Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
T |
11: 110,205,384 (GRCm39) |
I299N |
probably damaging |
Het |
Abcc8 |
T |
C |
7: 45,803,936 (GRCm39) |
T413A |
probably benign |
Het |
Actc1 |
G |
A |
2: 113,880,010 (GRCm39) |
S201F |
probably damaging |
Het |
Adam30 |
G |
A |
3: 98,069,841 (GRCm39) |
C558Y |
probably damaging |
Het |
Adcy4 |
T |
A |
14: 56,016,396 (GRCm39) |
I352F |
probably damaging |
Het |
Adgrl4 |
A |
T |
3: 151,216,233 (GRCm39) |
D472V |
probably damaging |
Het |
Afap1l2 |
T |
A |
19: 56,918,583 (GRCm39) |
M117L |
probably benign |
Het |
AI597479 |
T |
C |
1: 43,152,389 (GRCm39) |
V229A |
probably damaging |
Het |
Ascc1 |
T |
C |
10: 59,898,338 (GRCm39) |
V267A |
probably benign |
Het |
Asxl3 |
A |
G |
18: 22,649,810 (GRCm39) |
S600G |
possibly damaging |
Het |
Atg14 |
T |
C |
14: 47,786,451 (GRCm39) |
I268V |
probably benign |
Het |
Bcas1 |
C |
T |
2: 170,260,584 (GRCm39) |
V32I |
probably benign |
Het |
Cacna1c |
G |
T |
6: 118,570,955 (GRCm39) |
D2106E |
probably benign |
Het |
Cacna1i |
A |
G |
15: 80,263,255 (GRCm39) |
H1440R |
possibly damaging |
Het |
Catsper2 |
G |
A |
2: 121,236,927 (GRCm39) |
T240M |
probably damaging |
Het |
Ccn4 |
T |
A |
15: 66,791,120 (GRCm39) |
N307K |
possibly damaging |
Het |
Cd163 |
A |
G |
6: 124,288,406 (GRCm39) |
E279G |
probably damaging |
Het |
Cdx2 |
C |
T |
5: 147,243,470 (GRCm39) |
S108N |
probably benign |
Het |
Cenpf |
A |
T |
1: 189,386,936 (GRCm39) |
N1781K |
probably damaging |
Het |
Cgref1 |
T |
A |
5: 31,093,338 (GRCm39) |
|
probably benign |
Het |
Clcn4 |
C |
T |
7: 7,299,763 (GRCm39) |
W22* |
probably null |
Het |
Cntn2 |
A |
G |
1: 132,448,875 (GRCm39) |
|
probably null |
Het |
Cntn5 |
C |
T |
9: 9,673,801 (GRCm39) |
|
probably null |
Het |
Cpeb3 |
A |
G |
19: 37,116,500 (GRCm39) |
M377T |
probably benign |
Het |
Cryge |
T |
A |
1: 65,087,997 (GRCm39) |
R135* |
probably null |
Het |
Ctdsp2 |
C |
A |
10: 126,829,790 (GRCm39) |
|
probably benign |
Het |
Ctsll3 |
G |
A |
13: 60,949,089 (GRCm39) |
|
probably benign |
Het |
Cuzd1 |
C |
A |
7: 130,918,371 (GRCm39) |
G189C |
probably damaging |
Het |
Dmbt1 |
T |
A |
7: 130,711,366 (GRCm39) |
|
probably null |
Het |
Dnai4 |
T |
A |
4: 102,944,615 (GRCm39) |
L245F |
possibly damaging |
Het |
Dnajc13 |
A |
T |
9: 104,056,139 (GRCm39) |
S1587R |
probably damaging |
Het |
Dock6 |
T |
C |
9: 21,743,202 (GRCm39) |
H701R |
probably damaging |
Het |
Edem3 |
A |
G |
1: 151,683,261 (GRCm39) |
T646A |
possibly damaging |
Het |
Esrra |
A |
C |
19: 6,889,823 (GRCm39) |
D160E |
probably benign |
Het |
Fbn2 |
T |
C |
18: 58,143,452 (GRCm39) |
T2868A |
probably benign |
Het |
Galnt7 |
T |
A |
8: 58,105,892 (GRCm39) |
M41L |
probably benign |
Het |
Gbf1 |
T |
C |
19: 46,259,984 (GRCm39) |
|
probably benign |
Het |
Glyat |
A |
G |
19: 12,625,467 (GRCm39) |
N63S |
probably damaging |
Het |
Gm9376 |
A |
T |
14: 118,504,894 (GRCm39) |
M109L |
probably benign |
Het |
H2-M10.3 |
A |
G |
17: 36,677,612 (GRCm39) |
V222A |
probably damaging |
Het |
Ifna12 |
T |
G |
4: 88,521,193 (GRCm39) |
D118A |
possibly damaging |
Het |
Inpp5j |
T |
C |
11: 3,451,147 (GRCm39) |
M501V |
probably benign |
Het |
Itpr3 |
C |
T |
17: 27,336,128 (GRCm39) |
|
probably benign |
Het |
Ivns1abp |
A |
G |
1: 151,237,291 (GRCm39) |
N527S |
probably benign |
Het |
Kif13a |
T |
C |
13: 47,083,088 (GRCm39) |
T4A |
possibly damaging |
Het |
Kif3b |
T |
C |
2: 153,172,073 (GRCm39) |
*748Q |
probably null |
Het |
Klf8 |
C |
T |
X: 152,167,677 (GRCm39) |
Q241* |
probably null |
Het |
Kras |
A |
T |
6: 145,170,787 (GRCm39) |
|
probably benign |
Het |
Lamc3 |
C |
A |
2: 31,777,423 (GRCm39) |
T23K |
probably benign |
Het |
Lrrc74b |
T |
A |
16: 17,377,737 (GRCm39) |
H47L |
probably benign |
Het |
Ly75 |
A |
G |
2: 60,199,101 (GRCm39) |
|
probably null |
Het |
Map3k21 |
G |
A |
8: 126,668,876 (GRCm39) |
G821S |
probably benign |
Het |
Mettl14 |
A |
G |
3: 123,167,722 (GRCm39) |
|
probably benign |
Het |
Mettl5 |
T |
C |
2: 69,715,590 (GRCm39) |
|
probably benign |
Het |
Mier3 |
A |
G |
13: 111,848,289 (GRCm39) |
D301G |
probably damaging |
Het |
Mipep |
T |
C |
14: 61,025,595 (GRCm39) |
|
probably benign |
Het |
Mmp21 |
T |
C |
7: 133,277,588 (GRCm39) |
|
probably null |
Het |
Msh4 |
A |
G |
3: 153,563,207 (GRCm39) |
L723P |
probably damaging |
Het |
Muc5b |
T |
C |
7: 141,412,817 (GRCm39) |
V1921A |
unknown |
Het |
Myo1e |
G |
A |
9: 70,246,038 (GRCm39) |
E410K |
possibly damaging |
Het |
Nav2 |
T |
G |
7: 49,185,710 (GRCm39) |
I951S |
probably damaging |
Het |
Npc1 |
G |
A |
18: 12,324,887 (GRCm39) |
T1202I |
probably damaging |
Het |
Or10j3 |
A |
G |
1: 173,030,934 (GRCm39) |
K4E |
probably benign |
Het |
Or2ab1 |
A |
G |
11: 58,488,947 (GRCm39) |
R242G |
probably damaging |
Het |
Or5a3 |
C |
T |
19: 12,400,252 (GRCm39) |
T193I |
probably benign |
Het |
Pacc1 |
T |
C |
1: 191,060,486 (GRCm39) |
|
probably benign |
Het |
Patl2 |
C |
T |
2: 121,954,216 (GRCm39) |
V452M |
probably benign |
Het |
Pcdh18 |
A |
G |
3: 49,709,854 (GRCm39) |
V487A |
probably damaging |
Het |
Pdzph1 |
C |
T |
17: 59,239,440 (GRCm39) |
A963T |
probably damaging |
Het |
Pkd1l1 |
C |
T |
11: 8,866,302 (GRCm39) |
V518M |
probably damaging |
Het |
Plcd3 |
A |
G |
11: 102,969,199 (GRCm39) |
F256S |
probably damaging |
Het |
Proc |
T |
C |
18: 32,266,491 (GRCm39) |
D112G |
possibly damaging |
Het |
Ptges2 |
T |
A |
2: 32,290,874 (GRCm39) |
|
probably null |
Het |
Pth2r |
A |
T |
1: 65,402,436 (GRCm39) |
R312W |
probably damaging |
Het |
Pttg1ip2 |
C |
A |
5: 5,502,073 (GRCm39) |
|
probably benign |
Het |
Rbbp6 |
C |
T |
7: 122,591,676 (GRCm39) |
H546Y |
possibly damaging |
Het |
Retreg2 |
A |
G |
1: 75,123,164 (GRCm39) |
E364G |
probably damaging |
Het |
Rxrb |
G |
A |
17: 34,253,134 (GRCm39) |
C185Y |
probably damaging |
Het |
Septin2 |
T |
A |
1: 93,427,037 (GRCm39) |
N133K |
possibly damaging |
Het |
Serpina3b |
T |
A |
12: 104,104,969 (GRCm39) |
S382T |
probably benign |
Het |
Serpinb9e |
T |
C |
13: 33,439,099 (GRCm39) |
F175S |
probably benign |
Het |
Slc19a2 |
C |
T |
1: 164,084,766 (GRCm39) |
H219Y |
probably damaging |
Het |
Slfn9 |
A |
T |
11: 82,872,524 (GRCm39) |
D737E |
possibly damaging |
Het |
Snx31 |
T |
C |
15: 36,539,444 (GRCm39) |
E144G |
probably null |
Het |
Sp2 |
A |
G |
11: 96,854,282 (GRCm39) |
|
probably benign |
Het |
Spag9 |
C |
T |
11: 94,007,663 (GRCm39) |
L1117F |
probably damaging |
Het |
Spata31e2 |
G |
T |
1: 26,721,222 (GRCm39) |
Y1319* |
probably null |
Het |
Syndig1l |
A |
T |
12: 84,727,137 (GRCm39) |
|
probably benign |
Het |
Sypl1 |
A |
T |
12: 33,024,332 (GRCm39) |
|
probably benign |
Het |
Tmem169 |
T |
C |
1: 72,339,855 (GRCm39) |
M95T |
probably benign |
Het |
Tnfrsf17 |
A |
G |
16: 11,133,066 (GRCm39) |
Y48C |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,657,859 (GRCm39) |
|
probably benign |
Het |
Uap1 |
G |
C |
1: 169,977,952 (GRCm39) |
H366Q |
probably benign |
Het |
Ulbp1 |
A |
G |
10: 7,396,557 (GRCm39) |
|
probably benign |
Het |
Urb2 |
T |
C |
8: 124,757,647 (GRCm39) |
V1118A |
probably benign |
Het |
Usp54 |
T |
C |
14: 20,600,258 (GRCm39) |
N1493S |
probably benign |
Het |
Vmn1r129 |
C |
A |
7: 21,094,655 (GRCm39) |
V188F |
probably benign |
Het |
Vmn1r226 |
A |
T |
17: 20,907,994 (GRCm39) |
L75F |
probably benign |
Het |
Yes1 |
T |
A |
5: 32,809,046 (GRCm39) |
S137R |
probably benign |
Het |
Zfp804b |
A |
G |
5: 7,229,372 (GRCm39) |
|
probably benign |
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 |
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 |
|