Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001C19Rik |
T |
C |
17: 47,413,776 |
E140G |
probably benign |
Het |
4932431P20Rik |
T |
C |
7: 29,532,517 |
|
noncoding transcript |
Het |
Ablim2 |
C |
T |
5: 35,866,780 |
|
probably benign |
Het |
Aire |
T |
C |
10: 78,034,493 |
|
probably benign |
Het |
Akap12 |
T |
C |
10: 4,353,315 |
S42P |
probably benign |
Het |
Amigo1 |
T |
C |
3: 108,191,669 |
|
probably benign |
Het |
Angptl3 |
A |
G |
4: 99,033,262 |
T206A |
probably benign |
Het |
Ank1 |
T |
A |
8: 23,110,384 |
|
probably benign |
Het |
Ano5 |
A |
T |
7: 51,574,810 |
T472S |
probably damaging |
Het |
Arid3c |
T |
C |
4: 41,725,958 |
D215G |
probably damaging |
Het |
Cd200 |
T |
C |
16: 45,397,110 |
I73V |
probably benign |
Het |
Cd47 |
T |
C |
16: 49,906,799 |
I318T |
possibly damaging |
Het |
Cep290 |
A |
G |
10: 100,568,813 |
|
probably null |
Het |
Cep350 |
A |
G |
1: 155,959,753 |
S66P |
possibly damaging |
Het |
Cfap46 |
C |
T |
7: 139,676,034 |
C300Y |
probably damaging |
Het |
Chd1 |
T |
A |
17: 15,758,261 |
|
probably benign |
Het |
Chd5 |
C |
A |
4: 152,385,950 |
T1913K |
probably benign |
Het |
Clec4b1 |
A |
G |
6: 123,071,446 |
Y180C |
probably damaging |
Het |
Cntnap5c |
A |
T |
17: 58,034,995 |
D227V |
probably damaging |
Het |
Col19a1 |
C |
G |
1: 24,575,455 |
|
probably benign |
Het |
Cyp2c66 |
T |
A |
19: 39,186,616 |
F487I |
possibly damaging |
Het |
Dpp8 |
T |
C |
9: 65,066,502 |
|
probably benign |
Het |
Duoxa1 |
A |
T |
2: 122,306,380 |
|
probably benign |
Het |
Edil3 |
A |
G |
13: 89,177,280 |
K263E |
probably damaging |
Het |
Fat2 |
A |
G |
11: 55,309,209 |
L1013P |
probably damaging |
Het |
Fras1 |
T |
C |
5: 96,667,387 |
|
probably benign |
Het |
Gab1 |
A |
G |
8: 80,769,668 |
S668P |
probably damaging |
Het |
Galnt14 |
T |
C |
17: 73,545,035 |
T130A |
probably damaging |
Het |
Gm10192 |
G |
A |
4: 97,182,872 |
H99Y |
unknown |
Het |
Gm5592 |
A |
G |
7: 41,289,387 |
T698A |
possibly damaging |
Het |
Gm6605 |
C |
A |
7: 38,448,275 |
|
noncoding transcript |
Het |
Gsdma3 |
A |
G |
11: 98,631,191 |
K149R |
probably benign |
Het |
Igkv4-71 |
A |
G |
6: 69,243,427 |
S29P |
probably damaging |
Het |
Igsf10 |
C |
T |
3: 59,328,594 |
V1389I |
probably benign |
Het |
Ik |
T |
C |
18: 36,747,333 |
|
probably benign |
Het |
Ino80 |
G |
A |
2: 119,383,481 |
P1203S |
probably damaging |
Het |
Iqsec2 |
G |
A |
X: 152,204,124 |
E398K |
possibly damaging |
Het |
Jmjd6 |
A |
G |
11: 116,840,527 |
V232A |
probably damaging |
Het |
Klhdc9 |
G |
A |
1: 171,360,327 |
T112M |
possibly damaging |
Het |
Marcks |
A |
G |
10: 37,141,185 |
|
probably benign |
Het |
Mctp2 |
T |
A |
7: 72,083,170 |
T829S |
probably damaging |
Het |
Mroh2a |
C |
A |
1: 88,228,380 |
A78E |
probably damaging |
Het |
Mroh2a |
G |
A |
1: 88,250,342 |
D1053N |
probably damaging |
Het |
Mtmr14 |
A |
T |
6: 113,270,647 |
H518L |
probably damaging |
Het |
Mum1 |
T |
A |
10: 80,230,080 |
V56E |
probably damaging |
Het |
Myo5c |
T |
C |
9: 75,278,289 |
M978T |
probably benign |
Het |
Nlrc3 |
T |
C |
16: 3,948,911 |
I1015V |
probably benign |
Het |
Nlrp5 |
C |
A |
7: 23,417,417 |
Q189K |
possibly damaging |
Het |
Olfr1082 |
T |
C |
2: 86,594,079 |
I250V |
probably benign |
Het |
Olfr385 |
A |
C |
11: 73,589,252 |
L162R |
probably damaging |
Het |
Olfr583 |
A |
G |
7: 103,051,702 |
I135V |
probably benign |
Het |
Olfr92 |
G |
C |
17: 37,111,455 |
L176V |
probably benign |
Het |
Otof |
T |
A |
5: 30,382,361 |
Y1051F |
probably benign |
Het |
Pcdhb14 |
C |
A |
18: 37,448,339 |
T166K |
possibly damaging |
Het |
Pla2g4e |
A |
G |
2: 120,200,198 |
|
probably benign |
Het |
Polr3gl |
T |
C |
3: 96,582,155 |
E20G |
probably damaging |
Het |
Psmd1 |
A |
G |
1: 86,082,039 |
D295G |
probably benign |
Het |
Ptpn21 |
C |
A |
12: 98,688,216 |
A831S |
probably benign |
Het |
Rd3l |
T |
C |
12: 111,980,162 |
D60G |
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,110,324 |
|
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,441,834 |
D2624G |
probably benign |
Het |
Sec31a |
T |
C |
5: 100,393,207 |
D347G |
probably damaging |
Het |
Sema4g |
G |
A |
19: 44,997,587 |
R289H |
probably damaging |
Het |
Sema5b |
C |
T |
16: 35,660,333 |
T761I |
probably benign |
Het |
Sept1 |
A |
T |
7: 127,216,999 |
F86L |
probably damaging |
Het |
Shank3 |
T |
C |
15: 89,531,388 |
V627A |
possibly damaging |
Het |
Slc25a46 |
C |
A |
18: 31,609,588 |
G75V |
probably benign |
Het |
Slc45a2 |
T |
A |
15: 11,025,778 |
Y405N |
probably damaging |
Het |
Spidr |
T |
C |
16: 16,037,634 |
E339G |
probably damaging |
Het |
Sptbn1 |
A |
T |
11: 30,117,903 |
H1770Q |
probably damaging |
Het |
Srgap1 |
T |
C |
10: 121,792,235 |
Y944C |
probably damaging |
Het |
Supt20 |
C |
T |
3: 54,706,969 |
T169I |
probably damaging |
Het |
Tie1 |
G |
A |
4: 118,479,769 |
Q587* |
probably null |
Het |
Tmem214 |
A |
G |
5: 30,871,825 |
T203A |
possibly damaging |
Het |
Tmprss15 |
C |
A |
16: 78,985,950 |
S742I |
probably damaging |
Het |
Zfhx2 |
A |
G |
14: 55,063,163 |
V2377A |
probably damaging |
Het |
Zfp763 |
G |
A |
17: 33,019,800 |
H124Y |
possibly damaging |
Het |
Zfp846 |
T |
C |
9: 20,593,557 |
S238P |
probably benign |
Het |
|