Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110004F10Rik |
C |
A |
7: 115,692,757 (GRCm39) |
D20E |
probably benign |
Het |
Abcb9 |
T |
A |
5: 124,216,853 (GRCm39) |
M455L |
probably benign |
Het |
Add2 |
G |
A |
6: 86,095,752 (GRCm39) |
V475M |
probably benign |
Het |
Apoh |
T |
A |
11: 108,300,064 (GRCm39) |
Y238N |
probably damaging |
Het |
Arpp21 |
A |
G |
9: 111,896,360 (GRCm39) |
S681P |
probably benign |
Het |
Atp1a3 |
A |
C |
7: 24,698,389 (GRCm39) |
F149C |
probably damaging |
Het |
B9d1 |
A |
G |
11: 61,397,186 (GRCm39) |
D27G |
probably benign |
Het |
Bfar |
T |
A |
16: 13,503,001 (GRCm39) |
M1K |
probably null |
Het |
Bok |
T |
C |
1: 93,616,963 (GRCm39) |
V103A |
probably damaging |
Het |
Brca1 |
A |
C |
11: 101,414,758 (GRCm39) |
H1125Q |
probably benign |
Het |
Card9 |
T |
A |
2: 26,247,632 (GRCm39) |
M218L |
probably damaging |
Het |
Cers1 |
T |
C |
8: 70,776,018 (GRCm39) |
V303A |
probably damaging |
Het |
Col6a5 |
T |
C |
9: 105,814,534 (GRCm39) |
I493V |
unknown |
Het |
Coro7 |
T |
C |
16: 4,446,085 (GRCm39) |
Y880C |
probably damaging |
Het |
Cyp2b19 |
T |
C |
7: 26,463,801 (GRCm39) |
Y318H |
probably benign |
Het |
Dennd3 |
T |
A |
15: 73,394,131 (GRCm39) |
L52Q |
probably damaging |
Het |
Dlat |
A |
T |
9: 50,570,670 (GRCm39) |
C33S |
probably benign |
Het |
Dmxl2 |
T |
A |
9: 54,287,099 (GRCm39) |
Q2646L |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,610,295 (GRCm39) |
N1703D |
probably damaging |
Het |
Dock10 |
T |
A |
1: 80,518,998 (GRCm39) |
H1241L |
probably damaging |
Het |
Fbxl17 |
T |
G |
17: 63,794,910 (GRCm39) |
I391L |
probably benign |
Het |
Fdxacb1 |
A |
G |
9: 50,681,418 (GRCm39) |
D113G |
possibly damaging |
Het |
Flii |
A |
G |
11: 60,605,919 (GRCm39) |
S1185P |
probably benign |
Het |
Gm14496 |
A |
T |
2: 181,637,577 (GRCm39) |
Q217L |
possibly damaging |
Het |
Heatr9 |
A |
T |
11: 83,410,018 (GRCm39) |
D74E |
probably benign |
Het |
Heca |
C |
A |
10: 17,783,895 (GRCm39) |
E91* |
probably null |
Het |
Ikzf4 |
T |
G |
10: 128,468,575 (GRCm39) |
T635P |
probably benign |
Het |
Kif17 |
C |
T |
4: 138,008,688 (GRCm39) |
P382S |
probably damaging |
Het |
Kmt5b |
T |
C |
19: 3,865,330 (GRCm39) |
V775A |
probably benign |
Het |
Mapk8ip2 |
T |
A |
15: 89,343,241 (GRCm39) |
F661Y |
probably damaging |
Het |
Mapkap1 |
A |
G |
2: 34,423,859 (GRCm39) |
E111G |
possibly damaging |
Het |
Med9 |
T |
A |
11: 59,839,266 (GRCm39) |
N58K |
probably benign |
Het |
Mid2 |
T |
A |
X: 139,578,981 (GRCm39) |
Y61N |
probably damaging |
Het |
Mief1 |
T |
A |
15: 80,132,080 (GRCm39) |
Y50* |
probably null |
Het |
Mios |
T |
C |
6: 8,235,429 (GRCm39) |
M859T |
probably benign |
Het |
Muc5ac |
G |
T |
7: 141,352,619 (GRCm39) |
C702F |
possibly damaging |
Het |
Nkiras1 |
T |
C |
14: 18,276,935 (GRCm38) |
|
probably benign |
Het |
Or11i1 |
A |
C |
3: 106,729,608 (GRCm39) |
I89R |
possibly damaging |
Het |
Or11i1 |
T |
A |
3: 106,729,624 (GRCm39) |
M84L |
possibly damaging |
Het |
Or56a3b |
T |
G |
7: 104,771,520 (GRCm39) |
H285Q |
probably null |
Het |
Or5ae2 |
T |
A |
7: 84,506,509 (GRCm39) |
C311S |
probably benign |
Het |
Pcsk5 |
C |
T |
19: 17,410,963 (GRCm39) |
V1810M |
probably benign |
Het |
Pex1 |
T |
C |
5: 3,680,270 (GRCm39) |
V964A |
probably damaging |
Het |
Pgm2l1 |
A |
T |
7: 99,916,794 (GRCm39) |
M471L |
probably benign |
Het |
Pkd1l2 |
T |
C |
8: 117,738,314 (GRCm39) |
T2182A |
probably damaging |
Het |
Plscr1l1 |
G |
A |
9: 92,233,084 (GRCm39) |
C69Y |
probably damaging |
Het |
Polr1b |
T |
A |
2: 128,951,257 (GRCm39) |
I290K |
probably benign |
Het |
Prkg1 |
T |
A |
19: 31,563,045 (GRCm39) |
M119L |
probably damaging |
Het |
Rbl1 |
A |
G |
2: 157,019,275 (GRCm39) |
V490A |
probably benign |
Het |
Shtn1 |
G |
C |
19: 59,039,305 (GRCm39) |
R45G |
probably damaging |
Het |
Slc10a6 |
T |
A |
5: 103,776,848 (GRCm39) |
Y84F |
probably benign |
Het |
Slc25a23 |
T |
C |
17: 57,366,597 (GRCm39) |
D26G |
probably damaging |
Het |
Slc41a2 |
T |
C |
10: 83,152,320 (GRCm39) |
K52E |
probably damaging |
Het |
Slc4a5 |
T |
C |
6: 83,247,951 (GRCm39) |
F501L |
probably benign |
Het |
Slfn5 |
T |
A |
11: 82,847,226 (GRCm39) |
M37K |
probably benign |
Het |
Taf3 |
T |
C |
2: 9,956,770 (GRCm39) |
T466A |
probably damaging |
Het |
Thbs2 |
C |
T |
17: 14,891,750 (GRCm39) |
G929D |
probably damaging |
Het |
Tmc3 |
A |
T |
7: 83,271,746 (GRCm39) |
D995V |
probably damaging |
Het |
Tmem262 |
T |
C |
19: 6,130,452 (GRCm39) |
F59L |
possibly damaging |
Het |
Triobp |
A |
G |
15: 78,875,228 (GRCm39) |
D137G |
probably damaging |
Het |
Tspear |
T |
C |
10: 77,702,199 (GRCm39) |
F211L |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,728,670 (GRCm39) |
|
probably benign |
Het |
Ugt2b5 |
T |
A |
5: 87,287,550 (GRCm39) |
M206L |
probably benign |
Het |
Ush1g |
A |
T |
11: 115,209,466 (GRCm39) |
S243T |
probably damaging |
Het |
Usp19 |
A |
T |
9: 108,370,433 (GRCm39) |
T86S |
possibly damaging |
Het |
Wdhd1 |
A |
G |
14: 47,506,149 (GRCm39) |
V255A |
probably benign |
Het |
Wdr11 |
G |
A |
7: 129,220,394 (GRCm39) |
W594* |
probably null |
Het |
Wnk3 |
T |
A |
X: 149,993,933 (GRCm39) |
Y331* |
probably null |
Het |
Zfp429 |
A |
T |
13: 67,538,523 (GRCm39) |
I307K |
probably benign |
Het |
Zkscan14 |
T |
A |
5: 145,132,444 (GRCm39) |
K362N |
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 |
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 |
R5966:Sptbn1
|
UTSW |
11 |
30,074,873 (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 |
|