Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930009A15Rik |
A |
T |
10: 115,415,717 (GRCm39) |
|
probably benign |
Het |
Acaa2 |
T |
C |
18: 74,937,223 (GRCm39) |
L369S |
probably damaging |
Het |
Akna |
A |
G |
4: 63,313,140 (GRCm39) |
S328P |
probably damaging |
Het |
Albfm1 |
A |
G |
5: 90,719,546 (GRCm39) |
Y214C |
probably damaging |
Het |
Apc |
A |
G |
18: 34,354,140 (GRCm39) |
|
probably benign |
Het |
Brca2 |
C |
T |
5: 150,466,716 (GRCm39) |
T2160I |
probably damaging |
Het |
Camsap2 |
A |
G |
1: 136,204,330 (GRCm39) |
S1251P |
probably damaging |
Het |
Ccdc110 |
A |
G |
8: 46,395,573 (GRCm39) |
E488G |
probably damaging |
Het |
Ccdc158 |
T |
A |
5: 92,797,908 (GRCm39) |
I411F |
probably damaging |
Het |
Cd163 |
C |
T |
6: 124,297,595 (GRCm39) |
Q914* |
probably null |
Het |
Cd22 |
T |
C |
7: 30,566,083 (GRCm39) |
D827G |
probably damaging |
Het |
Ces1e |
A |
G |
8: 93,946,001 (GRCm39) |
|
probably null |
Het |
Col14a1 |
T |
C |
15: 55,315,779 (GRCm39) |
|
probably null |
Het |
Csmd3 |
T |
A |
15: 47,713,135 (GRCm39) |
D1509V |
probably damaging |
Het |
Ddx51 |
A |
G |
5: 110,804,717 (GRCm39) |
D543G |
probably damaging |
Het |
Diaph3 |
T |
A |
14: 87,222,261 (GRCm39) |
I408F |
probably damaging |
Het |
Dld |
G |
A |
12: 31,390,325 (GRCm39) |
P213L |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,037,262 (GRCm39) |
T3327A |
probably benign |
Het |
Dnttip2 |
T |
A |
3: 122,078,817 (GRCm39) |
|
probably benign |
Het |
Dock10 |
T |
C |
1: 80,546,225 (GRCm39) |
E791G |
possibly damaging |
Het |
Ehd3 |
G |
T |
17: 74,134,356 (GRCm39) |
W238C |
probably damaging |
Het |
Ehd3 |
T |
G |
17: 74,134,361 (GRCm39) |
L240R |
probably damaging |
Het |
Ep400 |
A |
G |
5: 110,824,766 (GRCm39) |
V2357A |
unknown |
Het |
Fam20c |
T |
C |
5: 138,741,932 (GRCm39) |
V181A |
probably damaging |
Het |
Gm4781 |
T |
C |
10: 100,232,814 (GRCm39) |
|
noncoding transcript |
Het |
Gpatch8 |
A |
T |
11: 102,371,058 (GRCm39) |
S827T |
unknown |
Het |
Grm3 |
A |
T |
5: 9,561,930 (GRCm39) |
I640N |
probably damaging |
Het |
Gstm7 |
A |
G |
3: 107,838,747 (GRCm39) |
|
probably benign |
Het |
Hdac7 |
G |
T |
15: 97,700,372 (GRCm39) |
H572Q |
probably damaging |
Het |
Ift140 |
C |
T |
17: 25,313,735 (GRCm39) |
Q1389* |
probably null |
Het |
Igfn1 |
A |
G |
1: 135,893,152 (GRCm39) |
V2099A |
probably damaging |
Het |
Ik |
A |
G |
18: 36,888,531 (GRCm39) |
N443S |
possibly damaging |
Het |
Impact |
A |
G |
18: 13,123,601 (GRCm39) |
K315E |
probably benign |
Het |
Insr |
C |
A |
8: 3,308,697 (GRCm39) |
R113L |
probably benign |
Het |
Jak2 |
T |
A |
19: 29,260,954 (GRCm39) |
Y317N |
possibly damaging |
Het |
Kif18a |
T |
A |
2: 109,122,411 (GRCm39) |
V162E |
probably damaging |
Het |
L3mbtl3 |
A |
G |
10: 26,207,762 (GRCm39) |
V319A |
unknown |
Het |
Lepr |
T |
C |
4: 101,649,324 (GRCm39) |
|
probably benign |
Het |
Lmo7 |
C |
T |
14: 102,137,938 (GRCm39) |
T647I |
possibly damaging |
Het |
Mindy3 |
C |
T |
2: 12,405,854 (GRCm39) |
R147Q |
probably benign |
Het |
Mtr |
T |
C |
13: 12,230,453 (GRCm39) |
|
probably null |
Het |
Muc4 |
A |
T |
16: 32,576,652 (GRCm39) |
|
probably benign |
Het |
Nrip1 |
G |
A |
16: 76,090,471 (GRCm39) |
T362M |
possibly damaging |
Het |
Or1j17 |
G |
T |
2: 36,578,074 (GRCm39) |
R20L |
probably null |
Het |
Or1q1 |
T |
C |
2: 36,886,957 (GRCm39) |
I45T |
possibly damaging |
Het |
Or5d45 |
A |
G |
2: 88,153,222 (GRCm39) |
S276P |
probably benign |
Het |
Ovol1 |
G |
A |
19: 5,601,630 (GRCm39) |
R131C |
probably damaging |
Het |
Pcca |
T |
C |
14: 122,905,998 (GRCm39) |
V323A |
probably damaging |
Het |
Pcdhb14 |
A |
T |
18: 37,581,295 (GRCm39) |
M134L |
probably benign |
Het |
Pecam1 |
G |
A |
11: 106,581,887 (GRCm39) |
T252M |
probably benign |
Het |
Rnd3 |
T |
A |
2: 51,022,536 (GRCm39) |
I169F |
probably damaging |
Het |
Rnmt |
T |
A |
18: 68,444,689 (GRCm39) |
D219E |
probably benign |
Het |
Rufy1 |
A |
T |
11: 50,292,315 (GRCm39) |
F491L |
probably benign |
Het |
Ryr2 |
G |
T |
13: 11,677,124 (GRCm39) |
C3242* |
probably null |
Het |
Smurf2 |
G |
T |
11: 106,766,727 (GRCm39) |
R31S |
possibly damaging |
Het |
Stard9 |
G |
A |
2: 120,527,580 (GRCm39) |
C1279Y |
probably damaging |
Het |
Sugp2 |
T |
C |
8: 70,704,753 (GRCm39) |
|
probably null |
Het |
Sulf1 |
A |
T |
1: 12,929,636 (GRCm39) |
D301V |
probably benign |
Het |
Tbcd |
G |
T |
11: 121,492,737 (GRCm39) |
|
probably benign |
Het |
Tlr11 |
T |
C |
14: 50,599,712 (GRCm39) |
I566T |
probably benign |
Het |
Tm9sf2 |
T |
A |
14: 122,374,921 (GRCm39) |
|
probably benign |
Het |
Tnfaip8l1 |
T |
C |
17: 56,478,799 (GRCm39) |
F30L |
probably benign |
Het |
Trav15-2-dv6-2 |
T |
A |
14: 53,887,433 (GRCm39) |
C118S |
probably damaging |
Het |
Ttc13 |
A |
G |
8: 125,408,959 (GRCm39) |
|
probably benign |
Het |
Ubqln3 |
A |
T |
7: 103,790,906 (GRCm39) |
S395T |
probably benign |
Het |
Urb2 |
A |
G |
8: 124,754,827 (GRCm39) |
D178G |
probably benign |
Het |
Usf3 |
A |
G |
16: 44,041,222 (GRCm39) |
I1901V |
probably benign |
Het |
Vmn1r173 |
A |
T |
7: 23,402,112 (GRCm39) |
I116F |
probably benign |
Het |
Vmn1r69 |
T |
A |
7: 10,314,717 (GRCm39) |
T5S |
probably benign |
Het |
Wbp1l |
C |
T |
19: 46,642,619 (GRCm39) |
R191* |
probably null |
Het |
Wfikkn2 |
C |
T |
11: 94,129,688 (GRCm39) |
R151H |
probably damaging |
Het |
|
Other mutations in Sptbn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00227:Sptbn1
|
APN |
11 |
30,060,818 (GRCm39) |
nonsense |
probably null |
|
IGL01098:Sptbn1
|
APN |
11 |
30,109,385 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01843:Sptbn1
|
APN |
11 |
30,054,623 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02070:Sptbn1
|
APN |
11 |
30,095,979 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02075:Sptbn1
|
APN |
11 |
30,088,496 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02094:Sptbn1
|
APN |
11 |
30,050,659 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02102:Sptbn1
|
APN |
11 |
30,087,427 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02189:Sptbn1
|
APN |
11 |
30,067,871 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02256:Sptbn1
|
APN |
11 |
30,070,990 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02301:Sptbn1
|
APN |
11 |
30,092,129 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02354:Sptbn1
|
APN |
11 |
30,060,783 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02361:Sptbn1
|
APN |
11 |
30,060,783 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02377:Sptbn1
|
APN |
11 |
30,069,491 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02504:Sptbn1
|
APN |
11 |
30,092,293 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02672:Sptbn1
|
APN |
11 |
30,087,239 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02733:Sptbn1
|
APN |
11 |
30,147,747 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02755:Sptbn1
|
APN |
11 |
30,092,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Sptbn1
|
UTSW |
11 |
30,073,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Sptbn1
|
UTSW |
11 |
30,073,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Sptbn1
|
UTSW |
11 |
30,064,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0139:Sptbn1
|
UTSW |
11 |
30,092,289 (GRCm39) |
missense |
probably benign |
0.00 |
R0370:Sptbn1
|
UTSW |
11 |
30,071,545 (GRCm39) |
missense |
probably benign |
|
R0389:Sptbn1
|
UTSW |
11 |
30,089,250 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0415:Sptbn1
|
UTSW |
11 |
30,099,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R0552:Sptbn1
|
UTSW |
11 |
30,095,985 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0601:Sptbn1
|
UTSW |
11 |
30,100,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Sptbn1
|
UTSW |
11 |
30,088,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Sptbn1
|
UTSW |
11 |
30,067,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R0708:Sptbn1
|
UTSW |
11 |
30,064,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0711:Sptbn1
|
UTSW |
11 |
30,064,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0729:Sptbn1
|
UTSW |
11 |
30,060,902 (GRCm39) |
missense |
probably damaging |
0.96 |
R0755:Sptbn1
|
UTSW |
11 |
30,089,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R0892:Sptbn1
|
UTSW |
11 |
30,092,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R0927:Sptbn1
|
UTSW |
11 |
30,071,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R1102:Sptbn1
|
UTSW |
11 |
30,070,785 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1460:Sptbn1
|
UTSW |
11 |
30,088,637 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1479:Sptbn1
|
UTSW |
11 |
30,063,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Sptbn1
|
UTSW |
11 |
30,071,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R1649:Sptbn1
|
UTSW |
11 |
30,087,301 (GRCm39) |
missense |
probably damaging |
0.97 |
R1663:Sptbn1
|
UTSW |
11 |
30,070,783 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1671:Sptbn1
|
UTSW |
11 |
30,092,245 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1680:Sptbn1
|
UTSW |
11 |
30,109,371 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1695:Sptbn1
|
UTSW |
11 |
30,086,124 (GRCm39) |
missense |
probably benign |
0.13 |
R1868:Sptbn1
|
UTSW |
11 |
30,064,781 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1918:Sptbn1
|
UTSW |
11 |
30,092,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R1921:Sptbn1
|
UTSW |
11 |
30,054,469 (GRCm39) |
missense |
probably damaging |
0.98 |
R2026:Sptbn1
|
UTSW |
11 |
30,054,559 (GRCm39) |
missense |
probably benign |
0.02 |
R2038:Sptbn1
|
UTSW |
11 |
30,109,293 (GRCm39) |
critical splice donor site |
probably null |
|
R2047:Sptbn1
|
UTSW |
11 |
30,088,360 (GRCm39) |
splice site |
probably benign |
|
R2312:Sptbn1
|
UTSW |
11 |
30,104,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Sptbn1
|
UTSW |
11 |
30,169,686 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3624:Sptbn1
|
UTSW |
11 |
30,090,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R3723:Sptbn1
|
UTSW |
11 |
30,087,335 (GRCm39) |
missense |
possibly damaging |
0.59 |
R3862:Sptbn1
|
UTSW |
11 |
30,092,329 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4446:Sptbn1
|
UTSW |
11 |
30,089,114 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4582:Sptbn1
|
UTSW |
11 |
30,169,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R4705:Sptbn1
|
UTSW |
11 |
30,050,660 (GRCm39) |
missense |
probably benign |
|
R4707:Sptbn1
|
UTSW |
11 |
30,087,197 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4718:Sptbn1
|
UTSW |
11 |
30,104,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R4789:Sptbn1
|
UTSW |
11 |
30,067,759 (GRCm39) |
missense |
probably benign |
|
R4824:Sptbn1
|
UTSW |
11 |
30,068,295 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4855:Sptbn1
|
UTSW |
11 |
30,092,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R5009:Sptbn1
|
UTSW |
11 |
30,074,016 (GRCm39) |
missense |
probably benign |
0.05 |
R5071:Sptbn1
|
UTSW |
11 |
30,063,854 (GRCm39) |
critical splice donor site |
probably null |
|
R5153:Sptbn1
|
UTSW |
11 |
30,071,510 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5334:Sptbn1
|
UTSW |
11 |
30,087,364 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5462:Sptbn1
|
UTSW |
11 |
30,050,520 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5523:Sptbn1
|
UTSW |
11 |
30,087,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R5707:Sptbn1
|
UTSW |
11 |
30,093,174 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5724:Sptbn1
|
UTSW |
11 |
30,094,113 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5738:Sptbn1
|
UTSW |
11 |
30,095,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R5864:Sptbn1
|
UTSW |
11 |
30,095,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R5895:Sptbn1
|
UTSW |
11 |
30,073,978 (GRCm39) |
missense |
probably damaging |
0.99 |
R5932:Sptbn1
|
UTSW |
11 |
30,086,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R5984:Sptbn1
|
UTSW |
11 |
30,068,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R6155:Sptbn1
|
UTSW |
11 |
30,087,403 (GRCm39) |
missense |
probably damaging |
0.99 |
R6163:Sptbn1
|
UTSW |
11 |
30,109,443 (GRCm39) |
nonsense |
probably null |
|
R6226:Sptbn1
|
UTSW |
11 |
30,086,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R6271:Sptbn1
|
UTSW |
11 |
30,050,660 (GRCm39) |
missense |
probably benign |
0.00 |
R6443:Sptbn1
|
UTSW |
11 |
30,089,429 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6591:Sptbn1
|
UTSW |
11 |
30,063,984 (GRCm39) |
missense |
probably damaging |
0.99 |
R6616:Sptbn1
|
UTSW |
11 |
30,074,030 (GRCm39) |
missense |
probably benign |
0.08 |
R6691:Sptbn1
|
UTSW |
11 |
30,063,984 (GRCm39) |
missense |
probably damaging |
0.99 |
R6751:Sptbn1
|
UTSW |
11 |
30,067,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R6823:Sptbn1
|
UTSW |
11 |
30,064,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R6863:Sptbn1
|
UTSW |
11 |
30,096,777 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6885:Sptbn1
|
UTSW |
11 |
30,088,634 (GRCm39) |
missense |
probably benign |
0.26 |
R6892:Sptbn1
|
UTSW |
11 |
30,092,187 (GRCm39) |
missense |
probably benign |
0.27 |
R6998:Sptbn1
|
UTSW |
11 |
30,050,633 (GRCm39) |
missense |
probably damaging |
0.97 |
R7043:Sptbn1
|
UTSW |
11 |
30,053,323 (GRCm39) |
missense |
probably benign |
0.02 |
R7092:Sptbn1
|
UTSW |
11 |
30,087,119 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7272:Sptbn1
|
UTSW |
11 |
30,064,859 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7301:Sptbn1
|
UTSW |
11 |
30,067,798 (GRCm39) |
nonsense |
probably null |
|
R7379:Sptbn1
|
UTSW |
11 |
30,089,292 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7774:Sptbn1
|
UTSW |
11 |
30,092,142 (GRCm39) |
missense |
probably damaging |
0.99 |
R7813:Sptbn1
|
UTSW |
11 |
30,088,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R7837:Sptbn1
|
UTSW |
11 |
30,088,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R7843:Sptbn1
|
UTSW |
11 |
30,104,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R7846:Sptbn1
|
UTSW |
11 |
30,092,153 (GRCm39) |
missense |
probably damaging |
0.98 |
R7877:Sptbn1
|
UTSW |
11 |
30,079,601 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7902:Sptbn1
|
UTSW |
11 |
30,086,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R8060:Sptbn1
|
UTSW |
11 |
30,051,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R8116:Sptbn1
|
UTSW |
11 |
30,089,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R8169:Sptbn1
|
UTSW |
11 |
30,147,783 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8208:Sptbn1
|
UTSW |
11 |
30,074,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Sptbn1
|
UTSW |
11 |
30,063,906 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8412:Sptbn1
|
UTSW |
11 |
30,088,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R8470:Sptbn1
|
UTSW |
11 |
30,070,758 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8544:Sptbn1
|
UTSW |
11 |
30,169,750 (GRCm39) |
start gained |
probably benign |
|
R8674:Sptbn1
|
UTSW |
11 |
30,089,352 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8846:Sptbn1
|
UTSW |
11 |
30,075,009 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8889:Sptbn1
|
UTSW |
11 |
30,067,800 (GRCm39) |
missense |
probably benign |
0.03 |
R8892:Sptbn1
|
UTSW |
11 |
30,067,800 (GRCm39) |
missense |
probably benign |
0.03 |
R8927:Sptbn1
|
UTSW |
11 |
30,088,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Sptbn1
|
UTSW |
11 |
30,088,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R8975:Sptbn1
|
UTSW |
11 |
30,073,869 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9115:Sptbn1
|
UTSW |
11 |
30,087,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R9127:Sptbn1
|
UTSW |
11 |
30,104,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R9193:Sptbn1
|
UTSW |
11 |
30,087,551 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9237:Sptbn1
|
UTSW |
11 |
30,096,803 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Sptbn1
|
UTSW |
11 |
30,147,787 (GRCm39) |
missense |
probably benign |
0.13 |
Z1176:Sptbn1
|
UTSW |
11 |
30,087,439 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sptbn1
|
UTSW |
11 |
30,070,659 (GRCm39) |
missense |
probably benign |
0.27 |
Z1177:Sptbn1
|
UTSW |
11 |
30,064,734 (GRCm39) |
missense |
probably damaging |
1.00 |
|