Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aarsd1 |
A |
G |
11: 101,301,226 (GRCm39) |
V272A |
probably benign |
Het |
Acbd6 |
G |
A |
1: 155,562,706 (GRCm39) |
E236K |
probably damaging |
Het |
Actr1b |
T |
C |
1: 36,748,909 (GRCm39) |
N9S |
probably benign |
Het |
Adam17 |
A |
T |
12: 21,401,595 (GRCm39) |
D133E |
probably benign |
Het |
Adam6b |
G |
A |
12: 113,453,227 (GRCm39) |
V15M |
probably damaging |
Het |
Adam9 |
T |
A |
8: 25,457,235 (GRCm39) |
N631I |
probably damaging |
Het |
Albfm1 |
A |
G |
5: 90,714,461 (GRCm39) |
N157S |
probably benign |
Het |
Amy2a1 |
A |
T |
3: 113,325,276 (GRCm39) |
|
probably benign |
Het |
Aplnr |
A |
T |
2: 84,967,515 (GRCm39) |
Y180F |
probably benign |
Het |
Arhgef7 |
T |
C |
8: 11,831,216 (GRCm39) |
V105A |
probably benign |
Het |
Bambi |
G |
A |
18: 3,511,277 (GRCm39) |
D33N |
probably damaging |
Het |
Bicc1 |
G |
A |
10: 70,779,216 (GRCm39) |
T724I |
probably benign |
Het |
Brd2 |
T |
A |
17: 34,335,934 (GRCm39) |
Q93L |
probably damaging |
Het |
Cacnb2 |
A |
G |
2: 14,972,759 (GRCm39) |
D222G |
possibly damaging |
Het |
Cdh1 |
G |
T |
8: 107,386,336 (GRCm39) |
D420Y |
probably damaging |
Het |
Cep162 |
T |
C |
9: 87,109,314 (GRCm39) |
S430G |
probably benign |
Het |
Cfap161 |
T |
A |
7: 83,443,282 (GRCm39) |
R27S |
possibly damaging |
Het |
Chek1 |
C |
T |
9: 36,629,636 (GRCm39) |
A237T |
probably benign |
Het |
Coro7 |
A |
C |
16: 4,452,203 (GRCm39) |
V410G |
probably benign |
Het |
Crmp1 |
C |
A |
5: 37,441,440 (GRCm39) |
N507K |
probably damaging |
Het |
Crocc |
T |
C |
4: 140,761,369 (GRCm39) |
R755G |
possibly damaging |
Het |
Disc1 |
A |
G |
8: 125,881,796 (GRCm39) |
D577G |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,156,811 (GRCm39) |
Y649H |
possibly damaging |
Het |
Flywch1 |
A |
G |
17: 23,975,731 (GRCm39) |
S504P |
probably damaging |
Het |
Fpr1 |
A |
T |
17: 18,097,851 (GRCm39) |
V46D |
probably damaging |
Het |
Fpr-rs7 |
C |
T |
17: 20,333,789 (GRCm39) |
V234M |
probably benign |
Het |
Ighv5-16 |
T |
C |
12: 113,802,288 (GRCm39) |
N71D |
probably benign |
Het |
Kash5 |
G |
T |
7: 44,845,481 (GRCm39) |
D152E |
probably damaging |
Het |
Kdm3b |
A |
G |
18: 34,937,157 (GRCm39) |
M480V |
probably benign |
Het |
L3mbtl3 |
T |
A |
10: 26,152,121 (GRCm39) |
D825V |
probably damaging |
Het |
Lef1 |
T |
A |
3: 130,988,366 (GRCm39) |
M311K |
probably damaging |
Het |
Magi1 |
T |
A |
6: 93,792,789 (GRCm39) |
R150* |
probably null |
Het |
Magi3 |
C |
T |
3: 103,958,169 (GRCm39) |
V639I |
probably damaging |
Het |
Mocos |
A |
T |
18: 24,812,554 (GRCm39) |
R483W |
probably damaging |
Het |
Mrps11 |
G |
T |
7: 78,438,487 (GRCm39) |
V80F |
possibly damaging |
Het |
Myh2 |
A |
T |
11: 67,084,578 (GRCm39) |
R1706W |
probably damaging |
Het |
Neurod6 |
T |
A |
6: 55,656,228 (GRCm39) |
L136F |
probably damaging |
Het |
Nfe2l1 |
A |
T |
11: 96,711,306 (GRCm39) |
Y308N |
probably damaging |
Het |
Nptn |
T |
A |
9: 58,525,905 (GRCm39) |
|
probably benign |
Het |
Or1e28-ps1 |
G |
T |
11: 73,615,307 (GRCm39) |
T181N |
unknown |
Het |
Or5g25 |
A |
T |
2: 85,478,034 (GRCm39) |
S210R |
probably damaging |
Het |
Oscar |
A |
G |
7: 3,613,900 (GRCm39) |
S227P |
probably benign |
Het |
Phgdh |
A |
C |
3: 98,247,024 (GRCm39) |
I42R |
possibly damaging |
Het |
Pla2g4a |
C |
T |
1: 149,761,935 (GRCm39) |
G174D |
probably benign |
Het |
Plcd4 |
A |
G |
1: 74,591,213 (GRCm39) |
T203A |
possibly damaging |
Het |
Plk3 |
ACACTCAC |
ACAC |
4: 116,989,090 (GRCm39) |
|
probably benign |
Het |
Plppr4 |
A |
T |
3: 117,119,482 (GRCm39) |
V309D |
probably damaging |
Het |
Pltp |
T |
C |
2: 164,686,652 (GRCm39) |
K324E |
possibly damaging |
Het |
Pml |
C |
T |
9: 58,154,348 (GRCm39) |
R175H |
probably damaging |
Het |
Psg20 |
C |
A |
7: 18,408,557 (GRCm39) |
V388F |
probably benign |
Het |
Qrfprl |
T |
C |
6: 65,424,393 (GRCm39) |
V182A |
probably benign |
Het |
Rabgef1 |
A |
G |
5: 130,237,557 (GRCm39) |
D209G |
possibly damaging |
Het |
Rif1 |
A |
T |
2: 52,001,742 (GRCm39) |
N90I |
|
Het |
Sec31a |
T |
C |
5: 100,526,688 (GRCm39) |
H57R |
|
Het |
Sidt1 |
T |
C |
16: 44,152,707 (GRCm39) |
N62S |
probably benign |
Het |
Slc18a2 |
T |
A |
19: 59,261,355 (GRCm39) |
M172K |
probably benign |
Het |
Slc34a3 |
T |
C |
2: 25,121,003 (GRCm39) |
T362A |
probably benign |
Het |
Smtn |
T |
G |
11: 3,476,407 (GRCm39) |
D158A |
probably benign |
Het |
Spen |
C |
T |
4: 141,200,261 (GRCm39) |
V2789M |
probably damaging |
Het |
Taf2 |
A |
T |
15: 54,910,849 (GRCm39) |
N608K |
probably benign |
Het |
Tctn3 |
A |
G |
19: 40,595,636 (GRCm39) |
V383A |
unknown |
Het |
Themis3 |
A |
T |
17: 66,866,676 (GRCm39) |
M188K |
probably benign |
Het |
Trpv5 |
A |
G |
6: 41,652,313 (GRCm39) |
V124A |
probably benign |
Het |
Tshr |
G |
A |
12: 91,504,324 (GRCm39) |
V421M |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,539,426 (GRCm39) |
D34520V |
probably benign |
Het |
Ttn |
A |
C |
2: 76,608,294 (GRCm39) |
Y17876* |
probably null |
Het |
Zrsr2-ps1 |
T |
C |
11: 22,923,694 (GRCm39) |
L156P |
probably benign |
Het |
|
Other mutations in Chrna3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02469:Chrna3
|
APN |
9 |
54,923,290 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02484:Chrna3
|
APN |
9 |
54,922,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Chrna3
|
UTSW |
9 |
54,929,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Chrna3
|
UTSW |
9 |
54,923,290 (GRCm39) |
missense |
probably benign |
0.01 |
R0557:Chrna3
|
UTSW |
9 |
54,923,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R0674:Chrna3
|
UTSW |
9 |
54,922,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R1552:Chrna3
|
UTSW |
9 |
54,923,192 (GRCm39) |
missense |
probably benign |
0.16 |
R1750:Chrna3
|
UTSW |
9 |
54,923,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Chrna3
|
UTSW |
9 |
54,923,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R2989:Chrna3
|
UTSW |
9 |
54,923,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R3114:Chrna3
|
UTSW |
9 |
54,923,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R3153:Chrna3
|
UTSW |
9 |
54,923,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R3154:Chrna3
|
UTSW |
9 |
54,923,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R3434:Chrna3
|
UTSW |
9 |
54,931,610 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3732:Chrna3
|
UTSW |
9 |
54,923,178 (GRCm39) |
missense |
probably benign |
0.00 |
R3732:Chrna3
|
UTSW |
9 |
54,923,178 (GRCm39) |
missense |
probably benign |
0.00 |
R3733:Chrna3
|
UTSW |
9 |
54,923,178 (GRCm39) |
missense |
probably benign |
0.00 |
R4758:Chrna3
|
UTSW |
9 |
54,929,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4903:Chrna3
|
UTSW |
9 |
54,922,810 (GRCm39) |
missense |
probably benign |
0.01 |
R5430:Chrna3
|
UTSW |
9 |
54,920,192 (GRCm39) |
missense |
probably damaging |
0.98 |
R5795:Chrna3
|
UTSW |
9 |
54,922,552 (GRCm39) |
missense |
probably benign |
0.17 |
R6546:Chrna3
|
UTSW |
9 |
54,923,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R6806:Chrna3
|
UTSW |
9 |
54,923,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R7516:Chrna3
|
UTSW |
9 |
54,922,653 (GRCm39) |
missense |
probably benign |
0.00 |
R7703:Chrna3
|
UTSW |
9 |
54,923,408 (GRCm39) |
missense |
probably benign |
0.00 |
R8053:Chrna3
|
UTSW |
9 |
54,922,674 (GRCm39) |
missense |
probably benign |
0.25 |
R9170:Chrna3
|
UTSW |
9 |
54,933,671 (GRCm39) |
missense |
unknown |
|
|