Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930596D02Rik |
A |
G |
14: 35,810,117 (GRCm38) |
M167T |
probably benign |
Het |
Abcc4 |
G |
T |
14: 118,611,475 (GRCm38) |
S488R |
probably damaging |
Het |
Adprm |
G |
T |
11: 67,040,247 (GRCm38) |
D230E |
possibly damaging |
Het |
Atp2a3 |
C |
A |
11: 72,975,339 (GRCm38) |
H262N |
probably benign |
Het |
Casc1 |
G |
T |
6: 145,205,257 (GRCm38) |
R30S |
unknown |
Het |
Ccdc66 |
T |
C |
14: 27,497,341 (GRCm38) |
K309E |
possibly damaging |
Het |
Cyb561d2 |
C |
T |
9: 107,540,172 (GRCm38) |
A127T |
probably benign |
Het |
Dctn1 |
T |
A |
6: 83,191,048 (GRCm38) |
M357K |
possibly damaging |
Het |
Diras2 |
T |
C |
13: 52,507,770 (GRCm38) |
N167S |
probably benign |
Het |
Dmgdh |
T |
G |
13: 93,703,910 (GRCm38) |
V283G |
probably damaging |
Het |
Dmxl2 |
A |
T |
9: 54,416,945 (GRCm38) |
W1052R |
probably damaging |
Het |
Dnah6 |
A |
T |
6: 73,121,823 (GRCm38) |
V2083D |
possibly damaging |
Het |
Exoc4 |
T |
G |
6: 33,921,532 (GRCm38) |
F895L |
probably benign |
Het |
Fsip1 |
G |
T |
2: 118,251,725 (GRCm38) |
A76E |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,998,318 (GRCm38) |
I6820V |
probably benign |
Het |
Hdac10 |
G |
A |
15: 89,125,644 (GRCm38) |
P395L |
probably benign |
Het |
Ing3 |
A |
G |
6: 21,950,059 (GRCm38) |
D17G |
probably damaging |
Het |
Map3k4 |
A |
T |
17: 12,235,953 (GRCm38) |
F1383L |
possibly damaging |
Het |
Mpp6 |
C |
T |
6: 50,194,529 (GRCm38) |
T386I |
probably damaging |
Het |
Myct1 |
C |
A |
10: 5,604,513 (GRCm38) |
P127T |
probably damaging |
Het |
Olfr593 |
A |
T |
7: 103,212,735 (GRCm38) |
I281F |
possibly damaging |
Het |
Osbpl7 |
G |
T |
11: 97,067,205 (GRCm38) |
A625S |
possibly damaging |
Het |
Padi2 |
C |
T |
4: 140,949,880 (GRCm38) |
R660C |
probably benign |
Het |
Paip1 |
A |
T |
13: 119,438,071 (GRCm38) |
I185F |
probably damaging |
Het |
Phykpl |
G |
A |
11: 51,593,687 (GRCm38) |
|
probably null |
Het |
Plekhg6 |
G |
A |
6: 125,372,803 (GRCm38) |
|
probably benign |
Het |
Plxna1 |
A |
T |
6: 89,357,269 (GRCm38) |
L126* |
probably null |
Het |
Rchy1 |
A |
T |
5: 91,962,718 (GRCm38) |
M1K |
probably null |
Het |
Rfx3 |
T |
C |
19: 27,815,614 (GRCm38) |
|
probably benign |
Het |
Sdr9c7 |
T |
C |
10: 127,902,398 (GRCm38) |
F182L |
probably damaging |
Het |
Sgpl1 |
A |
C |
10: 61,105,450 (GRCm38) |
V294G |
probably damaging |
Het |
Sh2b1 |
A |
G |
7: 126,472,474 (GRCm38) |
S180P |
possibly damaging |
Het |
Sorbs1 |
T |
C |
19: 40,314,681 (GRCm38) |
D488G |
probably damaging |
Het |
Stab2 |
A |
G |
10: 86,846,163 (GRCm38) |
|
probably benign |
Het |
Sycp1 |
A |
C |
3: 102,820,531 (GRCm38) |
|
probably benign |
Het |
Tmem245 |
T |
C |
4: 56,925,081 (GRCm38) |
K347E |
possibly damaging |
Het |
Tnk1 |
A |
G |
11: 69,856,923 (GRCm38) |
M51T |
probably damaging |
Het |
Trpm2 |
C |
T |
10: 77,935,942 (GRCm38) |
R621H |
probably damaging |
Het |
Ubd |
G |
T |
17: 37,195,529 (GRCm38) |
R102L |
probably benign |
Het |
Uhrf1bp1 |
A |
C |
17: 27,886,575 (GRCm38) |
I692L |
possibly damaging |
Het |
Zfp324 |
T |
A |
7: 12,970,846 (GRCm38) |
C321S |
probably damaging |
Het |
Zfp488 |
G |
T |
14: 33,970,820 (GRCm38) |
Q129K |
probably benign |
Het |
Zmpste24 |
T |
A |
4: 121,061,100 (GRCm38) |
N442Y |
probably damaging |
Het |
|
Other mutations in Vmn2r103 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00333:Vmn2r103
|
APN |
17 |
19,793,102 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL00939:Vmn2r103
|
APN |
17 |
19,794,965 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01120:Vmn2r103
|
APN |
17 |
19,792,997 (GRCm38) |
missense |
probably benign |
0.06 |
IGL01403:Vmn2r103
|
APN |
17 |
19,792,967 (GRCm38) |
missense |
probably benign |
|
IGL01404:Vmn2r103
|
APN |
17 |
19,812,434 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01713:Vmn2r103
|
APN |
17 |
19,794,068 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01802:Vmn2r103
|
APN |
17 |
19,799,208 (GRCm38) |
missense |
probably benign |
|
IGL02251:Vmn2r103
|
APN |
17 |
19,793,969 (GRCm38) |
missense |
possibly damaging |
0.84 |
IGL02466:Vmn2r103
|
APN |
17 |
19,773,369 (GRCm38) |
missense |
probably benign |
|
IGL02555:Vmn2r103
|
APN |
17 |
19,811,611 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02715:Vmn2r103
|
APN |
17 |
19,793,956 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL02735:Vmn2r103
|
APN |
17 |
19,812,248 (GRCm38) |
missense |
probably benign |
0.27 |
IGL03101:Vmn2r103
|
APN |
17 |
19,773,520 (GRCm38) |
missense |
probably damaging |
0.98 |
R0003:Vmn2r103
|
UTSW |
17 |
19,811,979 (GRCm38) |
missense |
probably damaging |
0.99 |
R0052:Vmn2r103
|
UTSW |
17 |
19,811,641 (GRCm38) |
missense |
probably benign |
0.01 |
R0375:Vmn2r103
|
UTSW |
17 |
19,793,464 (GRCm38) |
missense |
probably benign |
0.12 |
R0375:Vmn2r103
|
UTSW |
17 |
19,792,859 (GRCm38) |
missense |
probably benign |
0.06 |
R0755:Vmn2r103
|
UTSW |
17 |
19,773,568 (GRCm38) |
missense |
probably benign |
0.01 |
R0837:Vmn2r103
|
UTSW |
17 |
19,793,927 (GRCm38) |
missense |
probably damaging |
0.99 |
R1345:Vmn2r103
|
UTSW |
17 |
19,794,247 (GRCm38) |
missense |
probably damaging |
1.00 |
R1396:Vmn2r103
|
UTSW |
17 |
19,792,968 (GRCm38) |
missense |
probably benign |
|
R1488:Vmn2r103
|
UTSW |
17 |
19,793,660 (GRCm38) |
missense |
probably damaging |
0.97 |
R1533:Vmn2r103
|
UTSW |
17 |
19,773,400 (GRCm38) |
missense |
probably benign |
0.01 |
R1590:Vmn2r103
|
UTSW |
17 |
19,794,234 (GRCm38) |
missense |
probably benign |
|
R1928:Vmn2r103
|
UTSW |
17 |
19,811,767 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1942:Vmn2r103
|
UTSW |
17 |
19,812,300 (GRCm38) |
missense |
probably benign |
0.02 |
R2071:Vmn2r103
|
UTSW |
17 |
19,793,794 (GRCm38) |
missense |
probably benign |
|
R2219:Vmn2r103
|
UTSW |
17 |
19,793,647 (GRCm38) |
missense |
probably damaging |
1.00 |
R2442:Vmn2r103
|
UTSW |
17 |
19,773,531 (GRCm38) |
missense |
probably benign |
0.00 |
R2889:Vmn2r103
|
UTSW |
17 |
19,793,600 (GRCm38) |
missense |
probably damaging |
1.00 |
R3762:Vmn2r103
|
UTSW |
17 |
19,812,149 (GRCm38) |
missense |
probably damaging |
0.98 |
R4014:Vmn2r103
|
UTSW |
17 |
19,793,604 (GRCm38) |
missense |
possibly damaging |
0.67 |
R4331:Vmn2r103
|
UTSW |
17 |
19,794,233 (GRCm38) |
missense |
probably benign |
0.00 |
R4630:Vmn2r103
|
UTSW |
17 |
19,793,696 (GRCm38) |
missense |
probably benign |
0.04 |
R4631:Vmn2r103
|
UTSW |
17 |
19,793,696 (GRCm38) |
missense |
probably benign |
0.04 |
R4632:Vmn2r103
|
UTSW |
17 |
19,793,696 (GRCm38) |
missense |
probably benign |
0.04 |
R4660:Vmn2r103
|
UTSW |
17 |
19,811,815 (GRCm38) |
missense |
probably damaging |
1.00 |
R4801:Vmn2r103
|
UTSW |
17 |
19,795,076 (GRCm38) |
missense |
probably benign |
0.06 |
R4802:Vmn2r103
|
UTSW |
17 |
19,795,076 (GRCm38) |
missense |
probably benign |
0.06 |
R4931:Vmn2r103
|
UTSW |
17 |
19,811,769 (GRCm38) |
missense |
probably benign |
0.01 |
R4995:Vmn2r103
|
UTSW |
17 |
19,773,511 (GRCm38) |
missense |
probably benign |
0.14 |
R5309:Vmn2r103
|
UTSW |
17 |
19,793,034 (GRCm38) |
missense |
probably benign |
0.01 |
R5312:Vmn2r103
|
UTSW |
17 |
19,793,034 (GRCm38) |
missense |
probably benign |
0.01 |
R5329:Vmn2r103
|
UTSW |
17 |
19,812,171 (GRCm38) |
missense |
probably damaging |
1.00 |
R5611:Vmn2r103
|
UTSW |
17 |
19,793,642 (GRCm38) |
missense |
probably damaging |
0.99 |
R5684:Vmn2r103
|
UTSW |
17 |
19,792,989 (GRCm38) |
missense |
probably benign |
0.02 |
R5715:Vmn2r103
|
UTSW |
17 |
19,794,939 (GRCm38) |
missense |
probably benign |
0.17 |
R5907:Vmn2r103
|
UTSW |
17 |
19,812,453 (GRCm38) |
missense |
possibly damaging |
0.67 |
R6029:Vmn2r103
|
UTSW |
17 |
19,794,216 (GRCm38) |
nonsense |
probably null |
|
R6114:Vmn2r103
|
UTSW |
17 |
19,812,325 (GRCm38) |
missense |
probably damaging |
0.99 |
R6285:Vmn2r103
|
UTSW |
17 |
19,812,144 (GRCm38) |
missense |
probably benign |
|
R6292:Vmn2r103
|
UTSW |
17 |
19,793,604 (GRCm38) |
missense |
possibly damaging |
0.67 |
R6334:Vmn2r103
|
UTSW |
17 |
19,794,082 (GRCm38) |
missense |
probably damaging |
0.97 |
R6501:Vmn2r103
|
UTSW |
17 |
19,811,904 (GRCm38) |
missense |
probably benign |
0.29 |
R6710:Vmn2r103
|
UTSW |
17 |
19,811,977 (GRCm38) |
missense |
probably damaging |
1.00 |
R6774:Vmn2r103
|
UTSW |
17 |
19,773,511 (GRCm38) |
missense |
probably benign |
0.14 |
R6981:Vmn2r103
|
UTSW |
17 |
19,793,477 (GRCm38) |
missense |
probably benign |
0.00 |
R7768:Vmn2r103
|
UTSW |
17 |
19,812,052 (GRCm38) |
missense |
probably damaging |
0.99 |
R7816:Vmn2r103
|
UTSW |
17 |
19,794,214 (GRCm38) |
missense |
probably benign |
0.06 |
R7885:Vmn2r103
|
UTSW |
17 |
19,793,123 (GRCm38) |
missense |
probably benign |
0.25 |
R8002:Vmn2r103
|
UTSW |
17 |
19,799,249 (GRCm38) |
missense |
probably damaging |
1.00 |
R8031:Vmn2r103
|
UTSW |
17 |
19,793,497 (GRCm38) |
missense |
probably benign |
0.00 |
R8140:Vmn2r103
|
UTSW |
17 |
19,811,796 (GRCm38) |
missense |
probably damaging |
1.00 |
R8186:Vmn2r103
|
UTSW |
17 |
19,811,943 (GRCm38) |
missense |
probably damaging |
1.00 |
R8559:Vmn2r103
|
UTSW |
17 |
19,812,384 (GRCm38) |
missense |
probably benign |
0.01 |
R9413:Vmn2r103
|
UTSW |
17 |
19,811,896 (GRCm38) |
missense |
possibly damaging |
0.54 |
R9591:Vmn2r103
|
UTSW |
17 |
19,811,659 (GRCm38) |
missense |
possibly damaging |
0.70 |
R9652:Vmn2r103
|
UTSW |
17 |
19,793,765 (GRCm38) |
missense |
probably benign |
0.01 |
R9680:Vmn2r103
|
UTSW |
17 |
19,799,263 (GRCm38) |
nonsense |
probably null |
|
R9743:Vmn2r103
|
UTSW |
17 |
19,812,213 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1088:Vmn2r103
|
UTSW |
17 |
19,795,047 (GRCm38) |
missense |
probably benign |
0.08 |
|