Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700013G24Rik |
T |
G |
4: 137,454,579 (GRCm38) |
L15W |
probably damaging |
Het |
4930550C14Rik |
G |
A |
9: 53,411,756 (GRCm38) |
V31I |
possibly damaging |
Het |
4932415D10Rik |
T |
C |
10: 82,291,899 (GRCm38) |
D1759G |
possibly damaging |
Het |
Adgre1 |
C |
T |
17: 57,408,445 (GRCm38) |
S255F |
probably benign |
Het |
Aff4 |
T |
G |
11: 53,398,237 (GRCm38) |
S404R |
probably damaging |
Het |
Akr1c19 |
A |
T |
13: 4,233,758 (GRCm38) |
|
probably benign |
Het |
Ankrd31 |
T |
A |
13: 96,878,249 (GRCm38) |
I1342K |
probably damaging |
Het |
Arhgap5 |
T |
A |
12: 52,518,125 (GRCm38) |
D626E |
possibly damaging |
Het |
Arhgef1 |
G |
A |
7: 24,916,923 (GRCm38) |
V332I |
probably benign |
Het |
AY358078 |
A |
G |
14: 51,826,187 (GRCm38) |
E430G |
probably damaging |
Het |
B4gat1 |
T |
A |
19: 5,040,434 (GRCm38) |
I395N |
probably benign |
Het |
Bub1b |
T |
A |
2: 118,636,830 (GRCm38) |
I878N |
probably damaging |
Het |
Ccdc150 |
C |
T |
1: 54,355,709 (GRCm38) |
Q745* |
probably null |
Het |
Ccl19 |
A |
T |
4: 42,754,885 (GRCm38) |
I87N |
probably damaging |
Het |
Ces2g |
G |
C |
8: 104,963,908 (GRCm38) |
G107A |
probably benign |
Het |
Chpt1 |
A |
G |
10: 88,488,406 (GRCm38) |
V180A |
probably damaging |
Het |
Col2a1 |
T |
C |
15: 98,004,454 (GRCm38) |
T14A |
unknown |
Het |
Dnah7a |
T |
C |
1: 53,582,625 (GRCm38) |
I1114V |
possibly damaging |
Het |
Dnah7c |
T |
C |
1: 46,666,213 (GRCm38) |
I2462T |
possibly damaging |
Het |
Dnah8 |
T |
C |
17: 30,643,275 (GRCm38) |
F208S |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,714,210 (GRCm38) |
E3993G |
probably damaging |
Het |
Erv3 |
C |
T |
2: 131,855,966 (GRCm38) |
D158N |
possibly damaging |
Het |
Exoc6 |
T |
A |
19: 37,609,091 (GRCm38) |
F647I |
probably damaging |
Het |
Fbrs |
G |
A |
7: 127,479,508 (GRCm38) |
|
probably benign |
Het |
Fgfr1op2 |
T |
C |
6: 146,589,965 (GRCm38) |
F109L |
probably damaging |
Het |
Fv1 |
T |
C |
4: 147,869,271 (GRCm38) |
F98S |
possibly damaging |
Het |
Gm436 |
A |
G |
4: 144,686,325 (GRCm38) |
F15S |
probably benign |
Het |
H2-M10.1 |
T |
C |
17: 36,325,592 (GRCm38) |
K107E |
probably benign |
Het |
Hspg2 |
A |
T |
4: 137,528,890 (GRCm38) |
Q1436L |
probably damaging |
Het |
Ighv1-74 |
T |
C |
12: 115,802,763 (GRCm38) |
Y79C |
probably damaging |
Het |
Kcnj1 |
G |
A |
9: 32,396,585 (GRCm38) |
V102I |
probably benign |
Het |
Mnt |
C |
A |
11: 74,842,809 (GRCm38) |
|
probably benign |
Het |
Mrpl15 |
T |
C |
1: 4,782,660 (GRCm38) |
T112A |
probably benign |
Het |
Ncdn |
T |
C |
4: 126,747,189 (GRCm38) |
D506G |
probably benign |
Het |
Ogdh |
C |
T |
11: 6,313,806 (GRCm38) |
R81* |
probably null |
Het |
Olfr815 |
G |
C |
10: 129,902,409 (GRCm38) |
F100L |
probably damaging |
Het |
Pole |
G |
T |
5: 110,329,583 (GRCm38) |
V1863F |
probably damaging |
Het |
Pramel5 |
T |
C |
4: 144,274,007 (GRCm38) |
|
probably benign |
Het |
Rabep1 |
A |
G |
11: 70,934,537 (GRCm38) |
K636E |
probably damaging |
Het |
Rasgrf2 |
T |
A |
13: 91,885,635 (GRCm38) |
Y1151F |
probably benign |
Het |
Rrad |
A |
G |
8: 104,630,636 (GRCm38) |
V93A |
probably damaging |
Het |
Sesn3 |
A |
T |
9: 14,310,257 (GRCm38) |
R118* |
probably null |
Het |
Slc27a3 |
T |
C |
3: 90,386,290 (GRCm38) |
N596S |
probably benign |
Het |
Snx19 |
C |
A |
9: 30,428,935 (GRCm38) |
D456E |
probably damaging |
Het |
Supt20 |
T |
C |
3: 54,698,597 (GRCm38) |
S35P |
probably damaging |
Het |
Syde2 |
G |
T |
3: 146,019,809 (GRCm38) |
R885L |
probably benign |
Het |
Synm |
G |
A |
7: 67,733,658 (GRCm38) |
L1419F |
probably damaging |
Het |
Tcrg-V6 |
G |
T |
13: 19,190,644 (GRCm38) |
G40W |
possibly damaging |
Het |
Tekt2 |
A |
G |
4: 126,323,443 (GRCm38) |
F221L |
probably benign |
Het |
Ticam1 |
C |
T |
17: 56,269,900 (GRCm38) |
E732K |
probably benign |
Het |
Tmem39b |
A |
G |
4: 129,693,148 (GRCm38) |
I90T |
possibly damaging |
Het |
Trib2 |
A |
G |
12: 15,815,338 (GRCm38) |
S79P |
probably damaging |
Het |
Usp32 |
T |
C |
11: 85,010,143 (GRCm38) |
M1084V |
probably benign |
Het |
Vmn1r181 |
T |
C |
7: 23,984,847 (GRCm38) |
F246L |
probably damaging |
Het |
Wnt16 |
A |
G |
6: 22,288,511 (GRCm38) |
D2G |
probably damaging |
Het |
Zfp462 |
A |
G |
4: 55,080,716 (GRCm38) |
E1357G |
probably benign |
Het |
Zhx3 |
A |
G |
2: 160,779,868 (GRCm38) |
M793T |
probably benign |
Het |
|
Other mutations in Olfr791 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01153:Olfr791
|
APN |
10 |
129,526,995 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL03034:Olfr791
|
APN |
10 |
129,526,658 (GRCm38) |
missense |
probably benign |
|
IGL03281:Olfr791
|
APN |
10 |
129,526,403 (GRCm38) |
missense |
probably benign |
0.31 |
R0555:Olfr791
|
UTSW |
10 |
129,526,896 (GRCm38) |
missense |
possibly damaging |
0.90 |
R1474:Olfr791
|
UTSW |
10 |
129,526,955 (GRCm38) |
missense |
probably benign |
0.03 |
R1638:Olfr791
|
UTSW |
10 |
129,526,619 (GRCm38) |
missense |
probably benign |
0.00 |
R1917:Olfr791
|
UTSW |
10 |
129,527,049 (GRCm38) |
missense |
probably damaging |
0.99 |
R1918:Olfr791
|
UTSW |
10 |
129,527,049 (GRCm38) |
missense |
probably damaging |
0.99 |
R1919:Olfr791
|
UTSW |
10 |
129,527,049 (GRCm38) |
missense |
probably damaging |
0.99 |
R2303:Olfr791
|
UTSW |
10 |
129,527,049 (GRCm38) |
missense |
probably benign |
0.10 |
R3113:Olfr791
|
UTSW |
10 |
129,527,143 (GRCm38) |
missense |
probably benign |
0.08 |
R3929:Olfr791
|
UTSW |
10 |
129,526,231 (GRCm38) |
start codon destroyed |
probably null |
1.00 |
R4704:Olfr791
|
UTSW |
10 |
129,526,302 (GRCm38) |
missense |
possibly damaging |
0.90 |
R4831:Olfr791
|
UTSW |
10 |
129,526,580 (GRCm38) |
missense |
probably damaging |
1.00 |
R5207:Olfr791
|
UTSW |
10 |
129,526,904 (GRCm38) |
missense |
probably benign |
0.08 |
R5313:Olfr791
|
UTSW |
10 |
129,527,081 (GRCm38) |
missense |
probably damaging |
1.00 |
R5644:Olfr791
|
UTSW |
10 |
129,527,103 (GRCm38) |
missense |
probably damaging |
1.00 |
R5661:Olfr791
|
UTSW |
10 |
129,526,749 (GRCm38) |
missense |
probably benign |
0.45 |
R5894:Olfr791
|
UTSW |
10 |
129,526,488 (GRCm38) |
missense |
probably damaging |
0.98 |
R6996:Olfr791
|
UTSW |
10 |
129,526,863 (GRCm38) |
missense |
probably damaging |
1.00 |
R7380:Olfr791
|
UTSW |
10 |
129,526,661 (GRCm38) |
missense |
probably benign |
|
R7539:Olfr791
|
UTSW |
10 |
129,527,105 (GRCm38) |
nonsense |
probably null |
|
R7552:Olfr791
|
UTSW |
10 |
129,526,560 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7635:Olfr791
|
UTSW |
10 |
129,526,682 (GRCm38) |
missense |
probably benign |
0.00 |
R8084:Olfr791
|
UTSW |
10 |
129,526,940 (GRCm38) |
missense |
probably damaging |
1.00 |
R8260:Olfr791
|
UTSW |
10 |
129,527,088 (GRCm38) |
missense |
possibly damaging |
0.55 |
R8755:Olfr791
|
UTSW |
10 |
129,526,463 (GRCm38) |
missense |
possibly damaging |
0.60 |
X0066:Olfr791
|
UTSW |
10 |
129,526,745 (GRCm38) |
missense |
probably damaging |
1.00 |
|