Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam3 |
T |
C |
8: 25,171,539 (GRCm39) |
Y764C |
probably benign |
Het |
Atxn1 |
C |
T |
13: 45,721,095 (GRCm39) |
V267M |
probably benign |
Het |
Cadps |
T |
A |
14: 12,505,793 (GRCm38) |
H759L |
possibly damaging |
Het |
Calcoco2 |
GGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC |
GGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC |
11: 95,990,808 (GRCm39) |
|
probably benign |
Het |
Caprin2 |
A |
G |
6: 148,779,474 (GRCm39) |
L111P |
probably damaging |
Het |
Ccl8 |
A |
T |
11: 82,006,865 (GRCm39) |
D26V |
possibly damaging |
Het |
Cdh19 |
T |
C |
1: 110,882,596 (GRCm39) |
|
probably benign |
Het |
Cnga3 |
C |
A |
1: 37,283,965 (GRCm39) |
H89Q |
probably benign |
Het |
Cnga4 |
A |
T |
7: 105,056,190 (GRCm39) |
Q264L |
probably damaging |
Het |
Coil |
A |
G |
11: 88,872,673 (GRCm39) |
T345A |
probably benign |
Het |
Cyp11b2 |
A |
G |
15: 74,723,281 (GRCm39) |
L461P |
probably damaging |
Het |
Dsc1 |
C |
T |
18: 20,219,701 (GRCm39) |
|
probably null |
Het |
Dync2h1 |
A |
T |
9: 7,168,743 (GRCm39) |
C357S |
probably null |
Het |
Ebf3 |
A |
C |
7: 136,826,994 (GRCm39) |
I306R |
probably damaging |
Het |
Eprs1 |
A |
G |
1: 185,128,360 (GRCm39) |
H580R |
possibly damaging |
Het |
Ermap |
A |
T |
4: 119,035,810 (GRCm39) |
F393I |
probably damaging |
Het |
Flii |
T |
C |
11: 60,613,151 (GRCm39) |
T217A |
probably benign |
Het |
Fras1 |
C |
T |
5: 96,762,732 (GRCm39) |
Q745* |
probably null |
Het |
Gja8 |
A |
G |
3: 96,826,657 (GRCm39) |
V335A |
probably benign |
Het |
Gm21560 |
A |
T |
14: 6,218,333 (GRCm38) |
N48K |
probably damaging |
Het |
Gpr158 |
C |
T |
2: 21,653,802 (GRCm39) |
T457I |
possibly damaging |
Het |
Kcnv1 |
A |
T |
15: 44,977,997 (GRCm39) |
S14T |
unknown |
Het |
Lamb2 |
T |
C |
9: 108,358,496 (GRCm39) |
Y178H |
probably damaging |
Het |
Lamc2 |
G |
A |
1: 153,012,508 (GRCm39) |
T722M |
probably benign |
Het |
Map1b |
T |
C |
13: 99,567,142 (GRCm39) |
T1860A |
unknown |
Het |
Map2k7 |
T |
C |
8: 4,294,035 (GRCm39) |
Y194H |
possibly damaging |
Het |
Map4 |
T |
A |
9: 109,881,982 (GRCm39) |
M282K |
probably benign |
Het |
Mmp10 |
A |
G |
9: 7,503,531 (GRCm39) |
I134V |
probably benign |
Het |
Mrtfa |
G |
T |
15: 80,902,649 (GRCm39) |
S220* |
probably null |
Het |
Msh5 |
A |
T |
17: 35,248,978 (GRCm39) |
L685Q |
probably damaging |
Het |
Myh1 |
T |
A |
11: 67,111,463 (GRCm39) |
I1634N |
possibly damaging |
Het |
Myh13 |
C |
T |
11: 67,217,980 (GRCm39) |
R18* |
probably null |
Het |
Myo3b |
A |
T |
2: 69,957,329 (GRCm39) |
I185L |
probably damaging |
Het |
Ninl |
G |
T |
2: 150,808,145 (GRCm39) |
H294Q |
probably benign |
Het |
Or4a79 |
G |
A |
2: 89,552,269 (GRCm39) |
A62V |
possibly damaging |
Het |
Or51b17 |
A |
T |
7: 103,542,238 (GRCm39) |
S235T |
probably benign |
Het |
Or8b44 |
T |
C |
9: 38,410,607 (GRCm39) |
I214T |
possibly damaging |
Het |
Orm3 |
T |
A |
4: 63,275,180 (GRCm39) |
L97Q |
probably damaging |
Het |
Osbpl1a |
T |
C |
18: 12,889,281 (GRCm39) |
N432S |
probably benign |
Het |
Pikfyve |
T |
A |
1: 65,285,822 (GRCm39) |
D1020E |
probably damaging |
Het |
Pxk |
T |
A |
14: 8,122,371 (GRCm38) |
D60E |
probably benign |
Het |
Rack1 |
T |
A |
11: 48,694,752 (GRCm39) |
V198E |
probably damaging |
Het |
Ripk1 |
C |
T |
13: 34,201,100 (GRCm39) |
A271V |
probably benign |
Het |
Rsrc1 |
C |
T |
3: 66,901,982 (GRCm39) |
P44L |
unknown |
Het |
Ryr2 |
G |
T |
13: 11,669,266 (GRCm39) |
H3513N |
possibly damaging |
Het |
Scn7a |
A |
T |
2: 66,534,147 (GRCm39) |
D509E |
probably damaging |
Het |
Selplg |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
5: 113,957,756 (GRCm39) |
|
probably benign |
Het |
Sfxn5 |
A |
G |
6: 85,233,414 (GRCm39) |
V181A |
probably benign |
Het |
Slc5a4b |
C |
T |
10: 75,925,812 (GRCm39) |
A198T |
probably damaging |
Het |
Sp2 |
C |
T |
11: 96,848,552 (GRCm39) |
R357H |
possibly damaging |
Het |
Tchh |
CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC |
CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC |
3: 93,354,015 (GRCm39) |
|
probably benign |
Het |
Tnfrsf11b |
G |
A |
15: 54,115,770 (GRCm39) |
L276F |
probably damaging |
Het |
Usp37 |
A |
G |
1: 74,493,118 (GRCm39) |
V723A |
probably benign |
Het |
Usp45 |
G |
T |
4: 21,781,844 (GRCm39) |
R36I |
probably damaging |
Het |
Vcan |
T |
C |
13: 89,838,737 (GRCm39) |
D2269G |
probably damaging |
Het |
Vmn2r18 |
T |
A |
5: 151,485,338 (GRCm39) |
M719L |
possibly damaging |
Het |
Vmn2r52 |
C |
T |
7: 9,902,998 (GRCm39) |
G477R |
probably benign |
Het |
Vmn2r60 |
C |
A |
7: 41,791,716 (GRCm39) |
N546K |
probably benign |
Het |
Wnt8b |
G |
A |
19: 44,500,280 (GRCm39) |
C289Y |
probably damaging |
Het |
Zdbf2 |
T |
G |
1: 63,329,925 (GRCm39) |
M10R |
probably benign |
Het |
Zfp945 |
T |
A |
17: 23,071,543 (GRCm39) |
K140* |
probably null |
Het |
|
Other mutations in Dock2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Dock2
|
APN |
11 |
34,595,488 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00469:Dock2
|
APN |
11 |
34,179,603 (GRCm39) |
splice site |
probably benign |
|
IGL01061:Dock2
|
APN |
11 |
34,596,653 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01319:Dock2
|
APN |
11 |
34,589,617 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01451:Dock2
|
APN |
11 |
34,260,390 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01490:Dock2
|
APN |
11 |
34,596,608 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01601:Dock2
|
APN |
11 |
34,189,528 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01800:Dock2
|
APN |
11 |
34,647,100 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01804:Dock2
|
APN |
11 |
34,212,433 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01823:Dock2
|
APN |
11 |
34,212,391 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01829:Dock2
|
APN |
11 |
34,596,668 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01830:Dock2
|
APN |
11 |
34,582,744 (GRCm39) |
nonsense |
probably null |
|
IGL01835:Dock2
|
APN |
11 |
34,260,435 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01845:Dock2
|
APN |
11 |
34,599,692 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01953:Dock2
|
APN |
11 |
34,623,183 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01989:Dock2
|
APN |
11 |
34,218,053 (GRCm39) |
missense |
probably benign |
|
IGL02081:Dock2
|
APN |
11 |
34,204,355 (GRCm39) |
missense |
probably benign |
|
IGL02105:Dock2
|
APN |
11 |
34,605,352 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02153:Dock2
|
APN |
11 |
34,180,670 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02170:Dock2
|
APN |
11 |
34,217,949 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02344:Dock2
|
APN |
11 |
34,622,337 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02389:Dock2
|
APN |
11 |
34,589,567 (GRCm39) |
splice site |
probably benign |
|
IGL02409:Dock2
|
APN |
11 |
34,451,204 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02472:Dock2
|
APN |
11 |
34,199,801 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02625:Dock2
|
APN |
11 |
34,451,168 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02929:Dock2
|
APN |
11 |
34,218,048 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02951:Dock2
|
APN |
11 |
34,260,448 (GRCm39) |
unclassified |
probably benign |
|
IGL02999:Dock2
|
APN |
11 |
34,583,086 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03165:Dock2
|
APN |
11 |
34,578,360 (GRCm39) |
missense |
probably damaging |
0.99 |
Arches
|
UTSW |
11 |
34,580,587 (GRCm39) |
missense |
probably damaging |
1.00 |
capitol_reef
|
UTSW |
11 |
34,244,170 (GRCm39) |
critical splice acceptor site |
probably null |
|
Croesus
|
UTSW |
11 |
34,611,854 (GRCm39) |
missense |
probably damaging |
1.00 |
denali
|
UTSW |
11 |
34,179,472 (GRCm39) |
critical splice donor site |
probably null |
|
dew
|
UTSW |
11 |
34,198,636 (GRCm39) |
nonsense |
probably null |
|
Dinghy
|
UTSW |
11 |
34,212,460 (GRCm39) |
missense |
possibly damaging |
0.70 |
Dry
|
UTSW |
11 |
34,181,652 (GRCm39) |
missense |
possibly damaging |
0.79 |
frazz
|
UTSW |
11 |
34,198,572 (GRCm39) |
critical splice donor site |
probably benign |
|
frizz
|
UTSW |
11 |
34,208,184 (GRCm39) |
splice site |
probably benign |
|
gildenstern
|
UTSW |
11 |
34,623,166 (GRCm39) |
critical splice donor site |
probably null |
|
godsgrace
|
UTSW |
11 |
34,586,280 (GRCm39) |
missense |
probably damaging |
1.00 |
Harborside
|
UTSW |
11 |
34,212,445 (GRCm39) |
missense |
probably benign |
|
Landing
|
UTSW |
11 |
34,605,328 (GRCm39) |
missense |
possibly damaging |
0.83 |
latest
|
UTSW |
11 |
34,647,049 (GRCm39) |
missense |
probably damaging |
1.00 |
Launch
|
UTSW |
11 |
34,206,562 (GRCm39) |
missense |
probably damaging |
1.00 |
liaoning
|
UTSW |
11 |
34,599,620 (GRCm39) |
missense |
probably damaging |
1.00 |
lucre
|
UTSW |
11 |
34,595,436 (GRCm39) |
frame shift |
probably null |
|
midas
|
UTSW |
11 |
34,244,323 (GRCm39) |
missense |
probably damaging |
0.99 |
muelle
|
UTSW |
11 |
34,578,365 (GRCm39) |
missense |
probably damaging |
1.00 |
narrowest
|
UTSW |
11 |
34,232,652 (GRCm39) |
missense |
probably damaging |
0.98 |
pier
|
UTSW |
11 |
34,580,593 (GRCm39) |
missense |
probably damaging |
1.00 |
Plank
|
UTSW |
11 |
34,674,622 (GRCm39) |
missense |
possibly damaging |
0.51 |
resplendent
|
UTSW |
11 |
34,618,287 (GRCm39) |
nonsense |
probably null |
|
riches
|
UTSW |
11 |
34,579,279 (GRCm39) |
critical splice donor site |
probably null |
|
skiff
|
UTSW |
11 |
34,212,388 (GRCm39) |
missense |
probably null |
0.80 |
Slip
|
UTSW |
11 |
34,244,286 (GRCm39) |
missense |
probably benign |
0.25 |
toothskin
|
UTSW |
11 |
34,414,922 (GRCm39) |
missense |
probably damaging |
1.00 |
Touch
|
UTSW |
11 |
34,223,750 (GRCm39) |
missense |
possibly damaging |
0.95 |
wassup
|
UTSW |
11 |
34,453,413 (GRCm39) |
missense |
probably damaging |
1.00 |
Wharf
|
UTSW |
11 |
34,623,198 (GRCm39) |
missense |
possibly damaging |
0.81 |
BB009:Dock2
|
UTSW |
11 |
34,217,998 (GRCm39) |
missense |
probably benign |
0.00 |
BB019:Dock2
|
UTSW |
11 |
34,217,998 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03052:Dock2
|
UTSW |
11 |
34,182,853 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4377001:Dock2
|
UTSW |
11 |
34,611,835 (GRCm39) |
missense |
probably benign |
0.02 |
R0006:Dock2
|
UTSW |
11 |
34,262,453 (GRCm39) |
unclassified |
probably benign |
|
R0012:Dock2
|
UTSW |
11 |
34,674,622 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0063:Dock2
|
UTSW |
11 |
34,647,111 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0063:Dock2
|
UTSW |
11 |
34,647,111 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0116:Dock2
|
UTSW |
11 |
34,579,392 (GRCm39) |
intron |
probably benign |
|
R0149:Dock2
|
UTSW |
11 |
34,388,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R0361:Dock2
|
UTSW |
11 |
34,388,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R0462:Dock2
|
UTSW |
11 |
34,218,052 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0471:Dock2
|
UTSW |
11 |
34,579,380 (GRCm39) |
missense |
probably benign |
0.30 |
R0538:Dock2
|
UTSW |
11 |
34,595,545 (GRCm39) |
splice site |
probably benign |
|
R0543:Dock2
|
UTSW |
11 |
34,244,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R0660:Dock2
|
UTSW |
11 |
34,198,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R0676:Dock2
|
UTSW |
11 |
34,586,063 (GRCm39) |
missense |
probably damaging |
0.99 |
R0722:Dock2
|
UTSW |
11 |
34,414,970 (GRCm39) |
splice site |
probably benign |
|
R0801:Dock2
|
UTSW |
11 |
34,599,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1110:Dock2
|
UTSW |
11 |
34,206,535 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1171:Dock2
|
UTSW |
11 |
34,586,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R1387:Dock2
|
UTSW |
11 |
34,223,309 (GRCm39) |
splice site |
probably benign |
|
R1445:Dock2
|
UTSW |
11 |
34,189,705 (GRCm39) |
missense |
probably benign |
|
R1494:Dock2
|
UTSW |
11 |
34,232,761 (GRCm39) |
nonsense |
probably null |
|
R1589:Dock2
|
UTSW |
11 |
34,597,288 (GRCm39) |
missense |
probably damaging |
0.99 |
R1597:Dock2
|
UTSW |
11 |
34,595,474 (GRCm39) |
missense |
probably benign |
0.00 |
R1629:Dock2
|
UTSW |
11 |
34,212,480 (GRCm39) |
splice site |
probably null |
|
R1749:Dock2
|
UTSW |
11 |
34,182,767 (GRCm39) |
critical splice donor site |
probably null |
|
R1888:Dock2
|
UTSW |
11 |
34,598,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R1888:Dock2
|
UTSW |
11 |
34,598,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Dock2
|
UTSW |
11 |
34,244,286 (GRCm39) |
missense |
probably benign |
0.25 |
R1924:Dock2
|
UTSW |
11 |
34,414,934 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2031:Dock2
|
UTSW |
11 |
34,618,297 (GRCm39) |
splice site |
probably benign |
|
R2045:Dock2
|
UTSW |
11 |
34,244,106 (GRCm39) |
splice site |
probably null |
|
R2098:Dock2
|
UTSW |
11 |
34,609,832 (GRCm39) |
missense |
probably damaging |
0.99 |
R2098:Dock2
|
UTSW |
11 |
34,216,279 (GRCm39) |
missense |
probably benign |
0.16 |
R2129:Dock2
|
UTSW |
11 |
34,618,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R2147:Dock2
|
UTSW |
11 |
34,179,472 (GRCm39) |
critical splice donor site |
probably null |
|
R2149:Dock2
|
UTSW |
11 |
34,179,472 (GRCm39) |
critical splice donor site |
probably null |
|
R2150:Dock2
|
UTSW |
11 |
34,179,472 (GRCm39) |
critical splice donor site |
probably null |
|
R2176:Dock2
|
UTSW |
11 |
34,586,044 (GRCm39) |
missense |
probably benign |
0.00 |
R2230:Dock2
|
UTSW |
11 |
34,244,323 (GRCm39) |
missense |
probably damaging |
0.99 |
R2508:Dock2
|
UTSW |
11 |
34,262,485 (GRCm39) |
missense |
probably benign |
0.04 |
R2875:Dock2
|
UTSW |
11 |
34,609,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R2885:Dock2
|
UTSW |
11 |
34,580,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R2910:Dock2
|
UTSW |
11 |
34,182,910 (GRCm39) |
splice site |
probably benign |
|
R3081:Dock2
|
UTSW |
11 |
34,181,610 (GRCm39) |
missense |
probably benign |
|
R3418:Dock2
|
UTSW |
11 |
34,580,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R3552:Dock2
|
UTSW |
11 |
34,611,787 (GRCm39) |
missense |
probably benign |
0.22 |
R3731:Dock2
|
UTSW |
11 |
34,599,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R3846:Dock2
|
UTSW |
11 |
34,623,198 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4135:Dock2
|
UTSW |
11 |
34,605,328 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4598:Dock2
|
UTSW |
11 |
34,189,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R4599:Dock2
|
UTSW |
11 |
34,189,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R4715:Dock2
|
UTSW |
11 |
34,244,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R4722:Dock2
|
UTSW |
11 |
34,586,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R4742:Dock2
|
UTSW |
11 |
34,244,170 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4830:Dock2
|
UTSW |
11 |
34,223,767 (GRCm39) |
splice site |
probably null |
|
R4884:Dock2
|
UTSW |
11 |
34,216,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4990:Dock2
|
UTSW |
11 |
34,586,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R5334:Dock2
|
UTSW |
11 |
34,178,643 (GRCm39) |
missense |
probably benign |
0.00 |
R5570:Dock2
|
UTSW |
11 |
34,618,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R5602:Dock2
|
UTSW |
11 |
34,204,391 (GRCm39) |
missense |
probably benign |
0.16 |
R5681:Dock2
|
UTSW |
11 |
34,199,836 (GRCm39) |
missense |
probably benign |
0.06 |
R5809:Dock2
|
UTSW |
11 |
34,212,445 (GRCm39) |
missense |
probably benign |
|
R5860:Dock2
|
UTSW |
11 |
34,206,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R6111:Dock2
|
UTSW |
11 |
34,599,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R6155:Dock2
|
UTSW |
11 |
34,244,123 (GRCm39) |
missense |
probably benign |
0.06 |
R6156:Dock2
|
UTSW |
11 |
34,197,789 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6173:Dock2
|
UTSW |
11 |
34,212,388 (GRCm39) |
missense |
probably null |
0.80 |
R6182:Dock2
|
UTSW |
11 |
34,179,476 (GRCm39) |
missense |
probably damaging |
0.97 |
R6188:Dock2
|
UTSW |
11 |
34,453,396 (GRCm39) |
missense |
probably damaging |
0.98 |
R6191:Dock2
|
UTSW |
11 |
34,181,652 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6283:Dock2
|
UTSW |
11 |
34,598,152 (GRCm39) |
missense |
probably damaging |
0.99 |
R6395:Dock2
|
UTSW |
11 |
34,182,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R6465:Dock2
|
UTSW |
11 |
34,453,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R6500:Dock2
|
UTSW |
11 |
34,312,822 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6561:Dock2
|
UTSW |
11 |
34,578,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R6745:Dock2
|
UTSW |
11 |
34,596,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R6745:Dock2
|
UTSW |
11 |
34,596,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R6880:Dock2
|
UTSW |
11 |
34,579,279 (GRCm39) |
critical splice donor site |
probably null |
|
R6913:Dock2
|
UTSW |
11 |
34,647,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R7057:Dock2
|
UTSW |
11 |
34,586,044 (GRCm39) |
missense |
probably benign |
0.00 |
R7057:Dock2
|
UTSW |
11 |
34,177,684 (GRCm39) |
missense |
probably benign |
0.10 |
R7134:Dock2
|
UTSW |
11 |
34,260,363 (GRCm39) |
missense |
probably benign |
0.03 |
R7188:Dock2
|
UTSW |
11 |
34,189,675 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7239:Dock2
|
UTSW |
11 |
34,181,677 (GRCm39) |
missense |
probably benign |
0.00 |
R7247:Dock2
|
UTSW |
11 |
34,605,340 (GRCm39) |
nonsense |
probably null |
|
R7250:Dock2
|
UTSW |
11 |
34,586,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:Dock2
|
UTSW |
11 |
34,586,032 (GRCm39) |
missense |
probably benign |
0.01 |
R7271:Dock2
|
UTSW |
11 |
34,223,750 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7284:Dock2
|
UTSW |
11 |
34,180,672 (GRCm39) |
missense |
probably benign |
0.01 |
R7397:Dock2
|
UTSW |
11 |
34,609,816 (GRCm39) |
missense |
probably benign |
0.00 |
R7464:Dock2
|
UTSW |
11 |
34,586,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R7512:Dock2
|
UTSW |
11 |
34,262,542 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7556:Dock2
|
UTSW |
11 |
34,611,778 (GRCm39) |
missense |
probably benign |
0.43 |
R7663:Dock2
|
UTSW |
11 |
34,611,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R7779:Dock2
|
UTSW |
11 |
34,605,282 (GRCm39) |
missense |
probably benign |
0.38 |
R7797:Dock2
|
UTSW |
11 |
34,232,652 (GRCm39) |
missense |
probably damaging |
0.98 |
R7855:Dock2
|
UTSW |
11 |
34,223,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R7922:Dock2
|
UTSW |
11 |
34,598,154 (GRCm39) |
missense |
probably benign |
0.29 |
R7932:Dock2
|
UTSW |
11 |
34,217,998 (GRCm39) |
missense |
probably benign |
0.00 |
R8013:Dock2
|
UTSW |
11 |
34,596,677 (GRCm39) |
missense |
probably damaging |
0.96 |
R8192:Dock2
|
UTSW |
11 |
34,623,166 (GRCm39) |
critical splice donor site |
probably null |
|
R8244:Dock2
|
UTSW |
11 |
34,586,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R8307:Dock2
|
UTSW |
11 |
34,260,362 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8418:Dock2
|
UTSW |
11 |
34,609,795 (GRCm39) |
missense |
probably benign |
0.01 |
R8460:Dock2
|
UTSW |
11 |
34,180,825 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8495:Dock2
|
UTSW |
11 |
34,181,622 (GRCm39) |
missense |
probably benign |
0.14 |
R8556:Dock2
|
UTSW |
11 |
34,212,457 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8690:Dock2
|
UTSW |
11 |
34,618,287 (GRCm39) |
nonsense |
probably null |
|
R8743:Dock2
|
UTSW |
11 |
34,223,252 (GRCm39) |
nonsense |
probably null |
|
R8757:Dock2
|
UTSW |
11 |
34,586,067 (GRCm39) |
missense |
probably benign |
0.13 |
R8759:Dock2
|
UTSW |
11 |
34,586,067 (GRCm39) |
missense |
probably benign |
0.13 |
R8793:Dock2
|
UTSW |
11 |
34,451,215 (GRCm39) |
missense |
probably benign |
0.00 |
R8882:Dock2
|
UTSW |
11 |
34,595,436 (GRCm39) |
frame shift |
probably null |
|
R8885:Dock2
|
UTSW |
11 |
34,260,396 (GRCm39) |
missense |
probably benign |
0.01 |
R8943:Dock2
|
UTSW |
11 |
34,599,646 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9171:Dock2
|
UTSW |
11 |
34,589,670 (GRCm39) |
missense |
probably benign |
0.12 |
R9182:Dock2
|
UTSW |
11 |
34,260,398 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9203:Dock2
|
UTSW |
11 |
34,622,366 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9310:Dock2
|
UTSW |
11 |
34,244,139 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9388:Dock2
|
UTSW |
11 |
34,212,460 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9490:Dock2
|
UTSW |
11 |
34,589,582 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9568:Dock2
|
UTSW |
11 |
34,599,638 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9593:Dock2
|
UTSW |
11 |
34,178,607 (GRCm39) |
missense |
probably benign |
0.34 |
R9694:Dock2
|
UTSW |
11 |
34,218,054 (GRCm39) |
missense |
probably benign |
|
R9697:Dock2
|
UTSW |
11 |
34,204,417 (GRCm39) |
missense |
probably benign |
|
R9753:Dock2
|
UTSW |
11 |
34,223,673 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9783:Dock2
|
UTSW |
11 |
34,208,128 (GRCm39) |
missense |
possibly damaging |
0.83 |
X0017:Dock2
|
UTSW |
11 |
34,216,271 (GRCm39) |
missense |
probably benign |
0.08 |
X0018:Dock2
|
UTSW |
11 |
34,182,833 (GRCm39) |
missense |
possibly damaging |
0.65 |
X0058:Dock2
|
UTSW |
11 |
34,206,564 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Dock2
|
UTSW |
11 |
34,260,357 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1088:Dock2
|
UTSW |
11 |
34,583,209 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dock2
|
UTSW |
11 |
34,388,300 (GRCm39) |
missense |
probably benign |
0.14 |
Z1088:Dock2
|
UTSW |
11 |
34,586,039 (GRCm39) |
nonsense |
probably null |
|
Z1176:Dock2
|
UTSW |
11 |
34,609,751 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Dock2
|
UTSW |
11 |
34,262,553 (GRCm39) |
missense |
possibly damaging |
0.68 |
|