Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
A |
G |
17: 24,328,632 (GRCm38) |
V256A |
probably benign |
Het |
Acap1 |
T |
C |
11: 69,889,491 (GRCm38) |
N42S |
possibly damaging |
Het |
Apoo-ps |
C |
A |
13: 107,414,640 (GRCm38) |
|
noncoding transcript |
Het |
Bri3 |
C |
T |
5: 144,244,601 (GRCm38) |
T39I |
probably benign |
Het |
Bsn |
A |
G |
9: 108,106,920 (GRCm38) |
S3312P |
unknown |
Het |
Camkmt |
C |
A |
17: 85,090,775 (GRCm38) |
A17E |
possibly damaging |
Het |
Cc2d2a |
G |
T |
5: 43,671,305 (GRCm38) |
|
probably null |
Het |
Ccdc122 |
G |
T |
14: 77,091,958 (GRCm38) |
M150I |
possibly damaging |
Het |
Celf4 |
A |
G |
18: 25,753,459 (GRCm38) |
F57L |
probably damaging |
Het |
Cep192 |
T |
A |
18: 67,824,688 (GRCm38) |
F564Y |
possibly damaging |
Het |
Ces1c |
T |
C |
8: 93,123,212 (GRCm38) |
D38G |
probably damaging |
Het |
Cts7 |
C |
A |
13: 61,355,617 (GRCm38) |
G178* |
probably null |
Het |
Dcc |
A |
T |
18: 71,456,883 (GRCm38) |
Y681N |
probably damaging |
Het |
Dhx29 |
A |
G |
13: 112,946,974 (GRCm38) |
E521G |
possibly damaging |
Het |
Dnase2a |
T |
C |
8: 84,908,993 (GRCm38) |
V35A |
probably damaging |
Het |
Eif3l |
A |
G |
15: 79,085,607 (GRCm38) |
M268V |
probably damaging |
Het |
Foxc1 |
A |
G |
13: 31,808,798 (GRCm38) |
M531V |
unknown |
Het |
Grin2c |
A |
G |
11: 115,251,134 (GRCm38) |
Y820H |
probably damaging |
Het |
Ifit1bl1 |
G |
A |
19: 34,594,889 (GRCm38) |
A56V |
probably benign |
Het |
Iqsec1 |
T |
C |
6: 90,689,883 (GRCm38) |
E524G |
possibly damaging |
Het |
Kcnt2 |
A |
G |
1: 140,376,353 (GRCm38) |
I154V |
possibly damaging |
Het |
Kdm1b |
T |
A |
13: 47,062,975 (GRCm38) |
Y274N |
probably benign |
Het |
Kntc1 |
T |
A |
5: 123,810,859 (GRCm38) |
L1889Q |
probably damaging |
Het |
Lama1 |
A |
G |
17: 67,768,317 (GRCm38) |
T1010A |
probably benign |
Het |
Mmp11 |
T |
C |
10: 75,927,245 (GRCm38) |
N171S |
probably benign |
Het |
Myom1 |
A |
G |
17: 71,110,735 (GRCm38) |
E1409G |
probably damaging |
Het |
N4bp1 |
A |
G |
8: 86,862,040 (GRCm38) |
I90T |
probably damaging |
Het |
Olfr1263 |
T |
C |
2: 90,015,341 (GRCm38) |
V137A |
probably benign |
Het |
Plcb4 |
T |
C |
2: 135,950,382 (GRCm38) |
S342P |
probably damaging |
Het |
Plg |
A |
G |
17: 12,410,960 (GRCm38) |
E627G |
probably benign |
Het |
Rsf1 |
CG |
CGACGGCGGAG |
7: 97,579,908 (GRCm38) |
|
probably benign |
Het |
Sla2 |
G |
A |
2: 156,875,942 (GRCm38) |
R137C |
probably damaging |
Het |
Slc7a14 |
A |
G |
3: 31,230,320 (GRCm38) |
I289T |
probably damaging |
Het |
Srpr |
G |
A |
9: 35,212,001 (GRCm38) |
G43S |
possibly damaging |
Het |
Tbc1d9 |
T |
C |
8: 83,166,076 (GRCm38) |
M1T |
probably null |
Het |
Tcte2 |
A |
T |
17: 13,714,077 (GRCm38) |
I90N |
possibly damaging |
Het |
Trim30c |
G |
A |
7: 104,382,274 (GRCm38) |
P445S |
probably damaging |
Het |
Trrap |
A |
G |
5: 144,817,966 (GRCm38) |
Q1984R |
probably damaging |
Het |
Ubn2 |
T |
C |
6: 38,491,005 (GRCm38) |
S885P |
probably benign |
Het |
Unc45a |
A |
G |
7: 80,339,669 (GRCm38) |
F17S |
probably damaging |
Het |
Uts2b |
C |
T |
16: 27,361,032 (GRCm38) |
V75I |
probably benign |
Het |
Vmn2r82 |
A |
G |
10: 79,385,376 (GRCm38) |
S524G |
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 |
IGL02668:Vmn2r103
|
APN |
17 |
19,794,127 (GRCm38) |
missense |
probably benign |
0.03 |
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 |
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 |
|