Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afdn |
T |
A |
17: 13,881,299 (GRCm38) |
D1016E |
probably damaging |
Het |
Aplnr |
A |
T |
2: 85,136,673 (GRCm38) |
Q14L |
probably benign |
Het |
Aspm |
T |
C |
1: 139,473,683 (GRCm38) |
L1147S |
probably damaging |
Het |
Atad2b |
A |
G |
12: 4,952,642 (GRCm38) |
T337A |
possibly damaging |
Het |
Atrn |
A |
G |
2: 131,023,027 (GRCm38) |
E1358G |
probably damaging |
Het |
Caml |
C |
A |
13: 55,623,249 (GRCm38) |
S53R |
possibly damaging |
Het |
Cd180 |
T |
G |
13: 102,705,633 (GRCm38) |
S396A |
probably benign |
Het |
Cdhr2 |
A |
G |
13: 54,718,512 (GRCm38) |
T344A |
probably damaging |
Het |
Cyp4a31 |
A |
C |
4: 115,570,269 (GRCm38) |
D224A |
probably damaging |
Het |
Dhx36 |
T |
C |
3: 62,484,974 (GRCm38) |
T544A |
probably damaging |
Het |
Dnpep |
T |
A |
1: 75,315,378 (GRCm38) |
K199N |
probably benign |
Het |
Dsc2 |
C |
T |
18: 20,051,175 (GRCm38) |
|
probably null |
Het |
Efl1 |
T |
A |
7: 82,674,568 (GRCm38) |
D239E |
probably damaging |
Het |
Elovl4 |
A |
G |
9: 83,785,178 (GRCm38) |
V42A |
possibly damaging |
Het |
Exoc3 |
T |
C |
13: 74,189,187 (GRCm38) |
T432A |
possibly damaging |
Het |
Fam98c |
A |
G |
7: 29,156,128 (GRCm38) |
|
probably null |
Het |
Fbln2 |
G |
A |
6: 91,233,272 (GRCm38) |
G66D |
probably damaging |
Het |
Fchsd1 |
G |
A |
18: 37,964,084 (GRCm38) |
T410I |
possibly damaging |
Het |
Flcn |
T |
C |
11: 59,801,082 (GRCm38) |
D247G |
probably damaging |
Het |
Galnt16 |
T |
C |
12: 80,575,903 (GRCm38) |
V127A |
probably benign |
Het |
H2-Ob |
A |
T |
17: 34,243,886 (GRCm38) |
|
probably null |
Het |
Has2 |
G |
A |
15: 56,667,798 (GRCm38) |
S507F |
possibly damaging |
Het |
Ido2 |
T |
A |
8: 24,533,923 (GRCm38) |
M300L |
probably damaging |
Het |
Itga10 |
T |
C |
3: 96,658,041 (GRCm38) |
|
probably null |
Het |
Klra9 |
G |
T |
6: 130,179,032 (GRCm38) |
Y253* |
probably null |
Het |
Mfsd2a |
A |
G |
4: 122,950,457 (GRCm38) |
V299A |
probably benign |
Het |
Mybpc1 |
T |
C |
10: 88,560,355 (GRCm38) |
D210G |
probably damaging |
Het |
Ndrg1 |
A |
T |
15: 66,933,872 (GRCm38) |
M128K |
probably damaging |
Het |
Obscn |
T |
A |
11: 59,051,558 (GRCm38) |
T5091S |
probably benign |
Het |
Or2j3 |
A |
G |
17: 38,305,413 (GRCm38) |
L16P |
probably damaging |
Het |
Pex5 |
A |
T |
6: 124,413,613 (GRCm38) |
M91K |
possibly damaging |
Het |
Phlpp2 |
G |
T |
8: 109,934,685 (GRCm38) |
A810S |
probably benign |
Het |
Pla2g7 |
G |
C |
17: 43,599,126 (GRCm38) |
A174P |
probably damaging |
Het |
Plxna4 |
C |
T |
6: 32,215,678 (GRCm38) |
V783M |
probably damaging |
Het |
Poll |
A |
T |
19: 45,553,604 (GRCm38) |
M421K |
probably benign |
Het |
Ppfia2 |
C |
A |
10: 106,913,698 (GRCm38) |
S1148R |
possibly damaging |
Het |
Prkg1 |
A |
G |
19: 30,781,346 (GRCm38) |
F280S |
probably benign |
Het |
Rdh10 |
G |
A |
1: 16,107,855 (GRCm38) |
C117Y |
probably damaging |
Het |
Rtl1 |
C |
A |
12: 109,595,196 (GRCm38) |
A70S |
unknown |
Het |
Scgb2b3 |
A |
T |
7: 31,359,067 (GRCm38) |
L104I |
probably benign |
Het |
Sh3tc1 |
T |
C |
5: 35,706,597 (GRCm38) |
R749G |
probably damaging |
Het |
Skint4 |
A |
G |
4: 112,146,510 (GRCm38) |
K380R |
probably benign |
Het |
Smtnl1 |
A |
C |
2: 84,818,368 (GRCm38) |
S181A |
probably benign |
Het |
Spata31d1b |
T |
C |
13: 59,717,185 (GRCm38) |
S716P |
probably damaging |
Het |
Spc25 |
A |
G |
2: 69,206,102 (GRCm38) |
|
probably benign |
Het |
Stab2 |
C |
T |
10: 86,901,567 (GRCm38) |
|
probably null |
Het |
Timm22 |
T |
C |
11: 76,409,744 (GRCm38) |
V114A |
possibly damaging |
Het |
Timp4 |
A |
G |
6: 115,247,220 (GRCm38) |
C163R |
probably damaging |
Het |
Toporsl |
T |
A |
4: 52,611,548 (GRCm38) |
N480K |
possibly damaging |
Het |
Tpo |
T |
C |
12: 30,084,754 (GRCm38) |
E735G |
probably benign |
Het |
Trpm3 |
A |
G |
19: 22,901,305 (GRCm38) |
D692G |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,751,714 (GRCm38) |
H22945R |
probably damaging |
Het |
Vmn2r6 |
A |
T |
3: 64,547,380 (GRCm38) |
Y499* |
probably null |
Het |
Vwa1 |
G |
A |
4: 155,772,769 (GRCm38) |
H191Y |
probably benign |
Het |
|
Other mutations in Dnah14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01086:Dnah14
|
APN |
1 |
181,752,046 (GRCm38) |
missense |
probably benign |
0.17 |
IGL01764:Dnah14
|
APN |
1 |
181,744,777 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03218:Dnah14
|
APN |
1 |
181,755,269 (GRCm38) |
missense |
probably benign |
0.02 |
IGL03290:Dnah14
|
APN |
1 |
181,763,978 (GRCm38) |
splice site |
probably benign |
|
IGL03384:Dnah14
|
APN |
1 |
181,745,949 (GRCm38) |
missense |
probably benign |
0.03 |
R0009:Dnah14
|
UTSW |
1 |
181,769,407 (GRCm38) |
splice site |
probably benign |
|
R0125:Dnah14
|
UTSW |
1 |
181,752,063 (GRCm38) |
missense |
probably damaging |
0.99 |
R0579:Dnah14
|
UTSW |
1 |
181,744,747 (GRCm38) |
missense |
possibly damaging |
0.72 |
R0973:Dnah14
|
UTSW |
1 |
181,752,145 (GRCm38) |
missense |
probably damaging |
1.00 |
R0973:Dnah14
|
UTSW |
1 |
181,752,145 (GRCm38) |
missense |
probably damaging |
1.00 |
R0974:Dnah14
|
UTSW |
1 |
181,752,145 (GRCm38) |
missense |
probably damaging |
1.00 |
R1609:Dnah14
|
UTSW |
1 |
181,750,177 (GRCm38) |
missense |
probably damaging |
0.97 |
R1860:Dnah14
|
UTSW |
1 |
181,763,960 (GRCm38) |
missense |
probably damaging |
1.00 |
R2050:Dnah14
|
UTSW |
1 |
181,752,562 (GRCm38) |
missense |
probably damaging |
1.00 |
R2974:Dnah14
|
UTSW |
1 |
181,755,241 (GRCm38) |
critical splice acceptor site |
probably null |
|
R4715:Dnah14
|
UTSW |
1 |
181,757,223 (GRCm38) |
missense |
probably damaging |
1.00 |
R5076:Dnah14
|
UTSW |
1 |
181,757,234 (GRCm38) |
missense |
probably benign |
0.01 |
R5424:Dnah14
|
UTSW |
1 |
181,763,310 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5808:Dnah14
|
UTSW |
1 |
181,741,159 (GRCm38) |
missense |
possibly damaging |
0.72 |
R5997:Dnah14
|
UTSW |
1 |
181,770,105 (GRCm38) |
missense |
probably benign |
0.00 |
R6052:Dnah14
|
UTSW |
1 |
181,666,487 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6061:Dnah14
|
UTSW |
1 |
181,709,051 (GRCm38) |
missense |
probably damaging |
1.00 |
R6089:Dnah14
|
UTSW |
1 |
181,750,154 (GRCm38) |
missense |
probably damaging |
1.00 |
R6092:Dnah14
|
UTSW |
1 |
181,621,833 (GRCm38) |
missense |
probably benign |
0.13 |
R6145:Dnah14
|
UTSW |
1 |
181,666,417 (GRCm38) |
missense |
probably benign |
0.00 |
R6163:Dnah14
|
UTSW |
1 |
181,666,361 (GRCm38) |
missense |
probably benign |
0.33 |
R6246:Dnah14
|
UTSW |
1 |
181,680,888 (GRCm38) |
missense |
probably benign |
0.00 |
R6302:Dnah14
|
UTSW |
1 |
181,601,206 (GRCm38) |
missense |
possibly damaging |
0.96 |
R6306:Dnah14
|
UTSW |
1 |
181,585,024 (GRCm38) |
frame shift |
probably null |
|
R6326:Dnah14
|
UTSW |
1 |
181,783,556 (GRCm38) |
missense |
probably damaging |
1.00 |
R6348:Dnah14
|
UTSW |
1 |
181,626,720 (GRCm38) |
missense |
possibly damaging |
0.83 |
R6367:Dnah14
|
UTSW |
1 |
181,755,386 (GRCm38) |
splice site |
probably null |
|
R6376:Dnah14
|
UTSW |
1 |
181,605,894 (GRCm38) |
missense |
possibly damaging |
0.79 |
R6389:Dnah14
|
UTSW |
1 |
181,651,202 (GRCm38) |
critical splice donor site |
probably null |
|
R6454:Dnah14
|
UTSW |
1 |
181,783,705 (GRCm38) |
missense |
probably damaging |
1.00 |
R6476:Dnah14
|
UTSW |
1 |
181,744,768 (GRCm38) |
missense |
probably benign |
0.26 |
R6523:Dnah14
|
UTSW |
1 |
181,643,621 (GRCm38) |
missense |
probably benign |
0.00 |
R6529:Dnah14
|
UTSW |
1 |
181,666,469 (GRCm38) |
missense |
probably damaging |
0.98 |
R6538:Dnah14
|
UTSW |
1 |
181,584,985 (GRCm38) |
missense |
unknown |
|
R6546:Dnah14
|
UTSW |
1 |
181,738,987 (GRCm38) |
missense |
probably damaging |
1.00 |
R6752:Dnah14
|
UTSW |
1 |
181,593,452 (GRCm38) |
missense |
probably benign |
0.07 |
R6762:Dnah14
|
UTSW |
1 |
181,757,259 (GRCm38) |
missense |
probably damaging |
1.00 |
R6786:Dnah14
|
UTSW |
1 |
181,641,405 (GRCm38) |
missense |
probably benign |
0.21 |
R6849:Dnah14
|
UTSW |
1 |
181,808,945 (GRCm38) |
missense |
probably benign |
0.00 |
R6877:Dnah14
|
UTSW |
1 |
181,628,432 (GRCm38) |
missense |
possibly damaging |
0.82 |
R6912:Dnah14
|
UTSW |
1 |
181,750,183 (GRCm38) |
missense |
possibly damaging |
0.83 |
R6919:Dnah14
|
UTSW |
1 |
181,585,066 (GRCm38) |
missense |
probably benign |
0.04 |
R6924:Dnah14
|
UTSW |
1 |
181,627,952 (GRCm38) |
missense |
probably benign |
0.04 |
R6957:Dnah14
|
UTSW |
1 |
181,785,175 (GRCm38) |
missense |
possibly damaging |
0.92 |
R6980:Dnah14
|
UTSW |
1 |
181,648,230 (GRCm38) |
missense |
probably benign |
0.00 |
R7018:Dnah14
|
UTSW |
1 |
181,626,944 (GRCm38) |
missense |
possibly damaging |
0.55 |
R7046:Dnah14
|
UTSW |
1 |
181,623,003 (GRCm38) |
missense |
probably benign |
0.01 |
R7058:Dnah14
|
UTSW |
1 |
181,698,049 (GRCm38) |
missense |
probably benign |
0.00 |
R7068:Dnah14
|
UTSW |
1 |
181,769,790 (GRCm38) |
missense |
probably benign |
0.35 |
R7115:Dnah14
|
UTSW |
1 |
181,720,145 (GRCm38) |
missense |
probably damaging |
1.00 |
R7130:Dnah14
|
UTSW |
1 |
181,745,958 (GRCm38) |
nonsense |
probably null |
|
R7165:Dnah14
|
UTSW |
1 |
181,704,535 (GRCm38) |
missense |
probably benign |
0.00 |
R7169:Dnah14
|
UTSW |
1 |
181,702,365 (GRCm38) |
missense |
probably benign |
0.00 |
R7184:Dnah14
|
UTSW |
1 |
181,704,529 (GRCm38) |
nonsense |
probably null |
|
R7232:Dnah14
|
UTSW |
1 |
181,757,363 (GRCm38) |
missense |
probably damaging |
1.00 |
R7260:Dnah14
|
UTSW |
1 |
181,706,744 (GRCm38) |
missense |
probably damaging |
0.99 |
R7276:Dnah14
|
UTSW |
1 |
181,685,807 (GRCm38) |
missense |
probably benign |
0.41 |
R7290:Dnah14
|
UTSW |
1 |
181,628,174 (GRCm38) |
missense |
probably benign |
0.20 |
R7314:Dnah14
|
UTSW |
1 |
181,785,254 (GRCm38) |
splice site |
probably null |
|
R7326:Dnah14
|
UTSW |
1 |
181,598,403 (GRCm38) |
missense |
probably benign |
0.02 |
R7336:Dnah14
|
UTSW |
1 |
181,797,734 (GRCm38) |
missense |
probably damaging |
0.96 |
R7363:Dnah14
|
UTSW |
1 |
181,690,524 (GRCm38) |
splice site |
probably null |
|
R7371:Dnah14
|
UTSW |
1 |
181,626,885 (GRCm38) |
missense |
probably benign |
0.05 |
R7376:Dnah14
|
UTSW |
1 |
181,763,402 (GRCm38) |
missense |
probably benign |
0.03 |
R7418:Dnah14
|
UTSW |
1 |
181,616,742 (GRCm38) |
missense |
possibly damaging |
0.92 |
R7473:Dnah14
|
UTSW |
1 |
181,752,139 (GRCm38) |
missense |
probably damaging |
0.99 |
R7514:Dnah14
|
UTSW |
1 |
181,628,067 (GRCm38) |
missense |
probably damaging |
0.96 |
R7555:Dnah14
|
UTSW |
1 |
181,770,054 (GRCm38) |
missense |
probably benign |
0.26 |
R7641:Dnah14
|
UTSW |
1 |
181,707,533 (GRCm38) |
missense |
probably benign |
0.01 |
R7663:Dnah14
|
UTSW |
1 |
181,752,155 (GRCm38) |
splice site |
probably null |
|
R7674:Dnah14
|
UTSW |
1 |
181,707,533 (GRCm38) |
missense |
probably benign |
0.01 |
R7680:Dnah14
|
UTSW |
1 |
181,685,800 (GRCm38) |
missense |
probably benign |
0.15 |
R7709:Dnah14
|
UTSW |
1 |
181,702,484 (GRCm38) |
critical splice donor site |
probably null |
|
R7842:Dnah14
|
UTSW |
1 |
181,627,898 (GRCm38) |
missense |
probably damaging |
0.99 |
R7861:Dnah14
|
UTSW |
1 |
181,616,759 (GRCm38) |
missense |
probably damaging |
1.00 |
R7988:Dnah14
|
UTSW |
1 |
181,783,574 (GRCm38) |
missense |
probably damaging |
0.97 |
R8016:Dnah14
|
UTSW |
1 |
181,648,311 (GRCm38) |
missense |
probably benign |
0.05 |
R8042:Dnah14
|
UTSW |
1 |
181,643,631 (GRCm38) |
critical splice donor site |
probably null |
|
R8071:Dnah14
|
UTSW |
1 |
181,615,894 (GRCm38) |
missense |
possibly damaging |
0.84 |
R8086:Dnah14
|
UTSW |
1 |
181,766,232 (GRCm38) |
missense |
probably damaging |
1.00 |
R8095:Dnah14
|
UTSW |
1 |
181,806,032 (GRCm38) |
nonsense |
probably null |
|
R8139:Dnah14
|
UTSW |
1 |
181,755,288 (GRCm38) |
missense |
probably damaging |
1.00 |
R8176:Dnah14
|
UTSW |
1 |
181,657,033 (GRCm38) |
missense |
probably damaging |
0.96 |
R8193:Dnah14
|
UTSW |
1 |
181,688,205 (GRCm38) |
missense |
probably damaging |
1.00 |
R8197:Dnah14
|
UTSW |
1 |
181,690,101 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8209:Dnah14
|
UTSW |
1 |
181,795,545 (GRCm38) |
missense |
possibly damaging |
0.69 |
R8226:Dnah14
|
UTSW |
1 |
181,795,545 (GRCm38) |
missense |
possibly damaging |
0.69 |
R8251:Dnah14
|
UTSW |
1 |
181,664,865 (GRCm38) |
missense |
probably damaging |
1.00 |
R8264:Dnah14
|
UTSW |
1 |
181,744,792 (GRCm38) |
missense |
probably damaging |
0.99 |
R8284:Dnah14
|
UTSW |
1 |
181,773,811 (GRCm38) |
missense |
probably benign |
0.03 |
R8289:Dnah14
|
UTSW |
1 |
181,716,215 (GRCm38) |
nonsense |
probably null |
|
R8323:Dnah14
|
UTSW |
1 |
181,704,544 (GRCm38) |
missense |
probably benign |
0.01 |
R8442:Dnah14
|
UTSW |
1 |
181,741,284 (GRCm38) |
missense |
probably damaging |
0.97 |
R8458:Dnah14
|
UTSW |
1 |
181,806,012 (GRCm38) |
missense |
|
|
R8507:Dnah14
|
UTSW |
1 |
181,641,414 (GRCm38) |
missense |
probably benign |
0.02 |
R8509:Dnah14
|
UTSW |
1 |
181,814,655 (GRCm38) |
missense |
|
|
R8520:Dnah14
|
UTSW |
1 |
181,653,638 (GRCm38) |
missense |
probably damaging |
1.00 |
R8530:Dnah14
|
UTSW |
1 |
181,664,946 (GRCm38) |
missense |
probably damaging |
1.00 |
R8703:Dnah14
|
UTSW |
1 |
181,666,011 (GRCm38) |
nonsense |
probably null |
|
R8710:Dnah14
|
UTSW |
1 |
181,690,311 (GRCm38) |
missense |
probably benign |
0.04 |
R8752:Dnah14
|
UTSW |
1 |
181,628,016 (GRCm38) |
missense |
probably benign |
0.00 |
R8792:Dnah14
|
UTSW |
1 |
181,814,624 (GRCm38) |
missense |
|
|
R8797:Dnah14
|
UTSW |
1 |
181,637,847 (GRCm38) |
missense |
probably benign |
0.19 |
R8821:Dnah14
|
UTSW |
1 |
181,792,004 (GRCm38) |
nonsense |
probably null |
|
R8834:Dnah14
|
UTSW |
1 |
181,616,750 (GRCm38) |
missense |
possibly damaging |
0.83 |
R8913:Dnah14
|
UTSW |
1 |
181,725,498 (GRCm38) |
missense |
probably benign |
0.01 |
R8925:Dnah14
|
UTSW |
1 |
181,680,756 (GRCm38) |
missense |
probably damaging |
1.00 |
R8927:Dnah14
|
UTSW |
1 |
181,680,756 (GRCm38) |
missense |
probably damaging |
1.00 |
R8934:Dnah14
|
UTSW |
1 |
181,622,723 (GRCm38) |
missense |
possibly damaging |
0.84 |
R9090:Dnah14
|
UTSW |
1 |
181,769,760 (GRCm38) |
missense |
probably benign |
0.33 |
R9169:Dnah14
|
UTSW |
1 |
181,605,816 (GRCm38) |
missense |
probably benign |
0.06 |
R9199:Dnah14
|
UTSW |
1 |
181,651,001 (GRCm38) |
missense |
possibly damaging |
0.50 |
R9212:Dnah14
|
UTSW |
1 |
181,801,287 (GRCm38) |
missense |
possibly damaging |
0.95 |
R9213:Dnah14
|
UTSW |
1 |
181,616,640 (GRCm38) |
critical splice donor site |
probably null |
|
R9271:Dnah14
|
UTSW |
1 |
181,769,760 (GRCm38) |
missense |
probably benign |
0.33 |
R9282:Dnah14
|
UTSW |
1 |
181,814,512 (GRCm38) |
missense |
|
|
R9350:Dnah14
|
UTSW |
1 |
181,734,804 (GRCm38) |
missense |
possibly damaging |
0.79 |
R9358:Dnah14
|
UTSW |
1 |
181,709,033 (GRCm38) |
missense |
probably benign |
0.01 |
R9436:Dnah14
|
UTSW |
1 |
181,680,783 (GRCm38) |
missense |
probably damaging |
1.00 |
R9484:Dnah14
|
UTSW |
1 |
181,797,746 (GRCm38) |
missense |
probably benign |
0.01 |
R9484:Dnah14
|
UTSW |
1 |
181,690,208 (GRCm38) |
missense |
probably benign |
0.45 |
R9486:Dnah14
|
UTSW |
1 |
181,680,929 (GRCm38) |
missense |
possibly damaging |
0.68 |
R9546:Dnah14
|
UTSW |
1 |
181,593,427 (GRCm38) |
critical splice acceptor site |
probably null |
|
R9547:Dnah14
|
UTSW |
1 |
181,593,427 (GRCm38) |
critical splice acceptor site |
probably null |
|
R9578:Dnah14
|
UTSW |
1 |
181,674,442 (GRCm38) |
missense |
probably benign |
0.16 |
R9654:Dnah14
|
UTSW |
1 |
181,766,339 (GRCm38) |
missense |
probably benign |
0.01 |
R9681:Dnah14
|
UTSW |
1 |
181,734,849 (GRCm38) |
missense |
possibly damaging |
0.91 |
R9683:Dnah14
|
UTSW |
1 |
181,598,944 (GRCm38) |
missense |
probably benign |
0.01 |
R9687:Dnah14
|
UTSW |
1 |
181,598,413 (GRCm38) |
missense |
probably benign |
0.01 |
R9718:Dnah14
|
UTSW |
1 |
181,622,979 (GRCm38) |
missense |
probably benign |
0.08 |
R9751:Dnah14
|
UTSW |
1 |
181,792,045 (GRCm38) |
missense |
probably damaging |
1.00 |
R9757:Dnah14
|
UTSW |
1 |
181,685,784 (GRCm38) |
missense |
probably benign |
0.03 |
RF007:Dnah14
|
UTSW |
1 |
181,685,809 (GRCm38) |
missense |
probably benign |
0.00 |
RF012:Dnah14
|
UTSW |
1 |
181,627,898 (GRCm38) |
missense |
probably damaging |
0.99 |
Z1176:Dnah14
|
UTSW |
1 |
181,757,351 (GRCm38) |
missense |
possibly damaging |
0.83 |
Z1177:Dnah14
|
UTSW |
1 |
181,690,320 (GRCm38) |
missense |
probably benign |
0.03 |
Z1177:Dnah14
|
UTSW |
1 |
181,766,304 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Dnah14
|
UTSW |
1 |
181,763,334 (GRCm38) |
missense |
probably damaging |
1.00 |
|