Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110082I17Rik |
G |
A |
5: 139,364,073 (GRCm38) |
R74W |
probably damaging |
Het |
4933407L21Rik |
T |
G |
1: 85,931,274 (GRCm38) |
|
probably null |
Het |
Adcy8 |
A |
T |
15: 64,920,471 (GRCm38) |
I212N |
possibly damaging |
Het |
Cobll1 |
T |
C |
2: 65,098,457 (GRCm38) |
T879A |
probably damaging |
Het |
Copb2 |
T |
C |
9: 98,574,111 (GRCm38) |
S233P |
probably damaging |
Het |
Cpa5 |
T |
A |
6: 30,630,437 (GRCm38) |
M330K |
probably damaging |
Het |
Dgcr8 |
A |
T |
16: 18,280,443 (GRCm38) |
N361K |
probably benign |
Het |
Dmxl1 |
A |
G |
18: 49,846,586 (GRCm38) |
E96G |
probably benign |
Het |
Dock8 |
T |
A |
19: 25,130,397 (GRCm38) |
N830K |
probably benign |
Het |
Ephb1 |
C |
T |
9: 102,195,434 (GRCm38) |
D49N |
probably benign |
Het |
Fam19a1 |
G |
A |
6: 96,649,185 (GRCm38) |
R128Q |
probably damaging |
Het |
Fer1l6 |
A |
G |
15: 58,571,389 (GRCm38) |
I514V |
probably benign |
Het |
Fpr1 |
A |
G |
17: 17,877,082 (GRCm38) |
I215T |
probably benign |
Het |
Hectd4 |
G |
A |
5: 121,353,502 (GRCm38) |
V3668M |
possibly damaging |
Het |
Ighv3-4 |
T |
A |
12: 114,253,768 (GRCm38) |
I68L |
probably benign |
Het |
Intu |
A |
G |
3: 40,692,972 (GRCm38) |
|
probably null |
Het |
Kel |
C |
T |
6: 41,699,027 (GRCm38) |
G243E |
probably damaging |
Het |
Mycbp2 |
A |
C |
14: 103,156,453 (GRCm38) |
S2781A |
possibly damaging |
Het |
Myom2 |
T |
A |
8: 15,122,705 (GRCm38) |
S1211T |
probably benign |
Het |
Nrp1 |
A |
T |
8: 128,468,448 (GRCm38) |
I462F |
probably benign |
Het |
Olfr787 |
T |
A |
10: 129,463,438 (GRCm38) |
I254N |
probably damaging |
Het |
Olfr958 |
T |
C |
9: 39,550,691 (GRCm38) |
Y60C |
probably damaging |
Het |
Pcsk1 |
A |
C |
13: 75,131,960 (GRCm38) |
S635R |
probably benign |
Het |
Pms1 |
A |
T |
1: 53,207,702 (GRCm38) |
Y280* |
probably null |
Het |
Rsf1 |
CGGCGGCGG |
CGGCGGCGGGGGCGGCGG |
7: 97,579,920 (GRCm38) |
|
probably benign |
Het |
Sema3b |
C |
A |
9: 107,601,429 (GRCm38) |
A356S |
probably damaging |
Het |
Shoc2 |
C |
A |
19: 54,029,892 (GRCm38) |
T485K |
probably benign |
Het |
Slc7a7 |
G |
A |
14: 54,377,835 (GRCm38) |
S235L |
possibly damaging |
Het |
Smcr8 |
A |
T |
11: 60,784,151 (GRCm38) |
T918S |
probably benign |
Het |
Tle3 |
C |
A |
9: 61,414,851 (GRCm38) |
F719L |
probably damaging |
Het |
Vmn2r57 |
A |
T |
7: 41,448,471 (GRCm38) |
H57Q |
possibly damaging |
Het |
|
Other mutations in Vmn2r45 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01287:Vmn2r45
|
APN |
7 |
8,485,623 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01322:Vmn2r45
|
APN |
7 |
8,481,333 (GRCm38) |
missense |
possibly damaging |
0.49 |
IGL01402:Vmn2r45
|
APN |
7 |
8,481,468 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01404:Vmn2r45
|
APN |
7 |
8,481,468 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01529:Vmn2r45
|
APN |
7 |
8,483,494 (GRCm38) |
missense |
probably benign |
|
IGL01596:Vmn2r45
|
APN |
7 |
8,483,273 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01646:Vmn2r45
|
APN |
7 |
8,483,338 (GRCm38) |
missense |
probably benign |
0.18 |
IGL01819:Vmn2r45
|
APN |
7 |
8,485,557 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02096:Vmn2r45
|
APN |
7 |
8,481,444 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02130:Vmn2r45
|
APN |
7 |
8,483,557 (GRCm38) |
missense |
possibly damaging |
0.46 |
IGL02409:Vmn2r45
|
APN |
7 |
8,485,728 (GRCm38) |
missense |
probably benign |
0.03 |
IGL02517:Vmn2r45
|
APN |
7 |
8,483,186 (GRCm38) |
nonsense |
probably null |
|
IGL02633:Vmn2r45
|
APN |
7 |
8,485,729 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02940:Vmn2r45
|
APN |
7 |
8,472,370 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL03281:Vmn2r45
|
APN |
7 |
8,483,604 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03358:Vmn2r45
|
APN |
7 |
8,471,716 (GRCm38) |
missense |
probably damaging |
1.00 |
BB004:Vmn2r45
|
UTSW |
7 |
8,483,514 (GRCm38) |
missense |
probably benign |
|
BB014:Vmn2r45
|
UTSW |
7 |
8,483,514 (GRCm38) |
missense |
probably benign |
|
R0382:Vmn2r45
|
UTSW |
7 |
8,483,099 (GRCm38) |
missense |
probably benign |
0.06 |
R0532:Vmn2r45
|
UTSW |
7 |
8,471,821 (GRCm38) |
missense |
probably damaging |
0.99 |
R0932:Vmn2r45
|
UTSW |
7 |
8,475,381 (GRCm38) |
missense |
probably damaging |
1.00 |
R1125:Vmn2r45
|
UTSW |
7 |
8,485,543 (GRCm38) |
missense |
probably benign |
0.00 |
R1580:Vmn2r45
|
UTSW |
7 |
8,471,747 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1817:Vmn2r45
|
UTSW |
7 |
8,472,373 (GRCm38) |
missense |
probably damaging |
1.00 |
R1996:Vmn2r45
|
UTSW |
7 |
8,472,025 (GRCm38) |
missense |
probably damaging |
1.00 |
R2050:Vmn2r45
|
UTSW |
7 |
8,472,022 (GRCm38) |
missense |
probably damaging |
1.00 |
R2284:Vmn2r45
|
UTSW |
7 |
8,485,766 (GRCm38) |
missense |
probably benign |
0.02 |
R4019:Vmn2r45
|
UTSW |
7 |
8,471,581 (GRCm38) |
nonsense |
probably null |
|
R4227:Vmn2r45
|
UTSW |
7 |
8,483,278 (GRCm38) |
missense |
probably damaging |
0.98 |
R4381:Vmn2r45
|
UTSW |
7 |
8,471,913 (GRCm38) |
nonsense |
probably null |
|
R4618:Vmn2r45
|
UTSW |
7 |
8,483,437 (GRCm38) |
missense |
probably benign |
0.00 |
R4624:Vmn2r45
|
UTSW |
7 |
8,481,342 (GRCm38) |
missense |
probably damaging |
1.00 |
R4704:Vmn2r45
|
UTSW |
7 |
8,483,536 (GRCm38) |
nonsense |
probably null |
|
R4735:Vmn2r45
|
UTSW |
7 |
8,483,473 (GRCm38) |
missense |
probably damaging |
1.00 |
R4868:Vmn2r45
|
UTSW |
7 |
8,481,481 (GRCm38) |
missense |
probably benign |
0.06 |
R4983:Vmn2r45
|
UTSW |
7 |
8,483,117 (GRCm38) |
missense |
probably damaging |
0.99 |
R5246:Vmn2r45
|
UTSW |
7 |
8,483,252 (GRCm38) |
missense |
probably benign |
0.00 |
R5430:Vmn2r45
|
UTSW |
7 |
8,483,334 (GRCm38) |
nonsense |
probably null |
|
R5504:Vmn2r45
|
UTSW |
7 |
8,483,177 (GRCm38) |
missense |
probably benign |
0.03 |
R5511:Vmn2r45
|
UTSW |
7 |
8,471,833 (GRCm38) |
missense |
probably benign |
0.19 |
R5814:Vmn2r45
|
UTSW |
7 |
8,471,476 (GRCm38) |
missense |
probably benign |
0.00 |
R6223:Vmn2r45
|
UTSW |
7 |
8,483,302 (GRCm38) |
missense |
probably benign |
|
R6267:Vmn2r45
|
UTSW |
7 |
8,472,208 (GRCm38) |
missense |
probably benign |
0.26 |
R6623:Vmn2r45
|
UTSW |
7 |
8,471,501 (GRCm38) |
missense |
probably benign |
0.09 |
R6999:Vmn2r45
|
UTSW |
7 |
8,483,220 (GRCm38) |
missense |
probably benign |
|
R7242:Vmn2r45
|
UTSW |
7 |
8,485,613 (GRCm38) |
nonsense |
probably null |
|
R7491:Vmn2r45
|
UTSW |
7 |
8,481,343 (GRCm38) |
missense |
probably benign |
0.27 |
R7620:Vmn2r45
|
UTSW |
7 |
8,483,223 (GRCm38) |
nonsense |
probably null |
|
R7719:Vmn2r45
|
UTSW |
7 |
8,483,461 (GRCm38) |
missense |
probably damaging |
0.99 |
R7720:Vmn2r45
|
UTSW |
7 |
8,483,461 (GRCm38) |
missense |
probably damaging |
0.99 |
R7853:Vmn2r45
|
UTSW |
7 |
8,482,988 (GRCm38) |
missense |
possibly damaging |
0.90 |
R7873:Vmn2r45
|
UTSW |
7 |
8,483,075 (GRCm38) |
missense |
probably benign |
0.00 |
R7882:Vmn2r45
|
UTSW |
7 |
8,483,410 (GRCm38) |
missense |
possibly damaging |
0.82 |
R7927:Vmn2r45
|
UTSW |
7 |
8,483,514 (GRCm38) |
missense |
probably benign |
|
R8684:Vmn2r45
|
UTSW |
7 |
8,483,512 (GRCm38) |
missense |
probably damaging |
0.99 |
R8780:Vmn2r45
|
UTSW |
7 |
8,481,372 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8811:Vmn2r45
|
UTSW |
7 |
8,471,882 (GRCm38) |
missense |
probably damaging |
1.00 |
R8893:Vmn2r45
|
UTSW |
7 |
8,485,620 (GRCm38) |
missense |
probably damaging |
1.00 |
R9043:Vmn2r45
|
UTSW |
7 |
8,471,905 (GRCm38) |
missense |
possibly damaging |
0.92 |
R9208:Vmn2r45
|
UTSW |
7 |
8,483,299 (GRCm38) |
missense |
probably damaging |
1.00 |
R9327:Vmn2r45
|
UTSW |
7 |
8,471,533 (GRCm38) |
missense |
probably damaging |
1.00 |
R9586:Vmn2r45
|
UTSW |
7 |
8,483,051 (GRCm38) |
missense |
probably benign |
0.01 |
R9599:Vmn2r45
|
UTSW |
7 |
8,475,458 (GRCm38) |
critical splice acceptor site |
probably null |
|
U24488:Vmn2r45
|
UTSW |
7 |
8,472,362 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1088:Vmn2r45
|
UTSW |
7 |
8,471,485 (GRCm38) |
missense |
probably benign |
0.16 |
|