Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9030612E09Rik |
T |
C |
10: 43,050,769 (GRCm39) |
L21P |
probably damaging |
Het |
Ank3 |
C |
T |
10: 69,728,240 (GRCm39) |
A642V |
probably damaging |
Het |
Bap1 |
A |
G |
14: 30,978,182 (GRCm39) |
N349S |
probably benign |
Het |
Brca1 |
G |
T |
11: 101,415,591 (GRCm39) |
Q32K |
probably damaging |
Het |
Ccdc39 |
A |
T |
3: 33,892,108 (GRCm39) |
N121K |
probably benign |
Het |
Champ1 |
A |
T |
8: 13,930,002 (GRCm39) |
N720I |
probably damaging |
Het |
Chd3 |
T |
A |
11: 69,252,886 (GRCm39) |
R216* |
probably null |
Het |
D630003M21Rik |
A |
G |
2: 158,047,619 (GRCm39) |
|
probably null |
Het |
Exoc2 |
A |
T |
13: 31,010,047 (GRCm39) |
V804E |
possibly damaging |
Het |
Fcgbp |
A |
G |
7: 27,791,343 (GRCm39) |
N868S |
probably benign |
Het |
Gm10376 |
T |
C |
14: 42,873,025 (GRCm39) |
M1V |
probably null |
Het |
Gpc2 |
G |
A |
5: 138,275,533 (GRCm39) |
|
probably null |
Het |
Gpr37 |
G |
A |
6: 25,688,812 (GRCm39) |
T95I |
probably benign |
Het |
Ints3 |
G |
A |
3: 90,299,431 (GRCm39) |
|
probably benign |
Het |
Krt28 |
T |
C |
11: 99,257,839 (GRCm39) |
E334G |
probably damaging |
Het |
Lrrc75a |
T |
A |
11: 62,496,921 (GRCm39) |
T214S |
probably damaging |
Het |
Lyar |
A |
G |
5: 38,385,202 (GRCm39) |
I81V |
probably benign |
Het |
Mon2 |
A |
T |
10: 122,871,998 (GRCm39) |
L342Q |
probably damaging |
Het |
Mug2 |
C |
T |
6: 122,024,401 (GRCm39) |
A491V |
probably damaging |
Het |
Myh2 |
A |
G |
11: 67,077,438 (GRCm39) |
T858A |
probably benign |
Het |
Net1 |
C |
T |
13: 3,936,074 (GRCm39) |
|
probably null |
Het |
Or52s1 |
T |
A |
7: 102,861,111 (GRCm39) |
Y4N |
probably benign |
Het |
Or5p76 |
T |
C |
7: 108,122,423 (GRCm39) |
T245A |
probably benign |
Het |
Platr25 |
A |
T |
13: 62,821,623 (GRCm39) |
I110N |
possibly damaging |
Het |
Plk5 |
T |
A |
10: 80,198,879 (GRCm39) |
L412H |
probably damaging |
Het |
Rasal1 |
A |
T |
5: 120,812,790 (GRCm39) |
T605S |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,683,707 (GRCm39) |
D3119V |
probably damaging |
Het |
Serpina1a |
G |
T |
12: 103,820,017 (GRCm39) |
H387N |
probably benign |
Het |
Serpina1d |
G |
T |
12: 103,733,811 (GRCm39) |
N164K |
probably damaging |
Het |
Smurf1 |
A |
G |
5: 144,836,307 (GRCm39) |
Y69H |
probably damaging |
Het |
Sod2 |
A |
G |
17: 13,227,250 (GRCm39) |
K68R |
probably benign |
Het |
Ssbp2 |
A |
G |
13: 91,687,470 (GRCm39) |
N51S |
possibly damaging |
Het |
Tcl1b1 |
A |
G |
12: 105,130,663 (GRCm39) |
R49G |
probably benign |
Het |
Tgfb1 |
A |
G |
7: 25,396,350 (GRCm39) |
I214M |
probably benign |
Het |
Tln1 |
A |
G |
4: 43,547,525 (GRCm39) |
I812T |
probably damaging |
Het |
Topaz1 |
T |
A |
9: 122,577,419 (GRCm39) |
C110S |
possibly damaging |
Het |
Ubap2l |
A |
G |
3: 89,930,867 (GRCm39) |
F393L |
probably damaging |
Het |
Wdr24 |
C |
A |
17: 26,046,899 (GRCm39) |
Q651K |
probably damaging |
Het |
Wdr7 |
A |
G |
18: 63,911,322 (GRCm39) |
T905A |
possibly damaging |
Het |
Zfyve26 |
A |
G |
12: 79,285,109 (GRCm39) |
F2382S |
probably damaging |
Het |
|
Other mutations in Vmn1r62 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01337:Vmn1r62
|
APN |
7 |
5,679,144 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01650:Vmn1r62
|
APN |
7 |
5,679,024 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02892:Vmn1r62
|
APN |
7 |
5,679,202 (GRCm39) |
missense |
probably benign |
|
IGL02970:Vmn1r62
|
APN |
7 |
5,678,567 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03282:Vmn1r62
|
APN |
7 |
5,678,547 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0470:Vmn1r62
|
UTSW |
7 |
5,679,066 (GRCm39) |
nonsense |
probably null |
|
R1416:Vmn1r62
|
UTSW |
7 |
5,678,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R2149:Vmn1r62
|
UTSW |
7 |
5,678,358 (GRCm39) |
missense |
probably benign |
0.18 |
R4093:Vmn1r62
|
UTSW |
7 |
5,678,943 (GRCm39) |
missense |
probably damaging |
0.96 |
R4596:Vmn1r62
|
UTSW |
7 |
5,678,306 (GRCm39) |
start gained |
probably benign |
|
R4809:Vmn1r62
|
UTSW |
7 |
5,678,866 (GRCm39) |
missense |
probably benign |
0.41 |
R5669:Vmn1r62
|
UTSW |
7 |
5,678,736 (GRCm39) |
nonsense |
probably null |
|
R6262:Vmn1r62
|
UTSW |
7 |
5,678,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R6312:Vmn1r62
|
UTSW |
7 |
5,679,083 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7624:Vmn1r62
|
UTSW |
7 |
5,678,600 (GRCm39) |
missense |
probably benign |
0.01 |
R7710:Vmn1r62
|
UTSW |
7 |
5,678,182 (GRCm39) |
start gained |
probably benign |
|
R7896:Vmn1r62
|
UTSW |
7 |
5,678,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R8117:Vmn1r62
|
UTSW |
7 |
5,678,726 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8673:Vmn1r62
|
UTSW |
7 |
5,678,277 (GRCm39) |
start gained |
probably benign |
|
R8714:Vmn1r62
|
UTSW |
7 |
5,678,629 (GRCm39) |
nonsense |
probably null |
|
R8962:Vmn1r62
|
UTSW |
7 |
5,678,601 (GRCm39) |
missense |
probably damaging |
0.99 |
R9133:Vmn1r62
|
UTSW |
7 |
5,679,062 (GRCm39) |
missense |
probably benign |
0.01 |
R9246:Vmn1r62
|
UTSW |
7 |
5,678,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R9360:Vmn1r62
|
UTSW |
7 |
5,678,952 (GRCm39) |
missense |
probably damaging |
0.99 |
RF007:Vmn1r62
|
UTSW |
7 |
5,678,669 (GRCm39) |
missense |
probably benign |
0.00 |
|