Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930523C07Rik |
T |
A |
1: 159,903,003 (GRCm39) |
M91K |
probably benign |
Het |
Abr |
T |
C |
11: 76,346,474 (GRCm39) |
R437G |
probably damaging |
Het |
Acaca |
T |
G |
11: 84,167,362 (GRCm39) |
D1045E |
probably benign |
Het |
Adam23 |
A |
T |
1: 63,573,521 (GRCm39) |
|
probably null |
Het |
Adam34 |
A |
G |
8: 44,105,538 (GRCm39) |
Y36H |
probably benign |
Het |
Alg11 |
G |
A |
8: 22,555,309 (GRCm39) |
G108D |
probably damaging |
Het |
Alox12e |
A |
T |
11: 70,210,771 (GRCm39) |
I316N |
probably damaging |
Het |
Arid1a |
A |
T |
4: 133,408,677 (GRCm39) |
F1943L |
unknown |
Het |
Armh4 |
T |
C |
14: 49,989,028 (GRCm39) |
D647G |
probably benign |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
BC035044 |
T |
C |
6: 128,867,867 (GRCm39) |
|
probably benign |
Het |
Bcor |
G |
A |
X: 11,923,862 (GRCm39) |
A578V |
possibly damaging |
Het |
C1qtnf12 |
A |
G |
4: 156,050,922 (GRCm39) |
N297S |
probably benign |
Het |
Cadps2 |
G |
T |
6: 23,838,998 (GRCm39) |
|
probably benign |
Het |
Ccnf |
A |
T |
17: 24,449,288 (GRCm39) |
|
probably null |
Het |
Cdadc1 |
A |
G |
14: 59,835,202 (GRCm39) |
|
probably null |
Het |
Cep57l1 |
A |
G |
10: 41,616,895 (GRCm39) |
Y131H |
probably damaging |
Het |
Cfap251 |
T |
C |
5: 123,394,254 (GRCm39) |
V381A |
probably benign |
Het |
Cfap44 |
A |
G |
16: 44,272,047 (GRCm39) |
R1267G |
probably benign |
Het |
Chd3 |
A |
T |
11: 69,239,854 (GRCm39) |
L1658Q |
probably benign |
Het |
Chl1 |
T |
C |
6: 103,692,362 (GRCm39) |
|
probably null |
Het |
Chpf2 |
T |
A |
5: 24,797,033 (GRCm39) |
F660I |
probably damaging |
Het |
Cmas |
T |
A |
6: 142,717,015 (GRCm39) |
D302E |
probably benign |
Het |
Cpne3 |
T |
A |
4: 19,536,562 (GRCm39) |
M233L |
probably benign |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
Dennd3 |
T |
G |
15: 73,395,336 (GRCm39) |
L143R |
probably damaging |
Het |
Dnah2 |
T |
C |
11: 69,406,587 (GRCm39) |
M552V |
probably benign |
Het |
Ergic1 |
A |
G |
17: 26,855,024 (GRCm39) |
|
probably null |
Het |
Fbxl15 |
A |
T |
19: 46,317,627 (GRCm39) |
D103V |
probably damaging |
Het |
Gm4781 |
C |
A |
10: 100,232,414 (GRCm39) |
|
noncoding transcript |
Het |
Hpca |
A |
G |
4: 129,012,278 (GRCm39) |
I86T |
possibly damaging |
Het |
Katnip |
T |
A |
7: 125,464,492 (GRCm39) |
H1286Q |
probably damaging |
Het |
Lamb3 |
T |
C |
1: 193,010,212 (GRCm39) |
V275A |
probably benign |
Het |
Lipe |
G |
T |
7: 25,087,946 (GRCm39) |
A38E |
probably benign |
Het |
Lrrk1 |
A |
T |
7: 65,935,159 (GRCm39) |
|
probably null |
Het |
Lrsam1 |
T |
C |
2: 32,835,891 (GRCm39) |
K292R |
probably damaging |
Het |
Mbtps1 |
A |
T |
8: 120,265,598 (GRCm39) |
H316Q |
probably benign |
Het |
Mms22l |
T |
A |
4: 24,580,063 (GRCm39) |
Y525* |
probably null |
Het |
Mrps14 |
T |
C |
1: 160,022,862 (GRCm39) |
L9P |
possibly damaging |
Het |
Mycbp2 |
G |
A |
14: 103,393,358 (GRCm39) |
H3068Y |
probably damaging |
Het |
Myo15a |
A |
G |
11: 60,401,055 (GRCm39) |
D2992G |
possibly damaging |
Het |
N4bp2 |
T |
A |
5: 65,966,543 (GRCm39) |
L1327Q |
probably damaging |
Het |
Nradd |
A |
T |
9: 110,451,243 (GRCm39) |
F42I |
probably benign |
Het |
Or5k8 |
T |
A |
16: 58,644,842 (GRCm39) |
I77F |
probably damaging |
Het |
Pank1 |
T |
C |
19: 34,804,754 (GRCm39) |
H134R |
probably benign |
Het |
Pcdh7 |
T |
A |
5: 58,286,458 (GRCm39) |
M1178K |
possibly damaging |
Het |
Pcnx3 |
A |
T |
19: 5,717,633 (GRCm39) |
I1084N |
probably damaging |
Het |
Pdcd11 |
A |
G |
19: 47,093,191 (GRCm39) |
M490V |
probably benign |
Het |
Phf2 |
T |
C |
13: 48,958,165 (GRCm39) |
K950E |
unknown |
Het |
Pitpnc1 |
C |
T |
11: 107,103,344 (GRCm39) |
A252T |
probably damaging |
Het |
Prickle2 |
A |
G |
6: 92,402,652 (GRCm39) |
L112P |
probably damaging |
Het |
Prpf8 |
A |
G |
11: 75,381,357 (GRCm39) |
I231V |
probably benign |
Het |
Scin |
T |
A |
12: 40,130,984 (GRCm39) |
M310L |
probably benign |
Het |
Serpina3m |
T |
A |
12: 104,355,483 (GRCm39) |
I50N |
probably benign |
Het |
Skint8 |
C |
G |
4: 111,794,274 (GRCm39) |
N221K |
probably damaging |
Het |
Slc22a23 |
C |
T |
13: 34,366,990 (GRCm39) |
V673M |
probably benign |
Het |
Slc24a5 |
A |
G |
2: 124,929,361 (GRCm39) |
D368G |
probably damaging |
Het |
Slc28a1 |
A |
T |
7: 80,776,015 (GRCm39) |
Q237L |
possibly damaging |
Het |
Smchd1 |
T |
A |
17: 71,705,583 (GRCm39) |
K1005N |
possibly damaging |
Het |
Stim2 |
T |
C |
5: 54,262,717 (GRCm39) |
Y320H |
probably damaging |
Het |
Syne3 |
T |
A |
12: 104,919,357 (GRCm39) |
D512V |
probably damaging |
Het |
Tada2a |
T |
C |
11: 83,970,455 (GRCm39) |
D432G |
probably damaging |
Het |
Tcp10a |
T |
C |
17: 7,601,701 (GRCm39) |
S216P |
probably damaging |
Het |
Tmem178b |
A |
T |
6: 40,184,435 (GRCm39) |
Q111L |
probably damaging |
Het |
Tmem236 |
A |
G |
2: 14,223,861 (GRCm39) |
I217V |
probably benign |
Het |
Tmem45b |
A |
G |
9: 31,340,277 (GRCm39) |
V128A |
probably benign |
Het |
Tnfaip2 |
T |
C |
12: 111,412,456 (GRCm39) |
Y286H |
probably damaging |
Het |
Tsc2 |
T |
A |
17: 24,840,116 (GRCm39) |
I427L |
possibly damaging |
Het |
Ttc17 |
T |
A |
2: 94,132,139 (GRCm39) |
N1180I |
possibly damaging |
Het |
Ubr1 |
T |
G |
2: 120,694,811 (GRCm39) |
D1707A |
probably damaging |
Het |
Vmn1r11 |
A |
G |
6: 57,114,583 (GRCm39) |
I82M |
probably benign |
Het |
Vmn2r129 |
T |
C |
4: 156,687,014 (GRCm39) |
|
noncoding transcript |
Het |
Vps41 |
G |
T |
13: 19,023,904 (GRCm39) |
|
probably null |
Het |
Wnt5a |
A |
G |
14: 28,235,274 (GRCm39) |
Y86C |
probably damaging |
Het |
Zfp629 |
T |
C |
7: 127,209,616 (GRCm39) |
H731R |
probably damaging |
Het |
Zfp712 |
T |
C |
13: 67,189,960 (GRCm39) |
E189G |
possibly damaging |
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 |
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 |
R6997:Dock2
|
UTSW |
11 |
34,414,922 (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 |
|