Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930486L24Rik |
C |
A |
13: 61,001,336 (GRCm39) |
K130N |
probably damaging |
Het |
Adam6a |
T |
A |
12: 113,508,013 (GRCm39) |
S129T |
probably damaging |
Het |
Adamts10 |
T |
A |
17: 33,772,112 (GRCm39) |
F1087I |
probably damaging |
Het |
Afp |
T |
A |
5: 90,651,541 (GRCm39) |
N385K |
possibly damaging |
Het |
Ahnak |
T |
G |
19: 8,990,296 (GRCm39) |
|
probably benign |
Het |
Akap6 |
A |
G |
12: 53,188,279 (GRCm39) |
T1898A |
probably benign |
Het |
Antxr2 |
C |
A |
5: 98,123,199 (GRCm39) |
V283F |
possibly damaging |
Het |
Asgr1 |
T |
C |
11: 69,946,919 (GRCm39) |
V55A |
possibly damaging |
Het |
Asxl3 |
A |
G |
18: 22,649,411 (GRCm39) |
K467E |
probably damaging |
Het |
Atp5f1a |
C |
A |
18: 77,868,969 (GRCm39) |
Q398K |
probably damaging |
Het |
Atxn2 |
T |
A |
5: 121,924,437 (GRCm39) |
D455E |
probably damaging |
Het |
B4galt6 |
C |
T |
18: 20,878,410 (GRCm39) |
A39T |
possibly damaging |
Het |
C130073F10Rik |
C |
T |
4: 101,747,535 (GRCm39) |
E165K |
probably benign |
Het |
Cabin1 |
A |
G |
10: 75,530,626 (GRCm39) |
C1519R |
probably damaging |
Het |
Casp8ap2 |
C |
T |
4: 32,639,386 (GRCm39) |
R147* |
probably null |
Het |
Ccdc88b |
A |
G |
19: 6,831,391 (GRCm39) |
L517P |
probably benign |
Het |
Cd109 |
G |
A |
9: 78,561,869 (GRCm39) |
V220I |
probably damaging |
Het |
Cd2ap |
T |
C |
17: 43,131,488 (GRCm39) |
K369R |
probably benign |
Het |
Cd300c |
A |
G |
11: 114,850,614 (GRCm39) |
V63A |
probably benign |
Het |
Cnot10 |
A |
G |
9: 114,420,619 (GRCm39) |
V741A |
probably benign |
Het |
Col18a1 |
G |
T |
10: 76,932,040 (GRCm39) |
Q350K |
unknown |
Het |
Crnkl1 |
T |
C |
2: 145,774,236 (GRCm39) |
K76E |
possibly damaging |
Het |
Cryzl2 |
A |
G |
1: 157,298,291 (GRCm39) |
K227E |
probably benign |
Het |
Cts6 |
G |
A |
13: 61,344,194 (GRCm39) |
T286I |
probably benign |
Het |
Cul1 |
T |
C |
6: 47,491,820 (GRCm39) |
V392A |
probably damaging |
Het |
Dcaf7 |
T |
A |
11: 105,937,573 (GRCm39) |
F65L |
probably benign |
Het |
Dgke |
A |
C |
11: 88,946,320 (GRCm39) |
V160G |
possibly damaging |
Het |
Dock8 |
C |
A |
19: 25,178,400 (GRCm39) |
Q2098K |
possibly damaging |
Het |
Efhb |
T |
A |
17: 53,706,140 (GRCm39) |
D799V |
possibly damaging |
Het |
Ephb2 |
T |
C |
4: 136,386,262 (GRCm39) |
D829G |
probably benign |
Het |
Exosc1 |
A |
T |
19: 41,913,157 (GRCm39) |
S117R |
probably damaging |
Het |
Fga |
T |
C |
3: 82,935,925 (GRCm39) |
S51P |
probably benign |
Het |
Fmn1 |
T |
C |
2: 113,523,439 (GRCm39) |
F1141L |
possibly damaging |
Het |
Foxm1 |
C |
T |
6: 128,350,837 (GRCm39) |
L713F |
probably damaging |
Het |
Galnt4 |
A |
G |
10: 98,944,536 (GRCm39) |
E87G |
probably benign |
Het |
Gamt |
T |
C |
10: 80,096,692 (GRCm39) |
D15G |
probably benign |
Het |
Gm15557 |
C |
A |
2: 155,784,174 (GRCm39) |
D154E |
possibly damaging |
Het |
Gnptab |
A |
G |
10: 88,281,625 (GRCm39) |
I1211V |
probably benign |
Het |
Greb1 |
A |
T |
12: 16,761,775 (GRCm39) |
M535K |
probably damaging |
Het |
Grm8 |
C |
A |
6: 27,363,308 (GRCm39) |
A736S |
possibly damaging |
Het |
Hspa14 |
T |
C |
2: 3,492,645 (GRCm39) |
I373M |
probably benign |
Het |
Ifi207 |
T |
A |
1: 173,557,629 (GRCm39) |
T370S |
unknown |
Het |
Igf1r |
A |
G |
7: 67,653,585 (GRCm39) |
N41S |
probably damaging |
Het |
Ikzf5 |
A |
T |
7: 130,993,496 (GRCm39) |
V224D |
probably damaging |
Het |
Il10 |
C |
A |
1: 130,949,110 (GRCm39) |
Y90* |
probably null |
Het |
Itga4 |
A |
G |
2: 79,117,376 (GRCm39) |
D394G |
probably benign |
Het |
Kif21a |
A |
T |
15: 90,840,622 (GRCm39) |
S1165T |
probably benign |
Het |
Krtap14 |
A |
G |
16: 88,622,515 (GRCm39) |
S155P |
probably damaging |
Het |
Loxl2 |
A |
G |
14: 69,930,546 (GRCm39) |
N770S |
probably benign |
Het |
Man2b1 |
A |
G |
8: 85,813,474 (GRCm39) |
D222G |
probably damaging |
Het |
Mcub |
T |
A |
3: 129,709,464 (GRCm39) |
Y283F |
probably damaging |
Het |
Meis3 |
T |
A |
7: 15,911,496 (GRCm39) |
Y64* |
probably null |
Het |
Mfsd6 |
T |
A |
1: 52,748,716 (GRCm39) |
I50F |
probably benign |
Het |
Micu2 |
T |
C |
14: 58,182,854 (GRCm39) |
T165A |
probably damaging |
Het |
Mtcl1 |
T |
C |
17: 66,686,143 (GRCm39) |
E921G |
probably damaging |
Het |
Muc5b |
A |
T |
7: 141,396,971 (GRCm39) |
N215Y |
unknown |
Het |
Muc6 |
A |
G |
7: 141,234,176 (GRCm39) |
F772L |
possibly damaging |
Het |
Myt1 |
A |
G |
2: 181,438,904 (GRCm39) |
D142G |
probably benign |
Het |
Nol6 |
C |
T |
4: 41,120,281 (GRCm39) |
V479I |
probably benign |
Het |
Nsun7 |
A |
G |
5: 66,441,572 (GRCm39) |
K414E |
probably benign |
Het |
Nup210l |
A |
C |
3: 90,077,869 (GRCm39) |
I914L |
probably benign |
Het |
Obox3 |
G |
A |
7: 15,360,875 (GRCm39) |
P88L |
probably benign |
Het |
Or10ag57 |
A |
G |
2: 87,218,862 (GRCm39) |
Y271C |
probably damaging |
Het |
Or4f4b |
T |
C |
2: 111,314,351 (GRCm39) |
L192P |
probably damaging |
Het |
Or8h8 |
C |
T |
2: 86,752,922 (GRCm39) |
|
probably null |
Het |
Or8w1 |
T |
C |
2: 87,466,014 (GRCm39) |
T26A |
probably benign |
Het |
Pclo |
T |
C |
5: 14,730,441 (GRCm39) |
|
probably benign |
Het |
Pcsk5 |
T |
C |
19: 17,545,688 (GRCm39) |
N745D |
probably damaging |
Het |
Pdzrn3 |
T |
A |
6: 101,128,473 (GRCm39) |
N731I |
possibly damaging |
Het |
Pkdrej |
T |
A |
15: 85,701,334 (GRCm39) |
Q1534L |
probably benign |
Het |
Pramel28 |
T |
C |
4: 143,691,523 (GRCm39) |
N400S |
probably benign |
Het |
Rell1 |
T |
A |
5: 64,093,428 (GRCm39) |
D109V |
probably damaging |
Het |
Rplp0 |
C |
T |
5: 115,701,403 (GRCm39) |
T285I |
probably damaging |
Het |
Sanbr |
A |
T |
11: 23,565,222 (GRCm39) |
M255K |
probably damaging |
Het |
Sema3g |
C |
T |
14: 30,950,002 (GRCm39) |
R728C |
probably damaging |
Het |
Slc15a2 |
A |
G |
16: 36,574,153 (GRCm39) |
Y536H |
probably damaging |
Het |
Slc26a5 |
T |
A |
5: 22,021,962 (GRCm39) |
Y488F |
probably benign |
Het |
Slc5a4a |
A |
T |
10: 76,022,362 (GRCm39) |
S566C |
probably damaging |
Het |
Spink7 |
C |
T |
18: 62,729,275 (GRCm39) |
E21K |
possibly damaging |
Het |
Src |
C |
T |
2: 157,299,107 (GRCm39) |
Q35* |
probably null |
Het |
Srrm2 |
T |
A |
17: 24,039,770 (GRCm39) |
V2234E |
probably damaging |
Het |
Stk36 |
A |
T |
1: 74,650,314 (GRCm39) |
Q282L |
probably benign |
Het |
Tas2r118 |
T |
G |
6: 23,969,170 (GRCm39) |
E297A |
probably damaging |
Het |
Terf1 |
A |
G |
1: 15,913,194 (GRCm39) |
Y385C |
probably damaging |
Het |
Tmc3 |
T |
C |
7: 83,247,498 (GRCm39) |
S198P |
probably damaging |
Het |
Tmprss11b |
C |
T |
5: 86,808,355 (GRCm39) |
R407H |
possibly damaging |
Het |
Tspyl4 |
G |
A |
10: 34,174,107 (GRCm39) |
E200K |
probably damaging |
Het |
Ttc21a |
T |
C |
9: 119,771,707 (GRCm39) |
Y169H |
probably damaging |
Het |
Ugt2b36 |
C |
T |
5: 87,239,930 (GRCm39) |
D152N |
probably damaging |
Het |
Unk |
T |
C |
11: 115,940,235 (GRCm39) |
I196T |
probably benign |
Het |
Uroc1 |
T |
G |
6: 90,321,153 (GRCm39) |
V243G |
probably damaging |
Het |
Vmn2r117 |
T |
A |
17: 23,697,447 (GRCm39) |
I82L |
probably benign |
Het |
Vmn2r44 |
A |
T |
7: 8,380,882 (GRCm39) |
V337E |
probably damaging |
Het |
Zbtb14 |
C |
A |
17: 69,695,497 (GRCm39) |
F398L |
probably damaging |
Het |
Zfp362 |
T |
C |
4: 128,680,993 (GRCm39) |
T111A |
probably benign |
Het |
Zfp598 |
T |
C |
17: 24,899,046 (GRCm39) |
V615A |
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 |
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 |
R6306:Usp34
|
UTSW |
11 |
23,362,260 (GRCm39) |
missense |
possibly damaging |
0.94 |
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 |
|