Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam33 |
A |
T |
2: 130,894,840 (GRCm39) |
L687Q |
probably damaging |
Het |
Adap1 |
A |
G |
5: 139,293,489 (GRCm39) |
|
probably benign |
Het |
Add2 |
T |
A |
6: 86,075,610 (GRCm39) |
V253E |
probably damaging |
Het |
Agtr1a |
A |
T |
13: 30,565,732 (GRCm39) |
I266F |
probably damaging |
Het |
Anxa9 |
A |
G |
3: 95,215,406 (GRCm39) |
|
probably benign |
Het |
Arap2 |
G |
A |
5: 62,840,827 (GRCm39) |
L680F |
probably damaging |
Het |
Bnip3 |
A |
G |
7: 138,500,401 (GRCm39) |
|
probably benign |
Het |
Brwd1 |
A |
C |
16: 95,860,852 (GRCm39) |
S311R |
probably damaging |
Het |
C2cd3 |
G |
A |
7: 100,067,729 (GRCm39) |
V871M |
possibly damaging |
Het |
Cacul1 |
A |
G |
19: 60,552,691 (GRCm39) |
W145R |
probably damaging |
Het |
Celf5 |
C |
A |
10: 81,305,346 (GRCm39) |
V141L |
probably damaging |
Het |
Cfap206 |
C |
A |
4: 34,714,519 (GRCm39) |
L392F |
possibly damaging |
Het |
Chd2 |
G |
T |
7: 73,105,267 (GRCm39) |
T192K |
probably damaging |
Het |
Chrna10 |
T |
C |
7: 101,764,264 (GRCm39) |
N40S |
possibly damaging |
Het |
Cic |
T |
A |
7: 24,986,565 (GRCm39) |
S1299T |
probably damaging |
Het |
Cic |
C |
A |
7: 24,986,566 (GRCm39) |
S1299Y |
probably damaging |
Het |
Clspn |
T |
A |
4: 126,458,722 (GRCm39) |
|
probably benign |
Het |
Clstn1 |
G |
A |
4: 149,719,253 (GRCm39) |
V361M |
probably damaging |
Het |
Col5a3 |
A |
T |
9: 20,688,404 (GRCm39) |
|
probably benign |
Het |
Copb1 |
T |
A |
7: 113,836,643 (GRCm39) |
K366N |
probably damaging |
Het |
Cul9 |
G |
A |
17: 46,849,436 (GRCm39) |
R570C |
probably benign |
Het |
Cyp2c70 |
A |
T |
19: 40,175,687 (GRCm39) |
L7Q |
probably null |
Het |
Dpysl4 |
T |
G |
7: 138,677,799 (GRCm39) |
I412S |
probably benign |
Het |
Eaf2 |
T |
A |
16: 36,628,536 (GRCm39) |
|
probably benign |
Het |
Fasl |
T |
C |
1: 161,615,733 (GRCm39) |
D41G |
probably benign |
Het |
Fat2 |
A |
G |
11: 55,153,697 (GRCm39) |
V3505A |
probably benign |
Het |
Fbxo24 |
A |
G |
5: 137,620,256 (GRCm39) |
F101S |
probably damaging |
Het |
Fdft1 |
T |
C |
14: 63,415,147 (GRCm39) |
I28M |
probably benign |
Het |
Gcnt3 |
T |
C |
9: 69,941,367 (GRCm39) |
I400M |
probably benign |
Het |
Get3 |
T |
C |
8: 85,751,725 (GRCm39) |
|
probably benign |
Het |
Gpd2 |
T |
A |
2: 57,228,880 (GRCm39) |
M228K |
probably damaging |
Het |
Gsap |
T |
A |
5: 21,431,227 (GRCm39) |
|
probably benign |
Het |
Hipk1 |
A |
G |
3: 103,670,996 (GRCm39) |
M467T |
probably damaging |
Het |
Hmgb4 |
T |
A |
4: 128,154,518 (GRCm39) |
I17F |
probably damaging |
Het |
Ints10 |
C |
A |
8: 69,260,127 (GRCm39) |
L284M |
probably benign |
Het |
Kif17 |
T |
G |
4: 138,021,059 (GRCm39) |
S606A |
probably damaging |
Het |
Lifr |
C |
A |
15: 7,205,089 (GRCm39) |
T442K |
possibly damaging |
Het |
Lypd4 |
A |
G |
7: 24,564,757 (GRCm39) |
L127P |
probably damaging |
Het |
Lyst |
A |
G |
13: 13,862,279 (GRCm39) |
H2605R |
probably benign |
Het |
Map3k4 |
A |
G |
17: 12,457,076 (GRCm39) |
S1289P |
probably damaging |
Het |
Mgam |
T |
A |
6: 40,742,190 (GRCm39) |
|
probably null |
Het |
Mob1b |
G |
A |
5: 88,903,943 (GRCm39) |
|
probably benign |
Het |
Mrgpra1 |
A |
G |
7: 46,985,218 (GRCm39) |
S154P |
probably damaging |
Het |
Ms4a4c |
C |
A |
19: 11,396,344 (GRCm39) |
|
probably benign |
Het |
Mthfd2l |
A |
T |
5: 91,109,242 (GRCm39) |
H224L |
probably damaging |
Het |
Myh8 |
T |
C |
11: 67,190,847 (GRCm39) |
Y1350H |
probably benign |
Het |
Nectin2 |
T |
C |
7: 19,464,669 (GRCm39) |
|
probably benign |
Het |
Nos1 |
A |
C |
5: 118,031,967 (GRCm39) |
N305T |
probably damaging |
Het |
Ogfrl1 |
T |
A |
1: 23,409,206 (GRCm39) |
Q340L |
possibly damaging |
Het |
Or2aj5 |
T |
C |
16: 19,425,190 (GRCm39) |
N76S |
probably benign |
Het |
Or4f62 |
A |
T |
2: 111,987,171 (GRCm39) |
N292Y |
possibly damaging |
Het |
Or6k14 |
T |
G |
1: 173,927,773 (GRCm39) |
F250V |
probably damaging |
Het |
Or9i1 |
C |
A |
19: 13,839,187 (GRCm39) |
T10K |
probably damaging |
Het |
Orc1 |
T |
C |
4: 108,452,843 (GRCm39) |
|
probably null |
Het |
Plekhg5 |
C |
A |
4: 152,189,207 (GRCm39) |
D249E |
probably benign |
Het |
Plet1 |
A |
G |
9: 50,410,430 (GRCm39) |
I74V |
probably benign |
Het |
Psmd2 |
T |
A |
16: 20,480,434 (GRCm39) |
D718E |
probably damaging |
Het |
Rab33b |
G |
T |
3: 51,391,737 (GRCm39) |
|
probably benign |
Het |
Rae1 |
T |
A |
2: 172,844,466 (GRCm39) |
F4I |
unknown |
Het |
Ralgapa2 |
A |
G |
2: 146,254,672 (GRCm39) |
Y821H |
probably benign |
Het |
Scd2 |
G |
A |
19: 44,289,685 (GRCm39) |
V227I |
probably benign |
Het |
Sharpin |
G |
T |
15: 76,232,543 (GRCm39) |
P156T |
possibly damaging |
Het |
Slc38a4 |
C |
T |
15: 96,897,510 (GRCm39) |
R435H |
probably damaging |
Het |
Snrnp200 |
T |
C |
2: 127,070,469 (GRCm39) |
V1061A |
probably benign |
Het |
Suclg1 |
A |
G |
6: 73,247,980 (GRCm39) |
T234A |
possibly damaging |
Het |
Swsap1 |
T |
C |
9: 21,868,318 (GRCm39) |
C197R |
probably benign |
Het |
Tbx15 |
A |
G |
3: 99,259,412 (GRCm39) |
T428A |
probably benign |
Het |
Tet2 |
T |
C |
3: 133,182,319 (GRCm39) |
Y1215C |
probably damaging |
Het |
Tjp1 |
A |
G |
7: 64,979,523 (GRCm39) |
|
probably benign |
Het |
Tmem209 |
G |
T |
6: 30,502,112 (GRCm39) |
|
probably benign |
Het |
Tnpo3 |
T |
C |
6: 29,589,176 (GRCm39) |
E58G |
probably damaging |
Het |
Trp53bp2 |
T |
A |
1: 182,272,283 (GRCm39) |
M464K |
probably damaging |
Het |
Ttc32 |
A |
G |
12: 9,085,897 (GRCm39) |
Y148C |
possibly damaging |
Het |
Unc80 |
T |
C |
1: 66,546,550 (GRCm39) |
S541P |
probably damaging |
Het |
Ushbp1 |
T |
C |
8: 71,847,684 (GRCm39) |
|
probably benign |
Het |
Vmn2r100 |
A |
G |
17: 19,725,136 (GRCm39) |
M22V |
probably benign |
Het |
Vmn2r100 |
A |
T |
17: 19,746,296 (GRCm39) |
E485V |
probably damaging |
Het |
Wdr24 |
G |
A |
17: 26,046,087 (GRCm39) |
V471I |
probably benign |
Het |
Zfp35 |
T |
A |
18: 24,136,001 (GRCm39) |
M115K |
probably benign |
Het |
Zfp429 |
G |
A |
13: 67,538,796 (GRCm39) |
S216L |
probably benign |
Het |
Zfp644 |
T |
G |
5: 106,782,909 (GRCm39) |
E1155A |
probably benign |
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 |
|
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 |
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 |
|