Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310034C09Rik |
A |
G |
16: 88,555,902 (GRCm39) |
T39A |
probably damaging |
Het |
Abca3 |
G |
A |
17: 24,596,681 (GRCm39) |
G378D |
probably damaging |
Het |
Abtb2 |
T |
C |
2: 103,397,565 (GRCm39) |
V165A |
possibly damaging |
Het |
Ache |
A |
G |
5: 137,288,504 (GRCm39) |
E70G |
probably damaging |
Het |
Adamtsl4 |
T |
C |
3: 95,588,119 (GRCm39) |
T623A |
probably benign |
Het |
Ahdc1 |
G |
A |
4: 132,791,935 (GRCm39) |
V1059I |
probably benign |
Het |
Ajuba |
G |
A |
14: 54,810,915 (GRCm39) |
Q357* |
probably null |
Het |
Ano7 |
A |
T |
1: 93,330,700 (GRCm39) |
D54V |
|
Het |
Apob |
A |
T |
12: 8,055,072 (GRCm39) |
D1357V |
probably damaging |
Het |
Atad2b |
T |
A |
12: 5,067,992 (GRCm39) |
Y997N |
probably damaging |
Het |
Bhlhe22 |
C |
A |
3: 18,110,006 (GRCm39) |
T352K |
probably damaging |
Het |
Bsn |
T |
C |
9: 107,992,533 (GRCm39) |
E1073G |
probably damaging |
Het |
Bzw2 |
G |
A |
12: 36,180,054 (GRCm39) |
R58* |
probably null |
Het |
C7 |
G |
T |
15: 5,023,725 (GRCm39) |
S694R |
probably benign |
Het |
Cbr2 |
T |
A |
11: 120,621,087 (GRCm39) |
H170L |
probably benign |
Het |
Cdcp3 |
G |
A |
7: 130,837,641 (GRCm39) |
W512* |
probably null |
Het |
Cgas |
C |
A |
9: 78,340,315 (GRCm39) |
K472N |
probably benign |
Het |
Ckap2l |
T |
C |
2: 129,126,975 (GRCm39) |
N401S |
probably benign |
Het |
Cldn1 |
A |
G |
16: 26,190,346 (GRCm39) |
F11L |
probably benign |
Het |
Cmtr1 |
A |
G |
17: 29,895,174 (GRCm39) |
T118A |
probably benign |
Het |
Cog6 |
T |
C |
3: 52,890,610 (GRCm39) |
E610G |
probably benign |
Het |
Col3a1 |
G |
T |
1: 45,371,301 (GRCm39) |
A451S |
probably null |
Het |
Cr1l |
T |
A |
1: 194,799,878 (GRCm39) |
R265S |
probably benign |
Het |
Dapk1 |
T |
C |
13: 60,902,024 (GRCm39) |
I951T |
probably benign |
Het |
Dnah9 |
T |
C |
11: 66,009,770 (GRCm39) |
N706D |
probably benign |
Het |
Dpysl5 |
A |
T |
5: 30,940,539 (GRCm39) |
T239S |
probably benign |
Het |
Ect2l |
T |
A |
10: 18,004,894 (GRCm39) |
Y913F |
probably benign |
Het |
Elf5 |
C |
A |
2: 103,269,641 (GRCm39) |
A74D |
possibly damaging |
Het |
Erap1 |
T |
C |
13: 74,814,258 (GRCm39) |
V399A |
probably benign |
Het |
Ercc4 |
A |
G |
16: 12,965,657 (GRCm39) |
D763G |
probably damaging |
Het |
Fam222b |
T |
A |
11: 78,045,683 (GRCm39) |
C415S |
possibly damaging |
Het |
Fat4 |
A |
C |
3: 39,031,511 (GRCm39) |
N2432T |
probably damaging |
Het |
Fbn2 |
G |
T |
18: 58,186,833 (GRCm39) |
C1689* |
probably null |
Het |
Frrs1l |
T |
A |
4: 56,972,282 (GRCm39) |
T140S |
probably damaging |
Het |
Gm5141 |
A |
T |
13: 62,924,877 (GRCm39) |
H10Q |
possibly damaging |
Het |
Inafm1 |
A |
T |
7: 16,007,079 (GRCm39) |
L46Q |
probably damaging |
Het |
Irak2 |
T |
C |
6: 113,650,045 (GRCm39) |
L260P |
probably damaging |
Het |
Kat2b |
T |
C |
17: 53,977,706 (GRCm39) |
L751P |
probably damaging |
Het |
Kcnh1 |
T |
A |
1: 192,019,913 (GRCm39) |
I413N |
probably benign |
Het |
Kirrel1 |
T |
C |
3: 86,990,695 (GRCm39) |
D709G |
probably benign |
Het |
Lama4 |
T |
C |
10: 38,956,536 (GRCm39) |
V1153A |
possibly damaging |
Het |
Lipg |
A |
T |
18: 75,088,655 (GRCm39) |
F98L |
probably benign |
Het |
Lman1 |
T |
C |
18: 66,127,936 (GRCm39) |
E236G |
probably damaging |
Het |
Lrp1 |
T |
A |
10: 127,409,325 (GRCm39) |
D1598V |
probably damaging |
Het |
Lrrc71 |
T |
A |
3: 87,650,384 (GRCm39) |
N230Y |
probably damaging |
Het |
Maneal |
T |
C |
4: 124,750,983 (GRCm39) |
S258G |
possibly damaging |
Het |
Marchf10 |
T |
A |
11: 105,281,532 (GRCm39) |
E251V |
probably damaging |
Het |
Mpdz |
A |
G |
4: 81,215,570 (GRCm39) |
I1484T |
probably damaging |
Het |
Mtcl1 |
T |
A |
17: 66,647,534 (GRCm39) |
N1882I |
probably benign |
Het |
Neb |
G |
A |
2: 52,110,212 (GRCm39) |
A212V |
probably benign |
Het |
Obscn |
G |
A |
11: 58,903,672 (GRCm39) |
S7434L |
probably benign |
Het |
Or14j8 |
A |
C |
17: 38,263,048 (GRCm39) |
I289S |
probably damaging |
Het |
Or1ad8 |
T |
A |
11: 50,898,223 (GRCm39) |
C141* |
probably null |
Het |
Or1j12 |
A |
T |
2: 36,342,872 (GRCm39) |
I92F |
probably damaging |
Het |
Or4k47 |
T |
C |
2: 111,451,538 (GRCm39) |
M294V |
probably benign |
Het |
Or8g2b |
A |
G |
9: 39,750,753 (GRCm39) |
M8V |
probably benign |
Het |
Orc6 |
T |
C |
8: 86,029,590 (GRCm39) |
|
probably null |
Het |
Otogl |
T |
G |
10: 107,710,394 (GRCm39) |
E565A |
possibly damaging |
Het |
Papss1 |
A |
G |
3: 131,290,899 (GRCm39) |
Q214R |
probably benign |
Het |
Pck2 |
G |
A |
14: 55,786,169 (GRCm39) |
V653M |
probably benign |
Het |
Plxna4 |
G |
A |
6: 32,192,113 (GRCm39) |
Q826* |
probably null |
Het |
Pms1 |
T |
A |
1: 53,295,889 (GRCm39) |
T161S |
probably benign |
Het |
Prkar2a |
C |
A |
9: 108,617,669 (GRCm39) |
N242K |
probably damaging |
Het |
Prss1 |
T |
A |
6: 41,439,690 (GRCm39) |
I141N |
probably damaging |
Het |
Puf60 |
A |
G |
15: 75,943,717 (GRCm39) |
V235A |
probably damaging |
Het |
Rapgef6 |
T |
A |
11: 54,437,252 (GRCm39) |
F65Y |
probably benign |
Het |
Rasgef1b |
T |
C |
5: 99,447,898 (GRCm39) |
E104G |
unknown |
Het |
Rcn3 |
T |
C |
7: 44,734,333 (GRCm39) |
Y225C |
probably damaging |
Het |
Rhot1 |
G |
C |
11: 80,137,560 (GRCm39) |
W354S |
probably damaging |
Het |
Rp1 |
T |
C |
1: 4,417,513 (GRCm39) |
S1200G |
possibly damaging |
Het |
Scaper |
T |
A |
9: 55,745,460 (GRCm39) |
K603* |
probably null |
Het |
Selenbp1 |
G |
A |
3: 94,851,745 (GRCm39) |
V429I |
possibly damaging |
Het |
Setd5 |
T |
G |
6: 113,098,099 (GRCm39) |
S713A |
probably benign |
Het |
Shank1 |
T |
C |
7: 44,002,564 (GRCm39) |
Y1428H |
possibly damaging |
Het |
Slc11a1 |
G |
T |
1: 74,422,830 (GRCm39) |
W361L |
possibly damaging |
Het |
Spta1 |
A |
T |
1: 174,050,837 (GRCm39) |
D1772V |
possibly damaging |
Het |
St8sia6 |
T |
C |
2: 13,661,721 (GRCm39) |
H370R |
probably damaging |
Het |
Stkld1 |
A |
T |
2: 26,842,726 (GRCm39) |
D566V |
probably damaging |
Het |
Tango6 |
T |
C |
8: 107,415,791 (GRCm39) |
V204A |
probably benign |
Het |
Tdrd5 |
G |
A |
1: 156,129,293 (GRCm39) |
A139V |
probably damaging |
Het |
Tfip11 |
A |
T |
5: 112,479,044 (GRCm39) |
Q204L |
probably benign |
Het |
Tlr4 |
A |
T |
4: 66,759,430 (GRCm39) |
Q741L |
probably damaging |
Het |
Tmem18 |
A |
G |
12: 30,638,654 (GRCm39) |
M111V |
probably benign |
Het |
Togaram1 |
A |
G |
12: 65,042,292 (GRCm39) |
N1167S |
probably benign |
Het |
Trappc3 |
C |
T |
4: 126,168,945 (GRCm39) |
A145V |
possibly damaging |
Het |
Trbj2-3 |
T |
C |
6: 41,520,176 (GRCm39) |
F7S |
probably damaging |
Het |
Vinac1 |
A |
G |
2: 128,880,238 (GRCm39) |
S563P |
|
Het |
Vmn1r212 |
T |
A |
13: 23,067,731 (GRCm39) |
M201L |
probably benign |
Het |
Xaf1 |
C |
A |
11: 72,194,201 (GRCm39) |
C27* |
probably null |
Het |
Zeb1 |
T |
C |
18: 5,767,703 (GRCm39) |
V738A |
probably benign |
Het |
Zfp524 |
A |
T |
7: 5,020,883 (GRCm39) |
H137L |
probably damaging |
Het |
Zfyve19 |
A |
T |
2: 119,047,118 (GRCm39) |
H367L |
probably damaging |
Het |
Zim1 |
G |
A |
7: 6,680,872 (GRCm39) |
Q264* |
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 |
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 |
|