Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad12 |
T |
C |
5: 121,742,322 (GRCm39) |
T429A |
probably benign |
Het |
Afmid |
A |
C |
11: 117,727,300 (GRCm39) |
I275L |
probably benign |
Het |
Aimp1 |
A |
C |
3: 132,382,860 (GRCm39) |
D5E |
possibly damaging |
Het |
Aldob |
G |
A |
4: 49,538,171 (GRCm39) |
A319V |
probably benign |
Het |
Ankar |
C |
T |
1: 72,697,600 (GRCm39) |
V1068I |
possibly damaging |
Het |
Ccr2 |
C |
T |
9: 123,906,830 (GRCm39) |
S370L |
probably benign |
Het |
Chrnb4 |
A |
G |
9: 54,942,102 (GRCm39) |
Y391H |
probably damaging |
Het |
Clip1 |
A |
G |
5: 123,761,281 (GRCm39) |
M873T |
possibly damaging |
Het |
Cspg4 |
G |
C |
9: 56,797,762 (GRCm39) |
G1409R |
probably damaging |
Het |
Dnah17 |
A |
T |
11: 117,987,362 (GRCm39) |
L1320* |
probably null |
Het |
Eml4 |
T |
C |
17: 83,717,622 (GRCm39) |
S65P |
probably benign |
Het |
Fblim1 |
A |
T |
4: 141,312,175 (GRCm39) |
D183E |
probably damaging |
Het |
Foxn1 |
T |
C |
11: 78,256,763 (GRCm39) |
|
probably benign |
Het |
Gm973 |
A |
T |
1: 59,601,930 (GRCm39) |
T515S |
possibly damaging |
Het |
Hdac7 |
G |
A |
15: 97,704,386 (GRCm39) |
Q495* |
probably null |
Het |
Hipk3 |
T |
C |
2: 104,301,518 (GRCm39) |
I225V |
probably benign |
Het |
Hrc |
A |
T |
7: 44,985,638 (GRCm39) |
D263V |
probably damaging |
Het |
Hs6st3 |
T |
C |
14: 119,375,888 (GRCm39) |
I21T |
probably benign |
Het |
Il15ra |
A |
G |
2: 11,728,334 (GRCm39) |
T133A |
possibly damaging |
Het |
Krt78 |
T |
C |
15: 101,854,603 (GRCm39) |
*1069W |
probably null |
Het |
Lama3 |
T |
A |
18: 12,586,920 (GRCm39) |
M761K |
probably damaging |
Het |
Lonp1 |
T |
C |
17: 56,922,068 (GRCm39) |
T771A |
possibly damaging |
Het |
Macf1 |
T |
C |
4: 123,383,005 (GRCm39) |
T1320A |
probably damaging |
Het |
Mark3 |
A |
T |
12: 111,581,875 (GRCm39) |
I115L |
probably damaging |
Het |
Mcph1 |
T |
G |
8: 18,739,081 (GRCm39) |
|
probably benign |
Het |
Med23 |
T |
A |
10: 24,786,664 (GRCm39) |
N923K |
probably benign |
Het |
Msrb2 |
T |
G |
2: 19,398,032 (GRCm39) |
Y97D |
probably damaging |
Het |
Muc6 |
C |
T |
7: 141,234,368 (GRCm39) |
G708S |
probably damaging |
Het |
Mylk |
T |
C |
16: 34,700,673 (GRCm39) |
|
probably null |
Het |
Nfrkb |
T |
A |
9: 31,325,980 (GRCm39) |
V1141E |
possibly damaging |
Het |
Obscn |
T |
C |
11: 58,958,555 (GRCm39) |
E3675G |
probably damaging |
Het |
Or11h7 |
T |
A |
14: 50,890,821 (GRCm39) |
N42K |
probably damaging |
Het |
Or2l5 |
G |
A |
16: 19,333,586 (GRCm39) |
P267S |
probably damaging |
Het |
Or2t6 |
A |
T |
14: 14,175,446 (GRCm38) |
V212E |
probably damaging |
Het |
Or51aa2 |
A |
T |
7: 103,188,201 (GRCm39) |
F80Y |
probably damaging |
Het |
Or52z14 |
A |
G |
7: 103,253,219 (GRCm39) |
|
probably null |
Het |
Or5ac21 |
T |
C |
16: 59,124,091 (GRCm39) |
S193P |
probably damaging |
Het |
Or8k21 |
C |
G |
2: 86,145,498 (GRCm39) |
G44A |
probably damaging |
Het |
Pan2 |
T |
C |
10: 128,156,282 (GRCm39) |
V1171A |
probably damaging |
Het |
Pdgfc |
C |
T |
3: 81,116,552 (GRCm39) |
T302I |
probably damaging |
Het |
Pkhd1l1 |
G |
T |
15: 44,393,109 (GRCm39) |
V1815F |
probably damaging |
Het |
Pnpt1 |
A |
G |
11: 29,091,256 (GRCm39) |
I337V |
probably benign |
Het |
Psma8 |
T |
G |
18: 14,864,033 (GRCm39) |
|
probably null |
Het |
Rbl2 |
T |
C |
8: 91,812,090 (GRCm39) |
S220P |
probably benign |
Het |
Rere |
T |
A |
4: 150,700,190 (GRCm39) |
D1091E |
probably damaging |
Het |
Rpa1 |
A |
G |
11: 75,197,002 (GRCm39) |
C540R |
probably damaging |
Het |
Sema3d |
T |
A |
5: 12,613,285 (GRCm39) |
V454E |
probably damaging |
Het |
Sema3d |
T |
C |
5: 12,634,965 (GRCm39) |
V677A |
probably benign |
Het |
Sgk2 |
A |
G |
2: 162,846,080 (GRCm39) |
N207S |
probably benign |
Het |
Sirpb1a |
T |
C |
3: 15,444,141 (GRCm39) |
I370V |
probably benign |
Het |
Slc22a19 |
A |
G |
19: 7,661,224 (GRCm39) |
|
probably benign |
Het |
Slc26a1 |
T |
A |
5: 108,820,338 (GRCm39) |
D287V |
probably damaging |
Het |
Slc36a4 |
T |
A |
9: 15,645,506 (GRCm39) |
V311D |
probably damaging |
Het |
Slco1b2 |
A |
T |
6: 141,628,951 (GRCm39) |
Y551F |
probably damaging |
Het |
Slco2a1 |
T |
A |
9: 102,956,653 (GRCm39) |
Y488* |
probably null |
Het |
Stab2 |
A |
C |
10: 86,732,360 (GRCm39) |
|
probably null |
Het |
Strn |
T |
C |
17: 78,999,928 (GRCm39) |
|
probably null |
Het |
Tbxas1 |
A |
G |
6: 38,925,575 (GRCm39) |
|
probably benign |
Het |
Thumpd3 |
A |
G |
6: 113,032,838 (GRCm39) |
N192S |
possibly damaging |
Het |
Tns3 |
T |
A |
11: 8,385,738 (GRCm39) |
I1386F |
probably benign |
Het |
Treml4 |
T |
A |
17: 48,579,821 (GRCm39) |
V219E |
probably damaging |
Het |
Triobp |
T |
C |
15: 78,850,908 (GRCm39) |
V354A |
probably benign |
Het |
Tspan8 |
A |
G |
10: 115,680,035 (GRCm39) |
I217V |
probably benign |
Het |
Tub |
G |
A |
7: 108,627,042 (GRCm39) |
G314R |
possibly damaging |
Het |
Ube3b |
C |
T |
5: 114,537,926 (GRCm39) |
T339M |
possibly damaging |
Het |
Vmn2r43 |
A |
G |
7: 8,258,550 (GRCm39) |
I221T |
possibly damaging |
Het |
Vmn2r5 |
C |
T |
3: 64,411,642 (GRCm39) |
E309K |
probably damaging |
Het |
Zfp110 |
C |
T |
7: 12,582,429 (GRCm39) |
T359I |
probably benign |
Het |
Zfp322a |
A |
T |
13: 23,541,074 (GRCm39) |
C223S |
probably damaging |
Het |
Zfp512b |
G |
A |
2: 181,228,878 (GRCm39) |
R696* |
probably null |
Het |
|
Other mutations in Dock4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Dock4
|
APN |
12 |
40,882,305 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL00726:Dock4
|
APN |
12 |
40,840,067 (GRCm39) |
splice site |
probably benign |
|
IGL00790:Dock4
|
APN |
12 |
40,884,390 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01061:Dock4
|
APN |
12 |
40,752,968 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01083:Dock4
|
APN |
12 |
40,838,380 (GRCm39) |
splice site |
probably benign |
|
IGL01412:Dock4
|
APN |
12 |
40,780,040 (GRCm39) |
splice site |
probably benign |
|
IGL01583:Dock4
|
APN |
12 |
40,860,466 (GRCm39) |
nonsense |
probably null |
|
IGL01603:Dock4
|
APN |
12 |
40,743,030 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01766:Dock4
|
APN |
12 |
40,496,378 (GRCm39) |
nonsense |
probably null |
|
IGL02067:Dock4
|
APN |
12 |
40,884,384 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02302:Dock4
|
APN |
12 |
40,775,776 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02406:Dock4
|
APN |
12 |
40,827,206 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02547:Dock4
|
APN |
12 |
40,787,478 (GRCm39) |
missense |
probably benign |
|
IGL02613:Dock4
|
APN |
12 |
40,860,465 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02643:Dock4
|
APN |
12 |
40,718,429 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02952:Dock4
|
APN |
12 |
40,760,902 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02994:Dock4
|
APN |
12 |
40,829,159 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03096:Dock4
|
APN |
12 |
40,798,000 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03144:Dock4
|
APN |
12 |
40,742,906 (GRCm39) |
splice site |
probably benign |
|
IGL03223:Dock4
|
APN |
12 |
40,867,593 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03296:Dock4
|
APN |
12 |
40,783,256 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03349:Dock4
|
APN |
12 |
40,783,309 (GRCm39) |
missense |
probably benign |
0.42 |
IGL03353:Dock4
|
APN |
12 |
40,867,757 (GRCm39) |
splice site |
probably null |
|
BB005:Dock4
|
UTSW |
12 |
40,838,302 (GRCm39) |
missense |
probably damaging |
0.98 |
BB015:Dock4
|
UTSW |
12 |
40,838,302 (GRCm39) |
missense |
probably damaging |
0.98 |
R0046:Dock4
|
UTSW |
12 |
40,787,359 (GRCm39) |
splice site |
probably benign |
|
R0046:Dock4
|
UTSW |
12 |
40,787,359 (GRCm39) |
splice site |
probably benign |
|
R0110:Dock4
|
UTSW |
12 |
40,671,311 (GRCm39) |
splice site |
probably benign |
|
R0238:Dock4
|
UTSW |
12 |
40,787,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R0238:Dock4
|
UTSW |
12 |
40,787,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R0239:Dock4
|
UTSW |
12 |
40,787,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R0239:Dock4
|
UTSW |
12 |
40,787,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R0472:Dock4
|
UTSW |
12 |
40,888,437 (GRCm39) |
intron |
probably benign |
|
R0616:Dock4
|
UTSW |
12 |
40,754,414 (GRCm39) |
missense |
probably benign |
0.31 |
R0647:Dock4
|
UTSW |
12 |
40,760,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R0706:Dock4
|
UTSW |
12 |
40,752,922 (GRCm39) |
missense |
probably damaging |
0.98 |
R0791:Dock4
|
UTSW |
12 |
40,754,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R0940:Dock4
|
UTSW |
12 |
40,681,626 (GRCm39) |
splice site |
probably benign |
|
R1087:Dock4
|
UTSW |
12 |
40,779,937 (GRCm39) |
missense |
probably benign |
0.40 |
R1180:Dock4
|
UTSW |
12 |
40,690,413 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1194:Dock4
|
UTSW |
12 |
40,879,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R1463:Dock4
|
UTSW |
12 |
40,866,324 (GRCm39) |
frame shift |
probably null |
|
R1468:Dock4
|
UTSW |
12 |
40,805,809 (GRCm39) |
missense |
probably benign |
0.00 |
R1468:Dock4
|
UTSW |
12 |
40,805,809 (GRCm39) |
missense |
probably benign |
0.00 |
R1523:Dock4
|
UTSW |
12 |
40,743,024 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1616:Dock4
|
UTSW |
12 |
40,719,044 (GRCm39) |
missense |
probably damaging |
0.99 |
R1682:Dock4
|
UTSW |
12 |
40,775,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R1691:Dock4
|
UTSW |
12 |
40,775,754 (GRCm39) |
missense |
probably benign |
0.26 |
R1693:Dock4
|
UTSW |
12 |
40,884,721 (GRCm39) |
missense |
probably benign |
0.07 |
R1737:Dock4
|
UTSW |
12 |
40,857,000 (GRCm39) |
splice site |
probably null |
|
R1802:Dock4
|
UTSW |
12 |
40,844,597 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1813:Dock4
|
UTSW |
12 |
40,686,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R1846:Dock4
|
UTSW |
12 |
40,783,267 (GRCm39) |
missense |
probably benign |
0.00 |
R1959:Dock4
|
UTSW |
12 |
40,760,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R1986:Dock4
|
UTSW |
12 |
40,780,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R2105:Dock4
|
UTSW |
12 |
40,742,988 (GRCm39) |
missense |
probably benign |
0.00 |
R2134:Dock4
|
UTSW |
12 |
40,795,667 (GRCm39) |
missense |
probably benign |
|
R2135:Dock4
|
UTSW |
12 |
40,795,667 (GRCm39) |
missense |
probably benign |
|
R2154:Dock4
|
UTSW |
12 |
40,894,547 (GRCm39) |
small insertion |
probably benign |
|
R2154:Dock4
|
UTSW |
12 |
40,870,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R2864:Dock4
|
UTSW |
12 |
40,780,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R2890:Dock4
|
UTSW |
12 |
40,673,800 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3086:Dock4
|
UTSW |
12 |
40,781,862 (GRCm39) |
missense |
probably benign |
0.02 |
R3808:Dock4
|
UTSW |
12 |
40,722,809 (GRCm39) |
missense |
probably damaging |
0.99 |
R3811:Dock4
|
UTSW |
12 |
40,829,123 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3836:Dock4
|
UTSW |
12 |
40,844,623 (GRCm39) |
critical splice donor site |
probably null |
|
R3838:Dock4
|
UTSW |
12 |
40,844,623 (GRCm39) |
critical splice donor site |
probably null |
|
R4091:Dock4
|
UTSW |
12 |
40,894,266 (GRCm39) |
missense |
probably damaging |
0.99 |
R4735:Dock4
|
UTSW |
12 |
40,681,525 (GRCm39) |
missense |
probably benign |
0.31 |
R4752:Dock4
|
UTSW |
12 |
40,496,364 (GRCm39) |
missense |
probably benign |
0.04 |
R4828:Dock4
|
UTSW |
12 |
40,718,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R5039:Dock4
|
UTSW |
12 |
40,867,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R5092:Dock4
|
UTSW |
12 |
40,894,440 (GRCm39) |
missense |
probably benign |
|
R5146:Dock4
|
UTSW |
12 |
40,699,491 (GRCm39) |
splice site |
probably null |
|
R5213:Dock4
|
UTSW |
12 |
40,726,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R5214:Dock4
|
UTSW |
12 |
40,754,465 (GRCm39) |
missense |
probably benign |
0.00 |
R5270:Dock4
|
UTSW |
12 |
40,783,270 (GRCm39) |
missense |
probably benign |
0.02 |
R5426:Dock4
|
UTSW |
12 |
40,795,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R5474:Dock4
|
UTSW |
12 |
40,795,730 (GRCm39) |
missense |
probably benign |
|
R5544:Dock4
|
UTSW |
12 |
40,884,701 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5615:Dock4
|
UTSW |
12 |
40,699,479 (GRCm39) |
missense |
probably benign |
0.22 |
R5649:Dock4
|
UTSW |
12 |
40,894,539 (GRCm39) |
missense |
probably benign |
0.03 |
R5702:Dock4
|
UTSW |
12 |
40,787,490 (GRCm39) |
missense |
probably benign |
0.02 |
R5846:Dock4
|
UTSW |
12 |
40,867,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R5847:Dock4
|
UTSW |
12 |
40,671,250 (GRCm39) |
missense |
probably damaging |
0.97 |
R5895:Dock4
|
UTSW |
12 |
40,805,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R5997:Dock4
|
UTSW |
12 |
40,805,833 (GRCm39) |
missense |
probably damaging |
0.99 |
R6011:Dock4
|
UTSW |
12 |
40,867,756 (GRCm39) |
critical splice donor site |
probably null |
|
R6022:Dock4
|
UTSW |
12 |
40,798,109 (GRCm39) |
missense |
probably benign |
0.04 |
R6038:Dock4
|
UTSW |
12 |
40,783,350 (GRCm39) |
splice site |
probably null |
|
R6038:Dock4
|
UTSW |
12 |
40,783,350 (GRCm39) |
splice site |
probably null |
|
R6179:Dock4
|
UTSW |
12 |
40,781,868 (GRCm39) |
missense |
probably benign |
0.00 |
R6479:Dock4
|
UTSW |
12 |
40,878,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R6516:Dock4
|
UTSW |
12 |
40,781,898 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6748:Dock4
|
UTSW |
12 |
40,754,465 (GRCm39) |
missense |
probably benign |
0.44 |
R6752:Dock4
|
UTSW |
12 |
40,870,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R6814:Dock4
|
UTSW |
12 |
40,862,325 (GRCm39) |
critical splice donor site |
probably null |
|
R6864:Dock4
|
UTSW |
12 |
40,795,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R6872:Dock4
|
UTSW |
12 |
40,862,325 (GRCm39) |
critical splice donor site |
probably null |
|
R6891:Dock4
|
UTSW |
12 |
40,829,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R6937:Dock4
|
UTSW |
12 |
40,884,634 (GRCm39) |
missense |
probably benign |
0.01 |
R6950:Dock4
|
UTSW |
12 |
40,783,313 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7081:Dock4
|
UTSW |
12 |
40,671,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R7129:Dock4
|
UTSW |
12 |
40,878,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R7140:Dock4
|
UTSW |
12 |
40,686,158 (GRCm39) |
missense |
probably benign |
0.06 |
R7241:Dock4
|
UTSW |
12 |
40,844,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R7378:Dock4
|
UTSW |
12 |
40,838,243 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7714:Dock4
|
UTSW |
12 |
40,775,648 (GRCm39) |
nonsense |
probably null |
|
R7720:Dock4
|
UTSW |
12 |
40,856,974 (GRCm39) |
missense |
probably damaging |
0.99 |
R7756:Dock4
|
UTSW |
12 |
40,760,878 (GRCm39) |
missense |
probably benign |
0.02 |
R7758:Dock4
|
UTSW |
12 |
40,760,878 (GRCm39) |
missense |
probably benign |
0.02 |
R7759:Dock4
|
UTSW |
12 |
40,867,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R7787:Dock4
|
UTSW |
12 |
40,775,676 (GRCm39) |
missense |
probably benign |
|
R7879:Dock4
|
UTSW |
12 |
40,780,083 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7928:Dock4
|
UTSW |
12 |
40,838,302 (GRCm39) |
missense |
probably damaging |
0.98 |
R8000:Dock4
|
UTSW |
12 |
40,883,118 (GRCm39) |
missense |
probably benign |
0.05 |
R8042:Dock4
|
UTSW |
12 |
40,795,759 (GRCm39) |
missense |
probably benign |
0.01 |
R8231:Dock4
|
UTSW |
12 |
40,752,950 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8234:Dock4
|
UTSW |
12 |
40,884,837 (GRCm39) |
splice site |
probably null |
|
R8758:Dock4
|
UTSW |
12 |
40,838,231 (GRCm39) |
missense |
probably benign |
0.12 |
R8871:Dock4
|
UTSW |
12 |
40,795,730 (GRCm39) |
missense |
probably benign |
|
R8873:Dock4
|
UTSW |
12 |
40,726,767 (GRCm39) |
nonsense |
probably null |
|
R8884:Dock4
|
UTSW |
12 |
40,856,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R9164:Dock4
|
UTSW |
12 |
40,754,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R9225:Dock4
|
UTSW |
12 |
40,879,669 (GRCm39) |
missense |
probably benign |
0.02 |
R9276:Dock4
|
UTSW |
12 |
40,699,404 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9307:Dock4
|
UTSW |
12 |
40,686,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R9675:Dock4
|
UTSW |
12 |
40,894,393 (GRCm39) |
small insertion |
probably benign |
|
R9675:Dock4
|
UTSW |
12 |
40,894,379 (GRCm39) |
small insertion |
probably benign |
|
R9676:Dock4
|
UTSW |
12 |
40,894,397 (GRCm39) |
small insertion |
probably benign |
|
R9676:Dock4
|
UTSW |
12 |
40,894,387 (GRCm39) |
small insertion |
probably benign |
|
R9676:Dock4
|
UTSW |
12 |
40,894,379 (GRCm39) |
small insertion |
probably benign |
|
R9676:Dock4
|
UTSW |
12 |
40,894,401 (GRCm39) |
small insertion |
probably benign |
|
R9678:Dock4
|
UTSW |
12 |
40,894,396 (GRCm39) |
small insertion |
probably benign |
|
R9678:Dock4
|
UTSW |
12 |
40,894,387 (GRCm39) |
small insertion |
probably benign |
|
R9678:Dock4
|
UTSW |
12 |
40,894,379 (GRCm39) |
small insertion |
probably benign |
|
R9691:Dock4
|
UTSW |
12 |
40,686,097 (GRCm39) |
missense |
probably damaging |
1.00 |
RF018:Dock4
|
UTSW |
12 |
40,894,398 (GRCm39) |
frame shift |
probably null |
|
RF025:Dock4
|
UTSW |
12 |
40,894,392 (GRCm39) |
frame shift |
probably null |
|
RF063:Dock4
|
UTSW |
12 |
40,894,398 (GRCm39) |
frame shift |
probably null |
|
X0028:Dock4
|
UTSW |
12 |
40,719,046 (GRCm39) |
missense |
probably benign |
0.25 |
Z1176:Dock4
|
UTSW |
12 |
40,681,615 (GRCm39) |
missense |
probably benign |
0.16 |
Z1176:Dock4
|
UTSW |
12 |
40,681,613 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Dock4
|
UTSW |
12 |
40,867,640 (GRCm39) |
missense |
possibly damaging |
0.88 |
|