Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adra1d |
C |
A |
2: 131,388,134 (GRCm39) |
V474F |
probably benign |
Het |
Alg8 |
A |
T |
7: 97,032,891 (GRCm39) |
|
probably null |
Het |
Ash1l |
A |
G |
3: 88,974,529 (GRCm39) |
D2618G |
possibly damaging |
Het |
Atp6v1c2 |
C |
A |
12: 17,344,676 (GRCm39) |
|
probably null |
Het |
Cacna1d |
A |
G |
14: 29,845,453 (GRCm39) |
V572A |
probably benign |
Het |
Camta1 |
A |
G |
4: 151,228,187 (GRCm39) |
W882R |
probably damaging |
Het |
Cd72 |
A |
G |
4: 43,453,163 (GRCm39) |
V91A |
probably benign |
Het |
Cdh12 |
T |
C |
15: 21,586,493 (GRCm39) |
W771R |
probably damaging |
Het |
Cdx2 |
G |
T |
5: 147,240,097 (GRCm39) |
T193K |
probably damaging |
Het |
Cfap70 |
A |
C |
14: 20,498,673 (GRCm39) |
S5A |
probably benign |
Het |
Chmp7 |
A |
G |
14: 69,958,446 (GRCm39) |
V241A |
probably damaging |
Het |
Col4a1 |
C |
T |
8: 11,268,780 (GRCm39) |
|
probably benign |
Het |
D3Ertd751e |
A |
G |
3: 41,708,313 (GRCm39) |
Y150C |
probably damaging |
Het |
Depdc5 |
T |
C |
5: 33,100,584 (GRCm39) |
S832P |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,370,738 (GRCm39) |
S4673G |
probably benign |
Het |
Dysf |
C |
T |
6: 84,041,461 (GRCm39) |
Q156* |
probably null |
Het |
Elp1 |
C |
A |
4: 56,784,596 (GRCm39) |
V466L |
probably benign |
Het |
Espnl |
T |
C |
1: 91,250,009 (GRCm39) |
V52A |
probably damaging |
Het |
Flcn |
T |
C |
11: 59,691,902 (GRCm39) |
N249S |
probably benign |
Het |
Gemin6 |
C |
A |
17: 80,533,139 (GRCm39) |
A24D |
probably damaging |
Het |
Gm5773 |
A |
G |
3: 93,681,339 (GRCm39) |
H337R |
probably benign |
Het |
Greb1l |
C |
T |
18: 10,458,567 (GRCm39) |
|
probably benign |
Het |
Hal |
T |
C |
10: 93,339,344 (GRCm39) |
S478P |
possibly damaging |
Het |
Hectd1 |
T |
A |
12: 51,816,101 (GRCm39) |
M1324L |
possibly damaging |
Het |
Hyal5 |
T |
A |
6: 24,876,343 (GRCm39) |
L72Q |
probably damaging |
Het |
Ift140 |
C |
A |
17: 25,264,497 (GRCm39) |
C557* |
probably null |
Het |
Il4ra |
T |
C |
7: 125,174,371 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,332,074 (GRCm39) |
|
probably benign |
Het |
Irag2 |
G |
A |
6: 145,117,704 (GRCm39) |
|
probably benign |
Het |
Kbtbd3 |
G |
T |
9: 4,330,144 (GRCm39) |
V173L |
possibly damaging |
Het |
Kif14 |
A |
G |
1: 136,455,131 (GRCm39) |
E1551G |
probably damaging |
Het |
Klc1 |
A |
G |
12: 111,751,758 (GRCm39) |
|
probably benign |
Het |
Krt17 |
G |
A |
11: 100,151,704 (GRCm39) |
R30* |
probably null |
Het |
Lamb3 |
A |
T |
1: 193,003,361 (GRCm39) |
D100V |
probably damaging |
Het |
Map2 |
A |
G |
1: 66,455,265 (GRCm39) |
D1385G |
probably damaging |
Het |
Mettl25 |
C |
T |
10: 105,662,386 (GRCm39) |
V195I |
probably damaging |
Het |
Micu2 |
G |
A |
14: 58,154,835 (GRCm39) |
|
probably benign |
Het |
Mrrf |
T |
C |
2: 36,067,293 (GRCm39) |
|
probably benign |
Het |
Myh8 |
A |
G |
11: 67,192,518 (GRCm39) |
T1466A |
probably benign |
Het |
Myo3b |
T |
A |
2: 69,935,769 (GRCm39) |
C61S |
probably benign |
Het |
Nacc2 |
T |
G |
2: 25,952,273 (GRCm39) |
N361T |
probably damaging |
Het |
Nf1 |
A |
T |
11: 79,309,400 (GRCm39) |
K438M |
possibly damaging |
Het |
Nipal4 |
A |
G |
11: 46,041,268 (GRCm39) |
V309A |
possibly damaging |
Het |
Nomo1 |
T |
C |
7: 45,729,018 (GRCm39) |
|
probably null |
Het |
Nubp2 |
T |
C |
17: 25,103,445 (GRCm39) |
E144G |
probably damaging |
Het |
Nwd2 |
A |
T |
5: 63,957,467 (GRCm39) |
I266F |
probably benign |
Het |
Or12e7 |
T |
C |
2: 87,288,381 (GRCm39) |
F291L |
probably benign |
Het |
Or2ag1b |
A |
G |
7: 106,288,462 (GRCm39) |
Y159H |
probably benign |
Het |
Or52s1 |
G |
A |
7: 102,861,933 (GRCm39) |
V289M |
possibly damaging |
Het |
Orc1 |
T |
C |
4: 108,452,843 (GRCm39) |
|
probably null |
Het |
Otogl |
T |
A |
10: 107,642,557 (GRCm39) |
N1291I |
probably damaging |
Het |
Pah |
C |
T |
10: 87,403,143 (GRCm39) |
P173S |
possibly damaging |
Het |
Pga5 |
A |
G |
19: 10,646,817 (GRCm39) |
Y305H |
probably damaging |
Het |
Plekha4 |
A |
G |
7: 45,181,782 (GRCm39) |
H62R |
probably damaging |
Het |
Plxnd1 |
G |
T |
6: 115,945,754 (GRCm39) |
D906E |
probably benign |
Het |
Ppfia4 |
T |
C |
1: 134,256,927 (GRCm39) |
E98G |
possibly damaging |
Het |
Ptk2 |
A |
T |
15: 73,215,132 (GRCm39) |
|
probably null |
Het |
Pzp |
C |
T |
6: 128,466,119 (GRCm39) |
|
probably benign |
Het |
Raet1c |
C |
A |
10: 22,056,761 (GRCm39) |
H112Q |
possibly damaging |
Het |
Scai |
T |
A |
2: 38,965,054 (GRCm39) |
I597F |
probably benign |
Het |
Scgb1b2 |
T |
A |
7: 30,991,155 (GRCm39) |
|
probably benign |
Het |
Sec31b |
G |
A |
19: 44,513,908 (GRCm39) |
|
probably benign |
Het |
Sirpd |
A |
G |
3: 15,361,661 (GRCm39) |
L163P |
probably damaging |
Het |
Slc35c2 |
C |
T |
2: 165,122,757 (GRCm39) |
G176S |
probably damaging |
Het |
Slc35f4 |
A |
T |
14: 49,541,713 (GRCm39) |
I347N |
possibly damaging |
Het |
Slc49a3 |
G |
T |
5: 108,591,882 (GRCm39) |
|
probably benign |
Het |
Slc52a3 |
T |
C |
2: 151,850,076 (GRCm39) |
*461Q |
probably null |
Het |
Slc6a1 |
G |
A |
6: 114,279,761 (GRCm39) |
V142I |
probably benign |
Het |
Tbc1d31 |
C |
A |
15: 57,804,149 (GRCm39) |
T388N |
probably benign |
Het |
Tmem131 |
T |
C |
1: 36,867,131 (GRCm39) |
|
probably benign |
Het |
Tmem63c |
T |
C |
12: 87,122,413 (GRCm39) |
W404R |
probably damaging |
Het |
Tmem79 |
A |
G |
3: 88,240,628 (GRCm39) |
S107P |
probably benign |
Het |
Trip11 |
C |
T |
12: 101,850,987 (GRCm39) |
E741K |
probably damaging |
Het |
Trpm5 |
G |
T |
7: 142,636,695 (GRCm39) |
T414N |
probably damaging |
Het |
Tsnaxip1 |
T |
A |
8: 106,571,120 (GRCm39) |
I660N |
possibly damaging |
Het |
Ube2q2 |
T |
C |
9: 55,070,291 (GRCm39) |
S78P |
probably damaging |
Het |
Vac14 |
A |
T |
8: 111,362,007 (GRCm39) |
|
probably null |
Het |
Vps51 |
G |
T |
19: 6,121,467 (GRCm39) |
S185* |
probably null |
Het |
Zfp11 |
C |
T |
5: 129,735,302 (GRCm39) |
G53E |
possibly damaging |
Het |
Zfp532 |
A |
T |
18: 65,816,056 (GRCm39) |
I810F |
possibly damaging |
Het |
Zfp599 |
C |
T |
9: 22,161,055 (GRCm39) |
C370Y |
probably damaging |
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 |
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 |
R1975:Dock4
|
UTSW |
12 |
40,829,641 (GRCm39) |
splice site |
probably benign |
|
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 |
|