Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110059G10Rik |
T |
A |
9: 122,778,008 (GRCm39) |
I79L |
probably benign |
Het |
Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
Acaa1a |
G |
A |
9: 119,177,772 (GRCm39) |
S218N |
probably benign |
Het |
Acsm5 |
A |
T |
7: 119,137,314 (GRCm39) |
I377F |
probably damaging |
Het |
Ahnak2 |
T |
C |
12: 112,741,706 (GRCm39) |
T789A |
probably benign |
Het |
Ak9 |
A |
T |
10: 41,296,678 (GRCm39) |
T1475S |
unknown |
Het |
AU040320 |
A |
T |
4: 126,747,081 (GRCm39) |
N1028Y |
probably damaging |
Het |
Bahcc1 |
T |
A |
11: 120,178,580 (GRCm39) |
S2380T |
probably benign |
Het |
Cadps |
A |
G |
14: 12,536,386 (GRCm38) |
Y525H |
probably damaging |
Het |
Ccdc138 |
A |
G |
10: 58,380,817 (GRCm39) |
N483D |
possibly damaging |
Het |
Ccdc39 |
G |
A |
3: 33,893,242 (GRCm39) |
|
probably null |
Het |
Cd300c2 |
T |
C |
11: 114,887,772 (GRCm39) |
N210S |
probably damaging |
Het |
Cd84 |
A |
G |
1: 171,700,432 (GRCm39) |
D183G |
probably damaging |
Het |
Cep95 |
C |
T |
11: 106,702,172 (GRCm39) |
P390S |
probably damaging |
Het |
Chd9 |
A |
T |
8: 91,741,877 (GRCm39) |
H1622L |
possibly damaging |
Het |
Cilp |
C |
A |
9: 65,185,302 (GRCm39) |
Q466K |
probably benign |
Het |
Cinp |
T |
A |
12: 110,850,487 (GRCm39) |
T5S |
probably damaging |
Het |
Clec4a2 |
T |
C |
6: 123,119,462 (GRCm39) |
L238S |
probably damaging |
Het |
Cntrob |
T |
C |
11: 69,211,732 (GRCm39) |
Y164C |
probably damaging |
Het |
Col6a3 |
A |
G |
1: 90,735,246 (GRCm39) |
L1408P |
probably damaging |
Het |
Cul3 |
G |
A |
1: 80,258,632 (GRCm39) |
S468L |
possibly damaging |
Het |
Dnah11 |
T |
A |
12: 118,090,618 (GRCm39) |
D1081V |
probably benign |
Het |
Dnah2 |
C |
A |
11: 69,411,973 (GRCm39) |
V263L |
probably benign |
Het |
Efna3 |
C |
G |
3: 89,222,805 (GRCm39) |
R185P |
probably damaging |
Het |
F5 |
A |
T |
1: 164,039,389 (GRCm39) |
I2000F |
probably damaging |
Het |
Fancm |
G |
A |
12: 65,141,645 (GRCm39) |
G422E |
probably benign |
Het |
Gcnt2 |
A |
T |
13: 41,014,210 (GRCm39) |
D127V |
probably damaging |
Het |
Gm21798 |
G |
T |
15: 64,689,618 (GRCm39) |
|
probably benign |
Het |
Gramd1a |
A |
C |
7: 30,838,292 (GRCm39) |
S320R |
probably benign |
Het |
Grn |
T |
C |
11: 102,327,344 (GRCm39) |
|
probably benign |
Het |
Helq |
A |
T |
5: 100,910,507 (GRCm39) |
|
probably null |
Het |
Herc2 |
A |
G |
7: 55,827,660 (GRCm39) |
I2914V |
probably benign |
Het |
Hnrnph1 |
T |
C |
11: 50,269,237 (GRCm39) |
V27A |
probably damaging |
Het |
Hs1bp3 |
G |
T |
12: 8,374,007 (GRCm39) |
G182C |
probably damaging |
Het |
Idnk |
C |
T |
13: 58,311,267 (GRCm39) |
P78L |
probably benign |
Het |
Il10ra |
T |
C |
9: 45,166,919 (GRCm39) |
D544G |
probably benign |
Het |
Inpp5e |
T |
C |
2: 26,290,918 (GRCm39) |
D383G |
probably damaging |
Het |
Jak1 |
A |
T |
4: 101,036,911 (GRCm39) |
V243D |
probably damaging |
Het |
Kcnma1 |
A |
T |
14: 23,359,220 (GRCm39) |
S1036T |
probably damaging |
Het |
Kif26a |
G |
A |
12: 112,123,776 (GRCm39) |
C127Y |
probably damaging |
Het |
Kif2c |
T |
C |
4: 117,023,608 (GRCm39) |
E368G |
probably damaging |
Het |
Lasp1 |
T |
A |
11: 97,724,530 (GRCm39) |
|
probably null |
Het |
Lcor |
T |
A |
19: 41,572,601 (GRCm39) |
V452D |
probably benign |
Het |
Lrrtm1 |
C |
G |
6: 77,221,661 (GRCm39) |
H373D |
probably benign |
Het |
Matr3 |
T |
A |
18: 35,705,754 (GRCm39) |
D226E |
probably damaging |
Het |
Mmp17 |
G |
A |
5: 129,682,730 (GRCm39) |
W456* |
probably null |
Het |
Mpp4 |
T |
C |
1: 59,164,748 (GRCm39) |
E463G |
probably damaging |
Het |
Myh6 |
A |
C |
14: 55,194,419 (GRCm39) |
F737V |
probably damaging |
Het |
Nars2 |
T |
A |
7: 96,672,948 (GRCm39) |
D271E |
probably benign |
Het |
Nav2 |
A |
G |
7: 49,254,258 (GRCm39) |
E2352G |
probably damaging |
Het |
Nckap1 |
A |
G |
2: 80,353,718 (GRCm39) |
|
probably null |
Het |
Nckap5 |
A |
T |
1: 125,955,324 (GRCm39) |
S477R |
probably damaging |
Het |
Nek11 |
T |
G |
9: 105,175,488 (GRCm39) |
I319L |
probably benign |
Het |
Neto2 |
A |
G |
8: 86,396,393 (GRCm39) |
I84T |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,250,369 (GRCm39) |
I45F |
probably damaging |
Het |
Numa1 |
G |
A |
7: 101,662,012 (GRCm39) |
R548H |
probably damaging |
Het |
Or10a5 |
A |
C |
7: 106,635,364 (GRCm39) |
M1L |
probably benign |
Het |
Or14c39 |
A |
C |
7: 86,344,395 (GRCm39) |
I244L |
probably benign |
Het |
Or2ag1b |
A |
T |
7: 106,288,740 (GRCm39) |
L66H |
probably damaging |
Het |
Or4c10 |
A |
T |
2: 89,760,923 (GRCm39) |
M257L |
probably benign |
Het |
Or4c100 |
T |
A |
2: 88,356,254 (GRCm39) |
I109N |
probably damaging |
Het |
Or4k36 |
T |
A |
2: 111,146,574 (GRCm39) |
F250Y |
probably benign |
Het |
Or7g25 |
A |
G |
9: 19,160,149 (GRCm39) |
V182A |
probably benign |
Het |
Or9m1 |
A |
T |
2: 87,733,533 (GRCm39) |
N162K |
probably damaging |
Het |
Pcdhb16 |
T |
A |
18: 37,612,894 (GRCm39) |
|
probably null |
Het |
Pdcd10 |
T |
C |
3: 75,448,553 (GRCm39) |
T4A |
probably damaging |
Het |
Pgc |
A |
T |
17: 48,039,819 (GRCm39) |
Y71F |
probably damaging |
Het |
Phlpp1 |
G |
A |
1: 106,317,481 (GRCm39) |
G1234E |
probably damaging |
Het |
Prr27 |
T |
C |
5: 87,990,888 (GRCm39) |
F167L |
probably benign |
Het |
Prrc2b |
T |
A |
2: 32,116,330 (GRCm39) |
S1421T |
possibly damaging |
Het |
Pxmp2 |
A |
G |
5: 110,431,518 (GRCm39) |
V75A |
probably benign |
Het |
Pygl |
A |
T |
12: 70,243,807 (GRCm39) |
M545K |
probably null |
Het |
Ranbp9 |
A |
G |
13: 43,574,733 (GRCm39) |
Y412H |
possibly damaging |
Het |
Rcc1 |
A |
G |
4: 132,065,064 (GRCm39) |
V140A |
probably damaging |
Het |
Reln |
A |
G |
5: 22,184,718 (GRCm39) |
V1599A |
probably benign |
Het |
Rhebl1 |
A |
T |
15: 98,776,903 (GRCm39) |
D122E |
probably damaging |
Het |
Rock2 |
C |
T |
12: 17,009,492 (GRCm39) |
L676F |
probably benign |
Het |
Scn9a |
A |
T |
2: 66,357,087 (GRCm39) |
D1062E |
probably benign |
Het |
Sec63 |
T |
C |
10: 42,681,186 (GRCm39) |
I390T |
probably damaging |
Het |
Slc10a6 |
T |
C |
5: 103,754,493 (GRCm39) |
E346G |
probably benign |
Het |
Slc12a3 |
G |
A |
8: 95,075,216 (GRCm39) |
V737M |
possibly damaging |
Het |
Slc12a8 |
T |
C |
16: 33,426,629 (GRCm39) |
|
probably null |
Het |
Slc25a38 |
T |
A |
9: 119,949,354 (GRCm39) |
I102N |
probably damaging |
Het |
Spg7 |
T |
A |
8: 123,807,394 (GRCm39) |
V390E |
probably damaging |
Het |
Tbc1d20 |
T |
C |
2: 152,144,228 (GRCm39) |
V75A |
probably benign |
Het |
Tesk1 |
T |
A |
4: 43,445,555 (GRCm39) |
C243* |
probably null |
Het |
Ttk |
T |
A |
9: 83,725,739 (GRCm39) |
N220K |
possibly damaging |
Het |
Ttll5 |
A |
G |
12: 85,965,948 (GRCm39) |
E651G |
probably benign |
Het |
Tubd1 |
T |
C |
11: 86,457,879 (GRCm39) |
Y426H |
probably damaging |
Het |
Uba6 |
T |
C |
5: 86,288,293 (GRCm39) |
|
silent |
Het |
Ube2ql1 |
G |
A |
13: 69,852,289 (GRCm39) |
R263W |
probably damaging |
Het |
Vmn2r117 |
C |
T |
17: 23,678,812 (GRCm39) |
G804D |
probably damaging |
Het |
Vmn2r25 |
C |
T |
6: 123,805,406 (GRCm39) |
E484K |
probably benign |
Het |
Vmn2r4 |
T |
A |
3: 64,296,476 (GRCm39) |
I770F |
possibly damaging |
Het |
Vmn2r82 |
G |
A |
10: 79,214,589 (GRCm39) |
V191M |
probably benign |
Het |
Zbtb45 |
C |
T |
7: 12,742,037 (GRCm39) |
V74M |
probably damaging |
Het |
Zfp366 |
T |
C |
13: 99,370,609 (GRCm39) |
V443A |
possibly damaging |
Het |
Zfyve1 |
A |
T |
12: 83,598,345 (GRCm39) |
C628S |
probably damaging |
Het |
Zfyve26 |
A |
T |
12: 79,296,469 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Casp8ap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00686:Casp8ap2
|
APN |
4 |
32,641,433 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00714:Casp8ap2
|
APN |
4 |
32,649,192 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00754:Casp8ap2
|
APN |
4 |
32,641,036 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00954:Casp8ap2
|
APN |
4 |
32,645,403 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00970:Casp8ap2
|
APN |
4 |
32,646,182 (GRCm39) |
missense |
probably benign |
|
IGL01534:Casp8ap2
|
APN |
4 |
32,648,134 (GRCm39) |
splice site |
probably benign |
|
IGL01596:Casp8ap2
|
APN |
4 |
32,646,365 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01686:Casp8ap2
|
APN |
4 |
32,641,294 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02002:Casp8ap2
|
APN |
4 |
32,639,391 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02273:Casp8ap2
|
APN |
4 |
32,643,974 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02510:Casp8ap2
|
APN |
4 |
32,639,704 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02600:Casp8ap2
|
APN |
4 |
32,630,246 (GRCm39) |
missense |
probably null |
1.00 |
IGL02929:Casp8ap2
|
APN |
4 |
32,624,105 (GRCm39) |
utr 5 prime |
probably benign |
|
F5770:Casp8ap2
|
UTSW |
4 |
32,639,944 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02988:Casp8ap2
|
UTSW |
4 |
32,644,590 (GRCm39) |
missense |
probably benign |
0.14 |
R0023:Casp8ap2
|
UTSW |
4 |
32,640,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R0027:Casp8ap2
|
UTSW |
4 |
32,643,810 (GRCm39) |
missense |
probably benign |
0.01 |
R0090:Casp8ap2
|
UTSW |
4 |
32,640,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R0117:Casp8ap2
|
UTSW |
4 |
32,640,817 (GRCm39) |
missense |
probably benign |
0.00 |
R0144:Casp8ap2
|
UTSW |
4 |
32,643,797 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0268:Casp8ap2
|
UTSW |
4 |
32,644,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R0344:Casp8ap2
|
UTSW |
4 |
32,644,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R0555:Casp8ap2
|
UTSW |
4 |
32,640,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R1051:Casp8ap2
|
UTSW |
4 |
32,640,790 (GRCm39) |
missense |
probably benign |
0.28 |
R1165:Casp8ap2
|
UTSW |
4 |
32,640,563 (GRCm39) |
missense |
probably benign |
0.01 |
R1243:Casp8ap2
|
UTSW |
4 |
32,645,687 (GRCm39) |
missense |
probably benign |
0.03 |
R1311:Casp8ap2
|
UTSW |
4 |
32,648,111 (GRCm39) |
missense |
probably damaging |
0.98 |
R1337:Casp8ap2
|
UTSW |
4 |
32,645,721 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1471:Casp8ap2
|
UTSW |
4 |
32,639,386 (GRCm39) |
nonsense |
probably null |
|
R1497:Casp8ap2
|
UTSW |
4 |
32,639,938 (GRCm39) |
missense |
probably benign |
0.00 |
R1521:Casp8ap2
|
UTSW |
4 |
32,631,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R1588:Casp8ap2
|
UTSW |
4 |
32,640,541 (GRCm39) |
missense |
probably benign |
0.00 |
R1625:Casp8ap2
|
UTSW |
4 |
32,648,068 (GRCm39) |
missense |
probably benign |
0.04 |
R1731:Casp8ap2
|
UTSW |
4 |
32,641,442 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1899:Casp8ap2
|
UTSW |
4 |
32,643,647 (GRCm39) |
missense |
probably damaging |
0.98 |
R2000:Casp8ap2
|
UTSW |
4 |
32,634,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R2021:Casp8ap2
|
UTSW |
4 |
32,644,560 (GRCm39) |
missense |
probably benign |
0.05 |
R2022:Casp8ap2
|
UTSW |
4 |
32,644,560 (GRCm39) |
missense |
probably benign |
0.05 |
R2023:Casp8ap2
|
UTSW |
4 |
32,644,560 (GRCm39) |
missense |
probably benign |
0.05 |
R2088:Casp8ap2
|
UTSW |
4 |
32,631,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R2104:Casp8ap2
|
UTSW |
4 |
32,644,727 (GRCm39) |
missense |
probably benign |
0.00 |
R2128:Casp8ap2
|
UTSW |
4 |
32,640,142 (GRCm39) |
missense |
probably benign |
0.06 |
R2129:Casp8ap2
|
UTSW |
4 |
32,640,142 (GRCm39) |
missense |
probably benign |
0.06 |
R2305:Casp8ap2
|
UTSW |
4 |
32,646,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R2316:Casp8ap2
|
UTSW |
4 |
32,643,781 (GRCm39) |
missense |
probably benign |
0.31 |
R2919:Casp8ap2
|
UTSW |
4 |
32,645,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R4091:Casp8ap2
|
UTSW |
4 |
32,643,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R4357:Casp8ap2
|
UTSW |
4 |
32,646,150 (GRCm39) |
missense |
probably benign |
0.00 |
R4807:Casp8ap2
|
UTSW |
4 |
32,644,505 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4828:Casp8ap2
|
UTSW |
4 |
32,639,807 (GRCm39) |
missense |
probably benign |
|
R4945:Casp8ap2
|
UTSW |
4 |
32,631,163 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4962:Casp8ap2
|
UTSW |
4 |
32,640,554 (GRCm39) |
missense |
probably damaging |
0.99 |
R6014:Casp8ap2
|
UTSW |
4 |
32,641,400 (GRCm39) |
missense |
probably damaging |
0.97 |
R6092:Casp8ap2
|
UTSW |
4 |
32,639,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Casp8ap2
|
UTSW |
4 |
32,641,364 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6289:Casp8ap2
|
UTSW |
4 |
32,639,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R6482:Casp8ap2
|
UTSW |
4 |
32,634,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R6496:Casp8ap2
|
UTSW |
4 |
32,641,553 (GRCm39) |
missense |
probably benign |
0.05 |
R6515:Casp8ap2
|
UTSW |
4 |
32,646,423 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7015:Casp8ap2
|
UTSW |
4 |
32,644,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Casp8ap2
|
UTSW |
4 |
32,639,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7072:Casp8ap2
|
UTSW |
4 |
32,644,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Casp8ap2
|
UTSW |
4 |
32,643,974 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7944:Casp8ap2
|
UTSW |
4 |
32,645,909 (GRCm39) |
missense |
probably benign |
0.12 |
R7945:Casp8ap2
|
UTSW |
4 |
32,645,909 (GRCm39) |
missense |
probably benign |
0.12 |
R8170:Casp8ap2
|
UTSW |
4 |
32,615,490 (GRCm39) |
splice site |
probably benign |
|
R8179:Casp8ap2
|
UTSW |
4 |
32,643,939 (GRCm39) |
nonsense |
probably null |
|
R8207:Casp8ap2
|
UTSW |
4 |
32,646,446 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8263:Casp8ap2
|
UTSW |
4 |
32,644,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R8298:Casp8ap2
|
UTSW |
4 |
32,640,429 (GRCm39) |
missense |
probably benign |
0.30 |
R9441:Casp8ap2
|
UTSW |
4 |
32,645,873 (GRCm39) |
missense |
probably benign |
0.00 |
R9455:Casp8ap2
|
UTSW |
4 |
32,643,924 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9729:Casp8ap2
|
UTSW |
4 |
32,643,807 (GRCm39) |
missense |
possibly damaging |
0.71 |
V7580:Casp8ap2
|
UTSW |
4 |
32,639,944 (GRCm39) |
missense |
probably benign |
0.00 |
X0018:Casp8ap2
|
UTSW |
4 |
32,643,738 (GRCm39) |
missense |
probably benign |
0.03 |
|