Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610021A01Rik |
T |
C |
7: 41,275,667 (GRCm39) |
S457P |
probably damaging |
Het |
Aak1 |
A |
G |
6: 86,964,234 (GRCm39) |
N945S |
unknown |
Het |
Actr1a |
C |
A |
19: 46,369,438 (GRCm39) |
R192L |
possibly damaging |
Het |
Adgrl2 |
T |
A |
3: 148,534,119 (GRCm39) |
N1036I |
probably damaging |
Het |
Ak5 |
A |
G |
3: 152,361,511 (GRCm39) |
V137A |
probably damaging |
Het |
Aldh1a2 |
T |
C |
9: 71,169,055 (GRCm39) |
V179A |
probably damaging |
Het |
Ap2b1 |
A |
T |
11: 83,237,579 (GRCm39) |
I548F |
probably damaging |
Het |
Arhgef10l |
A |
G |
4: 140,292,550 (GRCm39) |
Y352H |
probably damaging |
Het |
Atad5 |
C |
T |
11: 79,986,524 (GRCm39) |
T537M |
possibly damaging |
Het |
Atoh7 |
A |
G |
10: 62,935,938 (GRCm39) |
K2E |
possibly damaging |
Het |
BC061237 |
A |
G |
14: 44,741,658 (GRCm39) |
I134V |
probably benign |
Het |
Cadm1 |
T |
C |
9: 47,701,136 (GRCm39) |
I141T |
probably damaging |
Het |
Capn10 |
T |
C |
1: 92,871,454 (GRCm39) |
S351P |
probably damaging |
Het |
Cct6b |
T |
C |
11: 82,654,959 (GRCm39) |
|
probably benign |
Het |
Cd19 |
T |
C |
7: 126,011,330 (GRCm39) |
T284A |
probably benign |
Het |
Cfap53 |
A |
G |
18: 74,432,253 (GRCm39) |
Y47C |
probably damaging |
Het |
Cldn18 |
T |
C |
9: 99,578,162 (GRCm39) |
M194V |
probably benign |
Het |
Dgkb |
T |
A |
12: 38,652,777 (GRCm39) |
Y721N |
probably damaging |
Het |
Dmbt1 |
A |
G |
7: 130,721,372 (GRCm39) |
Q1880R |
possibly damaging |
Het |
Dock2 |
T |
C |
11: 34,599,646 (GRCm39) |
N311S |
possibly damaging |
Het |
Dpysl5 |
G |
T |
5: 30,935,375 (GRCm39) |
M159I |
probably benign |
Het |
Eif2b3 |
G |
A |
4: 116,901,778 (GRCm39) |
G147E |
probably damaging |
Het |
Fam193a |
A |
G |
5: 34,597,796 (GRCm39) |
D531G |
probably benign |
Het |
Fndc3b |
T |
C |
3: 27,555,329 (GRCm39) |
|
probably benign |
Het |
Foxe3 |
C |
A |
4: 114,782,523 (GRCm39) |
A230S |
unknown |
Het |
Gm5591 |
A |
T |
7: 38,219,727 (GRCm39) |
V382E |
probably benign |
Het |
Gm7995 |
A |
T |
14: 42,132,228 (GRCm39) |
N21I |
probably damaging |
Het |
Ipo8 |
G |
A |
6: 148,676,547 (GRCm39) |
P981S |
probably benign |
Het |
Kcnh8 |
A |
G |
17: 53,104,486 (GRCm39) |
D161G |
probably benign |
Het |
Krt71 |
A |
G |
15: 101,645,180 (GRCm39) |
I377T |
possibly damaging |
Het |
Krt75 |
A |
T |
15: 101,476,767 (GRCm39) |
M374K |
probably benign |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Lpcat1 |
A |
G |
13: 73,662,029 (GRCm39) |
T409A |
probably benign |
Het |
Lrch1 |
A |
T |
14: 75,032,808 (GRCm39) |
I514K |
probably benign |
Het |
Mc4r |
A |
C |
18: 66,993,110 (GRCm39) |
M1R |
probably null |
Het |
Mthfd1l |
A |
T |
10: 3,978,466 (GRCm39) |
H442L |
probably damaging |
Het |
Or5d38 |
T |
A |
2: 87,954,718 (GRCm39) |
I204F |
probably damaging |
Het |
Pdcd1lg2 |
T |
C |
19: 29,423,553 (GRCm39) |
M199T |
probably benign |
Het |
Pigg |
G |
A |
5: 108,484,066 (GRCm39) |
V438M |
probably damaging |
Het |
Pira12 |
T |
C |
7: 3,898,365 (GRCm39) |
E319G |
probably benign |
Het |
Ppfibp1 |
T |
A |
6: 146,920,681 (GRCm39) |
|
probably null |
Het |
Rbm15 |
T |
A |
3: 107,239,372 (GRCm39) |
Y342F |
possibly damaging |
Het |
Rhbdl1 |
A |
T |
17: 26,054,116 (GRCm39) |
V278E |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,465,669 (GRCm39) |
N4781S |
probably damaging |
Het |
Scn7a |
A |
T |
2: 66,525,206 (GRCm39) |
|
silent |
Het |
Sfswap |
A |
G |
5: 129,581,168 (GRCm39) |
R114G |
probably damaging |
Het |
Sohlh2 |
C |
A |
3: 55,104,282 (GRCm39) |
A258D |
possibly damaging |
Het |
Sstr4 |
T |
A |
2: 148,237,782 (GRCm39) |
V131D |
possibly damaging |
Het |
Tmem131l |
A |
T |
3: 83,831,479 (GRCm39) |
F818I |
probably damaging |
Het |
Trappc6b |
A |
G |
12: 59,097,149 (GRCm39) |
F58L |
probably damaging |
Het |
Vmn1r229 |
A |
T |
17: 21,035,418 (GRCm39) |
H221L |
possibly damaging |
Het |
Vmn1r33 |
T |
A |
6: 66,588,783 (GRCm39) |
Y257F |
probably damaging |
Het |
Wdfy3 |
T |
C |
5: 101,993,231 (GRCm39) |
|
probably benign |
Het |
Zfp446 |
C |
T |
7: 12,713,564 (GRCm39) |
Q177* |
probably null |
Het |
Zup1 |
A |
G |
10: 33,795,301 (GRCm39) |
*552Q |
probably null |
Het |
|
Other mutations in Tenm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Tenm2
|
APN |
11 |
36,097,726 (GRCm39) |
splice site |
probably benign |
|
IGL00834:Tenm2
|
APN |
11 |
35,915,085 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00911:Tenm2
|
APN |
11 |
35,899,560 (GRCm39) |
nonsense |
probably null |
|
IGL00937:Tenm2
|
APN |
11 |
35,915,450 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01154:Tenm2
|
APN |
11 |
35,932,371 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01313:Tenm2
|
APN |
11 |
35,915,075 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01346:Tenm2
|
APN |
11 |
35,918,232 (GRCm39) |
nonsense |
probably null |
|
IGL01539:Tenm2
|
APN |
11 |
35,997,654 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01629:Tenm2
|
APN |
11 |
36,755,711 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01780:Tenm2
|
APN |
11 |
35,937,768 (GRCm39) |
missense |
probably benign |
|
IGL01821:Tenm2
|
APN |
11 |
35,914,710 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01988:Tenm2
|
APN |
11 |
35,918,078 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02002:Tenm2
|
APN |
11 |
36,097,922 (GRCm39) |
missense |
probably benign |
|
IGL02449:Tenm2
|
APN |
11 |
35,914,449 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02505:Tenm2
|
APN |
11 |
35,942,743 (GRCm39) |
nonsense |
probably null |
|
IGL02649:Tenm2
|
APN |
11 |
36,097,912 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02688:Tenm2
|
APN |
11 |
35,959,285 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02801:Tenm2
|
APN |
11 |
35,937,857 (GRCm39) |
nonsense |
probably null |
|
IGL02928:Tenm2
|
APN |
11 |
35,917,997 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02940:Tenm2
|
APN |
11 |
35,932,471 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03202:Tenm2
|
APN |
11 |
35,915,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03213:Tenm2
|
APN |
11 |
35,914,157 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03276:Tenm2
|
APN |
11 |
35,963,603 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03296:Tenm2
|
APN |
11 |
35,942,852 (GRCm39) |
splice site |
probably null |
|
IGL03381:Tenm2
|
APN |
11 |
35,959,238 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03398:Tenm2
|
APN |
11 |
35,915,370 (GRCm39) |
missense |
probably damaging |
1.00 |
browser
|
UTSW |
11 |
35,937,592 (GRCm39) |
critical splice donor site |
probably null |
|
mosaic
|
UTSW |
11 |
35,954,602 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02799:Tenm2
|
UTSW |
11 |
36,164,235 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4260001:Tenm2
|
UTSW |
11 |
36,054,557 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4382001:Tenm2
|
UTSW |
11 |
35,954,729 (GRCm39) |
missense |
probably damaging |
0.99 |
R0004:Tenm2
|
UTSW |
11 |
35,914,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R0420:Tenm2
|
UTSW |
11 |
36,097,951 (GRCm39) |
splice site |
probably benign |
|
R0537:Tenm2
|
UTSW |
11 |
36,054,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R0599:Tenm2
|
UTSW |
11 |
35,915,607 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0636:Tenm2
|
UTSW |
11 |
36,834,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R0693:Tenm2
|
UTSW |
11 |
35,915,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R0991:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0992:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1167:Tenm2
|
UTSW |
11 |
36,755,511 (GRCm39) |
missense |
probably benign |
0.30 |
R1177:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1178:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1179:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1180:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1181:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1193:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1194:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1195:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1195:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1195:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1259:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1265:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1267:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1268:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1269:Tenm2
|
UTSW |
11 |
35,899,185 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1270:Tenm2
|
UTSW |
11 |
35,932,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1272:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1273:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1311:Tenm2
|
UTSW |
11 |
35,959,421 (GRCm39) |
splice site |
probably benign |
|
R1374:Tenm2
|
UTSW |
11 |
35,899,281 (GRCm39) |
missense |
probably benign |
0.00 |
R1542:Tenm2
|
UTSW |
11 |
36,191,047 (GRCm39) |
missense |
probably damaging |
0.99 |
R1573:Tenm2
|
UTSW |
11 |
35,937,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R1579:Tenm2
|
UTSW |
11 |
35,997,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R1697:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1722:Tenm2
|
UTSW |
11 |
35,898,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R1756:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1793:Tenm2
|
UTSW |
11 |
35,914,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R1950:Tenm2
|
UTSW |
11 |
35,954,004 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1954:Tenm2
|
UTSW |
11 |
35,938,374 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2025:Tenm2
|
UTSW |
11 |
35,938,091 (GRCm39) |
nonsense |
probably null |
|
R2117:Tenm2
|
UTSW |
11 |
35,915,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R2244:Tenm2
|
UTSW |
11 |
36,755,689 (GRCm39) |
missense |
probably damaging |
0.98 |
R2298:Tenm2
|
UTSW |
11 |
35,937,604 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2432:Tenm2
|
UTSW |
11 |
35,918,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R3014:Tenm2
|
UTSW |
11 |
35,914,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R3115:Tenm2
|
UTSW |
11 |
35,914,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R3684:Tenm2
|
UTSW |
11 |
35,942,644 (GRCm39) |
missense |
probably benign |
0.00 |
R3685:Tenm2
|
UTSW |
11 |
35,942,644 (GRCm39) |
missense |
probably benign |
0.00 |
R3705:Tenm2
|
UTSW |
11 |
35,959,153 (GRCm39) |
missense |
probably damaging |
0.97 |
R3820:Tenm2
|
UTSW |
11 |
35,915,147 (GRCm39) |
missense |
probably damaging |
0.98 |
R3821:Tenm2
|
UTSW |
11 |
35,915,147 (GRCm39) |
missense |
probably damaging |
0.98 |
R3822:Tenm2
|
UTSW |
11 |
35,915,147 (GRCm39) |
missense |
probably damaging |
0.98 |
R3844:Tenm2
|
UTSW |
11 |
35,938,365 (GRCm39) |
missense |
probably damaging |
0.98 |
R3878:Tenm2
|
UTSW |
11 |
36,030,401 (GRCm39) |
critical splice donor site |
probably null |
|
R4019:Tenm2
|
UTSW |
11 |
35,937,901 (GRCm39) |
missense |
probably benign |
0.04 |
R4062:Tenm2
|
UTSW |
11 |
35,899,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R4367:Tenm2
|
UTSW |
11 |
35,918,225 (GRCm39) |
missense |
probably benign |
|
R4395:Tenm2
|
UTSW |
11 |
35,915,451 (GRCm39) |
missense |
probably benign |
0.23 |
R4508:Tenm2
|
UTSW |
11 |
35,899,172 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4534:Tenm2
|
UTSW |
11 |
35,953,931 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4539:Tenm2
|
UTSW |
11 |
35,937,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R4644:Tenm2
|
UTSW |
11 |
35,937,963 (GRCm39) |
missense |
probably benign |
0.00 |
R4661:Tenm2
|
UTSW |
11 |
35,915,275 (GRCm39) |
missense |
probably damaging |
0.99 |
R4669:Tenm2
|
UTSW |
11 |
35,901,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R4687:Tenm2
|
UTSW |
11 |
35,939,924 (GRCm39) |
missense |
probably benign |
|
R4711:Tenm2
|
UTSW |
11 |
36,191,039 (GRCm39) |
missense |
probably damaging |
0.98 |
R4816:Tenm2
|
UTSW |
11 |
35,918,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R4843:Tenm2
|
UTSW |
11 |
35,914,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R4850:Tenm2
|
UTSW |
11 |
35,914,315 (GRCm39) |
nonsense |
probably null |
|
R4870:Tenm2
|
UTSW |
11 |
35,969,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R5058:Tenm2
|
UTSW |
11 |
36,097,907 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5071:Tenm2
|
UTSW |
11 |
35,959,208 (GRCm39) |
missense |
probably damaging |
0.99 |
R5073:Tenm2
|
UTSW |
11 |
35,959,208 (GRCm39) |
missense |
probably damaging |
0.99 |
R5074:Tenm2
|
UTSW |
11 |
35,959,208 (GRCm39) |
missense |
probably damaging |
0.99 |
R5081:Tenm2
|
UTSW |
11 |
35,915,460 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5093:Tenm2
|
UTSW |
11 |
36,834,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R5170:Tenm2
|
UTSW |
11 |
35,915,633 (GRCm39) |
missense |
probably damaging |
0.98 |
R5253:Tenm2
|
UTSW |
11 |
35,938,028 (GRCm39) |
nonsense |
probably null |
|
R5343:Tenm2
|
UTSW |
11 |
35,960,330 (GRCm39) |
missense |
probably benign |
0.00 |
R5493:Tenm2
|
UTSW |
11 |
36,755,503 (GRCm39) |
missense |
probably benign |
0.01 |
R5600:Tenm2
|
UTSW |
11 |
36,054,541 (GRCm39) |
splice site |
probably null |
|
R5677:Tenm2
|
UTSW |
11 |
36,032,510 (GRCm39) |
missense |
probably damaging |
0.98 |
R5703:Tenm2
|
UTSW |
11 |
35,914,626 (GRCm39) |
missense |
probably benign |
0.34 |
R5707:Tenm2
|
UTSW |
11 |
35,938,009 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6026:Tenm2
|
UTSW |
11 |
35,963,556 (GRCm39) |
critical splice donor site |
probably null |
|
R6063:Tenm2
|
UTSW |
11 |
36,054,544 (GRCm39) |
critical splice donor site |
probably null |
|
R6086:Tenm2
|
UTSW |
11 |
35,899,473 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6151:Tenm2
|
UTSW |
11 |
35,899,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R6169:Tenm2
|
UTSW |
11 |
36,030,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R6193:Tenm2
|
UTSW |
11 |
35,937,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R6405:Tenm2
|
UTSW |
11 |
36,755,686 (GRCm39) |
missense |
probably benign |
0.44 |
R6477:Tenm2
|
UTSW |
11 |
35,901,334 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6607:Tenm2
|
UTSW |
11 |
35,954,602 (GRCm39) |
critical splice donor site |
probably null |
|
R6668:Tenm2
|
UTSW |
11 |
35,937,592 (GRCm39) |
critical splice donor site |
probably null |
|
R6825:Tenm2
|
UTSW |
11 |
35,937,711 (GRCm39) |
missense |
probably benign |
0.02 |
R6885:Tenm2
|
UTSW |
11 |
35,914,407 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7017:Tenm2
|
UTSW |
11 |
36,062,236 (GRCm39) |
missense |
probably damaging |
0.98 |
R7115:Tenm2
|
UTSW |
11 |
36,054,644 (GRCm39) |
missense |
probably damaging |
0.99 |
R7153:Tenm2
|
UTSW |
11 |
35,915,009 (GRCm39) |
missense |
probably damaging |
0.98 |
R7173:Tenm2
|
UTSW |
11 |
35,932,378 (GRCm39) |
missense |
probably damaging |
0.99 |
R7199:Tenm2
|
UTSW |
11 |
36,062,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R7205:Tenm2
|
UTSW |
11 |
35,939,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R7250:Tenm2
|
UTSW |
11 |
35,963,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R7290:Tenm2
|
UTSW |
11 |
35,914,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R7366:Tenm2
|
UTSW |
11 |
35,960,241 (GRCm39) |
missense |
probably benign |
0.09 |
R7432:Tenm2
|
UTSW |
11 |
36,755,768 (GRCm39) |
missense |
probably benign |
|
R7504:Tenm2
|
UTSW |
11 |
36,030,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R7513:Tenm2
|
UTSW |
11 |
35,942,727 (GRCm39) |
missense |
probably benign |
0.34 |
R7523:Tenm2
|
UTSW |
11 |
35,969,408 (GRCm39) |
splice site |
probably null |
|
R7527:Tenm2
|
UTSW |
11 |
36,097,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R7648:Tenm2
|
UTSW |
11 |
35,997,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R7653:Tenm2
|
UTSW |
11 |
35,938,174 (GRCm39) |
missense |
probably benign |
0.09 |
R7717:Tenm2
|
UTSW |
11 |
36,755,762 (GRCm39) |
missense |
probably damaging |
0.97 |
R7739:Tenm2
|
UTSW |
11 |
35,960,388 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7762:Tenm2
|
UTSW |
11 |
35,914,133 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7786:Tenm2
|
UTSW |
11 |
35,901,276 (GRCm39) |
missense |
probably damaging |
0.99 |
R7803:Tenm2
|
UTSW |
11 |
35,937,943 (GRCm39) |
missense |
probably damaging |
0.98 |
R7834:Tenm2
|
UTSW |
11 |
35,915,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R7838:Tenm2
|
UTSW |
11 |
35,997,626 (GRCm39) |
missense |
probably benign |
0.02 |
R8073:Tenm2
|
UTSW |
11 |
36,030,471 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8076:Tenm2
|
UTSW |
11 |
35,918,048 (GRCm39) |
missense |
probably benign |
0.23 |
R8109:Tenm2
|
UTSW |
11 |
35,899,137 (GRCm39) |
missense |
probably benign |
|
R8306:Tenm2
|
UTSW |
11 |
35,960,196 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8352:Tenm2
|
UTSW |
11 |
35,914,428 (GRCm39) |
missense |
probably damaging |
0.98 |
R8452:Tenm2
|
UTSW |
11 |
35,914,428 (GRCm39) |
missense |
probably damaging |
0.98 |
R8864:Tenm2
|
UTSW |
11 |
35,918,022 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8880:Tenm2
|
UTSW |
11 |
35,942,788 (GRCm39) |
missense |
probably damaging |
0.99 |
R8969:Tenm2
|
UTSW |
11 |
35,942,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R9168:Tenm2
|
UTSW |
11 |
35,930,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R9279:Tenm2
|
UTSW |
11 |
35,959,303 (GRCm39) |
missense |
probably benign |
0.00 |
R9294:Tenm2
|
UTSW |
11 |
35,915,327 (GRCm39) |
missense |
probably damaging |
0.98 |
R9320:Tenm2
|
UTSW |
11 |
35,914,474 (GRCm39) |
missense |
probably damaging |
0.99 |
R9373:Tenm2
|
UTSW |
11 |
35,930,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R9408:Tenm2
|
UTSW |
11 |
35,960,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R9410:Tenm2
|
UTSW |
11 |
36,032,396 (GRCm39) |
missense |
probably damaging |
0.99 |
R9454:Tenm2
|
UTSW |
11 |
36,112,286 (GRCm39) |
missense |
probably benign |
|
R9489:Tenm2
|
UTSW |
11 |
36,834,791 (GRCm39) |
missense |
probably damaging |
0.99 |
R9711:Tenm2
|
UTSW |
11 |
35,915,341 (GRCm39) |
missense |
probably damaging |
0.99 |
RF021:Tenm2
|
UTSW |
11 |
35,915,030 (GRCm39) |
missense |
possibly damaging |
0.95 |
X0018:Tenm2
|
UTSW |
11 |
35,915,027 (GRCm39) |
missense |
probably damaging |
1.00 |
X0063:Tenm2
|
UTSW |
11 |
35,915,557 (GRCm39) |
missense |
probably benign |
|
Z1088:Tenm2
|
UTSW |
11 |
36,164,094 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tenm2
|
UTSW |
11 |
36,191,162 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Tenm2
|
UTSW |
11 |
35,899,061 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Tenm2
|
UTSW |
11 |
36,275,957 (GRCm39) |
missense |
probably benign |
0.01 |
|