Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,510,620 (GRCm38) |
L4210P |
probably damaging |
Het |
Adcy6 |
T |
C |
15: 98,598,741 (GRCm38) |
T518A |
probably damaging |
Het |
Adgb |
C |
T |
10: 10,391,757 (GRCm38) |
V940I |
probably damaging |
Het |
Aqp11 |
A |
G |
7: 97,737,428 (GRCm38) |
V187A |
possibly damaging |
Het |
Arhgef15 |
A |
G |
11: 68,954,715 (GRCm38) |
S104P |
probably damaging |
Het |
Birc6 |
T |
A |
17: 74,696,404 (GRCm38) |
N4762K |
probably damaging |
Het |
Cacna1e |
T |
C |
1: 154,633,717 (GRCm38) |
D264G |
probably damaging |
Het |
Cela3b |
G |
T |
4: 137,424,856 (GRCm38) |
Q97K |
probably damaging |
Het |
Cenpc1 |
T |
A |
5: 86,035,434 (GRCm38) |
R499W |
possibly damaging |
Het |
Chct1 |
A |
G |
11: 85,173,312 (GRCm38) |
N93S |
probably benign |
Het |
Cnr1 |
C |
A |
4: 33,944,330 (GRCm38) |
C239* |
probably null |
Het |
Col6a2 |
T |
C |
10: 76,611,031 (GRCm38) |
K348E |
possibly damaging |
Het |
Ctnnb1 |
C |
A |
9: 120,955,168 (GRCm38) |
L368I |
probably benign |
Het |
Diras1 |
T |
C |
10: 81,022,081 (GRCm38) |
E112G |
probably benign |
Het |
Dop1a |
T |
A |
9: 86,502,997 (GRCm38) |
M332K |
possibly damaging |
Het |
Dpy19l1 |
T |
C |
9: 24,414,267 (GRCm38) |
*747W |
probably null |
Het |
Dydc2 |
T |
G |
14: 41,061,954 (GRCm38) |
T71P |
probably damaging |
Het |
Elapor2 |
A |
G |
5: 9,441,698 (GRCm38) |
Y686C |
probably damaging |
Het |
Ggt1 |
T |
A |
10: 75,585,238 (GRCm38) |
I429N |
probably benign |
Het |
Gm5114 |
G |
C |
7: 39,411,276 (GRCm38) |
L50V |
probably benign |
Het |
Gm5121 |
T |
G |
9: 57,334,483 (GRCm38) |
|
noncoding transcript |
Het |
Kidins220 |
A |
G |
12: 25,013,391 (GRCm38) |
D933G |
probably damaging |
Het |
Kirrel3 |
A |
G |
9: 35,013,276 (GRCm38) |
K286R |
probably damaging |
Het |
Klf5 |
T |
C |
14: 99,301,508 (GRCm38) |
I39T |
probably benign |
Het |
Krt14 |
C |
T |
11: 100,204,758 (GRCm38) |
V274I |
possibly damaging |
Het |
Meiob |
A |
G |
17: 24,835,051 (GRCm38) |
D364G |
probably benign |
Het |
Mroh7 |
T |
A |
4: 106,681,885 (GRCm38) |
E1190D |
possibly damaging |
Het |
Mtmr7 |
T |
C |
8: 40,558,162 (GRCm38) |
E285G |
possibly damaging |
Het |
Nhsl1 |
C |
T |
10: 18,526,503 (GRCm38) |
T1159M |
probably damaging |
Het |
Odad4 |
G |
A |
11: 100,554,061 (GRCm38) |
A348T |
probably damaging |
Het |
Or1af1 |
C |
A |
2: 37,219,889 (GRCm38) |
N133K |
probably benign |
Het |
Or1e23 |
G |
T |
11: 73,516,625 (GRCm38) |
D191E |
probably damaging |
Het |
Or2b2b |
A |
G |
13: 21,674,599 (GRCm38) |
L115P |
probably damaging |
Het |
Pcare |
G |
T |
17: 71,751,572 (GRCm38) |
A370E |
possibly damaging |
Het |
Pdlim5 |
T |
A |
3: 142,304,299 (GRCm38) |
H294L |
probably damaging |
Het |
Pdzd8 |
A |
T |
19: 59,299,625 (GRCm38) |
D1114E |
probably benign |
Het |
Phf20 |
T |
G |
2: 156,296,771 (GRCm38) |
|
probably null |
Het |
Plec |
C |
T |
15: 76,199,671 (GRCm38) |
|
probably benign |
Het |
Ppp1r18 |
T |
C |
17: 35,867,236 (GRCm38) |
M1T |
probably null |
Het |
Ppp4r3a |
G |
A |
12: 101,058,511 (GRCm38) |
T243I |
probably damaging |
Het |
Prss41 |
C |
T |
17: 23,842,416 (GRCm38) |
V134I |
probably benign |
Het |
Pter |
T |
C |
2: 12,978,180 (GRCm38) |
|
probably benign |
Het |
Rasgef1b |
T |
G |
5: 99,234,602 (GRCm38) |
K176N |
possibly damaging |
Het |
Reps1 |
T |
A |
10: 18,056,010 (GRCm38) |
D16E |
probably benign |
Het |
Slc4a5 |
T |
A |
6: 83,261,415 (GRCm38) |
D73E |
probably benign |
Het |
Smgc |
A |
T |
15: 91,860,663 (GRCm38) |
T146S |
possibly damaging |
Het |
Sptbn1 |
A |
T |
11: 30,143,174 (GRCm38) |
W396R |
possibly damaging |
Het |
Stkld1 |
A |
G |
2: 26,943,987 (GRCm38) |
E162G |
probably damaging |
Het |
Tanc1 |
T |
C |
2: 59,758,530 (GRCm38) |
F106L |
probably benign |
Het |
Tarbp1 |
A |
G |
8: 126,467,144 (GRCm38) |
Y340H |
probably damaging |
Het |
Tmem64 |
T |
C |
4: 15,266,288 (GRCm38) |
C113R |
probably damaging |
Het |
Try4 |
T |
C |
6: 41,305,043 (GRCm38) |
F188L |
possibly damaging |
Het |
Ucn3 |
A |
G |
13: 3,941,556 (GRCm38) |
V32A |
probably benign |
Het |
Vmn2r83 |
T |
A |
10: 79,491,349 (GRCm38) |
M597K |
possibly damaging |
Het |
Wdr90 |
A |
G |
17: 25,857,192 (GRCm38) |
V491A |
probably benign |
Het |
Xylt1 |
T |
A |
7: 117,656,494 (GRCm38) |
M763K |
possibly damaging |
Het |
Zfp507 |
G |
T |
7: 35,794,163 (GRCm38) |
A485E |
probably damaging |
Het |
|
Other mutations in Tenm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Tenm2
|
APN |
11 |
36,206,899 (GRCm38) |
splice site |
probably benign |
|
IGL00834:Tenm2
|
APN |
11 |
36,024,258 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00911:Tenm2
|
APN |
11 |
36,008,733 (GRCm38) |
nonsense |
probably null |
|
IGL00937:Tenm2
|
APN |
11 |
36,024,623 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01154:Tenm2
|
APN |
11 |
36,041,544 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01313:Tenm2
|
APN |
11 |
36,024,248 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01346:Tenm2
|
APN |
11 |
36,027,405 (GRCm38) |
nonsense |
probably null |
|
IGL01539:Tenm2
|
APN |
11 |
36,106,827 (GRCm38) |
missense |
possibly damaging |
0.89 |
IGL01629:Tenm2
|
APN |
11 |
36,864,884 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01780:Tenm2
|
APN |
11 |
36,046,941 (GRCm38) |
missense |
probably benign |
|
IGL01821:Tenm2
|
APN |
11 |
36,023,883 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01988:Tenm2
|
APN |
11 |
36,027,251 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02002:Tenm2
|
APN |
11 |
36,207,095 (GRCm38) |
missense |
probably benign |
|
IGL02449:Tenm2
|
APN |
11 |
36,023,622 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02505:Tenm2
|
APN |
11 |
36,051,916 (GRCm38) |
nonsense |
probably null |
|
IGL02649:Tenm2
|
APN |
11 |
36,207,085 (GRCm38) |
missense |
possibly damaging |
0.85 |
IGL02688:Tenm2
|
APN |
11 |
36,068,458 (GRCm38) |
missense |
probably benign |
0.05 |
IGL02801:Tenm2
|
APN |
11 |
36,047,030 (GRCm38) |
nonsense |
probably null |
|
IGL02928:Tenm2
|
APN |
11 |
36,027,170 (GRCm38) |
missense |
possibly damaging |
0.69 |
IGL02940:Tenm2
|
APN |
11 |
36,041,644 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03202:Tenm2
|
APN |
11 |
36,024,548 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03213:Tenm2
|
APN |
11 |
36,023,330 (GRCm38) |
missense |
probably benign |
0.05 |
IGL03276:Tenm2
|
APN |
11 |
36,072,776 (GRCm38) |
missense |
possibly damaging |
0.95 |
IGL03296:Tenm2
|
APN |
11 |
36,052,025 (GRCm38) |
splice site |
probably null |
|
IGL03381:Tenm2
|
APN |
11 |
36,068,411 (GRCm38) |
missense |
probably benign |
0.01 |
IGL03398:Tenm2
|
APN |
11 |
36,024,543 (GRCm38) |
missense |
probably damaging |
1.00 |
browser
|
UTSW |
11 |
36,046,765 (GRCm38) |
critical splice donor site |
probably null |
|
mosaic
|
UTSW |
11 |
36,063,775 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02799:Tenm2
|
UTSW |
11 |
36,273,408 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4260001:Tenm2
|
UTSW |
11 |
36,163,730 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4382001:Tenm2
|
UTSW |
11 |
36,063,902 (GRCm38) |
missense |
probably damaging |
0.99 |
R0004:Tenm2
|
UTSW |
11 |
36,023,357 (GRCm38) |
missense |
probably damaging |
1.00 |
R0420:Tenm2
|
UTSW |
11 |
36,207,124 (GRCm38) |
splice site |
probably benign |
|
R0537:Tenm2
|
UTSW |
11 |
36,163,730 (GRCm38) |
missense |
probably damaging |
1.00 |
R0599:Tenm2
|
UTSW |
11 |
36,024,780 (GRCm38) |
missense |
possibly damaging |
0.93 |
R0636:Tenm2
|
UTSW |
11 |
36,943,976 (GRCm38) |
missense |
probably damaging |
1.00 |
R0693:Tenm2
|
UTSW |
11 |
36,024,809 (GRCm38) |
missense |
probably damaging |
1.00 |
R0991:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0992:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1167:Tenm2
|
UTSW |
11 |
36,864,684 (GRCm38) |
missense |
probably benign |
0.30 |
R1177:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1178:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1179:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1180:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1181:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1193:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1194:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1195:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1195:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1195:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1259:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1265:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1267:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1268:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1269:Tenm2
|
UTSW |
11 |
36,008,358 (GRCm38) |
missense |
possibly damaging |
0.64 |
R1270:Tenm2
|
UTSW |
11 |
36,041,659 (GRCm38) |
missense |
probably damaging |
1.00 |
R1272:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1273:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1311:Tenm2
|
UTSW |
11 |
36,068,594 (GRCm38) |
splice site |
probably benign |
|
R1374:Tenm2
|
UTSW |
11 |
36,008,454 (GRCm38) |
missense |
probably benign |
0.00 |
R1542:Tenm2
|
UTSW |
11 |
36,300,220 (GRCm38) |
missense |
probably damaging |
0.99 |
R1573:Tenm2
|
UTSW |
11 |
36,047,069 (GRCm38) |
missense |
probably damaging |
1.00 |
R1579:Tenm2
|
UTSW |
11 |
36,106,783 (GRCm38) |
missense |
probably damaging |
1.00 |
R1697:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1722:Tenm2
|
UTSW |
11 |
36,008,103 (GRCm38) |
missense |
probably damaging |
1.00 |
R1756:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1793:Tenm2
|
UTSW |
11 |
36,023,382 (GRCm38) |
missense |
probably damaging |
0.99 |
R1950:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1954:Tenm2
|
UTSW |
11 |
36,047,547 (GRCm38) |
missense |
possibly damaging |
0.87 |
R2025:Tenm2
|
UTSW |
11 |
36,047,264 (GRCm38) |
nonsense |
probably null |
|
R2117:Tenm2
|
UTSW |
11 |
36,024,854 (GRCm38) |
missense |
probably damaging |
1.00 |
R2244:Tenm2
|
UTSW |
11 |
36,864,862 (GRCm38) |
missense |
probably damaging |
0.98 |
R2298:Tenm2
|
UTSW |
11 |
36,046,777 (GRCm38) |
missense |
possibly damaging |
0.62 |
R2432:Tenm2
|
UTSW |
11 |
36,027,191 (GRCm38) |
missense |
probably damaging |
1.00 |
R3014:Tenm2
|
UTSW |
11 |
36,023,973 (GRCm38) |
missense |
probably damaging |
1.00 |
R3115:Tenm2
|
UTSW |
11 |
36,023,366 (GRCm38) |
missense |
probably damaging |
1.00 |
R3684:Tenm2
|
UTSW |
11 |
36,051,817 (GRCm38) |
missense |
probably benign |
0.00 |
R3685:Tenm2
|
UTSW |
11 |
36,051,817 (GRCm38) |
missense |
probably benign |
0.00 |
R3705:Tenm2
|
UTSW |
11 |
36,068,326 (GRCm38) |
missense |
probably damaging |
0.97 |
R3820:Tenm2
|
UTSW |
11 |
36,024,320 (GRCm38) |
missense |
probably damaging |
0.98 |
R3821:Tenm2
|
UTSW |
11 |
36,024,320 (GRCm38) |
missense |
probably damaging |
0.98 |
R3822:Tenm2
|
UTSW |
11 |
36,024,320 (GRCm38) |
missense |
probably damaging |
0.98 |
R3844:Tenm2
|
UTSW |
11 |
36,047,538 (GRCm38) |
missense |
probably damaging |
0.98 |
R3878:Tenm2
|
UTSW |
11 |
36,139,574 (GRCm38) |
critical splice donor site |
probably null |
|
R4019:Tenm2
|
UTSW |
11 |
36,047,074 (GRCm38) |
missense |
probably benign |
0.04 |
R4062:Tenm2
|
UTSW |
11 |
36,008,655 (GRCm38) |
missense |
probably damaging |
1.00 |
R4367:Tenm2
|
UTSW |
11 |
36,027,398 (GRCm38) |
missense |
probably benign |
|
R4395:Tenm2
|
UTSW |
11 |
36,024,624 (GRCm38) |
missense |
probably benign |
0.23 |
R4508:Tenm2
|
UTSW |
11 |
36,008,345 (GRCm38) |
missense |
possibly damaging |
0.82 |
R4534:Tenm2
|
UTSW |
11 |
36,063,104 (GRCm38) |
missense |
possibly damaging |
0.64 |
R4539:Tenm2
|
UTSW |
11 |
36,046,780 (GRCm38) |
missense |
probably damaging |
1.00 |
R4644:Tenm2
|
UTSW |
11 |
36,047,136 (GRCm38) |
missense |
probably benign |
0.00 |
R4661:Tenm2
|
UTSW |
11 |
36,024,448 (GRCm38) |
missense |
probably damaging |
0.99 |
R4669:Tenm2
|
UTSW |
11 |
36,010,487 (GRCm38) |
missense |
probably damaging |
1.00 |
R4687:Tenm2
|
UTSW |
11 |
36,049,097 (GRCm38) |
missense |
probably benign |
|
R4711:Tenm2
|
UTSW |
11 |
36,300,212 (GRCm38) |
missense |
probably damaging |
0.98 |
R4816:Tenm2
|
UTSW |
11 |
36,027,290 (GRCm38) |
missense |
probably damaging |
1.00 |
R4843:Tenm2
|
UTSW |
11 |
36,024,020 (GRCm38) |
missense |
probably damaging |
1.00 |
R4850:Tenm2
|
UTSW |
11 |
36,023,488 (GRCm38) |
nonsense |
probably null |
|
R4870:Tenm2
|
UTSW |
11 |
36,078,569 (GRCm38) |
missense |
probably damaging |
1.00 |
R5058:Tenm2
|
UTSW |
11 |
36,207,080 (GRCm38) |
missense |
possibly damaging |
0.80 |
R5071:Tenm2
|
UTSW |
11 |
36,068,381 (GRCm38) |
missense |
probably damaging |
0.99 |
R5073:Tenm2
|
UTSW |
11 |
36,068,381 (GRCm38) |
missense |
probably damaging |
0.99 |
R5074:Tenm2
|
UTSW |
11 |
36,068,381 (GRCm38) |
missense |
probably damaging |
0.99 |
R5081:Tenm2
|
UTSW |
11 |
36,024,633 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5093:Tenm2
|
UTSW |
11 |
36,944,162 (GRCm38) |
missense |
probably damaging |
1.00 |
R5170:Tenm2
|
UTSW |
11 |
36,024,806 (GRCm38) |
missense |
probably damaging |
0.98 |
R5253:Tenm2
|
UTSW |
11 |
36,047,201 (GRCm38) |
nonsense |
probably null |
|
R5343:Tenm2
|
UTSW |
11 |
36,069,503 (GRCm38) |
missense |
probably benign |
0.00 |
R5493:Tenm2
|
UTSW |
11 |
36,864,676 (GRCm38) |
missense |
probably benign |
0.01 |
R5600:Tenm2
|
UTSW |
11 |
36,163,714 (GRCm38) |
splice site |
probably null |
|
R5677:Tenm2
|
UTSW |
11 |
36,141,683 (GRCm38) |
missense |
probably damaging |
0.98 |
R5703:Tenm2
|
UTSW |
11 |
36,023,799 (GRCm38) |
missense |
probably benign |
0.34 |
R6026:Tenm2
|
UTSW |
11 |
36,072,729 (GRCm38) |
critical splice donor site |
probably null |
|
R6063:Tenm2
|
UTSW |
11 |
36,163,717 (GRCm38) |
critical splice donor site |
probably null |
|
R6086:Tenm2
|
UTSW |
11 |
36,008,646 (GRCm38) |
missense |
possibly damaging |
0.64 |
R6151:Tenm2
|
UTSW |
11 |
36,008,783 (GRCm38) |
missense |
probably damaging |
1.00 |
R6169:Tenm2
|
UTSW |
11 |
36,139,690 (GRCm38) |
missense |
probably damaging |
0.99 |
R6193:Tenm2
|
UTSW |
11 |
36,046,794 (GRCm38) |
missense |
probably damaging |
1.00 |
R6405:Tenm2
|
UTSW |
11 |
36,864,859 (GRCm38) |
missense |
probably benign |
0.44 |
R6477:Tenm2
|
UTSW |
11 |
36,010,507 (GRCm38) |
critical splice acceptor site |
probably null |
|
R6607:Tenm2
|
UTSW |
11 |
36,063,775 (GRCm38) |
critical splice donor site |
probably null |
|
R6668:Tenm2
|
UTSW |
11 |
36,046,765 (GRCm38) |
critical splice donor site |
probably null |
|
R6825:Tenm2
|
UTSW |
11 |
36,046,884 (GRCm38) |
missense |
probably benign |
0.02 |
R6885:Tenm2
|
UTSW |
11 |
36,023,580 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7017:Tenm2
|
UTSW |
11 |
36,171,409 (GRCm38) |
missense |
probably damaging |
0.98 |
R7115:Tenm2
|
UTSW |
11 |
36,163,817 (GRCm38) |
missense |
probably damaging |
0.99 |
R7153:Tenm2
|
UTSW |
11 |
36,024,182 (GRCm38) |
missense |
probably damaging |
0.98 |
R7173:Tenm2
|
UTSW |
11 |
36,041,551 (GRCm38) |
missense |
probably damaging |
0.99 |
R7199:Tenm2
|
UTSW |
11 |
36,171,436 (GRCm38) |
missense |
probably damaging |
1.00 |
R7205:Tenm2
|
UTSW |
11 |
36,049,129 (GRCm38) |
missense |
probably damaging |
0.99 |
R7250:Tenm2
|
UTSW |
11 |
36,072,798 (GRCm38) |
missense |
probably damaging |
1.00 |
R7290:Tenm2
|
UTSW |
11 |
36,023,471 (GRCm38) |
missense |
probably damaging |
1.00 |
R7366:Tenm2
|
UTSW |
11 |
36,069,414 (GRCm38) |
missense |
probably benign |
0.09 |
R7432:Tenm2
|
UTSW |
11 |
36,864,941 (GRCm38) |
missense |
probably benign |
|
R7504:Tenm2
|
UTSW |
11 |
36,139,743 (GRCm38) |
missense |
probably damaging |
1.00 |
R7513:Tenm2
|
UTSW |
11 |
36,051,900 (GRCm38) |
missense |
probably benign |
0.34 |
R7523:Tenm2
|
UTSW |
11 |
36,078,581 (GRCm38) |
splice site |
probably null |
|
R7527:Tenm2
|
UTSW |
11 |
36,206,976 (GRCm38) |
missense |
probably damaging |
1.00 |
R7648:Tenm2
|
UTSW |
11 |
36,106,736 (GRCm38) |
missense |
probably damaging |
1.00 |
R7653:Tenm2
|
UTSW |
11 |
36,047,347 (GRCm38) |
missense |
probably benign |
0.09 |
R7717:Tenm2
|
UTSW |
11 |
36,864,935 (GRCm38) |
missense |
probably damaging |
0.97 |
R7739:Tenm2
|
UTSW |
11 |
36,069,561 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7762:Tenm2
|
UTSW |
11 |
36,023,306 (GRCm38) |
missense |
possibly damaging |
0.74 |
R7786:Tenm2
|
UTSW |
11 |
36,010,449 (GRCm38) |
missense |
probably damaging |
0.99 |
R7803:Tenm2
|
UTSW |
11 |
36,047,116 (GRCm38) |
missense |
probably damaging |
0.98 |
R7834:Tenm2
|
UTSW |
11 |
36,024,854 (GRCm38) |
missense |
probably damaging |
1.00 |
R7838:Tenm2
|
UTSW |
11 |
36,106,799 (GRCm38) |
missense |
probably benign |
0.02 |
R8073:Tenm2
|
UTSW |
11 |
36,139,644 (GRCm38) |
missense |
possibly damaging |
0.56 |
R8076:Tenm2
|
UTSW |
11 |
36,027,221 (GRCm38) |
missense |
probably benign |
0.23 |
R8109:Tenm2
|
UTSW |
11 |
36,008,310 (GRCm38) |
missense |
probably benign |
|
R8306:Tenm2
|
UTSW |
11 |
36,069,369 (GRCm38) |
missense |
possibly damaging |
0.52 |
R8352:Tenm2
|
UTSW |
11 |
36,023,601 (GRCm38) |
missense |
probably damaging |
0.98 |
R8452:Tenm2
|
UTSW |
11 |
36,023,601 (GRCm38) |
missense |
probably damaging |
0.98 |
R8864:Tenm2
|
UTSW |
11 |
36,027,195 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8880:Tenm2
|
UTSW |
11 |
36,051,961 (GRCm38) |
missense |
probably damaging |
0.99 |
R8943:Tenm2
|
UTSW |
11 |
36,944,034 (GRCm38) |
missense |
probably damaging |
0.98 |
R8969:Tenm2
|
UTSW |
11 |
36,051,861 (GRCm38) |
missense |
probably damaging |
0.99 |
R9168:Tenm2
|
UTSW |
11 |
36,039,895 (GRCm38) |
missense |
probably damaging |
1.00 |
R9279:Tenm2
|
UTSW |
11 |
36,068,476 (GRCm38) |
missense |
probably benign |
0.00 |
R9294:Tenm2
|
UTSW |
11 |
36,024,500 (GRCm38) |
missense |
probably damaging |
0.98 |
R9320:Tenm2
|
UTSW |
11 |
36,023,647 (GRCm38) |
missense |
probably damaging |
0.99 |
R9373:Tenm2
|
UTSW |
11 |
36,039,886 (GRCm38) |
missense |
probably damaging |
1.00 |
R9408:Tenm2
|
UTSW |
11 |
36,069,419 (GRCm38) |
missense |
probably damaging |
1.00 |
R9410:Tenm2
|
UTSW |
11 |
36,141,569 (GRCm38) |
missense |
probably damaging |
0.99 |
R9454:Tenm2
|
UTSW |
11 |
36,221,459 (GRCm38) |
missense |
probably benign |
|
R9489:Tenm2
|
UTSW |
11 |
36,943,964 (GRCm38) |
missense |
probably damaging |
0.99 |
R9711:Tenm2
|
UTSW |
11 |
36,024,514 (GRCm38) |
missense |
probably damaging |
0.99 |
RF021:Tenm2
|
UTSW |
11 |
36,024,203 (GRCm38) |
missense |
possibly damaging |
0.95 |
X0018:Tenm2
|
UTSW |
11 |
36,024,200 (GRCm38) |
missense |
probably damaging |
1.00 |
X0063:Tenm2
|
UTSW |
11 |
36,024,730 (GRCm38) |
missense |
probably benign |
|
Z1088:Tenm2
|
UTSW |
11 |
36,273,267 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Tenm2
|
UTSW |
11 |
36,300,335 (GRCm38) |
missense |
probably damaging |
0.98 |
Z1177:Tenm2
|
UTSW |
11 |
36,008,234 (GRCm38) |
missense |
possibly damaging |
0.95 |
Z1177:Tenm2
|
UTSW |
11 |
36,385,130 (GRCm38) |
missense |
probably benign |
0.01 |
|