Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb9 |
T |
A |
5: 124,227,909 (GRCm39) |
I111F |
probably benign |
Het |
Abcc12 |
A |
C |
8: 87,255,048 (GRCm39) |
|
probably benign |
Het |
Adgre1 |
G |
T |
17: 57,754,860 (GRCm39) |
V653L |
probably damaging |
Het |
Aebp2 |
T |
A |
6: 140,593,707 (GRCm39) |
D230E |
probably damaging |
Het |
Asap3 |
A |
G |
4: 135,956,768 (GRCm39) |
|
probably benign |
Het |
Bod1l |
T |
C |
5: 41,974,441 (GRCm39) |
E2291G |
probably damaging |
Het |
Casp8 |
A |
T |
1: 58,872,864 (GRCm39) |
S267C |
probably damaging |
Het |
Cchcr1 |
T |
C |
17: 35,836,233 (GRCm39) |
V341A |
probably damaging |
Het |
Cd2ap |
T |
A |
17: 43,126,980 (GRCm39) |
|
probably null |
Het |
Cimip3 |
AC |
A |
17: 47,744,348 (GRCm39) |
|
probably benign |
Het |
Clip1 |
T |
A |
5: 123,728,897 (GRCm39) |
E1155D |
probably damaging |
Het |
Cnnm2 |
A |
G |
19: 46,866,375 (GRCm39) |
E841G |
probably damaging |
Het |
Cntrl |
G |
A |
2: 35,010,061 (GRCm39) |
R245H |
probably damaging |
Het |
Cyp2b23 |
A |
T |
7: 26,380,842 (GRCm39) |
S128T |
probably benign |
Het |
Dhrs11 |
A |
T |
11: 84,712,579 (GRCm39) |
I196N |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 117,971,675 (GRCm39) |
|
probably benign |
Het |
Edc3 |
A |
T |
9: 57,655,686 (GRCm39) |
I479F |
possibly damaging |
Het |
Emg1 |
T |
A |
6: 124,682,009 (GRCm39) |
M172L |
probably benign |
Het |
Epha7 |
G |
A |
4: 28,938,680 (GRCm39) |
V512I |
probably benign |
Het |
Exoc7 |
T |
C |
11: 116,197,731 (GRCm39) |
D27G |
probably benign |
Het |
Fasl |
C |
A |
1: 161,615,760 (GRCm39) |
C32F |
probably benign |
Het |
Flg |
A |
T |
3: 93,187,307 (GRCm39) |
H253L |
probably benign |
Het |
Fnip2 |
A |
T |
3: 79,386,812 (GRCm39) |
D971E |
possibly damaging |
Het |
Gab2 |
A |
G |
7: 96,948,280 (GRCm39) |
Y290C |
probably damaging |
Het |
Gm17067 |
T |
A |
7: 42,360,104 (GRCm39) |
I43L |
possibly damaging |
Het |
Gpld1 |
A |
G |
13: 25,146,305 (GRCm39) |
Y183C |
probably damaging |
Het |
Gpr137c |
C |
A |
14: 45,516,392 (GRCm39) |
P327T |
probably benign |
Het |
Hepacam2 |
A |
G |
6: 3,494,477 (GRCm39) |
M1T |
probably null |
Het |
Ighv5-4 |
A |
T |
12: 113,561,060 (GRCm39) |
|
probably benign |
Het |
Iqca1l |
A |
T |
5: 24,750,440 (GRCm39) |
|
probably benign |
Het |
Itgb8 |
T |
A |
12: 119,131,740 (GRCm39) |
E635V |
possibly damaging |
Het |
Kat14 |
T |
C |
2: 144,245,982 (GRCm39) |
V469A |
probably damaging |
Het |
Kcnj15 |
C |
T |
16: 95,097,329 (GRCm39) |
T317I |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Klhl18 |
A |
T |
9: 110,265,151 (GRCm39) |
L285Q |
probably damaging |
Het |
Krt90 |
G |
A |
15: 101,471,218 (GRCm39) |
R15W |
probably damaging |
Het |
Krtap4-8 |
A |
T |
11: 99,670,863 (GRCm39) |
C203S |
unknown |
Het |
Lsp1 |
C |
T |
7: 142,040,098 (GRCm39) |
S75F |
probably damaging |
Het |
Map1b |
A |
G |
13: 99,567,580 (GRCm39) |
S1714P |
unknown |
Het |
Mcm2 |
A |
G |
6: 88,865,234 (GRCm39) |
I481T |
probably damaging |
Het |
Mcpt9 |
T |
C |
14: 56,265,136 (GRCm39) |
T122A |
probably benign |
Het |
Megf10 |
A |
T |
18: 57,422,465 (GRCm39) |
R947W |
probably damaging |
Het |
Or2ag18 |
A |
T |
7: 106,405,072 (GRCm39) |
V199D |
probably damaging |
Het |
Or51ai2 |
A |
T |
7: 103,586,616 (GRCm39) |
N10Y |
possibly damaging |
Het |
Pank4 |
A |
G |
4: 155,054,058 (GRCm39) |
Y79C |
probably damaging |
Het |
Pds5b |
T |
A |
5: 150,670,171 (GRCm39) |
N386K |
probably benign |
Het |
Pfkm |
A |
G |
15: 98,022,928 (GRCm39) |
M362V |
probably benign |
Het |
Phc2 |
T |
C |
4: 128,637,351 (GRCm39) |
|
probably null |
Het |
Pou4f1 |
C |
T |
14: 104,703,611 (GRCm39) |
A274T |
unknown |
Het |
Proc |
A |
G |
18: 32,256,758 (GRCm39) |
L303P |
probably damaging |
Het |
Ptk2b |
C |
T |
14: 66,394,517 (GRCm39) |
G821D |
possibly damaging |
Het |
Rlim |
T |
C |
X: 103,006,267 (GRCm39) |
T545A |
probably benign |
Het |
Serpinb6c |
T |
C |
13: 34,077,888 (GRCm39) |
N161D |
probably benign |
Het |
Sf3b1 |
G |
A |
1: 55,058,548 (GRCm39) |
Q14* |
probably null |
Het |
Sh3d19 |
G |
A |
3: 86,014,534 (GRCm39) |
V442M |
possibly damaging |
Het |
Slc30a8 |
A |
G |
15: 52,185,097 (GRCm39) |
I140V |
probably benign |
Het |
Spata1 |
T |
A |
3: 146,181,079 (GRCm39) |
N293I |
probably damaging |
Het |
Strap |
T |
G |
6: 137,712,380 (GRCm39) |
C10G |
probably damaging |
Het |
Tcf7 |
C |
A |
11: 52,173,793 (GRCm39) |
|
probably benign |
Het |
Tmem114 |
A |
T |
16: 8,230,054 (GRCm39) |
M116K |
probably damaging |
Het |
Tmem63b |
A |
G |
17: 45,988,884 (GRCm39) |
S113P |
probably damaging |
Het |
Tmtc3 |
A |
C |
10: 100,284,888 (GRCm39) |
N582K |
probably damaging |
Het |
Tnfrsf11b |
G |
A |
15: 54,119,578 (GRCm39) |
|
probably benign |
Het |
Trim30a |
A |
G |
7: 104,060,348 (GRCm39) |
V476A |
probably damaging |
Het |
Ush2a |
T |
A |
1: 188,132,151 (GRCm39) |
V791D |
probably benign |
Het |
Vmn2r99 |
T |
C |
17: 19,614,635 (GRCm39) |
F785S |
possibly damaging |
Het |
Vps35l |
A |
G |
7: 118,345,613 (GRCm39) |
T49A |
possibly damaging |
Het |
Wdr35 |
A |
T |
12: 9,036,077 (GRCm39) |
I283F |
probably benign |
Het |
Wnt10b |
G |
T |
15: 98,672,219 (GRCm39) |
A166E |
possibly damaging |
Het |
|
Other mutations in Tns2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01575:Tns2
|
APN |
15 |
102,021,626 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01935:Tns2
|
APN |
15 |
102,020,069 (GRCm39) |
splice site |
probably null |
|
IGL01994:Tns2
|
APN |
15 |
102,019,814 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02025:Tns2
|
APN |
15 |
102,020,484 (GRCm39) |
nonsense |
probably null |
|
IGL02135:Tns2
|
APN |
15 |
102,021,461 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02355:Tns2
|
APN |
15 |
102,020,725 (GRCm39) |
missense |
probably benign |
|
IGL02362:Tns2
|
APN |
15 |
102,020,725 (GRCm39) |
missense |
probably benign |
|
IGL02439:Tns2
|
APN |
15 |
102,022,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02488:Tns2
|
APN |
15 |
102,021,178 (GRCm39) |
missense |
probably benign |
|
IGL02546:Tns2
|
APN |
15 |
102,019,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02616:Tns2
|
APN |
15 |
102,019,850 (GRCm39) |
missense |
probably benign |
|
IGL02628:Tns2
|
APN |
15 |
102,020,263 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02658:Tns2
|
APN |
15 |
102,016,231 (GRCm39) |
splice site |
probably benign |
|
IGL03267:Tns2
|
APN |
15 |
102,013,813 (GRCm39) |
critical splice donor site |
probably null |
|
P0005:Tns2
|
UTSW |
15 |
102,022,491 (GRCm39) |
missense |
probably damaging |
0.98 |
R0586:Tns2
|
UTSW |
15 |
102,018,020 (GRCm39) |
splice site |
probably benign |
|
R0791:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0817:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0818:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0819:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0820:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1451:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1452:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1453:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1454:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1455:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1487:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1510:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1579:Tns2
|
UTSW |
15 |
102,019,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R1698:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1772:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1843:Tns2
|
UTSW |
15 |
102,021,568 (GRCm39) |
splice site |
probably null |
|
R1923:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1924:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1927:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1980:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2051:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2087:Tns2
|
UTSW |
15 |
102,015,554 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2100:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2103:Tns2
|
UTSW |
15 |
102,021,100 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2105:Tns2
|
UTSW |
15 |
102,015,941 (GRCm39) |
missense |
probably benign |
0.27 |
R2224:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2225:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2227:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2252:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2253:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Tns2
|
UTSW |
15 |
102,020,458 (GRCm39) |
missense |
probably damaging |
0.99 |
R2304:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2318:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2446:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2447:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2448:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2566:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2567:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2897:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2898:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3159:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3160:Tns2
|
UTSW |
15 |
102,021,771 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3162:Tns2
|
UTSW |
15 |
102,021,771 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3162:Tns2
|
UTSW |
15 |
102,021,771 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3196:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3237:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3426:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3427:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3428:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3695:Tns2
|
UTSW |
15 |
102,021,184 (GRCm39) |
missense |
probably null |
|
R3767:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4113:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4157:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4394:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4395:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4396:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4439:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4441:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4537:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4538:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4541:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4599:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4602:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4773:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4774:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4775:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4776:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4880:Tns2
|
UTSW |
15 |
102,020,474 (GRCm39) |
missense |
probably damaging |
0.98 |
R4989:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5014:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5058:Tns2
|
UTSW |
15 |
102,016,295 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5253:Tns2
|
UTSW |
15 |
102,019,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R5336:Tns2
|
UTSW |
15 |
102,019,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R5351:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5452:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5453:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5629:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5630:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5631:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5685:Tns2
|
UTSW |
15 |
102,015,538 (GRCm39) |
missense |
probably benign |
0.02 |
R5844:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6048:Tns2
|
UTSW |
15 |
102,019,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R6067:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6079:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6130:Tns2
|
UTSW |
15 |
102,019,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R6136:Tns2
|
UTSW |
15 |
102,015,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R6138:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6199:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6210:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6426:Tns2
|
UTSW |
15 |
102,015,472 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6544:Tns2
|
UTSW |
15 |
102,022,269 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6594:Tns2
|
UTSW |
15 |
102,018,994 (GRCm39) |
missense |
probably benign |
0.00 |
R6596:Tns2
|
UTSW |
15 |
102,018,994 (GRCm39) |
missense |
probably benign |
0.00 |
R6734:Tns2
|
UTSW |
15 |
102,011,551 (GRCm39) |
missense |
probably damaging |
0.96 |
R7061:Tns2
|
UTSW |
15 |
102,012,914 (GRCm39) |
start codon destroyed |
probably null |
|
R7070:Tns2
|
UTSW |
15 |
102,012,968 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7110:Tns2
|
UTSW |
15 |
102,013,801 (GRCm39) |
missense |
probably damaging |
0.99 |
R7410:Tns2
|
UTSW |
15 |
102,018,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R7447:Tns2
|
UTSW |
15 |
102,019,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R7751:Tns2
|
UTSW |
15 |
102,018,163 (GRCm39) |
missense |
probably benign |
0.02 |
R8052:Tns2
|
UTSW |
15 |
102,021,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R8114:Tns2
|
UTSW |
15 |
102,019,825 (GRCm39) |
missense |
probably benign |
0.01 |
R8906:Tns2
|
UTSW |
15 |
102,020,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8964:Tns2
|
UTSW |
15 |
102,011,553 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9192:Tns2
|
UTSW |
15 |
102,021,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R9273:Tns2
|
UTSW |
15 |
102,021,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R9307:Tns2
|
UTSW |
15 |
102,018,996 (GRCm39) |
missense |
probably damaging |
0.97 |
R9402:Tns2
|
UTSW |
15 |
102,021,623 (GRCm39) |
missense |
probably damaging |
0.99 |
R9612:Tns2
|
UTSW |
15 |
102,015,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:Tns2
|
UTSW |
15 |
102,012,933 (GRCm39) |
missense |
probably benign |
0.03 |
U15987:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
X0009:Tns2
|
UTSW |
15 |
102,020,900 (GRCm39) |
missense |
possibly damaging |
0.94 |
X0026:Tns2
|
UTSW |
15 |
102,018,937 (GRCm39) |
missense |
probably damaging |
1.00 |
|