Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl11 |
A |
G |
9: 107,929,633 |
N385S |
probably benign |
Het |
Ahctf1 |
A |
T |
1: 179,754,068 |
I1523N |
probably benign |
Het |
Akna |
C |
T |
4: 63,394,959 |
G309E |
probably benign |
Het |
Akna |
T |
C |
4: 63,395,566 |
N107D |
probably benign |
Het |
Arhgef15 |
G |
A |
11: 68,954,051 |
P240L |
probably benign |
Het |
Brd1 |
T |
A |
15: 88,701,122 |
E836D |
probably benign |
Het |
Brf2 |
A |
G |
8: 27,124,283 |
S292P |
possibly damaging |
Het |
C3 |
A |
G |
17: 57,222,976 |
L500P |
probably damaging |
Het |
Ccdc107 |
T |
C |
4: 43,495,685 |
L196P |
probably damaging |
Het |
Cdcp1 |
G |
T |
9: 123,178,029 |
P551Q |
probably damaging |
Het |
Ckap5 |
T |
C |
2: 91,594,816 |
L1224P |
probably damaging |
Het |
Csnk1g2 |
C |
A |
10: 80,638,398 |
T178K |
probably benign |
Het |
Ctsq |
A |
T |
13: 61,037,888 |
C146* |
probably null |
Het |
Cyp2ab1 |
T |
A |
16: 20,313,757 |
I264F |
probably damaging |
Het |
Daxx |
TGATGATGACGATGATGACGATGATGA |
TGATGATGACGATGATGA |
17: 33,912,641 |
|
probably benign |
Het |
Dnah11 |
G |
A |
12: 117,975,848 |
T3179M |
possibly damaging |
Het |
Eif4enif1 |
T |
C |
11: 3,243,989 |
V776A |
probably damaging |
Het |
Erbb4 |
G |
T |
1: 68,298,293 |
T622N |
probably damaging |
Het |
Erich6 |
A |
G |
3: 58,618,797 |
Y595H |
probably benign |
Het |
Fam107a |
C |
T |
14: 8,298,764 |
A121T |
probably benign |
Het |
Gif |
T |
C |
19: 11,748,495 |
S50P |
possibly damaging |
Het |
Gpatch11 |
C |
T |
17: 78,842,119 |
Q183* |
probably null |
Het |
Gpr161 |
C |
A |
1: 165,306,413 |
F81L |
possibly damaging |
Het |
Hook1 |
G |
T |
4: 96,002,528 |
E291D |
probably benign |
Het |
Hsf2bp |
T |
A |
17: 31,946,695 |
I309F |
probably damaging |
Het |
Hspg2 |
T |
C |
4: 137,548,174 |
|
probably null |
Het |
Ide |
T |
G |
19: 37,272,224 |
M910L |
unknown |
Het |
Igdcc4 |
A |
G |
9: 65,128,795 |
Y712C |
probably damaging |
Het |
Kmt2d |
T |
C |
15: 98,853,068 |
|
probably benign |
Het |
Lats1 |
T |
C |
10: 7,705,754 |
Y768H |
probably damaging |
Het |
Mageb3 |
A |
G |
2: 121,954,387 |
V278A |
probably damaging |
Het |
Mapkbp1 |
G |
A |
2: 120,019,243 |
R732H |
probably damaging |
Het |
Marveld2 |
T |
C |
13: 100,600,938 |
I148V |
probably benign |
Het |
Mast1 |
G |
C |
8: 84,916,260 |
P969A |
probably damaging |
Het |
Myh10 |
T |
G |
11: 68,798,380 |
V1261G |
possibly damaging |
Het |
Nlrp1b |
A |
T |
11: 71,217,276 |
H466Q |
probably benign |
Het |
Npr2 |
T |
G |
4: 43,650,150 |
V905G |
probably damaging |
Het |
Oip5 |
T |
A |
2: 119,610,327 |
I240F |
unknown |
Het |
Olfr1259 |
A |
G |
2: 89,943,585 |
C177R |
probably damaging |
Het |
Olfr175-ps1 |
G |
T |
16: 58,824,153 |
Y185* |
probably null |
Het |
Olfr874 |
T |
A |
9: 37,746,524 |
M130K |
probably benign |
Het |
Pcsk2 |
G |
A |
2: 143,546,560 |
A24T |
probably benign |
Het |
Plxnb1 |
G |
T |
9: 109,100,750 |
G225W |
probably damaging |
Het |
Polr1a |
T |
C |
6: 71,929,366 |
S389P |
possibly damaging |
Het |
Prkca |
A |
G |
11: 108,053,980 |
V175A |
probably benign |
Het |
Rassf7 |
C |
A |
7: 141,217,060 |
|
probably null |
Het |
Rbl2 |
A |
G |
8: 91,078,932 |
I206V |
probably benign |
Het |
Rnf111 |
A |
T |
9: 70,459,096 |
H353Q |
probably benign |
Het |
Rpn1 |
T |
G |
6: 88,093,859 |
V237G |
probably damaging |
Het |
Sec61a2 |
T |
A |
2: 5,876,540 |
I267F |
possibly damaging |
Het |
Spop |
G |
T |
11: 95,485,843 |
V241F |
probably damaging |
Het |
Sptbn2 |
C |
T |
19: 4,725,950 |
A178V |
probably damaging |
Het |
Stard13 |
A |
G |
5: 151,045,901 |
Y791H |
probably benign |
Het |
Susd2 |
T |
A |
10: 75,642,218 |
I113L |
probably benign |
Het |
Tcof1 |
T |
C |
18: 60,831,556 |
E666G |
possibly damaging |
Het |
Tekt5 |
G |
T |
16: 10,361,390 |
A371E |
possibly damaging |
Het |
Thap11 |
G |
A |
8: 105,855,916 |
E186K |
probably damaging |
Het |
Tk2 |
A |
T |
8: 104,247,683 |
D45E |
possibly damaging |
Het |
Tuba8 |
C |
A |
6: 121,222,913 |
Y185* |
probably null |
Het |
Usp24 |
T |
A |
4: 106,416,047 |
Y2210N |
probably damaging |
Het |
Wfdc8 |
A |
T |
2: 164,597,319 |
|
probably benign |
Het |
Zar1l |
T |
C |
5: 150,512,900 |
N237S |
probably damaging |
Het |
Zfp607b |
A |
T |
7: 27,702,607 |
T163S |
probably benign |
Het |
Zfp619 |
C |
A |
7: 39,535,153 |
H202Q |
probably benign |
Het |
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