Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310033P09Rik |
A |
G |
11: 59,100,806 (GRCm39) |
S181G |
possibly damaging |
Het |
5730596B20Rik |
A |
G |
6: 52,156,413 (GRCm39) |
R160G |
unknown |
Het |
Acy1 |
A |
G |
9: 106,311,952 (GRCm39) |
Y262H |
probably benign |
Het |
Adamts13 |
T |
C |
2: 26,880,379 (GRCm39) |
S681P |
possibly damaging |
Het |
Adgra3 |
C |
A |
5: 50,118,395 (GRCm39) |
C1051F |
probably damaging |
Het |
Agrn |
A |
T |
4: 156,261,514 (GRCm39) |
V568E |
probably damaging |
Het |
Ahnak |
A |
G |
19: 8,987,149 (GRCm39) |
E2811G |
probably damaging |
Het |
Ap1m1 |
C |
A |
8: 72,994,066 (GRCm39) |
Y7* |
probably null |
Het |
Apobec1 |
T |
A |
6: 122,555,837 (GRCm39) |
T207S |
probably benign |
Het |
Arhgap32 |
G |
A |
9: 32,157,309 (GRCm39) |
R102Q |
probably damaging |
Het |
Bcat2 |
T |
C |
7: 45,237,446 (GRCm39) |
|
probably null |
Het |
Cd209f |
T |
A |
8: 4,155,802 (GRCm39) |
|
probably benign |
Het |
Cox7c |
G |
A |
13: 86,194,837 (GRCm39) |
|
probably benign |
Het |
Cyp2d11 |
A |
G |
15: 82,276,203 (GRCm39) |
V156A |
possibly damaging |
Het |
Dhrs3 |
A |
T |
4: 144,653,769 (GRCm39) |
T297S |
probably benign |
Het |
Dip2c |
T |
C |
13: 9,660,766 (GRCm39) |
C876R |
probably damaging |
Het |
Eprs1 |
A |
T |
1: 185,129,273 (GRCm39) |
I587F |
probably damaging |
Het |
Fam13c |
A |
G |
10: 70,286,978 (GRCm39) |
T81A |
probably benign |
Het |
Flt4 |
A |
G |
11: 49,524,064 (GRCm39) |
Y548C |
probably damaging |
Het |
Garin2 |
T |
C |
12: 78,757,202 (GRCm39) |
|
probably null |
Het |
Gimap4 |
T |
A |
6: 48,667,629 (GRCm39) |
V128E |
probably benign |
Het |
Gm32742 |
A |
G |
9: 51,060,735 (GRCm39) |
L856P |
possibly damaging |
Het |
Gm5916 |
A |
G |
9: 36,032,258 (GRCm39) |
Y59H |
probably damaging |
Het |
Gnai3 |
A |
T |
3: 108,030,990 (GRCm39) |
H57Q |
|
Het |
Golga3 |
G |
T |
5: 110,333,757 (GRCm39) |
R131L |
probably benign |
Het |
Gpc6 |
A |
T |
14: 117,424,088 (GRCm39) |
I59F |
probably benign |
Het |
H2bc6 |
T |
C |
13: 23,769,753 (GRCm39) |
M63V |
possibly damaging |
Het |
Herc6 |
T |
C |
6: 57,596,604 (GRCm39) |
S515P |
probably damaging |
Het |
Ift74 |
T |
C |
4: 94,575,103 (GRCm39) |
I518T |
probably benign |
Het |
Kat6b |
T |
C |
14: 21,675,256 (GRCm39) |
S474P |
possibly damaging |
Het |
Klhl3 |
A |
C |
13: 58,248,212 (GRCm39) |
I28S |
unknown |
Het |
Klrh1 |
T |
A |
6: 129,743,697 (GRCm39) |
I196F |
probably benign |
Het |
Lipi |
A |
G |
16: 75,359,159 (GRCm39) |
F259S |
probably damaging |
Het |
Lrrc8a |
T |
A |
2: 30,145,782 (GRCm39) |
S199T |
probably damaging |
Het |
Map2 |
T |
A |
1: 66,472,723 (GRCm39) |
C1709* |
probably null |
Het |
Mrgprf |
A |
G |
7: 144,861,503 (GRCm39) |
S22G |
probably benign |
Het |
Myo1e |
G |
T |
9: 70,274,983 (GRCm39) |
R712L |
probably benign |
Het |
Nras |
A |
T |
3: 102,967,658 (GRCm39) |
N85Y |
probably benign |
Het |
Or4a71 |
C |
T |
2: 89,358,337 (GRCm39) |
C139Y |
probably damaging |
Het |
Or5b3 |
A |
T |
19: 13,388,475 (GRCm39) |
I181F |
probably benign |
Het |
Or6ae1 |
A |
G |
7: 139,742,660 (GRCm39) |
S68P |
|
Het |
Or9q2 |
T |
C |
19: 13,772,780 (GRCm39) |
H65R |
probably damaging |
Het |
Pcp2 |
T |
A |
8: 3,674,638 (GRCm39) |
|
probably benign |
Het |
Pigv |
T |
C |
4: 133,392,079 (GRCm39) |
R364G |
probably benign |
Het |
Plekhh3 |
T |
A |
11: 101,061,625 (GRCm39) |
S30C |
probably damaging |
Het |
Poglut3 |
A |
G |
9: 53,295,530 (GRCm39) |
Y44C |
probably damaging |
Het |
Pramel11 |
A |
C |
4: 143,623,334 (GRCm39) |
V280G |
possibly damaging |
Het |
Pramel51 |
C |
T |
12: 88,144,055 (GRCm39) |
A261T |
possibly damaging |
Het |
Rhof |
T |
C |
5: 123,258,571 (GRCm39) |
|
probably benign |
Het |
Rufy3 |
A |
T |
5: 88,780,336 (GRCm39) |
E361D |
|
Het |
Serpina1b |
T |
C |
12: 103,698,699 (GRCm39) |
D50G |
probably benign |
Het |
Sgsm2 |
G |
A |
11: 74,756,222 (GRCm39) |
Q376* |
probably null |
Het |
Slc18b1 |
A |
T |
10: 23,692,262 (GRCm39) |
I246F |
probably damaging |
Het |
Slc38a9 |
A |
T |
13: 112,850,777 (GRCm39) |
N387I |
probably damaging |
Het |
Synrg |
C |
G |
11: 83,862,409 (GRCm39) |
P35A |
probably damaging |
Het |
Tdrp |
T |
C |
8: 14,005,796 (GRCm39) |
K42E |
probably damaging |
Het |
Trappc10 |
A |
C |
10: 78,029,201 (GRCm39) |
M1112R |
probably damaging |
Het |
Ube2e1 |
A |
G |
14: 18,285,203 (GRCm38) |
V90A |
probably damaging |
Het |
Vwde |
C |
A |
6: 13,205,051 (GRCm39) |
V277F |
possibly damaging |
Het |
Zfyve16 |
A |
G |
13: 92,659,563 (GRCm39) |
M116T |
possibly damaging |
Het |
|
Other mutations in Afp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03261:Afp
|
APN |
5 |
90,639,610 (GRCm39) |
critical splice donor site |
probably null |
|
R0018:Afp
|
UTSW |
5 |
90,654,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R0387:Afp
|
UTSW |
5 |
90,645,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R0529:Afp
|
UTSW |
5 |
90,652,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R1401:Afp
|
UTSW |
5 |
90,649,486 (GRCm39) |
splice site |
probably benign |
|
R1471:Afp
|
UTSW |
5 |
90,651,541 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1666:Afp
|
UTSW |
5 |
90,652,927 (GRCm39) |
missense |
probably damaging |
0.99 |
R1800:Afp
|
UTSW |
5 |
90,638,655 (GRCm39) |
missense |
probably benign |
0.00 |
R2138:Afp
|
UTSW |
5 |
90,647,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R2248:Afp
|
UTSW |
5 |
90,649,429 (GRCm39) |
missense |
probably damaging |
0.99 |
R4324:Afp
|
UTSW |
5 |
90,655,764 (GRCm39) |
missense |
probably benign |
0.00 |
R4555:Afp
|
UTSW |
5 |
90,654,546 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5035:Afp
|
UTSW |
5 |
90,655,764 (GRCm39) |
missense |
probably benign |
0.00 |
R5241:Afp
|
UTSW |
5 |
90,649,473 (GRCm39) |
missense |
probably benign |
0.37 |
R5925:Afp
|
UTSW |
5 |
90,645,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R6220:Afp
|
UTSW |
5 |
90,652,269 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6719:Afp
|
UTSW |
5 |
90,651,562 (GRCm39) |
missense |
probably benign |
0.01 |
R8211:Afp
|
UTSW |
5 |
90,649,345 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8496:Afp
|
UTSW |
5 |
90,639,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R8960:Afp
|
UTSW |
5 |
90,651,500 (GRCm39) |
missense |
probably benign |
0.12 |
R9326:Afp
|
UTSW |
5 |
90,652,205 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Afp
|
UTSW |
5 |
90,652,874 (GRCm39) |
missense |
possibly damaging |
0.54 |
|