Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bahcc1 |
A |
G |
11: 120,289,512 |
T2565A |
probably damaging |
Het |
C8a |
A |
C |
4: 104,827,985 |
F354V |
probably benign |
Het |
Cadps |
C |
T |
14: 12,486,543 |
V876M |
possibly damaging |
Het |
Chmp7 |
A |
T |
14: 69,719,406 |
I351N |
probably damaging |
Het |
Clec7a |
A |
T |
6: 129,465,486 |
W193R |
probably damaging |
Het |
Clint1 |
T |
C |
11: 45,909,019 |
V535A |
probably benign |
Het |
Clu |
A |
G |
14: 65,975,588 |
E141G |
probably damaging |
Het |
Cmah |
A |
T |
13: 24,430,549 |
D159V |
probably damaging |
Het |
Cntn2 |
A |
T |
1: 132,518,905 |
|
probably null |
Het |
Cox6a1 |
C |
A |
5: 115,345,839 |
|
probably benign |
Het |
Cyp2d10 |
C |
T |
15: 82,403,841 |
A195T |
probably benign |
Het |
Dnah10 |
G |
T |
5: 124,777,212 |
K1901N |
probably damaging |
Het |
Dopey1 |
G |
A |
9: 86,551,677 |
D2329N |
possibly damaging |
Het |
Eipr1 |
A |
G |
12: 28,864,771 |
E308G |
probably damaging |
Het |
Exoc4 |
T |
C |
6: 33,305,400 |
|
probably benign |
Het |
Fancd2 |
A |
G |
6: 113,553,752 |
I449V |
probably benign |
Het |
Fbn2 |
T |
C |
18: 58,113,370 |
T487A |
possibly damaging |
Het |
Fbxo40 |
T |
C |
16: 36,970,454 |
E98G |
probably damaging |
Het |
Folh1 |
G |
A |
7: 86,726,098 |
T527I |
probably damaging |
Het |
Gls |
C |
T |
1: 52,188,708 |
D217N |
probably damaging |
Het |
Gm6994 |
A |
G |
14: 77,481,178 |
|
probably benign |
Het |
Gpr149 |
A |
T |
3: 62,604,297 |
W94R |
probably damaging |
Het |
Gpr158 |
A |
G |
2: 21,369,031 |
D259G |
possibly damaging |
Het |
Hcn2 |
T |
C |
10: 79,729,068 |
L438P |
probably damaging |
Het |
Hgd |
A |
C |
16: 37,631,730 |
T374P |
possibly damaging |
Het |
Ints3 |
A |
G |
3: 90,415,156 |
|
probably null |
Het |
Kctd5 |
A |
T |
17: 24,057,775 |
V172E |
probably damaging |
Het |
Lmcd1 |
A |
G |
6: 112,310,625 |
I91V |
probably benign |
Het |
Lrrc37a |
A |
G |
11: 103,497,937 |
S2221P |
unknown |
Het |
Ltk |
T |
A |
2: 119,752,974 |
D310V |
probably damaging |
Het |
Luzp1 |
T |
A |
4: 136,542,776 |
M770K |
probably damaging |
Het |
Mxd4 |
G |
A |
5: 34,184,346 |
|
probably benign |
Het |
Mzb1 |
T |
A |
18: 35,648,346 |
H71L |
probably benign |
Het |
Necap2 |
G |
A |
4: 141,074,965 |
T63I |
probably benign |
Het |
Nefl |
A |
G |
14: 68,086,482 |
|
probably benign |
Het |
Odam |
G |
A |
5: 87,885,896 |
|
probably null |
Het |
Pcdh18 |
A |
G |
3: 49,755,798 |
I356T |
probably benign |
Het |
Pcx |
T |
A |
19: 4,620,235 |
|
probably null |
Het |
Pde2a |
T |
C |
7: 101,507,159 |
S593P |
probably benign |
Het |
Rapgef3 |
A |
T |
15: 97,758,059 |
L359M |
probably damaging |
Het |
Rb1 |
T |
C |
14: 73,264,371 |
|
probably null |
Het |
Rbm44 |
A |
G |
1: 91,168,964 |
I976V |
probably benign |
Het |
Rdh13 |
A |
T |
7: 4,427,624 |
S278R |
probably damaging |
Het |
Rgma |
A |
G |
7: 73,417,483 |
E256G |
probably damaging |
Het |
Rnf112 |
A |
T |
11: 61,450,477 |
D402E |
probably benign |
Het |
Rnps1 |
T |
A |
17: 24,422,299 |
D224E |
probably damaging |
Het |
Scn10a |
C |
T |
9: 119,622,766 |
V1364M |
probably damaging |
Het |
Scn1a |
C |
T |
2: 66,325,960 |
R535H |
probably benign |
Het |
Scn8a |
A |
T |
15: 101,032,201 |
D1431V |
probably benign |
Het |
Setdb1 |
A |
T |
3: 95,338,580 |
L677* |
probably null |
Het |
Slc17a8 |
T |
A |
10: 89,591,244 |
I148F |
probably damaging |
Het |
Slx4ip |
T |
A |
2: 137,044,055 |
C98* |
probably null |
Het |
Sptbn2 |
T |
G |
19: 4,745,972 |
Y1726* |
probably null |
Het |
Tcof1 |
T |
C |
18: 60,818,095 |
|
probably benign |
Het |
Tdrd3 |
G |
A |
14: 87,480,794 |
V210I |
possibly damaging |
Het |
Tmod4 |
G |
A |
3: 95,128,297 |
R252H |
probably benign |
Het |
Tti1 |
G |
T |
2: 158,009,130 |
P63Q |
possibly damaging |
Het |
Tuft1 |
A |
T |
3: 94,628,287 |
D109E |
probably damaging |
Het |
Wdr63 |
T |
C |
3: 146,042,836 |
Y841C |
probably benign |
Het |
Zcchc2 |
T |
C |
1: 106,029,775 |
S659P |
probably damaging |
Het |
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