Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acly |
A |
G |
11: 100,410,576 (GRCm39) |
F134S |
probably damaging |
Het |
Acsl5 |
T |
C |
19: 55,257,262 (GRCm39) |
|
probably null |
Het |
Adam29 |
G |
T |
8: 56,325,463 (GRCm39) |
N330K |
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,677,033 (GRCm39) |
S1933P |
probably benign |
Het |
Afap1l2 |
T |
C |
19: 56,902,824 (GRCm39) |
H785R |
probably damaging |
Het |
Ahnak |
T |
A |
19: 8,987,800 (GRCm39) |
L3028* |
probably null |
Het |
Ajuba |
T |
C |
14: 54,807,847 (GRCm39) |
T462A |
possibly damaging |
Het |
Ankrd36 |
A |
G |
11: 5,534,016 (GRCm39) |
N289S |
possibly damaging |
Het |
Ankrd46 |
A |
T |
15: 36,486,001 (GRCm39) |
L84Q |
probably damaging |
Het |
Ankrd54 |
T |
G |
15: 78,940,270 (GRCm39) |
D163A |
probably damaging |
Het |
Arhgef28 |
A |
G |
13: 98,282,064 (GRCm39) |
L10P |
probably benign |
Het |
Atm |
A |
T |
9: 53,367,288 (GRCm39) |
|
probably null |
Het |
Azin1 |
G |
C |
15: 38,492,572 (GRCm39) |
F312L |
probably damaging |
Het |
C2cd4c |
A |
G |
10: 79,448,482 (GRCm39) |
S222P |
probably damaging |
Het |
Cdyl |
A |
G |
13: 36,000,147 (GRCm39) |
T143A |
probably benign |
Het |
Clhc1 |
G |
A |
11: 29,503,751 (GRCm39) |
V56I |
possibly damaging |
Het |
Cntn4 |
T |
C |
6: 106,486,471 (GRCm39) |
S300P |
probably benign |
Het |
Col12a1 |
A |
G |
9: 79,551,224 (GRCm39) |
Y2131H |
probably damaging |
Het |
Cyp3a41b |
A |
G |
5: 145,506,190 (GRCm39) |
S287P |
probably benign |
Het |
Dctn4 |
A |
G |
18: 60,689,401 (GRCm39) |
D424G |
probably benign |
Het |
Dnajb8 |
C |
T |
6: 88,199,940 (GRCm39) |
R159C |
possibly damaging |
Het |
E330034G19Rik |
A |
C |
14: 24,346,135 (GRCm39) |
|
probably null |
Het |
Ehhadh |
G |
A |
16: 21,581,373 (GRCm39) |
P540S |
possibly damaging |
Het |
Emsy |
T |
C |
7: 98,297,111 (GRCm39) |
E24G |
probably damaging |
Het |
F930015N05Rik |
A |
C |
11: 64,326,418 (GRCm39) |
L74W |
unknown |
Het |
Fat1 |
A |
G |
8: 45,406,390 (GRCm39) |
D1047G |
|
Het |
Galnt7 |
A |
G |
8: 58,005,600 (GRCm39) |
V211A |
possibly damaging |
Het |
Gdap2 |
T |
C |
3: 100,109,611 (GRCm39) |
C543R |
unknown |
Het |
Ghr |
A |
C |
15: 3,362,901 (GRCm39) |
D190E |
probably benign |
Het |
Glrx |
A |
G |
13: 75,995,346 (GRCm39) |
M89V |
probably benign |
Het |
Gm10323 |
A |
C |
13: 67,000,859 (GRCm39) |
Y91* |
noncoding transcript |
Het |
Gnb4 |
A |
T |
3: 32,644,184 (GRCm39) |
D153E |
possibly damaging |
Het |
Gnptab |
G |
T |
10: 88,276,254 (GRCm39) |
|
probably null |
Het |
Grip2 |
T |
C |
6: 91,762,665 (GRCm39) |
D193G |
possibly damaging |
Het |
Igsf3 |
T |
C |
3: 101,347,038 (GRCm39) |
W658R |
probably damaging |
Het |
Ip6k1 |
T |
A |
9: 107,923,115 (GRCm39) |
F416I |
probably benign |
Het |
Klhl1 |
T |
G |
14: 96,517,546 (GRCm39) |
T377P |
possibly damaging |
Het |
Lrrc38 |
G |
A |
4: 143,077,303 (GRCm39) |
G189R |
probably damaging |
Het |
Lrrfip1 |
T |
C |
1: 91,042,878 (GRCm39) |
S428P |
probably benign |
Het |
Megf10 |
A |
G |
18: 57,416,893 (GRCm39) |
D754G |
probably benign |
Het |
Mrgprx2 |
T |
A |
7: 48,132,527 (GRCm39) |
Y97F |
probably benign |
Het |
Msantd2 |
T |
G |
9: 37,400,684 (GRCm39) |
V22G |
probably damaging |
Het |
Myl6b |
T |
C |
10: 128,333,209 (GRCm39) |
K11R |
unknown |
Het |
Nab2 |
C |
A |
10: 127,498,645 (GRCm39) |
V475L |
probably benign |
Het |
Npas1 |
T |
C |
7: 16,189,890 (GRCm39) |
E552G |
probably damaging |
Het |
Pknox2 |
T |
C |
9: 36,821,040 (GRCm39) |
N274S |
possibly damaging |
Het |
Pmepa1 |
A |
T |
2: 173,069,700 (GRCm39) |
L247Q |
probably damaging |
Het |
Poll |
T |
C |
19: 45,542,047 (GRCm39) |
K420E |
probably damaging |
Het |
Polr2a |
A |
G |
11: 69,628,344 (GRCm39) |
V1283A |
probably benign |
Het |
Ppil4 |
A |
T |
10: 7,671,444 (GRCm39) |
Y36F |
probably benign |
Het |
Pramel20 |
T |
G |
4: 143,298,530 (GRCm39) |
Y158D |
probably benign |
Het |
Psd2 |
C |
T |
18: 36,113,478 (GRCm39) |
R317W |
probably damaging |
Het |
Pspc1 |
T |
A |
14: 57,015,616 (GRCm39) |
M1L |
probably benign |
Het |
Qrsl1 |
A |
T |
10: 43,758,080 (GRCm39) |
F338I |
possibly damaging |
Het |
Rcor3 |
A |
G |
1: 191,814,749 (GRCm39) |
Y77H |
unknown |
Het |
Sbno2 |
G |
A |
10: 79,905,845 (GRCm39) |
P157L |
probably benign |
Het |
Scn10a |
C |
T |
9: 119,446,829 (GRCm39) |
V1400I |
probably damaging |
Het |
Setd3 |
C |
G |
12: 108,073,612 (GRCm39) |
G555A |
possibly damaging |
Het |
Slc12a4 |
A |
T |
8: 106,678,601 (GRCm39) |
M245K |
probably benign |
Het |
Slc1a5 |
T |
A |
7: 16,515,902 (GRCm39) |
L26Q |
probably benign |
Het |
Slc38a3 |
T |
G |
9: 107,534,908 (GRCm39) |
M156L |
probably damaging |
Het |
Slc45a2 |
A |
T |
15: 11,001,233 (GRCm39) |
I111F |
probably benign |
Het |
Slc4a3 |
T |
A |
1: 75,528,810 (GRCm39) |
M491K |
probably benign |
Het |
Son |
A |
G |
16: 91,453,734 (GRCm39) |
D827G |
probably damaging |
Het |
Sppl2c |
A |
T |
11: 104,077,710 (GRCm39) |
H170L |
probably damaging |
Het |
St6gal2 |
T |
A |
17: 55,797,935 (GRCm39) |
|
probably null |
Het |
Taf4b |
T |
A |
18: 15,031,106 (GRCm39) |
L830H |
probably damaging |
Het |
Tex22 |
A |
G |
12: 113,038,696 (GRCm39) |
|
probably null |
Het |
Tiam2 |
C |
T |
17: 3,568,860 (GRCm39) |
R1669C |
probably damaging |
Het |
Tmprss15 |
T |
A |
16: 78,821,223 (GRCm39) |
N506I |
probably damaging |
Het |
Topors |
A |
T |
4: 40,260,686 (GRCm39) |
I866K |
unknown |
Het |
Trip12 |
G |
T |
1: 84,743,771 (GRCm39) |
T512K |
possibly damaging |
Het |
Ubr1 |
T |
A |
2: 120,791,585 (GRCm39) |
H133L |
probably damaging |
Het |
Wwtr1 |
T |
C |
3: 57,366,441 (GRCm39) |
D422G |
probably damaging |
Het |
Zfp689 |
A |
C |
7: 127,043,758 (GRCm39) |
C291G |
probably damaging |
Het |
Zfyve9 |
A |
G |
4: 108,576,877 (GRCm39) |
L68P |
possibly damaging |
Het |
Zswim5 |
G |
T |
4: 116,735,219 (GRCm39) |
R188L |
probably benign |
Het |
|
Other mutations in Dop1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00476:Dop1b
|
APN |
16 |
93,596,914 (GRCm39) |
unclassified |
probably benign |
|
IGL00492:Dop1b
|
APN |
16 |
93,577,670 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00753:Dop1b
|
APN |
16 |
93,566,512 (GRCm39) |
missense |
probably benign |
|
IGL00832:Dop1b
|
APN |
16 |
93,560,289 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00939:Dop1b
|
APN |
16 |
93,570,971 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01019:Dop1b
|
APN |
16 |
93,607,117 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01288:Dop1b
|
APN |
16 |
93,536,181 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01505:Dop1b
|
APN |
16 |
93,554,004 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01535:Dop1b
|
APN |
16 |
93,566,846 (GRCm39) |
nonsense |
probably null |
|
IGL01696:Dop1b
|
APN |
16 |
93,567,128 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02077:Dop1b
|
APN |
16 |
93,577,648 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02163:Dop1b
|
APN |
16 |
93,559,315 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02234:Dop1b
|
APN |
16 |
93,549,039 (GRCm39) |
missense |
probably benign |
|
IGL02302:Dop1b
|
APN |
16 |
93,607,005 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02485:Dop1b
|
APN |
16 |
93,567,710 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02563:Dop1b
|
APN |
16 |
93,574,293 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02733:Dop1b
|
APN |
16 |
93,536,079 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02792:Dop1b
|
APN |
16 |
93,598,460 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02941:Dop1b
|
APN |
16 |
93,552,361 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03143:Dop1b
|
APN |
16 |
93,556,543 (GRCm39) |
missense |
probably benign |
|
PIT4519001:Dop1b
|
UTSW |
16 |
93,558,942 (GRCm39) |
missense |
probably benign |
|
R0320:Dop1b
|
UTSW |
16 |
93,607,035 (GRCm39) |
missense |
probably benign |
0.02 |
R0499:Dop1b
|
UTSW |
16 |
93,567,325 (GRCm39) |
missense |
probably benign |
0.00 |
R0501:Dop1b
|
UTSW |
16 |
93,549,750 (GRCm39) |
missense |
probably benign |
0.00 |
R0534:Dop1b
|
UTSW |
16 |
93,559,393 (GRCm39) |
missense |
probably benign |
0.04 |
R0583:Dop1b
|
UTSW |
16 |
93,552,374 (GRCm39) |
missense |
probably benign |
0.30 |
R0626:Dop1b
|
UTSW |
16 |
93,560,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R0724:Dop1b
|
UTSW |
16 |
93,559,213 (GRCm39) |
missense |
probably benign |
0.01 |
R0907:Dop1b
|
UTSW |
16 |
93,598,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R1263:Dop1b
|
UTSW |
16 |
93,574,274 (GRCm39) |
missense |
probably benign |
|
R1378:Dop1b
|
UTSW |
16 |
93,567,280 (GRCm39) |
missense |
probably benign |
|
R1572:Dop1b
|
UTSW |
16 |
93,567,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R1604:Dop1b
|
UTSW |
16 |
93,559,458 (GRCm39) |
missense |
probably benign |
|
R1642:Dop1b
|
UTSW |
16 |
93,559,203 (GRCm39) |
missense |
probably benign |
0.00 |
R1668:Dop1b
|
UTSW |
16 |
93,562,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R1669:Dop1b
|
UTSW |
16 |
93,566,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R1702:Dop1b
|
UTSW |
16 |
93,544,509 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1711:Dop1b
|
UTSW |
16 |
93,596,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Dop1b
|
UTSW |
16 |
93,513,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Dop1b
|
UTSW |
16 |
93,579,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R1988:Dop1b
|
UTSW |
16 |
93,563,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Dop1b
|
UTSW |
16 |
93,566,323 (GRCm39) |
missense |
probably benign |
0.36 |
R2139:Dop1b
|
UTSW |
16 |
93,567,895 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2355:Dop1b
|
UTSW |
16 |
93,567,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R3609:Dop1b
|
UTSW |
16 |
93,536,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R3792:Dop1b
|
UTSW |
16 |
93,568,734 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4364:Dop1b
|
UTSW |
16 |
93,567,812 (GRCm39) |
missense |
probably benign |
0.00 |
R4380:Dop1b
|
UTSW |
16 |
93,513,120 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4455:Dop1b
|
UTSW |
16 |
93,563,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R4779:Dop1b
|
UTSW |
16 |
93,553,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Dop1b
|
UTSW |
16 |
93,589,978 (GRCm39) |
missense |
probably benign |
0.00 |
R4834:Dop1b
|
UTSW |
16 |
93,536,892 (GRCm39) |
start codon destroyed |
probably null |
0.70 |
R4866:Dop1b
|
UTSW |
16 |
93,560,318 (GRCm39) |
critical splice donor site |
probably null |
|
R4882:Dop1b
|
UTSW |
16 |
93,549,802 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4900:Dop1b
|
UTSW |
16 |
93,560,318 (GRCm39) |
critical splice donor site |
probably null |
|
R5153:Dop1b
|
UTSW |
16 |
93,570,891 (GRCm39) |
missense |
probably damaging |
0.98 |
R5176:Dop1b
|
UTSW |
16 |
93,536,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R5206:Dop1b
|
UTSW |
16 |
93,598,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R5320:Dop1b
|
UTSW |
16 |
93,536,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R5361:Dop1b
|
UTSW |
16 |
93,567,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R5380:Dop1b
|
UTSW |
16 |
93,560,298 (GRCm39) |
missense |
probably damaging |
0.96 |
R5476:Dop1b
|
UTSW |
16 |
93,570,801 (GRCm39) |
splice site |
probably null |
|
R5502:Dop1b
|
UTSW |
16 |
93,590,114 (GRCm39) |
missense |
probably benign |
0.00 |
R5543:Dop1b
|
UTSW |
16 |
93,595,808 (GRCm39) |
missense |
probably damaging |
0.98 |
R5557:Dop1b
|
UTSW |
16 |
93,560,819 (GRCm39) |
missense |
probably damaging |
0.96 |
R5901:Dop1b
|
UTSW |
16 |
93,566,639 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5907:Dop1b
|
UTSW |
16 |
93,598,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R6174:Dop1b
|
UTSW |
16 |
93,563,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R6256:Dop1b
|
UTSW |
16 |
93,604,102 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6383:Dop1b
|
UTSW |
16 |
93,579,136 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6525:Dop1b
|
UTSW |
16 |
93,606,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R6554:Dop1b
|
UTSW |
16 |
93,557,346 (GRCm39) |
missense |
probably benign |
0.22 |
R6823:Dop1b
|
UTSW |
16 |
93,552,373 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7036:Dop1b
|
UTSW |
16 |
93,574,378 (GRCm39) |
missense |
probably benign |
0.01 |
R7058:Dop1b
|
UTSW |
16 |
93,573,878 (GRCm39) |
missense |
probably benign |
0.00 |
R7061:Dop1b
|
UTSW |
16 |
93,558,951 (GRCm39) |
missense |
probably benign |
0.00 |
R7209:Dop1b
|
UTSW |
16 |
93,566,733 (GRCm39) |
missense |
probably benign |
|
R7214:Dop1b
|
UTSW |
16 |
93,607,023 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7232:Dop1b
|
UTSW |
16 |
93,557,373 (GRCm39) |
critical splice donor site |
probably null |
|
R7255:Dop1b
|
UTSW |
16 |
93,567,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R7335:Dop1b
|
UTSW |
16 |
93,544,396 (GRCm39) |
missense |
probably benign |
0.04 |
R7535:Dop1b
|
UTSW |
16 |
93,603,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R7700:Dop1b
|
UTSW |
16 |
93,595,649 (GRCm39) |
splice site |
probably null |
|
R7763:Dop1b
|
UTSW |
16 |
93,552,402 (GRCm39) |
missense |
probably benign |
0.00 |
R7814:Dop1b
|
UTSW |
16 |
93,596,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R7839:Dop1b
|
UTSW |
16 |
93,560,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R7862:Dop1b
|
UTSW |
16 |
93,546,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R7894:Dop1b
|
UTSW |
16 |
93,607,092 (GRCm39) |
missense |
probably benign |
0.01 |
R7952:Dop1b
|
UTSW |
16 |
93,546,848 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7956:Dop1b
|
UTSW |
16 |
93,567,916 (GRCm39) |
critical splice donor site |
probably null |
|
R8033:Dop1b
|
UTSW |
16 |
93,566,371 (GRCm39) |
missense |
probably benign |
|
R8061:Dop1b
|
UTSW |
16 |
93,546,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R8067:Dop1b
|
UTSW |
16 |
93,562,336 (GRCm39) |
nonsense |
probably null |
|
R8146:Dop1b
|
UTSW |
16 |
93,546,827 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8184:Dop1b
|
UTSW |
16 |
93,573,881 (GRCm39) |
missense |
probably benign |
0.13 |
R8263:Dop1b
|
UTSW |
16 |
93,559,083 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8329:Dop1b
|
UTSW |
16 |
93,568,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R8555:Dop1b
|
UTSW |
16 |
93,568,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R8683:Dop1b
|
UTSW |
16 |
93,570,809 (GRCm39) |
missense |
probably benign |
|
R8683:Dop1b
|
UTSW |
16 |
93,568,699 (GRCm39) |
missense |
probably damaging |
0.98 |
R8716:Dop1b
|
UTSW |
16 |
93,577,673 (GRCm39) |
nonsense |
probably null |
|
R8807:Dop1b
|
UTSW |
16 |
93,558,973 (GRCm39) |
missense |
probably benign |
0.03 |
R8840:Dop1b
|
UTSW |
16 |
93,607,005 (GRCm39) |
missense |
probably benign |
0.08 |
R8851:Dop1b
|
UTSW |
16 |
93,559,398 (GRCm39) |
missense |
probably benign |
0.39 |
R8884:Dop1b
|
UTSW |
16 |
93,556,550 (GRCm39) |
missense |
probably benign |
|
R8976:Dop1b
|
UTSW |
16 |
93,558,969 (GRCm39) |
missense |
probably benign |
0.01 |
R9219:Dop1b
|
UTSW |
16 |
93,567,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R9238:Dop1b
|
UTSW |
16 |
93,546,018 (GRCm39) |
missense |
probably benign |
0.14 |
R9284:Dop1b
|
UTSW |
16 |
93,557,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R9289:Dop1b
|
UTSW |
16 |
93,568,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R9298:Dop1b
|
UTSW |
16 |
93,597,087 (GRCm39) |
missense |
probably damaging |
0.96 |
R9338:Dop1b
|
UTSW |
16 |
93,600,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R9346:Dop1b
|
UTSW |
16 |
93,577,702 (GRCm39) |
critical splice donor site |
probably null |
|
R9444:Dop1b
|
UTSW |
16 |
93,607,127 (GRCm39) |
missense |
probably benign |
0.00 |
R9500:Dop1b
|
UTSW |
16 |
93,607,171 (GRCm39) |
missense |
probably benign |
|
R9601:Dop1b
|
UTSW |
16 |
93,544,531 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9793:Dop1b
|
UTSW |
16 |
93,598,503 (GRCm39) |
missense |
probably benign |
0.30 |
Z1088:Dop1b
|
UTSW |
16 |
93,560,214 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Dop1b
|
UTSW |
16 |
93,604,756 (GRCm39) |
missense |
possibly damaging |
0.82 |
Z1176:Dop1b
|
UTSW |
16 |
93,600,434 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dop1b
|
UTSW |
16 |
93,566,469 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Dop1b
|
UTSW |
16 |
93,560,783 (GRCm39) |
missense |
probably damaging |
1.00 |
|