Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
C |
9: 124,295,159 (GRCm38) |
|
probably benign |
Het |
4732465J04Rik |
GATCTATCTATCTATCTATCTATCTATCTATCTATCTATC |
GATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATC |
10: 95,794,578 (GRCm38) |
|
probably null |
Het |
4930522L14Rik |
T |
C |
5: 109,736,847 (GRCm38) |
K382E |
probably damaging |
Het |
Adck1 |
A |
G |
12: 88,455,510 (GRCm38) |
E297G |
probably damaging |
Het |
Ahrr |
G |
A |
13: 74,283,024 (GRCm38) |
|
probably benign |
Het |
Aldh3a2 |
C |
T |
11: 61,248,888 (GRCm38) |
V473I |
probably benign |
Het |
Arfgef3 |
A |
T |
10: 18,647,915 (GRCm38) |
I369K |
possibly damaging |
Het |
Atl2 |
A |
G |
17: 79,853,831 (GRCm38) |
|
probably benign |
Het |
Atp1b3 |
T |
C |
9: 96,338,709 (GRCm38) |
I178V |
possibly damaging |
Het |
Axdnd1 |
T |
C |
1: 156,378,386 (GRCm38) |
E520G |
possibly damaging |
Het |
Bahcc1 |
A |
T |
11: 120,285,074 (GRCm38) |
|
probably benign |
Het |
BB019430 |
A |
T |
10: 58,704,271 (GRCm38) |
|
noncoding transcript |
Het |
BC028528 |
A |
T |
3: 95,887,334 (GRCm38) |
|
probably benign |
Het |
Btbd1 |
T |
A |
7: 81,801,003 (GRCm38) |
Q343L |
probably benign |
Het |
Catsper1 |
A |
G |
19: 5,339,475 (GRCm38) |
T473A |
possibly damaging |
Het |
Chmp6 |
G |
A |
11: 119,915,523 (GRCm38) |
|
probably null |
Het |
D130040H23Rik |
T |
C |
8: 69,302,543 (GRCm38) |
V200A |
possibly damaging |
Het |
D830013O20Rik |
C |
T |
12: 73,364,331 (GRCm38) |
|
noncoding transcript |
Het |
Dcaf1 |
T |
A |
9: 106,844,145 (GRCm38) |
S379T |
possibly damaging |
Het |
Dcaf4 |
G |
A |
12: 83,535,988 (GRCm38) |
|
probably benign |
Het |
Dhx58 |
T |
C |
11: 100,695,324 (GRCm38) |
I624V |
probably benign |
Het |
Disp3 |
T |
C |
4: 148,254,251 (GRCm38) |
E821G |
probably damaging |
Het |
Dlc1 |
T |
A |
8: 36,599,440 (GRCm38) |
E464V |
probably damaging |
Het |
Dnah10 |
G |
A |
5: 124,783,834 (GRCm38) |
V2151I |
probably damaging |
Het |
Dnah6 |
C |
T |
6: 73,188,535 (GRCm38) |
|
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,748,665 (GRCm38) |
G2617D |
probably benign |
Het |
Dnah9 |
C |
A |
11: 65,918,804 (GRCm38) |
E872* |
probably null |
Het |
Dock9 |
T |
C |
14: 121,597,665 (GRCm38) |
Y99C |
probably damaging |
Het |
Dpy19l3 |
T |
A |
7: 35,716,646 (GRCm38) |
I310F |
probably damaging |
Het |
Fggy |
A |
T |
4: 95,837,654 (GRCm38) |
I137F |
probably damaging |
Het |
Gli2 |
A |
G |
1: 118,890,283 (GRCm38) |
|
probably benign |
Het |
Gm14421 |
A |
T |
2: 177,056,722 (GRCm38) |
|
noncoding transcript |
Het |
Gm5689 |
T |
A |
18: 42,173,543 (GRCm38) |
D58E |
probably damaging |
Het |
Grin2a |
A |
G |
16: 9,994,821 (GRCm38) |
|
probably null |
Het |
Grin2b |
A |
G |
6: 135,778,648 (GRCm38) |
|
probably benign |
Het |
Incenp |
A |
G |
19: 9,894,879 (GRCm38) |
S72P |
probably benign |
Het |
Ipo11 |
A |
G |
13: 106,910,194 (GRCm38) |
|
probably benign |
Het |
Klc3 |
T |
A |
7: 19,394,926 (GRCm38) |
N469Y |
possibly damaging |
Het |
Lrrc42 |
A |
G |
4: 107,247,505 (GRCm38) |
S88P |
probably benign |
Het |
Lrrc49 |
G |
A |
9: 60,680,600 (GRCm38) |
T93I |
probably benign |
Het |
Ltn1 |
G |
A |
16: 87,405,519 (GRCm38) |
|
probably benign |
Het |
Mlycd |
A |
T |
8: 119,407,641 (GRCm38) |
Q294L |
probably damaging |
Het |
Mmrn1 |
T |
A |
6: 60,975,815 (GRCm38) |
|
probably benign |
Het |
Mrpl22 |
T |
A |
11: 58,171,821 (GRCm38) |
I19N |
probably benign |
Het |
Msh3 |
T |
A |
13: 92,349,209 (GRCm38) |
K202N |
probably damaging |
Het |
N4bp2 |
T |
C |
5: 65,803,573 (GRCm38) |
|
probably benign |
Het |
Ncam1 |
C |
T |
9: 49,568,409 (GRCm38) |
D90N |
probably damaging |
Het |
Nckap5 |
A |
T |
1: 126,024,407 (GRCm38) |
D1405E |
possibly damaging |
Het |
Ncoa2 |
A |
G |
1: 13,186,731 (GRCm38) |
|
probably null |
Het |
Ncoa6 |
TGC |
TGCGC |
2: 155,408,291 (GRCm38) |
|
probably null |
Het |
Nlrp1b |
A |
T |
11: 71,164,099 (GRCm38) |
W844R |
probably damaging |
Het |
Nmnat1 |
G |
T |
4: 149,469,150 (GRCm38) |
N168K |
possibly damaging |
Het |
Olfr1446 |
A |
G |
19: 12,890,445 (GRCm38) |
L44P |
probably damaging |
Het |
Ost4 |
T |
C |
5: 30,907,459 (GRCm38) |
H26R |
probably damaging |
Het |
Otog |
G |
A |
7: 46,304,231 (GRCm38) |
V2638M |
probably damaging |
Het |
Otogl |
A |
T |
10: 107,874,530 (GRCm38) |
I566N |
probably damaging |
Het |
Pcyt1a |
T |
C |
16: 32,470,186 (GRCm38) |
S282P |
probably damaging |
Het |
Prkcg |
G |
A |
7: 3,329,119 (GRCm38) |
E581K |
probably damaging |
Het |
Ralgps2 |
A |
G |
1: 156,887,089 (GRCm38) |
|
probably null |
Het |
Rnf157 |
A |
G |
11: 116,354,810 (GRCm38) |
|
probably benign |
Het |
Scmh1 |
T |
C |
4: 120,529,865 (GRCm38) |
|
probably benign |
Het |
Sgo2b |
T |
C |
8: 63,938,383 (GRCm38) |
H150R |
possibly damaging |
Het |
Sh2b3 |
T |
G |
5: 121,829,037 (GRCm38) |
T5P |
probably damaging |
Het |
Skint6 |
A |
T |
4: 112,991,236 (GRCm38) |
|
probably benign |
Het |
Slfn10-ps |
T |
C |
11: 83,035,302 (GRCm38) |
|
noncoding transcript |
Het |
Sspo |
T |
A |
6: 48,494,194 (GRCm38) |
|
probably benign |
Het |
Tcp1 |
T |
A |
17: 12,922,747 (GRCm38) |
|
probably benign |
Het |
Tdp2 |
A |
G |
13: 24,838,239 (GRCm38) |
M214V |
probably damaging |
Het |
Tmem144 |
G |
A |
3: 79,839,273 (GRCm38) |
|
probably benign |
Het |
Tmem204 |
A |
G |
17: 25,058,350 (GRCm38) |
I187T |
probably damaging |
Het |
Tmem208 |
T |
G |
8: 105,334,694 (GRCm38) |
D117E |
probably benign |
Het |
Tnks1bp1 |
C |
T |
2: 85,059,221 (GRCm38) |
P631S |
possibly damaging |
Het |
Tomm70a |
T |
C |
16: 57,147,821 (GRCm38) |
V517A |
probably damaging |
Het |
Ttc7 |
T |
C |
17: 87,379,895 (GRCm38) |
V801A |
probably damaging |
Het |
Txndc5 |
A |
T |
13: 38,507,953 (GRCm38) |
C146S |
probably damaging |
Het |
Ubac2 |
A |
G |
14: 122,008,917 (GRCm38) |
|
probably benign |
Het |
Ube4b |
G |
T |
4: 149,360,324 (GRCm38) |
T493K |
probably damaging |
Het |
Ufl1 |
A |
T |
4: 25,256,008 (GRCm38) |
Y504N |
probably benign |
Het |
Ugt1a6a |
T |
C |
1: 88,139,270 (GRCm38) |
V266A |
possibly damaging |
Het |
Ugt1a6b |
T |
A |
1: 88,107,467 (GRCm38) |
C176S |
probably damaging |
Het |
Ulk3 |
T |
A |
9: 57,590,686 (GRCm38) |
I90N |
probably damaging |
Het |
Unc13c |
T |
C |
9: 73,694,892 (GRCm38) |
I1357M |
probably benign |
Het |
Vmn1r28 |
G |
A |
6: 58,265,717 (GRCm38) |
A182T |
probably benign |
Het |
Vmn2r114 |
A |
G |
17: 23,309,826 (GRCm38) |
|
probably null |
Het |
Vmn2r91 |
A |
C |
17: 18,106,137 (GRCm38) |
N228T |
probably benign |
Het |
Wdr43 |
T |
G |
17: 71,631,997 (GRCm38) |
|
probably benign |
Het |
Wisp1 |
T |
C |
15: 66,919,210 (GRCm38) |
L287P |
probably damaging |
Het |
Zbtb6 |
G |
T |
2: 37,429,588 (GRCm38) |
Y109* |
probably null |
Het |
Zfp980 |
A |
G |
4: 145,701,997 (GRCm38) |
D432G |
probably benign |
Het |
|
Other mutations in Tenm4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00228:Tenm4
|
APN |
7 |
96,868,009 (GRCm38) |
missense |
probably benign |
0.00 |
IGL00468:Tenm4
|
APN |
7 |
96,874,472 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL00519:Tenm4
|
APN |
7 |
96,805,138 (GRCm38) |
splice site |
probably benign |
|
IGL00979:Tenm4
|
APN |
7 |
96,729,391 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL01401:Tenm4
|
APN |
7 |
96,874,267 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01459:Tenm4
|
APN |
7 |
96,729,385 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01519:Tenm4
|
APN |
7 |
96,895,177 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01545:Tenm4
|
APN |
7 |
96,874,303 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01579:Tenm4
|
APN |
7 |
96,863,502 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01587:Tenm4
|
APN |
7 |
96,863,502 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01625:Tenm4
|
APN |
7 |
96,885,358 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01655:Tenm4
|
APN |
7 |
96,553,724 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01683:Tenm4
|
APN |
7 |
96,885,404 (GRCm38) |
missense |
possibly damaging |
0.84 |
IGL01728:Tenm4
|
APN |
7 |
96,896,064 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01732:Tenm4
|
APN |
7 |
96,895,509 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01924:Tenm4
|
APN |
7 |
96,895,212 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01966:Tenm4
|
APN |
7 |
96,553,550 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02177:Tenm4
|
APN |
7 |
96,895,662 (GRCm38) |
missense |
probably benign |
0.40 |
IGL02207:Tenm4
|
APN |
7 |
96,874,116 (GRCm38) |
missense |
possibly damaging |
0.85 |
IGL02269:Tenm4
|
APN |
7 |
96,823,822 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02274:Tenm4
|
APN |
7 |
96,854,734 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02375:Tenm4
|
APN |
7 |
96,704,137 (GRCm38) |
missense |
possibly damaging |
0.52 |
IGL02415:Tenm4
|
APN |
7 |
96,874,074 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02472:Tenm4
|
APN |
7 |
96,774,176 (GRCm38) |
unclassified |
probably benign |
|
IGL02656:Tenm4
|
APN |
7 |
96,885,433 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02678:Tenm4
|
APN |
7 |
96,896,219 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02829:Tenm4
|
APN |
7 |
96,894,998 (GRCm38) |
nonsense |
probably null |
|
IGL02863:Tenm4
|
APN |
7 |
96,873,706 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03145:Tenm4
|
APN |
7 |
96,842,968 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL03153:Tenm4
|
APN |
7 |
96,873,762 (GRCm38) |
missense |
probably damaging |
1.00 |
principium
|
UTSW |
7 |
96,797,481 (GRCm38) |
missense |
probably damaging |
0.98 |
toccata
|
UTSW |
7 |
96,902,989 (GRCm38) |
critical splice donor site |
probably null |
|
P0026:Tenm4
|
UTSW |
7 |
96,874,527 (GRCm38) |
missense |
probably damaging |
1.00 |
R0097:Tenm4
|
UTSW |
7 |
96,892,926 (GRCm38) |
missense |
probably damaging |
1.00 |
R0097:Tenm4
|
UTSW |
7 |
96,892,926 (GRCm38) |
missense |
probably damaging |
1.00 |
R0140:Tenm4
|
UTSW |
7 |
96,896,052 (GRCm38) |
missense |
possibly damaging |
0.78 |
R0277:Tenm4
|
UTSW |
7 |
96,694,950 (GRCm38) |
missense |
possibly damaging |
0.54 |
R0323:Tenm4
|
UTSW |
7 |
96,694,950 (GRCm38) |
missense |
possibly damaging |
0.54 |
R0362:Tenm4
|
UTSW |
7 |
96,772,035 (GRCm38) |
nonsense |
probably null |
|
R0381:Tenm4
|
UTSW |
7 |
96,905,881 (GRCm38) |
missense |
probably damaging |
1.00 |
R0420:Tenm4
|
UTSW |
7 |
96,873,766 (GRCm38) |
missense |
possibly damaging |
0.85 |
R0426:Tenm4
|
UTSW |
7 |
96,777,851 (GRCm38) |
missense |
probably damaging |
1.00 |
R0513:Tenm4
|
UTSW |
7 |
96,895,623 (GRCm38) |
missense |
probably benign |
0.35 |
R0624:Tenm4
|
UTSW |
7 |
96,774,020 (GRCm38) |
missense |
probably damaging |
1.00 |
R0837:Tenm4
|
UTSW |
7 |
96,896,275 (GRCm38) |
splice site |
probably benign |
|
R1037:Tenm4
|
UTSW |
7 |
96,797,481 (GRCm38) |
missense |
probably damaging |
0.98 |
R1172:Tenm4
|
UTSW |
7 |
96,848,044 (GRCm38) |
missense |
probably damaging |
1.00 |
R1422:Tenm4
|
UTSW |
7 |
96,550,051 (GRCm38) |
missense |
probably damaging |
0.99 |
R1427:Tenm4
|
UTSW |
7 |
96,843,048 (GRCm38) |
missense |
probably benign |
0.42 |
R1462:Tenm4
|
UTSW |
7 |
96,704,153 (GRCm38) |
missense |
probably damaging |
1.00 |
R1462:Tenm4
|
UTSW |
7 |
96,704,153 (GRCm38) |
missense |
probably damaging |
1.00 |
R1597:Tenm4
|
UTSW |
7 |
96,902,989 (GRCm38) |
critical splice donor site |
probably null |
|
R1701:Tenm4
|
UTSW |
7 |
96,902,889 (GRCm38) |
missense |
probably damaging |
1.00 |
R1707:Tenm4
|
UTSW |
7 |
96,888,685 (GRCm38) |
missense |
probably damaging |
1.00 |
R1809:Tenm4
|
UTSW |
7 |
96,873,780 (GRCm38) |
missense |
probably benign |
0.17 |
R1812:Tenm4
|
UTSW |
7 |
96,895,940 (GRCm38) |
missense |
probably damaging |
1.00 |
R1895:Tenm4
|
UTSW |
7 |
96,735,808 (GRCm38) |
missense |
probably damaging |
1.00 |
R1933:Tenm4
|
UTSW |
7 |
96,895,326 (GRCm38) |
missense |
probably damaging |
1.00 |
R1946:Tenm4
|
UTSW |
7 |
96,735,808 (GRCm38) |
missense |
probably damaging |
1.00 |
R2108:Tenm4
|
UTSW |
7 |
96,906,290 (GRCm38) |
missense |
probably damaging |
1.00 |
R2151:Tenm4
|
UTSW |
7 |
96,902,847 (GRCm38) |
missense |
probably damaging |
1.00 |
R2247:Tenm4
|
UTSW |
7 |
96,906,009 (GRCm38) |
missense |
probably benign |
0.03 |
R2329:Tenm4
|
UTSW |
7 |
96,895,862 (GRCm38) |
missense |
probably benign |
0.00 |
R2893:Tenm4
|
UTSW |
7 |
96,894,990 (GRCm38) |
missense |
probably damaging |
1.00 |
R2990:Tenm4
|
UTSW |
7 |
96,893,125 (GRCm38) |
splice site |
probably null |
|
R3409:Tenm4
|
UTSW |
7 |
96,895,160 (GRCm38) |
missense |
probably damaging |
1.00 |
R3410:Tenm4
|
UTSW |
7 |
96,852,530 (GRCm38) |
missense |
probably damaging |
0.99 |
R3411:Tenm4
|
UTSW |
7 |
96,852,530 (GRCm38) |
missense |
probably damaging |
0.99 |
R3440:Tenm4
|
UTSW |
7 |
96,553,516 (GRCm38) |
missense |
probably benign |
0.00 |
R3441:Tenm4
|
UTSW |
7 |
96,553,516 (GRCm38) |
missense |
probably benign |
0.00 |
R3719:Tenm4
|
UTSW |
7 |
96,863,563 (GRCm38) |
missense |
possibly damaging |
0.92 |
R3772:Tenm4
|
UTSW |
7 |
96,694,880 (GRCm38) |
missense |
probably damaging |
1.00 |
R3773:Tenm4
|
UTSW |
7 |
96,694,880 (GRCm38) |
missense |
probably damaging |
1.00 |
R4093:Tenm4
|
UTSW |
7 |
96,895,772 (GRCm38) |
missense |
probably damaging |
1.00 |
R4439:Tenm4
|
UTSW |
7 |
96,895,815 (GRCm38) |
missense |
probably benign |
0.01 |
R4441:Tenm4
|
UTSW |
7 |
96,895,815 (GRCm38) |
missense |
probably benign |
0.01 |
R4510:Tenm4
|
UTSW |
7 |
96,894,863 (GRCm38) |
missense |
probably benign |
|
R4511:Tenm4
|
UTSW |
7 |
96,894,863 (GRCm38) |
missense |
probably benign |
|
R4543:Tenm4
|
UTSW |
7 |
96,895,815 (GRCm38) |
missense |
probably benign |
0.01 |
R4645:Tenm4
|
UTSW |
7 |
96,895,742 (GRCm38) |
missense |
probably damaging |
1.00 |
R4701:Tenm4
|
UTSW |
7 |
96,895,349 (GRCm38) |
missense |
probably damaging |
1.00 |
R4707:Tenm4
|
UTSW |
7 |
96,774,046 (GRCm38) |
missense |
probably damaging |
0.99 |
R4714:Tenm4
|
UTSW |
7 |
96,894,924 (GRCm38) |
missense |
probably damaging |
1.00 |
R4742:Tenm4
|
UTSW |
7 |
96,797,484 (GRCm38) |
missense |
probably damaging |
0.99 |
R4784:Tenm4
|
UTSW |
7 |
96,774,046 (GRCm38) |
missense |
probably damaging |
0.99 |
R4785:Tenm4
|
UTSW |
7 |
96,774,046 (GRCm38) |
missense |
probably damaging |
0.99 |
R4801:Tenm4
|
UTSW |
7 |
96,906,245 (GRCm38) |
missense |
probably damaging |
0.97 |
R4802:Tenm4
|
UTSW |
7 |
96,906,245 (GRCm38) |
missense |
probably damaging |
0.97 |
R4880:Tenm4
|
UTSW |
7 |
96,905,818 (GRCm38) |
splice site |
probably null |
|
R5036:Tenm4
|
UTSW |
7 |
96,852,561 (GRCm38) |
missense |
probably damaging |
1.00 |
R5036:Tenm4
|
UTSW |
7 |
96,694,790 (GRCm38) |
missense |
probably damaging |
1.00 |
R5050:Tenm4
|
UTSW |
7 |
96,895,788 (GRCm38) |
missense |
probably damaging |
1.00 |
R5103:Tenm4
|
UTSW |
7 |
96,842,957 (GRCm38) |
missense |
probably damaging |
1.00 |
R5106:Tenm4
|
UTSW |
7 |
96,843,149 (GRCm38) |
missense |
probably damaging |
0.99 |
R5118:Tenm4
|
UTSW |
7 |
96,893,086 (GRCm38) |
missense |
probably damaging |
1.00 |
R5272:Tenm4
|
UTSW |
7 |
96,874,203 (GRCm38) |
missense |
probably damaging |
0.98 |
R5282:Tenm4
|
UTSW |
7 |
96,837,331 (GRCm38) |
missense |
possibly damaging |
0.90 |
R5403:Tenm4
|
UTSW |
7 |
96,888,827 (GRCm38) |
missense |
probably damaging |
1.00 |
R5404:Tenm4
|
UTSW |
7 |
96,894,680 (GRCm38) |
missense |
probably damaging |
1.00 |
R5567:Tenm4
|
UTSW |
7 |
96,896,209 (GRCm38) |
nonsense |
probably null |
|
R5590:Tenm4
|
UTSW |
7 |
96,797,401 (GRCm38) |
missense |
possibly damaging |
0.93 |
R5590:Tenm4
|
UTSW |
7 |
96,797,400 (GRCm38) |
missense |
possibly damaging |
0.73 |
R5597:Tenm4
|
UTSW |
7 |
96,553,517 (GRCm38) |
missense |
probably benign |
0.00 |
R5782:Tenm4
|
UTSW |
7 |
96,893,039 (GRCm38) |
missense |
probably benign |
0.00 |
R5861:Tenm4
|
UTSW |
7 |
96,843,217 (GRCm38) |
intron |
probably benign |
|
R5890:Tenm4
|
UTSW |
7 |
96,902,860 (GRCm38) |
missense |
probably damaging |
1.00 |
R5930:Tenm4
|
UTSW |
7 |
96,854,719 (GRCm38) |
missense |
probably damaging |
1.00 |
R5940:Tenm4
|
UTSW |
7 |
96,845,895 (GRCm38) |
missense |
probably damaging |
1.00 |
R6012:Tenm4
|
UTSW |
7 |
96,522,433 (GRCm38) |
intron |
probably benign |
|
R6060:Tenm4
|
UTSW |
7 |
96,873,711 (GRCm38) |
missense |
probably damaging |
1.00 |
R6104:Tenm4
|
UTSW |
7 |
96,837,289 (GRCm38) |
missense |
probably damaging |
0.97 |
R6283:Tenm4
|
UTSW |
7 |
96,874,494 (GRCm38) |
missense |
probably benign |
0.33 |
R6333:Tenm4
|
UTSW |
7 |
96,774,124 (GRCm38) |
missense |
probably damaging |
1.00 |
R6522:Tenm4
|
UTSW |
7 |
96,843,044 (GRCm38) |
missense |
possibly damaging |
0.88 |
R6616:Tenm4
|
UTSW |
7 |
96,553,496 (GRCm38) |
missense |
probably benign |
0.01 |
R6746:Tenm4
|
UTSW |
7 |
96,892,860 (GRCm38) |
missense |
probably damaging |
1.00 |
R6751:Tenm4
|
UTSW |
7 |
96,845,712 (GRCm38) |
missense |
possibly damaging |
0.95 |
R6806:Tenm4
|
UTSW |
7 |
96,811,959 (GRCm38) |
missense |
possibly damaging |
0.95 |
R6807:Tenm4
|
UTSW |
7 |
96,895,271 (GRCm38) |
missense |
probably damaging |
1.00 |
R6807:Tenm4
|
UTSW |
7 |
96,553,496 (GRCm38) |
missense |
probably benign |
0.01 |
R6809:Tenm4
|
UTSW |
7 |
96,553,496 (GRCm38) |
missense |
probably benign |
0.01 |
R6810:Tenm4
|
UTSW |
7 |
96,553,496 (GRCm38) |
missense |
probably benign |
0.01 |
R6811:Tenm4
|
UTSW |
7 |
96,553,496 (GRCm38) |
missense |
probably benign |
0.01 |
R6853:Tenm4
|
UTSW |
7 |
96,837,295 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6886:Tenm4
|
UTSW |
7 |
96,797,392 (GRCm38) |
missense |
possibly damaging |
0.85 |
R6920:Tenm4
|
UTSW |
7 |
96,895,550 (GRCm38) |
missense |
probably damaging |
1.00 |
R6937:Tenm4
|
UTSW |
7 |
96,553,496 (GRCm38) |
missense |
probably benign |
0.01 |
R6939:Tenm4
|
UTSW |
7 |
96,553,496 (GRCm38) |
missense |
probably benign |
0.01 |
R7011:Tenm4
|
UTSW |
7 |
96,896,135 (GRCm38) |
nonsense |
probably null |
|
R7033:Tenm4
|
UTSW |
7 |
96,895,223 (GRCm38) |
nonsense |
probably null |
|
R7040:Tenm4
|
UTSW |
7 |
96,553,496 (GRCm38) |
missense |
probably benign |
0.01 |
R7083:Tenm4
|
UTSW |
7 |
96,895,349 (GRCm38) |
missense |
probably damaging |
1.00 |
R7238:Tenm4
|
UTSW |
7 |
96,553,496 (GRCm38) |
missense |
probably benign |
0.01 |
R7239:Tenm4
|
UTSW |
7 |
96,735,813 (GRCm38) |
missense |
possibly damaging |
0.47 |
R7239:Tenm4
|
UTSW |
7 |
96,553,496 (GRCm38) |
missense |
probably benign |
0.01 |
R7337:Tenm4
|
UTSW |
7 |
96,874,126 (GRCm38) |
missense |
probably benign |
0.44 |
R7400:Tenm4
|
UTSW |
7 |
96,694,803 (GRCm38) |
missense |
probably damaging |
0.97 |
R7407:Tenm4
|
UTSW |
7 |
96,773,987 (GRCm38) |
missense |
possibly damaging |
0.89 |
R7449:Tenm4
|
UTSW |
7 |
96,874,213 (GRCm38) |
missense |
possibly damaging |
0.65 |
R7473:Tenm4
|
UTSW |
7 |
96,774,146 (GRCm38) |
missense |
probably damaging |
1.00 |
R7477:Tenm4
|
UTSW |
7 |
96,845,808 (GRCm38) |
missense |
probably damaging |
0.99 |
R7489:Tenm4
|
UTSW |
7 |
96,837,314 (GRCm38) |
missense |
possibly damaging |
0.90 |
R7498:Tenm4
|
UTSW |
7 |
96,848,017 (GRCm38) |
missense |
probably damaging |
1.00 |
R7562:Tenm4
|
UTSW |
7 |
96,888,814 (GRCm38) |
missense |
probably damaging |
1.00 |
R7615:Tenm4
|
UTSW |
7 |
96,845,926 (GRCm38) |
missense |
probably damaging |
1.00 |
R7624:Tenm4
|
UTSW |
7 |
96,895,985 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7626:Tenm4
|
UTSW |
7 |
96,893,014 (GRCm38) |
missense |
probably damaging |
1.00 |
R7690:Tenm4
|
UTSW |
7 |
96,863,533 (GRCm38) |
missense |
probably benign |
0.00 |
R7692:Tenm4
|
UTSW |
7 |
96,895,403 (GRCm38) |
missense |
probably damaging |
1.00 |
R7748:Tenm4
|
UTSW |
7 |
96,894,702 (GRCm38) |
missense |
probably damaging |
1.00 |
R7763:Tenm4
|
UTSW |
7 |
96,895,692 (GRCm38) |
missense |
probably benign |
0.38 |
R7792:Tenm4
|
UTSW |
7 |
96,774,014 (GRCm38) |
missense |
possibly damaging |
0.54 |
R7855:Tenm4
|
UTSW |
7 |
96,873,874 (GRCm38) |
missense |
probably damaging |
1.00 |
R7868:Tenm4
|
UTSW |
7 |
96,906,380 (GRCm38) |
missense |
possibly damaging |
0.79 |
R7878:Tenm4
|
UTSW |
7 |
96,852,357 (GRCm38) |
missense |
probably damaging |
1.00 |
R7997:Tenm4
|
UTSW |
7 |
96,874,305 (GRCm38) |
missense |
probably benign |
0.44 |
R8017:Tenm4
|
UTSW |
7 |
96,704,041 (GRCm38) |
missense |
probably damaging |
1.00 |
R8019:Tenm4
|
UTSW |
7 |
96,704,041 (GRCm38) |
missense |
probably damaging |
1.00 |
R8054:Tenm4
|
UTSW |
7 |
96,729,346 (GRCm38) |
splice site |
probably benign |
|
R8061:Tenm4
|
UTSW |
7 |
96,852,456 (GRCm38) |
missense |
probably damaging |
1.00 |
R8108:Tenm4
|
UTSW |
7 |
96,854,728 (GRCm38) |
missense |
probably benign |
0.39 |
R8140:Tenm4
|
UTSW |
7 |
96,895,176 (GRCm38) |
missense |
probably damaging |
1.00 |
R8214:Tenm4
|
UTSW |
7 |
96,895,407 (GRCm38) |
missense |
probably damaging |
1.00 |
R8258:Tenm4
|
UTSW |
7 |
96,867,991 (GRCm38) |
missense |
probably damaging |
1.00 |
R8259:Tenm4
|
UTSW |
7 |
96,867,991 (GRCm38) |
missense |
probably damaging |
1.00 |
R8364:Tenm4
|
UTSW |
7 |
96,772,106 (GRCm38) |
critical splice donor site |
probably null |
|
R8542:Tenm4
|
UTSW |
7 |
96,811,932 (GRCm38) |
missense |
probably damaging |
0.99 |
R8669:Tenm4
|
UTSW |
7 |
96,905,941 (GRCm38) |
missense |
probably benign |
|
R8670:Tenm4
|
UTSW |
7 |
96,905,941 (GRCm38) |
missense |
probably benign |
|
R8683:Tenm4
|
UTSW |
7 |
96,902,857 (GRCm38) |
missense |
probably damaging |
0.99 |
R8691:Tenm4
|
UTSW |
7 |
96,905,941 (GRCm38) |
missense |
probably benign |
|
R8692:Tenm4
|
UTSW |
7 |
96,905,941 (GRCm38) |
missense |
probably benign |
|
R8714:Tenm4
|
UTSW |
7 |
96,905,941 (GRCm38) |
missense |
probably benign |
|
R8716:Tenm4
|
UTSW |
7 |
96,905,941 (GRCm38) |
missense |
probably benign |
|
R8735:Tenm4
|
UTSW |
7 |
96,905,941 (GRCm38) |
missense |
probably benign |
|
R8736:Tenm4
|
UTSW |
7 |
96,905,941 (GRCm38) |
missense |
probably benign |
|
R8737:Tenm4
|
UTSW |
7 |
96,905,941 (GRCm38) |
missense |
probably benign |
|
R8738:Tenm4
|
UTSW |
7 |
96,905,941 (GRCm38) |
missense |
probably benign |
|
R8738:Tenm4
|
UTSW |
7 |
96,873,840 (GRCm38) |
missense |
probably damaging |
1.00 |
R8739:Tenm4
|
UTSW |
7 |
96,905,941 (GRCm38) |
missense |
probably benign |
|
R8776:Tenm4
|
UTSW |
7 |
96,895,032 (GRCm38) |
missense |
probably damaging |
1.00 |
R8776-TAIL:Tenm4
|
UTSW |
7 |
96,895,032 (GRCm38) |
missense |
probably damaging |
1.00 |
R8777:Tenm4
|
UTSW |
7 |
96,896,037 (GRCm38) |
missense |
probably damaging |
1.00 |
R8777-TAIL:Tenm4
|
UTSW |
7 |
96,896,037 (GRCm38) |
missense |
probably damaging |
1.00 |
R8817:Tenm4
|
UTSW |
7 |
96,874,128 (GRCm38) |
missense |
probably benign |
0.01 |
R8851:Tenm4
|
UTSW |
7 |
96,852,503 (GRCm38) |
missense |
probably damaging |
1.00 |
R8913:Tenm4
|
UTSW |
7 |
96,702,745 (GRCm38) |
splice site |
probably benign |
|
R8977:Tenm4
|
UTSW |
7 |
96,811,970 (GRCm38) |
missense |
probably damaging |
1.00 |
R9100:Tenm4
|
UTSW |
7 |
96,845,854 (GRCm38) |
missense |
probably damaging |
1.00 |
R9136:Tenm4
|
UTSW |
7 |
96,823,918 (GRCm38) |
missense |
possibly damaging |
0.69 |
R9163:Tenm4
|
UTSW |
7 |
96,823,873 (GRCm38) |
missense |
probably damaging |
1.00 |
R9188:Tenm4
|
UTSW |
7 |
96,772,027 (GRCm38) |
missense |
probably damaging |
1.00 |
R9195:Tenm4
|
UTSW |
7 |
96,892,919 (GRCm38) |
missense |
probably damaging |
1.00 |
R9217:Tenm4
|
UTSW |
7 |
96,885,439 (GRCm38) |
missense |
probably damaging |
1.00 |
R9344:Tenm4
|
UTSW |
7 |
96,896,145 (GRCm38) |
missense |
probably damaging |
1.00 |
R9414:Tenm4
|
UTSW |
7 |
96,896,160 (GRCm38) |
missense |
probably benign |
|
R9466:Tenm4
|
UTSW |
7 |
96,550,045 (GRCm38) |
missense |
possibly damaging |
0.79 |
R9559:Tenm4
|
UTSW |
7 |
96,823,849 (GRCm38) |
missense |
probably benign |
|
R9626:Tenm4
|
UTSW |
7 |
96,896,138 (GRCm38) |
missense |
probably damaging |
1.00 |
R9673:Tenm4
|
UTSW |
7 |
96,867,989 (GRCm38) |
missense |
probably damaging |
1.00 |
R9676:Tenm4
|
UTSW |
7 |
96,895,431 (GRCm38) |
missense |
probably damaging |
1.00 |
R9678:Tenm4
|
UTSW |
7 |
96,737,412 (GRCm38) |
missense |
possibly damaging |
0.94 |
R9775:Tenm4
|
UTSW |
7 |
96,906,554 (GRCm38) |
missense |
possibly damaging |
0.92 |
R9790:Tenm4
|
UTSW |
7 |
96,888,839 (GRCm38) |
missense |
probably damaging |
1.00 |
R9791:Tenm4
|
UTSW |
7 |
96,888,839 (GRCm38) |
missense |
probably damaging |
1.00 |
R9803:Tenm4
|
UTSW |
7 |
96,553,478 (GRCm38) |
missense |
probably damaging |
1.00 |
X0021:Tenm4
|
UTSW |
7 |
96,873,909 (GRCm38) |
nonsense |
probably null |
|
X0026:Tenm4
|
UTSW |
7 |
96,868,087 (GRCm38) |
missense |
probably damaging |
0.98 |
X0066:Tenm4
|
UTSW |
7 |
96,894,794 (GRCm38) |
missense |
probably damaging |
1.00 |
X0066:Tenm4
|
UTSW |
7 |
96,848,030 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Tenm4
|
UTSW |
7 |
96,905,914 (GRCm38) |
missense |
probably benign |
0.00 |
Z1177:Tenm4
|
UTSW |
7 |
96,863,585 (GRCm38) |
missense |
probably damaging |
0.96 |
|