Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
A |
G |
5: 8,946,587 (GRCm39) |
E29G |
probably benign |
Het |
Abi3bp |
T |
C |
16: 56,491,628 (GRCm39) |
S552P |
probably damaging |
Het |
Adgrg7 |
A |
G |
16: 56,593,829 (GRCm39) |
I129T |
probably benign |
Het |
Adhfe1 |
A |
G |
1: 9,623,943 (GRCm39) |
N148S |
probably damaging |
Het |
AI182371 |
A |
G |
2: 34,987,983 (GRCm39) |
Y77H |
probably damaging |
Het |
Aldh5a1 |
C |
T |
13: 25,103,661 (GRCm39) |
|
probably null |
Het |
Ankrd2 |
A |
G |
19: 42,028,544 (GRCm39) |
T67A |
possibly damaging |
Het |
Anln |
A |
T |
9: 22,287,604 (GRCm39) |
C232* |
probably null |
Het |
Cchcr1 |
A |
G |
17: 35,839,475 (GRCm39) |
D587G |
possibly damaging |
Het |
Cgn |
G |
T |
3: 94,674,435 (GRCm39) |
Q901K |
possibly damaging |
Het |
Cip2a |
A |
T |
16: 48,814,692 (GRCm39) |
K18* |
probably null |
Het |
Cluh |
G |
T |
11: 74,558,054 (GRCm39) |
|
probably null |
Het |
Crebbp |
G |
A |
16: 3,902,487 (GRCm39) |
Q2213* |
probably null |
Het |
Cyp2d22 |
T |
A |
15: 82,258,036 (GRCm39) |
|
probably null |
Het |
Dcdc2a |
T |
C |
13: 25,389,440 (GRCm39) |
V456A |
probably benign |
Het |
Depdc5 |
A |
G |
5: 33,126,075 (GRCm39) |
E569G |
probably benign |
Het |
Dnah5 |
T |
C |
15: 28,459,331 (GRCm39) |
F4517L |
probably benign |
Het |
Doc2b |
T |
C |
11: 75,664,421 (GRCm39) |
K317E |
probably damaging |
Het |
Dysf |
T |
A |
6: 84,180,181 (GRCm39) |
D1951E |
probably damaging |
Het |
Epha6 |
C |
A |
16: 60,245,198 (GRCm39) |
A334S |
possibly damaging |
Het |
F2rl2 |
A |
C |
13: 95,837,149 (GRCm39) |
I65L |
probably benign |
Het |
Fbxw17 |
A |
G |
13: 50,586,548 (GRCm39) |
K417E |
probably benign |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Fxr2 |
A |
G |
11: 69,532,165 (GRCm39) |
M96V |
possibly damaging |
Het |
Kcnj10 |
C |
A |
1: 172,196,892 (GRCm39) |
Y135* |
probably null |
Het |
Kidins220 |
G |
A |
12: 25,102,812 (GRCm39) |
R1238Q |
probably damaging |
Het |
Krt31 |
T |
C |
11: 99,939,056 (GRCm39) |
N255S |
probably benign |
Het |
Lrp2 |
T |
C |
2: 69,341,345 (GRCm39) |
D945G |
probably benign |
Het |
Lrrc66 |
T |
C |
5: 73,765,432 (GRCm39) |
D537G |
probably benign |
Het |
Ltbp4 |
T |
A |
7: 27,019,149 (GRCm39) |
I992F |
probably damaging |
Het |
Lzts1 |
A |
G |
8: 69,593,524 (GRCm39) |
S28P |
probably benign |
Het |
Mrc2 |
C |
A |
11: 105,216,470 (GRCm39) |
N86K |
probably damaging |
Het |
Mroh6 |
C |
A |
15: 75,758,486 (GRCm39) |
A302S |
possibly damaging |
Het |
Muc16 |
T |
A |
9: 18,409,093 (GRCm39) |
N198Y |
probably damaging |
Het |
Myo9a |
T |
C |
9: 59,778,512 (GRCm39) |
S1423P |
probably benign |
Het |
Or10ag58 |
A |
T |
2: 87,265,662 (GRCm39) |
D277V |
possibly damaging |
Het |
Or2b28 |
A |
T |
13: 21,531,164 (GRCm39) |
Y22F |
possibly damaging |
Het |
Or5h22 |
A |
G |
16: 58,895,077 (GRCm39) |
V122A |
probably benign |
Het |
Or5p56 |
G |
T |
7: 107,589,620 (GRCm39) |
G16V |
probably damaging |
Het |
Or5w17 |
A |
C |
2: 87,583,602 (GRCm39) |
L245R |
probably damaging |
Het |
Or9g4 |
T |
A |
2: 85,504,938 (GRCm39) |
K186* |
probably null |
Het |
Otogl |
G |
A |
10: 107,612,978 (GRCm39) |
|
silent |
Het |
Polg |
T |
C |
7: 79,100,260 (GRCm39) |
M1184V |
probably benign |
Het |
Prl8a8 |
T |
C |
13: 27,694,463 (GRCm39) |
Y108C |
probably damaging |
Het |
Proser1 |
T |
A |
3: 53,385,540 (GRCm39) |
I474N |
probably damaging |
Het |
Rab44 |
A |
G |
17: 29,354,391 (GRCm39) |
|
probably benign |
Het |
Rbp1 |
C |
A |
9: 98,307,669 (GRCm39) |
D79E |
possibly damaging |
Het |
Rnf213 |
T |
C |
11: 119,326,825 (GRCm39) |
V1605A |
probably benign |
Het |
Rps24 |
A |
T |
14: 24,540,803 (GRCm39) |
|
probably null |
Het |
Setd5 |
T |
C |
6: 113,098,773 (GRCm39) |
|
probably null |
Het |
Skic3 |
A |
G |
13: 76,333,359 (GRCm39) |
E1536G |
probably damaging |
Het |
Slc38a3 |
T |
C |
9: 107,532,228 (GRCm39) |
I435V |
probably benign |
Het |
Slco1a5 |
T |
A |
6: 142,180,534 (GRCm39) |
M623L |
probably benign |
Het |
Spaca9 |
G |
A |
2: 28,583,793 (GRCm39) |
R64W |
probably damaging |
Het |
Spn |
A |
G |
7: 126,735,479 (GRCm39) |
S343P |
possibly damaging |
Het |
Sptan1 |
A |
G |
2: 29,894,535 (GRCm39) |
T1168A |
probably benign |
Het |
Sptbn4 |
A |
T |
7: 27,064,012 (GRCm39) |
L2138* |
probably null |
Het |
Tigd5 |
T |
A |
15: 75,782,094 (GRCm39) |
L152Q |
probably damaging |
Het |
Tmem163 |
C |
T |
1: 127,447,126 (GRCm39) |
V170I |
probably benign |
Het |
Tpr |
T |
C |
1: 150,298,913 (GRCm39) |
C1068R |
possibly damaging |
Het |
Ubr1 |
A |
T |
2: 120,723,690 (GRCm39) |
Y1290N |
probably damaging |
Het |
Vmn1r184 |
T |
A |
7: 25,966,817 (GRCm39) |
F188I |
probably benign |
Het |
Vmn2r100 |
G |
A |
17: 19,742,522 (GRCm39) |
V299I |
probably benign |
Het |
Vmn2r91 |
T |
G |
17: 18,356,518 (GRCm39) |
H728Q |
probably benign |
Het |
Vta1 |
T |
C |
10: 14,581,096 (GRCm39) |
Y37C |
probably damaging |
Het |
Wbp2 |
C |
A |
11: 115,974,728 (GRCm39) |
M35I |
probably benign |
Het |
Zcchc9 |
G |
A |
13: 91,953,986 (GRCm39) |
Q90* |
probably null |
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 |
|
R0646:Tg
|
UTSW |
15 |
66,601,475 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
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 |
|