Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930486L24Rik |
A |
T |
13: 61,001,146 (GRCm39) |
|
probably benign |
Het |
6430548M08Rik |
G |
A |
8: 120,876,863 (GRCm39) |
R157H |
probably damaging |
Het |
Amer3 |
A |
G |
1: 34,627,206 (GRCm39) |
K482E |
probably damaging |
Het |
Ankrd11 |
A |
T |
8: 123,622,566 (GRCm39) |
S429T |
probably damaging |
Het |
Ano3 |
T |
A |
2: 110,569,157 (GRCm39) |
N125I |
probably damaging |
Het |
BC106179 |
T |
A |
16: 23,042,746 (GRCm39) |
|
probably benign |
Het |
Bclaf3 |
T |
C |
X: 158,338,524 (GRCm39) |
I457T |
possibly damaging |
Het |
Cd44 |
A |
G |
2: 102,662,826 (GRCm39) |
|
probably null |
Het |
Cd72 |
G |
A |
4: 43,448,332 (GRCm39) |
A316V |
probably benign |
Het |
Cdc27 |
A |
T |
11: 104,413,657 (GRCm39) |
|
probably benign |
Het |
Cdon |
A |
T |
9: 35,398,253 (GRCm39) |
Q990L |
probably damaging |
Het |
Clk2 |
T |
C |
3: 89,080,706 (GRCm39) |
W231R |
probably damaging |
Het |
Cpsf2 |
G |
A |
12: 101,965,825 (GRCm39) |
V597I |
probably benign |
Het |
D630003M21Rik |
A |
G |
2: 158,042,918 (GRCm39) |
V874A |
probably benign |
Het |
Daam2 |
A |
G |
17: 49,776,455 (GRCm39) |
F811L |
probably damaging |
Het |
Ddx54 |
T |
C |
5: 120,756,195 (GRCm39) |
|
probably benign |
Het |
Dysf |
T |
A |
6: 84,016,519 (GRCm39) |
L59Q |
probably damaging |
Het |
Eps8 |
A |
G |
6: 137,476,597 (GRCm39) |
Y601H |
probably damaging |
Het |
Faf2 |
T |
C |
13: 54,796,235 (GRCm39) |
Y131H |
probably damaging |
Het |
Hectd4 |
T |
A |
5: 121,445,067 (GRCm39) |
D101E |
possibly damaging |
Het |
Hk2 |
T |
C |
6: 82,737,139 (GRCm39) |
T30A |
possibly damaging |
Het |
Il27 |
A |
T |
7: 126,191,821 (GRCm39) |
L77Q |
probably damaging |
Het |
Klhdc1 |
T |
A |
12: 69,298,225 (GRCm39) |
V83D |
possibly damaging |
Het |
Manba |
T |
G |
3: 135,276,024 (GRCm39) |
S822A |
probably benign |
Het |
Mterf2 |
A |
C |
10: 84,956,195 (GRCm39) |
V143G |
probably damaging |
Het |
Ncapd3 |
A |
G |
9: 26,981,195 (GRCm39) |
D895G |
probably benign |
Het |
Or4c115 |
T |
A |
2: 88,927,801 (GRCm39) |
I157L |
probably benign |
Het |
Or6n1 |
T |
A |
1: 173,916,602 (GRCm39) |
|
probably benign |
Het |
Panx1 |
T |
C |
9: 14,919,101 (GRCm39) |
K253E |
probably benign |
Het |
Phc1 |
T |
A |
6: 122,300,748 (GRCm39) |
|
probably benign |
Het |
Pkd1l2 |
G |
A |
8: 117,792,484 (GRCm39) |
T436I |
probably benign |
Het |
Ptchd4 |
A |
G |
17: 42,688,208 (GRCm39) |
E250G |
probably damaging |
Het |
Rp1 |
G |
T |
1: 4,416,375 (GRCm39) |
S1579* |
probably null |
Het |
Rrp1 |
A |
G |
10: 78,245,056 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
A |
G |
2: 112,483,186 (GRCm39) |
L4187P |
possibly damaging |
Het |
Serpinc1 |
A |
T |
1: 160,827,561 (GRCm39) |
I387F |
probably damaging |
Het |
Slc2a7 |
G |
A |
4: 150,252,836 (GRCm39) |
C492Y |
probably benign |
Het |
Slf1 |
A |
G |
13: 77,274,478 (GRCm39) |
|
probably benign |
Het |
Spta1 |
T |
A |
1: 174,039,164 (GRCm39) |
L1169Q |
probably damaging |
Het |
Stap1 |
T |
A |
5: 86,219,824 (GRCm39) |
|
probably benign |
Het |
Taf6 |
A |
G |
5: 138,182,147 (GRCm39) |
L66P |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,632,841 (GRCm39) |
E14071G |
probably damaging |
Het |
Unk |
A |
G |
11: 115,947,125 (GRCm39) |
H586R |
possibly damaging |
Het |
Zfpm2 |
A |
C |
15: 40,966,662 (GRCm39) |
K917T |
probably damaging |
Het |
|
Other mutations in Cbr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01613:Cbr3
|
APN |
16 |
93,480,331 (GRCm39) |
missense |
probably benign |
0.00 |
R1764:Cbr3
|
UTSW |
16 |
93,487,370 (GRCm39) |
missense |
probably damaging |
0.98 |
R5154:Cbr3
|
UTSW |
16 |
93,482,027 (GRCm39) |
missense |
probably benign |
0.37 |
R5553:Cbr3
|
UTSW |
16 |
93,480,451 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5888:Cbr3
|
UTSW |
16 |
93,487,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R6644:Cbr3
|
UTSW |
16 |
93,487,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R6880:Cbr3
|
UTSW |
16 |
93,487,426 (GRCm39) |
missense |
probably benign |
0.21 |
R7050:Cbr3
|
UTSW |
16 |
93,487,282 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7121:Cbr3
|
UTSW |
16 |
93,487,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R8178:Cbr3
|
UTSW |
16 |
93,480,393 (GRCm39) |
missense |
probably benign |
0.05 |
R8440:Cbr3
|
UTSW |
16 |
93,480,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R9520:Cbr3
|
UTSW |
16 |
93,487,318 (GRCm39) |
missense |
probably benign |
0.00 |
R9715:Cbr3
|
UTSW |
16 |
93,481,941 (GRCm39) |
missense |
probably benign |
0.16 |
|