39) |
missense |
|
|
R8734:Usp34
|
UTSW |
11 |
23,394,184 (GRCm39) |
missense |
|
|
R8806:Usp34
|
UTSW |
11 |
23,434,143 (GRCm39) |
missense |
|
|
R8914:Usp34
|
UTSW |
11 |
23,293,604 (GRCm39) |
missense |
|
|
R8987:Usp34
|
UTSW |
11 |
23,414,267 (GRCm39) |
missense |
|
|
R9013:Usp34
|
UTSW |
11 |
23,320,302 (GRCm39) |
missense |
|
|
R9108:Usp34
|
UTSW |
11 |
23,320,528 (GRCm39) |
missense |
|
|
R9264:Usp34
|
UTSW |
11 |
23,439,064 (GRCm39) |
missense |
|
|
R9301:Usp34
|
UTSW |
11 |
23,422,951 (GRCm39) |
missense |
|
|
R9375:Usp34
|
UTSW |
11 |
23,437,203 (GRCm39) |
missense |
|
|
R9385:Usp34
|
UTSW |
11 |
23,399,223 (GRCm39) |
missense |
|
|
R9500:Usp34
|
UTSW |
11 |
23,331,337 (GRCm39) |
missense |
probably damaging |
0.99 |
R9566:Usp34
|
UTSW |
11 |
23,317,529 (GRCm39) |
missense |
|
|
R9629:Usp34
|
UTSW |
11 |
23,314,364 (GRCm39) |
missense |
|
|
R9679:Usp34
|
UTSW |
11 |
23,394,369 (GRCm39) |
missense |
|
|
R9680:Usp34
|
UTSW |
11 |
23,317,385 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9686:Usp34
|
UTSW |
11 |
23,424,351 (GRCm39) |
missense |
|
|
R9752:Usp34
|
UTSW |
11 |
23,409,182 (GRCm39) |
missense |
probably benign |
0.11 |
X0023:Usp34
|
UTSW |
11 |
23,325,028 (GRCm39) |
missense |
possibly damaging |
0.73 |
X0057:Usp34
|
UTSW |
11 |
23,407,824 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1176:Usp34
|
UTSW |
11 |
23,423,221 (GRCm39) |
missense |
probably damaging |
1.00 |
|