Other mutations in this stock |
Total: 107 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc8 |
C |
A |
7: 45,754,131 (GRCm39) |
A1562S |
probably benign |
Het |
Adam30 |
C |
A |
3: 98,070,061 (GRCm39) |
D631E |
possibly damaging |
Het |
Adgrv1 |
T |
C |
13: 81,676,793 (GRCm39) |
T2013A |
probably damaging |
Het |
Ark2n |
A |
T |
18: 77,740,995 (GRCm39) |
|
probably null |
Het |
Baiap3 |
T |
A |
17: 25,466,269 (GRCm39) |
|
probably benign |
Het |
Bicra |
T |
C |
7: 15,722,831 (GRCm39) |
T229A |
possibly damaging |
Het |
C1qbp |
A |
G |
11: 70,873,190 (GRCm39) |
|
probably benign |
Het |
C2cd3 |
C |
A |
7: 100,040,226 (GRCm39) |
T265K |
probably benign |
Het |
Cacna1s |
T |
A |
1: 136,043,007 (GRCm39) |
I1331K |
possibly damaging |
Het |
Cdadc1 |
AGACGGA |
AGA |
14: 59,806,440 (GRCm39) |
|
probably null |
Het |
Cdcp2 |
A |
G |
4: 106,963,969 (GRCm39) |
Y273C |
probably damaging |
Het |
Cdh23 |
A |
C |
10: 60,244,856 (GRCm39) |
V1013G |
possibly damaging |
Het |
Celf3 |
T |
A |
3: 94,386,529 (GRCm39) |
I39N |
probably damaging |
Het |
Cep152 |
A |
C |
2: 125,405,674 (GRCm39) |
S1619R |
probably damaging |
Het |
Cfap36 |
A |
G |
11: 29,195,108 (GRCm39) |
I42T |
probably damaging |
Het |
Cfap61 |
G |
T |
2: 145,985,020 (GRCm39) |
V955L |
probably damaging |
Het |
Cit |
G |
A |
5: 116,046,750 (GRCm39) |
D388N |
probably damaging |
Het |
Clca3a2 |
T |
C |
3: 144,516,613 (GRCm39) |
M328V |
probably benign |
Het |
Cntn4 |
A |
T |
6: 106,527,458 (GRCm39) |
I447L |
probably benign |
Het |
Csmd3 |
T |
C |
15: 47,721,330 (GRCm39) |
T1538A |
possibly damaging |
Het |
Cstf1 |
A |
G |
2: 172,214,905 (GRCm39) |
K9E |
probably damaging |
Het |
Dip2c |
T |
A |
13: 9,625,186 (GRCm39) |
M560K |
probably benign |
Het |
Dsg1a |
A |
T |
18: 20,466,779 (GRCm39) |
T550S |
probably benign |
Het |
Dtnb |
A |
G |
12: 3,799,505 (GRCm39) |
E460G |
probably damaging |
Het |
Dus1l |
GAGGTAAG |
GAG |
11: 120,680,584 (GRCm39) |
|
probably benign |
Het |
Efl1 |
T |
A |
7: 82,320,927 (GRCm39) |
V120E |
probably damaging |
Het |
Fbxl13 |
T |
C |
5: 21,689,001 (GRCm39) |
Y769C |
probably benign |
Het |
Fcho2 |
T |
C |
13: 98,942,874 (GRCm39) |
Y22C |
probably damaging |
Het |
Flacc1 |
G |
A |
1: 58,709,567 (GRCm39) |
A196V |
probably benign |
Het |
Gbp3 |
T |
C |
3: 142,273,335 (GRCm39) |
V294A |
probably damaging |
Het |
Gls |
A |
G |
1: 52,239,104 (GRCm39) |
|
probably benign |
Het |
Gm15130 |
A |
T |
2: 110,965,714 (GRCm39) |
|
probably benign |
Het |
Gm6185 |
A |
T |
1: 161,040,728 (GRCm39) |
|
noncoding transcript |
Het |
Gpr171 |
T |
A |
3: 59,005,517 (GRCm39) |
H86L |
probably damaging |
Het |
Gpr179 |
T |
C |
11: 97,230,074 (GRCm39) |
T694A |
probably damaging |
Het |
H2-Aa |
A |
T |
17: 34,502,794 (GRCm39) |
V124E |
probably damaging |
Het |
H2bc13 |
A |
G |
13: 21,900,135 (GRCm39) |
M60T |
probably benign |
Het |
H2-M5 |
A |
G |
17: 37,300,309 (GRCm39) |
|
probably benign |
Het |
Igf2r |
A |
T |
17: 12,902,984 (GRCm39) |
N2355K |
probably damaging |
Het |
Il9r |
A |
C |
11: 32,142,654 (GRCm39) |
S295A |
possibly damaging |
Het |
Ipo9 |
T |
C |
1: 135,334,288 (GRCm39) |
T313A |
probably benign |
Het |
Kalrn |
C |
T |
16: 34,334,389 (GRCm39) |
|
probably benign |
Het |
Lama3 |
G |
A |
18: 12,610,661 (GRCm39) |
V1175M |
possibly damaging |
Het |
Lhpp |
T |
A |
7: 132,272,104 (GRCm39) |
C242* |
probably null |
Het |
Lipe |
A |
G |
7: 25,079,568 (GRCm39) |
S1013P |
probably damaging |
Het |
Lrrc25 |
C |
T |
8: 71,070,726 (GRCm39) |
T169I |
probably benign |
Het |
Lrrc39 |
T |
C |
3: 116,362,515 (GRCm39) |
|
probably null |
Het |
Lrrd1 |
T |
A |
5: 3,901,126 (GRCm39) |
L477* |
probably null |
Het |
Lrriq4 |
A |
G |
3: 30,714,196 (GRCm39) |
I515V |
possibly damaging |
Het |
Magel2 |
A |
G |
7: 62,030,840 (GRCm39) |
Y1248C |
unknown |
Het |
Maml1 |
G |
T |
11: 50,149,162 (GRCm39) |
N859K |
possibly damaging |
Het |
Mdm1 |
A |
T |
10: 117,982,782 (GRCm39) |
H139L |
possibly damaging |
Het |
Mef2d |
C |
T |
3: 88,075,397 (GRCm39) |
P420S |
possibly damaging |
Het |
Mgat4b |
A |
G |
11: 50,101,848 (GRCm39) |
K38E |
probably benign |
Het |
Mtmr4 |
T |
C |
11: 87,494,923 (GRCm39) |
V405A |
probably damaging |
Het |
Naip5 |
G |
A |
13: 100,356,195 (GRCm39) |
T1140M |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,356,204 (GRCm39) |
Q1137R |
probably benign |
Het |
Naip5 |
G |
A |
13: 100,356,189 (GRCm39) |
S1142F |
probably benign |
Het |
Nfe2l3 |
T |
C |
6: 51,433,604 (GRCm39) |
S239P |
probably damaging |
Het |
Nlrp3 |
A |
G |
11: 59,439,127 (GRCm39) |
I235V |
probably benign |
Het |
Nyap2 |
T |
A |
1: 81,219,028 (GRCm39) |
L318Q |
probably damaging |
Het |
Nynrin |
G |
A |
14: 56,109,458 (GRCm39) |
V1522M |
probably damaging |
Het |
Oog3 |
A |
G |
4: 143,885,731 (GRCm39) |
L289P |
probably damaging |
Het |
Or52n20 |
C |
T |
7: 104,319,942 (GRCm39) |
P11L |
probably benign |
Het |
Or5b107 |
A |
G |
19: 13,142,488 (GRCm39) |
I37V |
probably benign |
Het |
Or6c69b |
T |
C |
10: 129,627,308 (GRCm39) |
D50G |
probably damaging |
Het |
Or8b12b |
T |
A |
9: 37,684,726 (GRCm39) |
M257K |
possibly damaging |
Het |
Or9g20 |
A |
T |
2: 85,630,391 (GRCm39) |
N74K |
probably benign |
Het |
Pax6 |
T |
C |
2: 105,514,129 (GRCm39) |
|
probably benign |
Het |
Pbrm1 |
G |
A |
14: 30,832,405 (GRCm39) |
R1441K |
probably benign |
Het |
Pcdha9 |
C |
T |
18: 37,132,511 (GRCm39) |
R527W |
probably damaging |
Het |
Pcdhb17 |
T |
C |
18: 37,620,450 (GRCm39) |
S747P |
probably benign |
Het |
Pcnx3 |
A |
C |
19: 5,738,023 (GRCm39) |
|
probably null |
Het |
Pds5a |
A |
T |
5: 65,808,632 (GRCm39) |
V413E |
probably damaging |
Het |
Phpt1 |
G |
T |
2: 25,464,332 (GRCm39) |
|
probably benign |
Het |
Phykpl |
A |
G |
11: 51,483,780 (GRCm39) |
E220G |
probably benign |
Het |
Pias2 |
T |
C |
18: 77,193,587 (GRCm39) |
|
probably null |
Het |
Pkhd1 |
T |
A |
1: 20,269,639 (GRCm39) |
I3302L |
probably damaging |
Het |
Poli |
A |
G |
18: 70,655,822 (GRCm39) |
L241P |
probably damaging |
Het |
Ppm1h |
T |
A |
10: 122,515,284 (GRCm39) |
I65N |
possibly damaging |
Het |
Ptpn14 |
T |
C |
1: 189,588,997 (GRCm39) |
L954P |
probably damaging |
Het |
Pxk |
T |
G |
14: 8,136,893 (GRCm38) |
M138R |
probably damaging |
Het |
Rasl11b |
G |
T |
5: 74,359,058 (GRCm39) |
D188Y |
probably damaging |
Het |
Rtraf |
A |
G |
14: 19,872,644 (GRCm39) |
F59S |
probably benign |
Het |
Sanbr |
A |
C |
11: 23,565,243 (GRCm39) |
I248S |
possibly damaging |
Het |
Serpinb5 |
G |
T |
1: 106,800,069 (GRCm39) |
L86F |
probably damaging |
Het |
Setdb2 |
G |
A |
14: 59,651,095 (GRCm39) |
T412I |
probably benign |
Het |
Shank2 |
C |
A |
7: 143,606,043 (GRCm39) |
N75K |
probably damaging |
Het |
Shank3 |
T |
A |
15: 89,427,318 (GRCm39) |
I791N |
probably damaging |
Het |
Slc25a13 |
T |
A |
6: 6,114,274 (GRCm39) |
M213L |
possibly damaging |
Het |
Slc25a21 |
T |
C |
12: 56,760,623 (GRCm39) |
Y298C |
probably damaging |
Het |
Slc34a2 |
A |
G |
5: 53,226,362 (GRCm39) |
N495S |
probably damaging |
Het |
Smc2 |
A |
G |
4: 52,451,231 (GRCm39) |
T292A |
probably benign |
Het |
Spag9 |
T |
C |
11: 93,939,425 (GRCm39) |
|
probably benign |
Het |
Tas2r113 |
C |
T |
6: 132,870,745 (GRCm39) |
P258S |
probably benign |
Het |
Tbkbp1 |
T |
C |
11: 97,029,567 (GRCm39) |
S530G |
probably benign |
Het |
Tm9sf1 |
C |
T |
14: 55,878,606 (GRCm39) |
R262Q |
possibly damaging |
Het |
Tmcc3 |
G |
T |
10: 94,414,646 (GRCm39) |
G147V |
possibly damaging |
Het |
Trim38 |
A |
T |
13: 23,972,264 (GRCm39) |
E195V |
probably damaging |
Het |
Try5 |
T |
C |
6: 41,290,349 (GRCm39) |
Y45C |
probably benign |
Het |
Umad1 |
A |
C |
6: 8,457,462 (GRCm39) |
|
probably benign |
Het |
Vmn2r105 |
T |
C |
17: 20,428,953 (GRCm39) |
I708V |
probably benign |
Het |
Zc3h12d |
A |
T |
10: 7,743,711 (GRCm39) |
S494C |
probably damaging |
Het |
Zeb2 |
A |
G |
2: 44,887,780 (GRCm39) |
S382P |
probably damaging |
Het |
Zfc3h1 |
A |
G |
10: 115,251,599 (GRCm39) |
S1304G |
probably benign |
Het |
Zfp287 |
G |
T |
11: 62,605,074 (GRCm39) |
T611K |
probably damaging |
Het |
Zfp534 |
G |
A |
4: 147,758,743 (GRCm39) |
T642I |
possibly 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 |
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 |
|