Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730049H05Rik |
A |
T |
6: 92,805,050 (GRCm39) |
Q70L |
unknown |
Het |
Adamts12 |
T |
A |
15: 11,257,115 (GRCm39) |
N489K |
probably benign |
Het |
Alms1 |
A |
G |
6: 85,597,577 (GRCm39) |
D801G |
possibly damaging |
Het |
Apex1 |
T |
G |
14: 51,163,995 (GRCm39) |
N173K |
probably damaging |
Het |
Arhgap32 |
A |
T |
9: 32,168,441 (GRCm39) |
N808I |
probably benign |
Het |
Arhgef28 |
T |
C |
13: 98,105,821 (GRCm39) |
Y706C |
probably benign |
Het |
Atg2b |
A |
T |
12: 105,602,731 (GRCm39) |
F1604Y |
possibly damaging |
Het |
Atm |
A |
T |
9: 53,401,602 (GRCm39) |
Y1422* |
probably null |
Het |
Bace2 |
T |
A |
16: 97,237,852 (GRCm39) |
V38E |
|
Het |
Birc6 |
C |
A |
17: 74,954,729 (GRCm39) |
L3442I |
possibly damaging |
Het |
C6 |
T |
A |
15: 4,844,244 (GRCm39) |
S889T |
|
Het |
Calcrl |
A |
T |
2: 84,175,529 (GRCm39) |
L275* |
probably null |
Het |
Casp6 |
T |
C |
3: 129,705,872 (GRCm39) |
Y180H |
probably benign |
Het |
Cd5 |
T |
C |
19: 10,703,910 (GRCm39) |
M51V |
probably benign |
Het |
Cdhr1 |
G |
T |
14: 36,804,158 (GRCm39) |
P500Q |
probably benign |
Het |
Celsr3 |
G |
A |
9: 108,712,269 (GRCm39) |
W1732* |
probably null |
Het |
Ces2g |
T |
C |
8: 105,689,285 (GRCm39) |
V87A |
probably damaging |
Het |
Chil6 |
T |
C |
3: 106,301,641 (GRCm39) |
N153S |
possibly damaging |
Het |
Chrna5 |
A |
T |
9: 54,909,718 (GRCm39) |
D113V |
probably benign |
Het |
Cimip2b |
T |
G |
4: 43,427,273 (GRCm39) |
|
probably null |
Het |
Cox20 |
A |
G |
1: 178,150,164 (GRCm39) |
T113A |
probably benign |
Het |
Cryl1 |
T |
C |
14: 57,541,148 (GRCm39) |
I179V |
probably benign |
Het |
Dennd3 |
A |
G |
15: 73,434,275 (GRCm39) |
T982A |
probably damaging |
Het |
Drosha |
G |
A |
15: 12,859,522 (GRCm39) |
V577I |
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,117,570 (GRCm39) |
S2240P |
probably benign |
Het |
Eif1ad14 |
T |
A |
12: 87,886,248 (GRCm39) |
D127V |
unknown |
Het |
Fbxl5 |
C |
T |
5: 43,916,116 (GRCm39) |
S432N |
probably benign |
Het |
Fez1 |
T |
A |
9: 36,772,146 (GRCm39) |
S150R |
probably benign |
Het |
Gabrb2 |
T |
G |
11: 42,378,039 (GRCm39) |
M85R |
probably damaging |
Het |
Lhx4 |
A |
G |
1: 155,580,617 (GRCm39) |
V203A |
probably damaging |
Het |
Med23 |
G |
A |
10: 24,780,282 (GRCm39) |
D977N |
probably damaging |
Het |
Mplkip |
T |
C |
13: 17,870,367 (GRCm39) |
F100L |
probably damaging |
Het |
Ncoa7 |
C |
T |
10: 30,570,239 (GRCm39) |
G240E |
probably damaging |
Het |
Nedd4 |
A |
G |
9: 72,650,910 (GRCm39) |
E827G |
probably damaging |
Het |
Nfatc2 |
A |
G |
2: 168,413,065 (GRCm39) |
F207L |
probably benign |
Het |
Nr2f1 |
A |
T |
13: 78,343,716 (GRCm39) |
S183T |
probably benign |
Het |
Ocel1 |
A |
G |
8: 71,824,560 (GRCm39) |
E81G |
probably benign |
Het |
Or10aa3 |
T |
C |
1: 173,878,488 (GRCm39) |
V183A |
probably benign |
Het |
Or10g3b |
C |
A |
14: 52,586,889 (GRCm39) |
G205* |
probably null |
Het |
Or4n4b |
C |
T |
14: 50,536,604 (GRCm39) |
G54E |
possibly damaging |
Het |
Pcdh8 |
G |
A |
14: 80,005,086 (GRCm39) |
P980S |
probably benign |
Het |
Pex26 |
A |
T |
6: 121,170,510 (GRCm39) |
Q285L |
possibly damaging |
Het |
Pgap6 |
T |
A |
17: 26,339,423 (GRCm39) |
M579K |
probably damaging |
Het |
Plce1 |
A |
T |
19: 38,737,763 (GRCm39) |
N1603I |
probably benign |
Het |
Poli |
A |
T |
18: 70,642,698 (GRCm39) |
C501S |
probably benign |
Het |
Ppp4r4 |
C |
T |
12: 103,550,404 (GRCm39) |
T276I |
probably damaging |
Het |
Rbpj |
T |
A |
5: 53,747,693 (GRCm39) |
M1K |
probably null |
Het |
Recql4 |
T |
A |
15: 76,587,982 (GRCm39) |
M1204L |
probably benign |
Het |
Ribc2 |
T |
C |
15: 85,025,876 (GRCm39) |
I284T |
probably benign |
Het |
Rreb1 |
C |
A |
13: 38,114,362 (GRCm39) |
Q574K |
probably benign |
Het |
Scn9a |
A |
T |
2: 66,357,424 (GRCm39) |
L959Q |
probably damaging |
Het |
Shank1 |
C |
A |
7: 43,969,093 (GRCm39) |
H329Q |
unknown |
Het |
Soat2 |
A |
T |
15: 102,071,013 (GRCm39) |
D469V |
probably damaging |
Het |
Spag7 |
T |
A |
11: 70,555,691 (GRCm39) |
H82L |
probably damaging |
Het |
Sptb |
T |
C |
12: 76,675,271 (GRCm39) |
I248V |
probably benign |
Het |
Tacr3 |
A |
G |
3: 134,566,843 (GRCm39) |
I239V |
probably benign |
Het |
Tbc1d1 |
T |
C |
5: 64,414,133 (GRCm39) |
F165L |
probably benign |
Het |
Tchhl1 |
A |
G |
3: 93,378,451 (GRCm39) |
E385G |
probably benign |
Het |
Tecta |
C |
T |
9: 42,248,532 (GRCm39) |
D1957N |
probably damaging |
Het |
Tet2 |
G |
T |
3: 133,192,146 (GRCm39) |
Q763K |
probably benign |
Het |
Timd6 |
A |
C |
11: 46,475,200 (GRCm39) |
S132R |
probably benign |
Het |
Tox3 |
G |
A |
8: 90,975,617 (GRCm39) |
T338I |
probably damaging |
Het |
Usp30 |
G |
A |
5: 114,259,730 (GRCm39) |
D479N |
probably damaging |
Het |
Vmn1r27 |
T |
C |
6: 58,192,785 (GRCm39) |
D73G |
possibly damaging |
Het |
Vmn1r27 |
A |
T |
6: 58,192,879 (GRCm39) |
S42T |
probably benign |
Het |
Vmn2r120 |
A |
T |
17: 57,816,258 (GRCm39) |
V699D |
possibly damaging |
Het |
Vwa2 |
A |
T |
19: 56,897,767 (GRCm39) |
T691S |
probably benign |
Het |
Wdr31 |
T |
A |
4: 62,381,666 (GRCm39) |
Q55L |
probably benign |
Het |
Xdh |
A |
G |
17: 74,204,040 (GRCm39) |
F1107L |
probably benign |
Het |
Zfp184 |
A |
G |
13: 22,143,887 (GRCm39) |
H531R |
probably damaging |
Het |
Zfp366 |
T |
C |
13: 99,365,709 (GRCm39) |
L290P |
probably damaging |
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 |
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 |
|