Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
A |
6: 121,625,125 (GRCm39) |
F501Y |
probably damaging |
Het |
Alk |
T |
C |
17: 72,204,906 (GRCm39) |
T1089A |
probably benign |
Het |
Ankrd12 |
G |
T |
17: 66,291,000 (GRCm39) |
P1478T |
probably benign |
Het |
Arhgap39 |
A |
G |
15: 76,636,088 (GRCm39) |
V49A |
probably benign |
Het |
Arid4b |
T |
C |
13: 14,307,069 (GRCm39) |
L108P |
probably damaging |
Het |
Atrn |
T |
A |
2: 130,836,127 (GRCm39) |
C1136S |
probably damaging |
Het |
Cacna1s |
T |
A |
1: 136,012,007 (GRCm39) |
M483K |
probably damaging |
Het |
Cacng1 |
C |
A |
11: 107,607,118 (GRCm39) |
V34L |
probably benign |
Het |
Casp8 |
T |
C |
1: 58,883,970 (GRCm39) |
S446P |
probably damaging |
Het |
Cngb3 |
G |
A |
4: 19,461,679 (GRCm39) |
C520Y |
probably damaging |
Het |
Crim1 |
C |
T |
17: 78,588,668 (GRCm39) |
|
probably benign |
Het |
F11 |
A |
G |
8: 45,701,675 (GRCm39) |
S353P |
probably damaging |
Het |
Fbxl17 |
G |
A |
17: 63,806,802 (GRCm39) |
P71S |
possibly damaging |
Het |
Fn1 |
C |
T |
1: 71,647,072 (GRCm39) |
G1482R |
probably damaging |
Het |
Gbp3 |
C |
T |
3: 142,272,099 (GRCm39) |
|
probably benign |
Het |
Golga4 |
A |
G |
9: 118,387,804 (GRCm39) |
D1642G |
possibly damaging |
Het |
Hspa1a |
C |
T |
17: 35,190,703 (GRCm39) |
V67M |
probably damaging |
Het |
Hyls1 |
T |
C |
9: 35,472,705 (GRCm39) |
D237G |
probably damaging |
Het |
Kmt2e |
A |
G |
5: 23,706,624 (GRCm39) |
N1396D |
probably benign |
Het |
Lasp1 |
G |
A |
11: 97,690,653 (GRCm39) |
V12M |
probably damaging |
Het |
Muc4 |
G |
C |
16: 32,753,919 (GRCm38) |
R1265P |
probably benign |
Het |
Muc5b |
C |
T |
7: 141,403,235 (GRCm39) |
T732M |
unknown |
Het |
Mxd1 |
G |
T |
6: 86,627,942 (GRCm39) |
Q199K |
probably benign |
Het |
Or14a258 |
T |
A |
7: 86,035,182 (GRCm39) |
T229S |
probably benign |
Het |
Or4a78 |
T |
C |
2: 89,497,357 (GRCm39) |
E291G |
probably damaging |
Het |
Or5w18 |
T |
A |
2: 87,633,031 (GRCm39) |
F95L |
probably benign |
Het |
Or5w20 |
T |
A |
2: 87,727,293 (GRCm39) |
|
probably null |
Het |
Prps1l1 |
A |
T |
12: 35,035,797 (GRCm39) |
H304L |
possibly damaging |
Het |
Psmd2 |
A |
G |
16: 20,474,392 (GRCm39) |
D316G |
probably benign |
Het |
Rlf |
G |
A |
4: 121,006,229 (GRCm39) |
T917I |
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,466,953 (GRCm39) |
D4704G |
probably damaging |
Het |
Scn1a |
T |
A |
2: 66,104,332 (GRCm39) |
I1643F |
probably damaging |
Het |
Zfc3h1 |
T |
C |
10: 115,255,806 (GRCm39) |
F1486L |
probably benign |
Het |
|
Other mutations in Vmn2r38 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02805:Vmn2r38
|
APN |
7 |
9,078,546 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03199:Vmn2r38
|
APN |
7 |
9,078,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R1619:Vmn2r38
|
UTSW |
7 |
9,078,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R3154:Vmn2r38
|
UTSW |
7 |
9,097,689 (GRCm39) |
missense |
probably benign |
0.03 |
R4302:Vmn2r38
|
UTSW |
7 |
9,100,562 (GRCm39) |
splice site |
probably null |
|
R5106:Vmn2r38
|
UTSW |
7 |
9,078,169 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5187:Vmn2r38
|
UTSW |
7 |
9,100,571 (GRCm39) |
missense |
probably benign |
0.03 |
R5575:Vmn2r38
|
UTSW |
7 |
9,078,635 (GRCm39) |
nonsense |
probably null |
|
R5653:Vmn2r38
|
UTSW |
7 |
9,100,764 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R6156:Vmn2r38
|
UTSW |
7 |
9,097,611 (GRCm39) |
missense |
probably damaging |
0.99 |
R6970:Vmn2r38
|
UTSW |
7 |
9,078,340 (GRCm39) |
nonsense |
probably null |
|
R7107:Vmn2r38
|
UTSW |
7 |
9,093,728 (GRCm39) |
missense |
probably benign |
0.00 |
R7231:Vmn2r38
|
UTSW |
7 |
9,100,637 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7419:Vmn2r38
|
UTSW |
7 |
9,078,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R7963:Vmn2r38
|
UTSW |
7 |
9,095,854 (GRCm39) |
missense |
probably benign |
0.17 |
R8788:Vmn2r38
|
UTSW |
7 |
9,078,482 (GRCm39) |
missense |
probably benign |
0.02 |
R9639:Vmn2r38
|
UTSW |
7 |
9,078,063 (GRCm39) |
missense |
probably damaging |
0.96 |
R9773:Vmn2r38
|
UTSW |
7 |
9,097,806 (GRCm39) |
missense |
probably damaging |
1.00 |
|