Other mutations in this stock |
Total: 125 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
C |
T |
7: 29,260,710 (GRCm39) |
|
noncoding transcript |
Het |
Abcb11 |
A |
G |
2: 69,115,627 (GRCm39) |
I579T |
probably damaging |
Het |
Abcc9 |
T |
C |
6: 142,627,830 (GRCm39) |
N400S |
probably benign |
Het |
Adarb2 |
T |
C |
13: 8,781,855 (GRCm39) |
L577P |
probably damaging |
Het |
Agt |
A |
C |
8: 125,283,852 (GRCm39) |
N422K |
probably damaging |
Het |
Ahnak |
A |
T |
19: 8,990,766 (GRCm39) |
K4017* |
probably null |
Het |
Akap13 |
C |
A |
7: 75,397,494 (GRCm39) |
Q2575K |
probably damaging |
Het |
Aldh3a2 |
A |
T |
11: 61,144,541 (GRCm39) |
I339K |
probably damaging |
Het |
Alox15 |
G |
T |
11: 70,236,450 (GRCm39) |
Y483* |
probably null |
Het |
Ampd1 |
A |
T |
3: 103,006,913 (GRCm39) |
I713F |
probably damaging |
Het |
Amph |
A |
T |
13: 19,297,286 (GRCm39) |
E344V |
possibly damaging |
Het |
Arhgef18 |
T |
C |
8: 3,436,959 (GRCm39) |
Y250H |
probably damaging |
Het |
Arid5b |
A |
G |
10: 67,932,807 (GRCm39) |
S1032P |
probably damaging |
Het |
Armc8 |
C |
A |
9: 99,387,741 (GRCm39) |
L393F |
probably damaging |
Het |
Bpnt1 |
A |
G |
1: 185,077,623 (GRCm39) |
|
probably null |
Het |
Cachd1 |
G |
A |
4: 100,845,418 (GRCm39) |
R970H |
probably damaging |
Het |
Cd207 |
T |
C |
6: 83,652,738 (GRCm39) |
T131A |
probably benign |
Het |
Cd83 |
G |
A |
13: 43,951,009 (GRCm39) |
V54I |
probably benign |
Het |
Cfap43 |
T |
C |
19: 47,752,115 (GRCm39) |
K1086E |
probably benign |
Het |
Cfap65 |
A |
T |
1: 74,941,328 (GRCm39) |
V1837E |
probably benign |
Het |
Clcnka |
T |
A |
4: 141,123,917 (GRCm39) |
H89L |
probably benign |
Het |
Cnga4 |
T |
C |
7: 105,054,182 (GRCm39) |
I50T |
possibly damaging |
Het |
Cog5 |
A |
G |
12: 31,887,358 (GRCm39) |
|
probably benign |
Het |
Col11a2 |
T |
A |
17: 34,278,322 (GRCm39) |
|
probably null |
Het |
Col28a1 |
T |
G |
6: 8,175,291 (GRCm39) |
I186L |
possibly damaging |
Het |
Col4a2 |
T |
A |
8: 11,481,252 (GRCm39) |
M808K |
probably benign |
Het |
Copb2 |
A |
G |
9: 98,445,528 (GRCm39) |
|
probably benign |
Het |
Dbnl |
G |
A |
11: 5,745,441 (GRCm39) |
|
probably benign |
Het |
Dbx2 |
T |
C |
15: 95,552,493 (GRCm39) |
T51A |
possibly damaging |
Het |
Dcp1a |
A |
T |
14: 30,224,842 (GRCm39) |
M123L |
probably damaging |
Het |
Ddx42 |
T |
A |
11: 106,123,659 (GRCm39) |
F217I |
probably benign |
Het |
Dlc1 |
T |
C |
8: 37,325,205 (GRCm39) |
T367A |
probably benign |
Het |
Dmgdh |
A |
T |
13: 93,888,863 (GRCm39) |
T834S |
probably benign |
Het |
Dnah8 |
T |
C |
17: 30,903,147 (GRCm39) |
S929P |
probably damaging |
Het |
Dnase1l2 |
C |
A |
17: 24,660,056 (GRCm39) |
V271L |
possibly damaging |
Het |
Dsc1 |
T |
C |
18: 20,229,114 (GRCm39) |
Y392C |
probably damaging |
Het |
Edn1 |
T |
C |
13: 42,458,718 (GRCm39) |
|
probably benign |
Het |
Efcab3 |
G |
A |
11: 104,611,327 (GRCm39) |
D390N |
probably benign |
Het |
Eps8l3 |
T |
C |
3: 107,792,126 (GRCm39) |
L351P |
probably damaging |
Het |
F12 |
G |
A |
13: 55,570,296 (GRCm39) |
|
probably benign |
Het |
Fam47e |
T |
C |
5: 92,726,317 (GRCm39) |
|
probably benign |
Het |
Fcrl5 |
C |
A |
3: 87,349,320 (GRCm39) |
Q32K |
probably benign |
Het |
Fndc1 |
C |
T |
17: 7,960,505 (GRCm39) |
V1637I |
possibly damaging |
Het |
Foxg1 |
G |
T |
12: 49,431,350 (GRCm39) |
|
probably benign |
Het |
Frrs1 |
A |
T |
3: 116,696,070 (GRCm39) |
I530F |
possibly damaging |
Het |
Galnt5 |
A |
T |
2: 57,889,097 (GRCm39) |
K232N |
probably benign |
Het |
Ggt5 |
G |
A |
10: 75,438,482 (GRCm39) |
V68M |
probably damaging |
Het |
Gm16519 |
T |
C |
17: 71,236,101 (GRCm39) |
C17R |
probably benign |
Het |
Gm17535 |
A |
G |
9: 3,035,804 (GRCm39) |
Y224C |
probably null |
Het |
Gm9631 |
T |
G |
11: 121,836,455 (GRCm39) |
D28A |
probably damaging |
Het |
Gpx2 |
T |
C |
12: 76,842,087 (GRCm39) |
I21M |
probably benign |
Het |
H2-Q2 |
T |
G |
17: 35,564,661 (GRCm39) |
D354E |
probably damaging |
Het |
Icam2 |
A |
T |
11: 106,271,717 (GRCm39) |
I71K |
probably damaging |
Het |
Il12a |
T |
C |
3: 68,605,223 (GRCm39) |
|
probably benign |
Het |
Insm2 |
C |
G |
12: 55,647,225 (GRCm39) |
A323G |
probably benign |
Het |
Itga1 |
T |
C |
13: 115,104,835 (GRCm39) |
T1064A |
probably benign |
Het |
Itgad |
T |
A |
7: 127,773,176 (GRCm39) |
V11E |
possibly damaging |
Het |
Kctd15 |
C |
T |
7: 34,344,306 (GRCm39) |
S115N |
probably damaging |
Het |
Klra5 |
A |
G |
6: 129,880,527 (GRCm39) |
W124R |
probably damaging |
Het |
Kng2 |
T |
A |
16: 22,806,486 (GRCm39) |
D571V |
probably benign |
Het |
Kpna6 |
A |
T |
4: 129,544,583 (GRCm39) |
F380I |
probably benign |
Het |
Lipo3 |
A |
T |
19: 33,762,169 (GRCm39) |
Y109* |
probably null |
Het |
Lrrc37 |
T |
A |
11: 103,503,986 (GRCm39) |
K485* |
probably null |
Het |
Man2a2 |
T |
C |
7: 80,012,945 (GRCm39) |
H540R |
possibly damaging |
Het |
Map2k4 |
T |
C |
11: 65,603,101 (GRCm39) |
E188G |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,895,252 (GRCm39) |
|
probably benign |
Het |
Mbtd1 |
A |
G |
11: 93,796,038 (GRCm39) |
D25G |
probably damaging |
Het |
Med13 |
T |
A |
11: 86,221,915 (GRCm39) |
Q238L |
possibly damaging |
Het |
Mmachc |
A |
G |
4: 116,560,851 (GRCm39) |
Y215H |
probably damaging |
Het |
Mtor |
T |
A |
4: 148,568,811 (GRCm39) |
Y1110* |
probably null |
Het |
Nek2 |
A |
G |
1: 191,554,331 (GRCm39) |
N57D |
probably damaging |
Het |
Nek7 |
ACCCC |
ACCC |
1: 138,443,431 (GRCm39) |
|
probably null |
Het |
Neo1 |
G |
T |
9: 58,838,317 (GRCm39) |
T489K |
probably damaging |
Het |
Neu1 |
T |
A |
17: 35,153,736 (GRCm39) |
Y387N |
probably damaging |
Het |
Nfasc |
A |
T |
1: 132,536,176 (GRCm39) |
C586* |
probably null |
Het |
Nle1 |
G |
A |
11: 82,795,671 (GRCm39) |
L259F |
probably damaging |
Het |
Nrde2 |
G |
A |
12: 100,110,105 (GRCm39) |
Q309* |
probably null |
Het |
Nufip2 |
C |
T |
11: 77,577,279 (GRCm39) |
H76Y |
probably benign |
Het |
Or10ak16 |
A |
C |
4: 118,750,687 (GRCm39) |
T136P |
probably damaging |
Het |
Or2y13 |
A |
T |
11: 49,415,405 (GRCm39) |
N285I |
probably damaging |
Het |
Or4k6 |
A |
T |
14: 50,476,096 (GRCm39) |
I82N |
probably damaging |
Het |
Or52e18 |
A |
T |
7: 104,609,018 (GRCm39) |
I307N |
probably benign |
Het |
Or52r1c |
T |
C |
7: 102,735,358 (GRCm39) |
F206S |
probably damaging |
Het |
Or9s18 |
A |
T |
13: 65,300,877 (GRCm39) |
I280F |
probably damaging |
Het |
Pcdhb5 |
A |
G |
18: 37,454,675 (GRCm39) |
T352A |
probably benign |
Het |
Pcdhb7 |
A |
T |
18: 37,476,442 (GRCm39) |
D526V |
probably damaging |
Het |
Phkg1 |
A |
T |
5: 129,893,394 (GRCm39) |
|
probably null |
Het |
Plg |
C |
T |
17: 12,637,623 (GRCm39) |
T744M |
probably damaging |
Het |
Plxnd1 |
A |
C |
6: 115,935,660 (GRCm39) |
|
probably benign |
Het |
Poglut1 |
A |
T |
16: 38,349,837 (GRCm39) |
I312N |
probably damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,574,999 (GRCm39) |
|
probably benign |
Het |
Ppt1 |
A |
G |
4: 122,737,892 (GRCm39) |
M77V |
probably benign |
Het |
Pramel26 |
A |
C |
4: 143,539,155 (GRCm39) |
S113A |
possibly damaging |
Het |
Pramel5 |
G |
T |
4: 143,998,190 (GRCm39) |
T351N |
probably damaging |
Het |
Psmb4 |
G |
A |
3: 94,792,275 (GRCm39) |
R216C |
probably benign |
Het |
Ptprd |
T |
C |
4: 76,002,640 (GRCm39) |
T699A |
probably damaging |
Het |
Retreg3 |
A |
T |
11: 100,989,455 (GRCm39) |
|
probably benign |
Het |
Sanbr |
C |
T |
11: 23,525,491 (GRCm39) |
R716H |
probably damaging |
Het |
Scaper |
G |
A |
9: 55,665,340 (GRCm39) |
A389V |
probably damaging |
Het |
Serinc5 |
G |
A |
13: 92,825,245 (GRCm39) |
D225N |
possibly damaging |
Het |
Slco1a1 |
T |
G |
6: 141,871,480 (GRCm39) |
|
probably benign |
Het |
Snapc1 |
C |
T |
12: 74,021,806 (GRCm39) |
R81C |
probably damaging |
Het |
Sod3 |
A |
T |
5: 52,525,421 (GRCm39) |
D40V |
probably benign |
Het |
Sorcs3 |
C |
A |
19: 48,194,734 (GRCm39) |
A39E |
probably benign |
Het |
Spon1 |
A |
T |
7: 113,639,056 (GRCm39) |
T761S |
probably benign |
Het |
Syde2 |
A |
G |
3: 145,720,004 (GRCm39) |
|
probably null |
Het |
Synm |
T |
A |
7: 67,408,916 (GRCm39) |
D154V |
probably benign |
Het |
Synpo2 |
T |
C |
3: 122,908,098 (GRCm39) |
E406G |
probably damaging |
Het |
Tcea3 |
T |
A |
4: 135,975,382 (GRCm39) |
L8* |
probably null |
Het |
Tec |
G |
A |
5: 72,980,840 (GRCm39) |
L33F |
probably damaging |
Het |
Tex15 |
T |
A |
8: 34,072,354 (GRCm39) |
S2634T |
possibly damaging |
Het |
Tmem8b |
G |
A |
4: 43,690,123 (GRCm39) |
V853I |
probably benign |
Het |
Togaram1 |
A |
G |
12: 65,068,240 (GRCm39) |
K1748E |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,728,822 (GRCm39) |
|
probably benign |
Het |
Usp36 |
C |
T |
11: 118,163,847 (GRCm39) |
D234N |
probably damaging |
Het |
Usp40 |
G |
A |
1: 87,906,244 (GRCm39) |
P664S |
probably benign |
Het |
Vmn1r54 |
T |
A |
6: 90,246,635 (GRCm39) |
L183H |
probably benign |
Het |
Vmn1r58 |
T |
G |
7: 5,413,676 (GRCm39) |
I185L |
probably benign |
Het |
Wnt8a |
A |
T |
18: 34,680,618 (GRCm39) |
R328W |
probably benign |
Het |
Yars1 |
A |
G |
4: 129,107,732 (GRCm39) |
|
probably benign |
Het |
Zbtb49 |
A |
C |
5: 38,358,018 (GRCm39) |
M745R |
probably damaging |
Het |
Zeb1 |
T |
G |
18: 5,759,027 (GRCm39) |
F162V |
probably damaging |
Het |
Zfp369 |
A |
T |
13: 65,445,362 (GRCm39) |
H835L |
probably damaging |
Het |
Zic5 |
A |
G |
14: 122,701,351 (GRCm39) |
V460A |
unknown |
Het |
Zp3 |
A |
G |
5: 136,013,210 (GRCm39) |
N181D |
possibly damaging |
Het |
|
Other mutations in Tg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00157:Tg
|
APN |
15 |
66,719,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00230:Tg
|
APN |
15 |
66,699,139 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00324:Tg
|
APN |
15 |
66,565,273 (GRCm39) |
missense |
probably benign |
|
IGL00428:Tg
|
APN |
15 |
66,645,273 (GRCm39) |
missense |
probably benign |
0.33 |
IGL00703:Tg
|
APN |
15 |
66,568,338 (GRCm39) |
missense |
probably benign |
0.34 |
IGL00808:Tg
|
APN |
15 |
66,555,662 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00833:Tg
|
APN |
15 |
66,560,650 (GRCm39) |
missense |
probably benign |
0.34 |
IGL00899:Tg
|
APN |
15 |
66,545,922 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00921:Tg
|
APN |
15 |
66,636,302 (GRCm39) |
missense |
probably benign |
0.28 |
IGL00975:Tg
|
APN |
15 |
66,553,731 (GRCm39) |
missense |
probably benign |
|
IGL01288:Tg
|
APN |
15 |
66,608,125 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01397:Tg
|
APN |
15 |
66,567,941 (GRCm39) |
splice site |
probably benign |
|
IGL01634:Tg
|
APN |
15 |
66,601,415 (GRCm39) |
missense |
probably benign |
0.34 |
IGL01646:Tg
|
APN |
15 |
66,549,936 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01704:Tg
|
APN |
15 |
66,543,200 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01958:Tg
|
APN |
15 |
66,631,335 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02093:Tg
|
APN |
15 |
66,564,223 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02113:Tg
|
APN |
15 |
66,577,179 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02138:Tg
|
APN |
15 |
66,589,082 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02156:Tg
|
APN |
15 |
66,577,197 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02169:Tg
|
APN |
15 |
66,629,792 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02342:Tg
|
APN |
15 |
66,636,140 (GRCm39) |
missense |
probably benign |
|
IGL02434:Tg
|
APN |
15 |
66,636,191 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02506:Tg
|
APN |
15 |
66,613,443 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02513:Tg
|
APN |
15 |
66,577,123 (GRCm39) |
missense |
probably benign |
|
IGL02549:Tg
|
APN |
15 |
66,711,210 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02669:Tg
|
APN |
15 |
66,620,575 (GRCm39) |
splice site |
probably benign |
|
IGL02756:Tg
|
APN |
15 |
66,606,435 (GRCm39) |
missense |
probably benign |
|
IGL02800:Tg
|
APN |
15 |
66,629,735 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02828:Tg
|
APN |
15 |
66,554,243 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02927:Tg
|
APN |
15 |
66,549,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03061:Tg
|
APN |
15 |
66,543,254 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03105:Tg
|
APN |
15 |
66,586,955 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03160:Tg
|
APN |
15 |
66,711,152 (GRCm39) |
nonsense |
probably null |
|
IGL03242:Tg
|
APN |
15 |
66,555,647 (GRCm39) |
missense |
probably damaging |
0.99 |
Also_ran
|
UTSW |
15 |
66,550,688 (GRCm39) |
missense |
probably damaging |
1.00 |
bedraggled
|
UTSW |
15 |
66,612,563 (GRCm39) |
missense |
probably damaging |
1.00 |
foster
|
UTSW |
15 |
66,565,109 (GRCm39) |
nonsense |
probably null |
|
hognose
|
UTSW |
15 |
66,589,057 (GRCm39) |
missense |
probably damaging |
0.99 |
ito
|
UTSW |
15 |
66,638,011 (GRCm39) |
nonsense |
probably null |
|
ito2
|
UTSW |
15 |
66,543,245 (GRCm39) |
missense |
probably damaging |
1.00 |
ito3
|
UTSW |
15 |
66,645,323 (GRCm39) |
missense |
probably damaging |
1.00 |
ito4
|
UTSW |
15 |
66,568,369 (GRCm39) |
missense |
possibly damaging |
0.47 |
Papua
|
UTSW |
15 |
66,545,899 (GRCm39) |
missense |
probably damaging |
1.00 |
Pipistrella
|
UTSW |
15 |
66,567,984 (GRCm39) |
missense |
probably damaging |
1.00 |
pluribus
|
UTSW |
15 |
66,587,012 (GRCm39) |
missense |
probably damaging |
0.98 |
samarai
|
UTSW |
15 |
66,629,855 (GRCm39) |
critical splice donor site |
probably null |
|
sariba
|
UTSW |
15 |
66,566,719 (GRCm39) |
missense |
probably benign |
0.01 |
ticker
|
UTSW |
15 |
66,699,231 (GRCm39) |
nonsense |
probably null |
|
Vampire
|
UTSW |
15 |
66,554,676 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03134:Tg
|
UTSW |
15 |
66,612,567 (GRCm39) |
missense |
probably damaging |
1.00 |
P0019:Tg
|
UTSW |
15 |
66,560,712 (GRCm39) |
missense |
probably benign |
0.01 |
R0121:Tg
|
UTSW |
15 |
66,612,630 (GRCm39) |
missense |
probably benign |
0.04 |
R0135:Tg
|
UTSW |
15 |
66,566,719 (GRCm39) |
missense |
probably benign |
0.01 |
R0227:Tg
|
UTSW |
15 |
66,570,295 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0448:Tg
|
UTSW |
15 |
66,636,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R0453:Tg
|
UTSW |
15 |
66,700,382 (GRCm39) |
missense |
probably benign |
0.09 |
R0504:Tg
|
UTSW |
15 |
66,554,253 (GRCm39) |
missense |
probably damaging |
0.97 |
R0543:Tg
|
UTSW |
15 |
66,601,446 (GRCm39) |
missense |
probably benign |
0.13 |
R0638:Tg
|
UTSW |
15 |
66,589,057 (GRCm39) |
missense |
probably damaging |
0.99 |
R0639:Tg
|
UTSW |
15 |
66,613,333 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0666:Tg
|
UTSW |
15 |
66,609,370 (GRCm39) |
missense |
probably benign |
|
R0673:Tg
|
UTSW |
15 |
66,613,333 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0689:Tg
|
UTSW |
15 |
66,711,253 (GRCm39) |
splice site |
probably benign |
|
R0704:Tg
|
UTSW |
15 |
66,629,729 (GRCm39) |
missense |
probably benign |
0.02 |
R0730:Tg
|
UTSW |
15 |
66,550,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R0830:Tg
|
UTSW |
15 |
66,596,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R0959:Tg
|
UTSW |
15 |
66,579,859 (GRCm39) |
missense |
probably damaging |
0.98 |
R1027:Tg
|
UTSW |
15 |
66,544,258 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1061:Tg
|
UTSW |
15 |
66,570,408 (GRCm39) |
missense |
probably benign |
0.09 |
R1086:Tg
|
UTSW |
15 |
66,555,911 (GRCm39) |
missense |
probably benign |
|
R1103:Tg
|
UTSW |
15 |
66,591,504 (GRCm39) |
missense |
probably benign |
0.45 |
R1240:Tg
|
UTSW |
15 |
66,700,397 (GRCm39) |
missense |
probably benign |
0.16 |
R1281:Tg
|
UTSW |
15 |
66,568,338 (GRCm39) |
missense |
probably benign |
0.34 |
R1470:Tg
|
UTSW |
15 |
66,721,312 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1470:Tg
|
UTSW |
15 |
66,721,312 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1531:Tg
|
UTSW |
15 |
66,722,351 (GRCm39) |
missense |
probably benign |
0.02 |
R1544:Tg
|
UTSW |
15 |
66,577,081 (GRCm39) |
missense |
probably benign |
0.04 |
R1550:Tg
|
UTSW |
15 |
66,565,279 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1575:Tg
|
UTSW |
15 |
66,601,534 (GRCm39) |
critical splice donor site |
probably null |
|
R1638:Tg
|
UTSW |
15 |
66,568,015 (GRCm39) |
nonsense |
probably null |
|
R1655:Tg
|
UTSW |
15 |
66,700,417 (GRCm39) |
critical splice donor site |
probably null |
|
R1671:Tg
|
UTSW |
15 |
66,564,236 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1789:Tg
|
UTSW |
15 |
66,609,397 (GRCm39) |
missense |
probably benign |
0.00 |
R1883:Tg
|
UTSW |
15 |
66,543,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R1984:Tg
|
UTSW |
15 |
66,554,691 (GRCm39) |
missense |
probably benign |
|
R2063:Tg
|
UTSW |
15 |
66,700,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R2092:Tg
|
UTSW |
15 |
66,721,456 (GRCm39) |
missense |
probably null |
0.26 |
R2109:Tg
|
UTSW |
15 |
66,601,443 (GRCm39) |
missense |
probably benign |
0.02 |
R2128:Tg
|
UTSW |
15 |
66,566,743 (GRCm39) |
missense |
probably benign |
0.10 |
R2129:Tg
|
UTSW |
15 |
66,566,743 (GRCm39) |
missense |
probably benign |
0.10 |
R2207:Tg
|
UTSW |
15 |
66,553,788 (GRCm39) |
missense |
probably benign |
0.15 |
R2219:Tg
|
UTSW |
15 |
66,553,782 (GRCm39) |
missense |
probably benign |
0.03 |
R2228:Tg
|
UTSW |
15 |
66,545,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R2229:Tg
|
UTSW |
15 |
66,545,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R2259:Tg
|
UTSW |
15 |
66,555,747 (GRCm39) |
missense |
probably benign |
|
R2994:Tg
|
UTSW |
15 |
66,553,802 (GRCm39) |
missense |
probably benign |
|
R3904:Tg
|
UTSW |
15 |
66,638,011 (GRCm39) |
nonsense |
probably null |
|
R3946:Tg
|
UTSW |
15 |
66,545,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R3965:Tg
|
UTSW |
15 |
66,556,039 (GRCm39) |
missense |
probably benign |
|
R4245:Tg
|
UTSW |
15 |
66,568,318 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4451:Tg
|
UTSW |
15 |
66,637,996 (GRCm39) |
missense |
probably benign |
0.01 |
R4487:Tg
|
UTSW |
15 |
66,543,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R4489:Tg
|
UTSW |
15 |
66,579,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R4623:Tg
|
UTSW |
15 |
66,607,120 (GRCm39) |
missense |
probably benign |
0.23 |
R4659:Tg
|
UTSW |
15 |
66,545,769 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4728:Tg
|
UTSW |
15 |
66,554,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R4760:Tg
|
UTSW |
15 |
66,565,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R4797:Tg
|
UTSW |
15 |
66,629,855 (GRCm39) |
critical splice donor site |
probably null |
|
R4944:Tg
|
UTSW |
15 |
66,636,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R4998:Tg
|
UTSW |
15 |
66,545,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R5009:Tg
|
UTSW |
15 |
66,568,435 (GRCm39) |
missense |
probably benign |
0.01 |
R5025:Tg
|
UTSW |
15 |
66,579,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R5035:Tg
|
UTSW |
15 |
66,553,662 (GRCm39) |
splice site |
probably null |
|
R5049:Tg
|
UTSW |
15 |
66,699,231 (GRCm39) |
nonsense |
probably null |
|
R5073:Tg
|
UTSW |
15 |
66,607,101 (GRCm39) |
missense |
probably benign |
0.05 |
R5169:Tg
|
UTSW |
15 |
66,550,629 (GRCm39) |
nonsense |
probably null |
|
R5185:Tg
|
UTSW |
15 |
66,645,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R5227:Tg
|
UTSW |
15 |
66,631,416 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5300:Tg
|
UTSW |
15 |
66,550,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R5334:Tg
|
UTSW |
15 |
66,549,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R5339:Tg
|
UTSW |
15 |
66,549,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R5402:Tg
|
UTSW |
15 |
66,611,017 (GRCm39) |
missense |
probably damaging |
0.98 |
R5441:Tg
|
UTSW |
15 |
66,568,369 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5509:Tg
|
UTSW |
15 |
66,699,142 (GRCm39) |
missense |
probably benign |
0.45 |
R5580:Tg
|
UTSW |
15 |
66,557,149 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5582:Tg
|
UTSW |
15 |
66,565,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R5624:Tg
|
UTSW |
15 |
66,709,906 (GRCm39) |
missense |
probably benign |
0.11 |
R5686:Tg
|
UTSW |
15 |
66,560,738 (GRCm39) |
missense |
probably benign |
0.28 |
R6042:Tg
|
UTSW |
15 |
66,555,842 (GRCm39) |
missense |
probably benign |
0.01 |
R6122:Tg
|
UTSW |
15 |
66,700,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R6146:Tg
|
UTSW |
15 |
66,545,216 (GRCm39) |
splice site |
probably null |
|
R6159:Tg
|
UTSW |
15 |
66,607,096 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6223:Tg
|
UTSW |
15 |
66,579,771 (GRCm39) |
missense |
probably benign |
0.15 |
R6480:Tg
|
UTSW |
15 |
66,543,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R6505:Tg
|
UTSW |
15 |
66,631,407 (GRCm39) |
missense |
probably damaging |
0.99 |
R6531:Tg
|
UTSW |
15 |
66,711,211 (GRCm39) |
missense |
probably damaging |
0.99 |
R6614:Tg
|
UTSW |
15 |
66,607,108 (GRCm39) |
missense |
probably damaging |
0.99 |
R6698:Tg
|
UTSW |
15 |
66,711,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Tg
|
UTSW |
15 |
66,550,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R6837:Tg
|
UTSW |
15 |
66,567,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6861:Tg
|
UTSW |
15 |
66,560,740 (GRCm39) |
missense |
probably benign |
0.00 |
R6888:Tg
|
UTSW |
15 |
66,568,095 (GRCm39) |
missense |
probably damaging |
0.99 |
R6933:Tg
|
UTSW |
15 |
66,636,158 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6983:Tg
|
UTSW |
15 |
66,565,207 (GRCm39) |
missense |
probably benign |
0.01 |
R7078:Tg
|
UTSW |
15 |
66,545,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7244:Tg
|
UTSW |
15 |
66,612,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R7320:Tg
|
UTSW |
15 |
66,566,633 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7334:Tg
|
UTSW |
15 |
66,597,121 (GRCm39) |
missense |
probably benign |
0.01 |
R7418:Tg
|
UTSW |
15 |
66,568,432 (GRCm39) |
missense |
probably damaging |
0.99 |
R7485:Tg
|
UTSW |
15 |
66,568,437 (GRCm39) |
missense |
probably benign |
0.04 |
R7524:Tg
|
UTSW |
15 |
66,568,010 (GRCm39) |
missense |
probably benign |
0.01 |
R7529:Tg
|
UTSW |
15 |
66,566,617 (GRCm39) |
missense |
probably damaging |
0.99 |
R7540:Tg
|
UTSW |
15 |
66,561,776 (GRCm39) |
missense |
probably benign |
0.16 |
R7583:Tg
|
UTSW |
15 |
66,636,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R7594:Tg
|
UTSW |
15 |
66,601,432 (GRCm39) |
missense |
probably benign |
0.20 |
R7667:Tg
|
UTSW |
15 |
66,587,012 (GRCm39) |
missense |
probably damaging |
0.98 |
R7722:Tg
|
UTSW |
15 |
66,636,158 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7790:Tg
|
UTSW |
15 |
66,721,453 (GRCm39) |
missense |
probably damaging |
0.99 |
R7838:Tg
|
UTSW |
15 |
66,565,112 (GRCm39) |
missense |
probably benign |
0.00 |
R7890:Tg
|
UTSW |
15 |
66,555,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R7904:Tg
|
UTSW |
15 |
66,577,128 (GRCm39) |
missense |
probably benign |
0.08 |
R7919:Tg
|
UTSW |
15 |
66,555,923 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7921:Tg
|
UTSW |
15 |
66,555,642 (GRCm39) |
missense |
probably benign |
0.08 |
R8037:Tg
|
UTSW |
15 |
66,560,724 (GRCm39) |
missense |
probably benign |
0.00 |
R8038:Tg
|
UTSW |
15 |
66,560,724 (GRCm39) |
missense |
probably benign |
0.00 |
R8214:Tg
|
UTSW |
15 |
66,645,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R8304:Tg
|
UTSW |
15 |
66,565,109 (GRCm39) |
nonsense |
probably null |
|
R8688:Tg
|
UTSW |
15 |
66,566,802 (GRCm39) |
critical splice donor site |
probably benign |
|
R8709:Tg
|
UTSW |
15 |
66,553,786 (GRCm39) |
missense |
probably benign |
0.08 |
R8714:Tg
|
UTSW |
15 |
66,555,891 (GRCm39) |
missense |
probably damaging |
0.97 |
R8901:Tg
|
UTSW |
15 |
66,557,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R8917:Tg
|
UTSW |
15 |
66,645,332 (GRCm39) |
critical splice donor site |
probably null |
|
R9023:Tg
|
UTSW |
15 |
66,555,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Tg
|
UTSW |
15 |
66,570,310 (GRCm39) |
missense |
probably benign |
0.01 |
R9310:Tg
|
UTSW |
15 |
66,699,118 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9361:Tg
|
UTSW |
15 |
66,557,246 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9389:Tg
|
UTSW |
15 |
66,561,173 (GRCm39) |
missense |
probably benign |
0.04 |
R9501:Tg
|
UTSW |
15 |
66,718,923 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9510:Tg
|
UTSW |
15 |
66,545,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R9594:Tg
|
UTSW |
15 |
66,607,109 (GRCm39) |
nonsense |
probably null |
|
R9629:Tg
|
UTSW |
15 |
66,555,587 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9701:Tg
|
UTSW |
15 |
66,637,991 (GRCm39) |
missense |
probably benign |
0.03 |
R9743:Tg
|
UTSW |
15 |
66,561,839 (GRCm39) |
missense |
probably benign |
0.18 |
R9748:Tg
|
UTSW |
15 |
66,719,008 (GRCm39) |
missense |
possibly damaging |
0.91 |
T0975:Tg
|
UTSW |
15 |
66,560,712 (GRCm39) |
missense |
probably benign |
0.01 |
X0005:Tg
|
UTSW |
15 |
66,560,712 (GRCm39) |
missense |
probably benign |
0.01 |
X0065:Tg
|
UTSW |
15 |
66,554,303 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Tg
|
UTSW |
15 |
66,620,592 (GRCm39) |
missense |
probably benign |
0.10 |
Z1177:Tg
|
UTSW |
15 |
66,721,396 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Tg
|
UTSW |
15 |
66,557,159 (GRCm39) |
missense |
possibly damaging |
0.49 |
|