Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aagab |
C |
A |
9: 63,524,096 (GRCm39) |
L68M |
probably damaging |
Het |
Abca13 |
T |
G |
11: 9,531,498 (GRCm39) |
L4575W |
probably damaging |
Het |
Abcb11 |
A |
T |
2: 69,076,105 (GRCm39) |
V1201D |
probably damaging |
Het |
Aldoa |
G |
T |
7: 126,395,166 (GRCm39) |
A252E |
probably damaging |
Het |
Ap1b1 |
C |
T |
11: 4,981,700 (GRCm39) |
A536V |
probably benign |
Het |
Arhgef3 |
A |
G |
14: 27,115,957 (GRCm39) |
H233R |
possibly damaging |
Het |
Arhgef40 |
A |
T |
14: 52,238,320 (GRCm39) |
E1266D |
probably damaging |
Het |
Atp1a4 |
C |
T |
1: 172,062,642 (GRCm39) |
V622M |
probably damaging |
Het |
Aup1 |
A |
G |
6: 83,032,258 (GRCm39) |
T142A |
probably benign |
Het |
Bcl6 |
A |
T |
16: 23,796,319 (GRCm39) |
I36N |
probably damaging |
Het |
Best1 |
A |
G |
19: 9,966,514 (GRCm39) |
S358P |
probably damaging |
Het |
Cadps |
T |
G |
14: 12,449,759 (GRCm38) |
Q1150P |
probably damaging |
Het |
Capn5 |
T |
A |
7: 97,780,403 (GRCm39) |
E322D |
possibly damaging |
Het |
Cd300ld2 |
A |
T |
11: 114,904,513 (GRCm39) |
M118K |
probably benign |
Het |
Cdh9 |
T |
C |
15: 16,856,075 (GRCm39) |
L705P |
probably damaging |
Het |
Cep170b |
T |
G |
12: 112,709,504 (GRCm39) |
N436K |
probably damaging |
Het |
Chil6 |
T |
A |
3: 106,313,278 (GRCm39) |
I24F |
probably benign |
Het |
Chmp2a |
T |
A |
7: 12,767,782 (GRCm39) |
K48* |
probably null |
Het |
Col19a1 |
C |
T |
1: 24,339,665 (GRCm39) |
|
probably benign |
Het |
Cops7b |
C |
A |
1: 86,520,043 (GRCm39) |
Q65K |
probably benign |
Het |
Cyp2e1 |
T |
A |
7: 140,349,069 (GRCm39) |
L133H |
probably damaging |
Het |
Dkc1 |
T |
C |
X: 74,152,339 (GRCm39) |
|
probably benign |
Het |
Erlec1 |
A |
G |
11: 30,900,767 (GRCm39) |
Y134H |
probably damaging |
Het |
F8 |
C |
A |
X: 74,423,204 (GRCm39) |
|
probably benign |
Het |
Fus |
G |
A |
7: 127,580,679 (GRCm39) |
R252Q |
possibly damaging |
Het |
Fzd3 |
A |
T |
14: 65,490,555 (GRCm39) |
D9E |
probably benign |
Het |
Gm15821 |
T |
C |
17: 34,433,259 (GRCm39) |
|
probably benign |
Het |
Gm5117 |
C |
A |
8: 32,228,344 (GRCm39) |
|
noncoding transcript |
Het |
H2-Q6 |
A |
G |
17: 35,644,152 (GRCm39) |
I45V |
probably benign |
Het |
Hectd1 |
A |
G |
12: 51,847,496 (GRCm39) |
|
probably null |
Het |
Ifi204 |
T |
C |
1: 173,583,220 (GRCm39) |
K333E |
probably benign |
Het |
Ildr1 |
G |
A |
16: 36,536,526 (GRCm39) |
G185D |
probably damaging |
Het |
Itgb2 |
G |
A |
10: 77,383,052 (GRCm39) |
D141N |
probably damaging |
Het |
Kdm1b |
G |
T |
13: 47,214,331 (GRCm39) |
D226Y |
probably damaging |
Het |
Krt77 |
A |
G |
15: 101,769,381 (GRCm39) |
L460P |
probably damaging |
Het |
Lamp3 |
A |
G |
16: 19,474,207 (GRCm39) |
I389T |
possibly damaging |
Het |
Macroh2a1 |
A |
G |
13: 56,222,143 (GRCm39) |
V336A |
probably damaging |
Het |
Mars1 |
C |
A |
10: 127,140,113 (GRCm39) |
E414* |
probably null |
Het |
Mpg |
T |
C |
11: 32,180,042 (GRCm39) |
V190A |
probably damaging |
Het |
Myh15 |
A |
G |
16: 48,937,626 (GRCm39) |
I742M |
possibly damaging |
Het |
Nell2 |
A |
T |
15: 95,194,144 (GRCm39) |
|
probably benign |
Het |
Nmur1 |
T |
C |
1: 86,314,057 (GRCm39) |
D370G |
probably benign |
Het |
Npsr1 |
A |
G |
9: 24,009,578 (GRCm39) |
E28G |
probably benign |
Het |
Or52r1 |
T |
C |
7: 102,536,814 (GRCm39) |
E182G |
probably damaging |
Het |
Or56a3 |
A |
T |
7: 104,735,540 (GRCm39) |
I206L |
probably benign |
Het |
Or7a42 |
G |
T |
10: 78,791,767 (GRCm39) |
V243F |
probably benign |
Het |
Or8b12c |
G |
A |
9: 37,715,627 (GRCm39) |
C140Y |
probably benign |
Het |
Pdzrn3 |
T |
C |
6: 101,128,899 (GRCm39) |
N589S |
possibly damaging |
Het |
Pkd1l3 |
T |
C |
8: 110,359,848 (GRCm39) |
L901P |
probably damaging |
Het |
Plekhg1 |
G |
T |
10: 3,907,139 (GRCm39) |
K685N |
probably damaging |
Het |
Prim1 |
T |
A |
10: 127,865,652 (GRCm39) |
*419R |
probably null |
Het |
Ptk2b |
G |
T |
14: 66,391,692 (GRCm39) |
N905K |
probably damaging |
Het |
Rbm34 |
T |
C |
8: 127,676,071 (GRCm39) |
I395V |
probably benign |
Het |
Rfx1 |
A |
G |
8: 84,822,438 (GRCm39) |
E912G |
possibly damaging |
Het |
Rngtt |
T |
C |
4: 33,337,936 (GRCm39) |
V253A |
possibly damaging |
Het |
Slc2a9 |
A |
G |
5: 38,594,002 (GRCm39) |
Y169H |
possibly damaging |
Het |
Slc49a4 |
G |
T |
16: 35,555,928 (GRCm39) |
D177E |
probably benign |
Het |
Susd4 |
C |
A |
1: 182,719,645 (GRCm39) |
T420K |
probably benign |
Het |
Tdrd3 |
G |
A |
14: 87,749,118 (GRCm39) |
G676D |
probably damaging |
Het |
Tec |
T |
C |
5: 72,946,587 (GRCm39) |
K47E |
probably damaging |
Het |
Tmprss15 |
A |
T |
16: 78,784,629 (GRCm39) |
D675E |
probably benign |
Het |
Vmn1r84 |
A |
G |
7: 12,096,346 (GRCm39) |
C104R |
probably damaging |
Het |
Vmn2r49 |
T |
A |
7: 9,710,378 (GRCm39) |
M785L |
probably benign |
Het |
Vmn2r85 |
G |
T |
10: 130,261,449 (GRCm39) |
T296K |
probably damaging |
Het |
Wdr3 |
C |
T |
3: 100,059,290 (GRCm39) |
S343N |
probably benign |
Het |
Yju2 |
G |
T |
17: 56,269,051 (GRCm39) |
G53V |
probably damaging |
Het |
Zfp143 |
A |
T |
7: 109,690,993 (GRCm39) |
M515L |
possibly damaging |
Het |
Zfp735 |
A |
G |
11: 73,580,626 (GRCm39) |
I42V |
probably benign |
Het |
Zswim5 |
A |
T |
4: 116,819,749 (GRCm39) |
M385L |
probably benign |
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 |
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 |
R8943:Tenm2
|
UTSW |
11 |
36,834,861 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
|