Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd24 |
A |
G |
10: 81,475,947 (GRCm39) |
H317R |
unknown |
Het |
Aox1 |
A |
T |
1: 58,080,638 (GRCm39) |
Y29F |
probably damaging |
Het |
Bnip2 |
T |
C |
9: 69,910,967 (GRCm39) |
F304S |
possibly damaging |
Het |
Bsn |
G |
A |
9: 107,988,651 (GRCm39) |
A2367V |
probably benign |
Het |
Ccdc18 |
T |
A |
5: 108,363,899 (GRCm39) |
V1198E |
probably damaging |
Het |
Cnot3 |
T |
C |
7: 3,661,687 (GRCm39) |
F660L |
probably benign |
Het |
Cntnap3 |
A |
G |
13: 64,886,479 (GRCm39) |
I1249T |
probably benign |
Het |
Ctnna3 |
A |
G |
10: 63,339,909 (GRCm39) |
I32V |
probably benign |
Het |
Dgkz |
A |
T |
2: 91,770,649 (GRCm39) |
S485T |
possibly damaging |
Het |
Dnaaf6rt |
A |
G |
1: 31,262,564 (GRCm39) |
N182S |
probably benign |
Het |
Dpagt1 |
C |
A |
9: 44,238,482 (GRCm39) |
N49K |
possibly damaging |
Het |
Dsg3 |
A |
T |
18: 20,656,765 (GRCm39) |
S212C |
probably damaging |
Het |
Epb41l1 |
C |
T |
2: 156,368,873 (GRCm39) |
A714V |
probably benign |
Het |
Eppk1 |
A |
G |
15: 75,995,831 (GRCm39) |
V350A |
probably benign |
Het |
Frem1 |
T |
G |
4: 82,918,499 (GRCm39) |
D481A |
probably damaging |
Het |
Git2 |
T |
C |
5: 114,871,989 (GRCm39) |
K532E |
possibly damaging |
Het |
Glyr1 |
T |
C |
16: 4,854,329 (GRCm39) |
H102R |
probably benign |
Het |
Hdgfl2 |
C |
T |
17: 56,400,712 (GRCm39) |
P160L |
probably benign |
Het |
Hivep1 |
T |
C |
13: 42,308,905 (GRCm39) |
S382P |
probably benign |
Het |
Hmcn2 |
C |
A |
2: 31,281,088 (GRCm39) |
L1867I |
probably benign |
Het |
Hydin |
G |
A |
8: 111,178,626 (GRCm39) |
G1074R |
probably damaging |
Het |
Ift140 |
A |
G |
17: 25,311,889 (GRCm39) |
I1271V |
probably damaging |
Het |
Krt28 |
T |
A |
11: 99,265,626 (GRCm39) |
I14L |
probably benign |
Het |
Lrtm2 |
A |
T |
6: 119,294,458 (GRCm39) |
D224E |
probably damaging |
Het |
Map1s |
G |
A |
8: 71,365,910 (GRCm39) |
V272M |
probably damaging |
Het |
Mast3 |
A |
G |
8: 71,233,866 (GRCm39) |
Y960H |
probably damaging |
Het |
Mettl25 |
G |
T |
10: 105,662,002 (GRCm39) |
Q323K |
probably benign |
Het |
Mlh3 |
A |
T |
12: 85,315,854 (GRCm39) |
S111T |
probably benign |
Het |
Muc17 |
A |
G |
5: 137,172,798 (GRCm39) |
L85P |
|
Het |
Myh6 |
C |
G |
14: 55,181,835 (GRCm39) |
R1822P |
probably damaging |
Het |
Myof |
C |
T |
19: 37,983,872 (GRCm39) |
G144E |
probably benign |
Het |
Nat8f2 |
A |
G |
6: 85,845,024 (GRCm39) |
S113P |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,256,925 (GRCm39) |
Y181F |
probably benign |
Het |
Nup85 |
A |
G |
11: 115,457,468 (GRCm39) |
I57V |
probably benign |
Het |
Or4c99 |
T |
A |
2: 88,329,710 (GRCm39) |
C94S |
probably damaging |
Het |
Or5p79 |
C |
T |
7: 108,221,163 (GRCm39) |
T48I |
probably damaging |
Het |
Or7e170 |
T |
A |
9: 19,795,409 (GRCm39) |
Y64F |
possibly damaging |
Het |
Pcdhb2 |
A |
G |
18: 37,429,110 (GRCm39) |
N361S |
probably damaging |
Het |
Peg10 |
T |
TCCA |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Phf20 |
C |
T |
2: 156,129,913 (GRCm39) |
T495M |
probably benign |
Het |
Pitpnm1 |
T |
C |
19: 4,155,454 (GRCm39) |
M368T |
probably benign |
Het |
Pter |
A |
G |
2: 13,005,700 (GRCm39) |
D291G |
probably damaging |
Het |
Rasgrp2 |
T |
G |
19: 6,454,781 (GRCm39) |
V207G |
probably damaging |
Het |
Rnd2 |
A |
T |
11: 101,362,011 (GRCm39) |
Q188L |
probably benign |
Het |
Sh3d19 |
T |
A |
3: 85,992,363 (GRCm39) |
D130E |
probably benign |
Het |
Slc7a2 |
A |
T |
8: 41,369,396 (GRCm39) |
Y617F |
probably damaging |
Het |
Snx29 |
T |
C |
16: 11,265,291 (GRCm39) |
L165P |
probably damaging |
Het |
St7 |
T |
C |
6: 17,848,080 (GRCm39) |
|
probably null |
Het |
Tead1 |
C |
A |
7: 112,456,135 (GRCm39) |
P164Q |
probably benign |
Het |
Thop1 |
A |
G |
10: 80,914,385 (GRCm39) |
Y224C |
probably damaging |
Het |
Twf1 |
T |
C |
15: 94,477,702 (GRCm39) |
*351W |
probably null |
Het |
Uck1 |
C |
A |
2: 32,150,153 (GRCm39) |
|
probably benign |
Het |
Utp20 |
A |
G |
10: 88,662,466 (GRCm39) |
|
probably null |
Het |
Vmn2r118 |
G |
T |
17: 55,915,057 (GRCm39) |
L530I |
probably benign |
Het |
Vmn2r30 |
A |
T |
7: 7,315,359 (GRCm39) |
C825S |
probably damaging |
Het |
Vps13d |
A |
T |
4: 144,818,549 (GRCm39) |
M3106K |
|
Het |
Wfdc15a |
A |
T |
2: 164,041,671 (GRCm39) |
C51S |
probably damaging |
Het |
Zc3hc1 |
T |
C |
6: 30,375,951 (GRCm39) |
D203G |
probably damaging |
Het |
Zfhx2 |
G |
T |
14: 55,308,079 (GRCm39) |
D932E |
probably benign |
Het |
Zfp267 |
G |
A |
3: 36,219,182 (GRCm39) |
G402S |
probably damaging |
Het |
|
Other mutations in Tas2r115 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00565:Tas2r115
|
APN |
6 |
132,714,741 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01285:Tas2r115
|
APN |
6 |
132,714,641 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01516:Tas2r115
|
APN |
6 |
132,714,576 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01637:Tas2r115
|
APN |
6 |
132,714,592 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02041:Tas2r115
|
APN |
6 |
132,714,430 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02178:Tas2r115
|
APN |
6 |
132,714,271 (GRCm39) |
missense |
probably benign |
0.11 |
R0467:Tas2r115
|
UTSW |
6 |
132,714,682 (GRCm39) |
missense |
probably benign |
0.02 |
R0553:Tas2r115
|
UTSW |
6 |
132,714,922 (GRCm39) |
missense |
probably benign |
0.18 |
R1425:Tas2r115
|
UTSW |
6 |
132,714,442 (GRCm39) |
missense |
probably benign |
0.02 |
R1770:Tas2r115
|
UTSW |
6 |
132,714,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R2120:Tas2r115
|
UTSW |
6 |
132,714,470 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2136:Tas2r115
|
UTSW |
6 |
132,714,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R2141:Tas2r115
|
UTSW |
6 |
132,714,321 (GRCm39) |
missense |
probably benign |
0.43 |
R2142:Tas2r115
|
UTSW |
6 |
132,714,321 (GRCm39) |
missense |
probably benign |
0.43 |
R4479:Tas2r115
|
UTSW |
6 |
132,714,495 (GRCm39) |
missense |
probably damaging |
0.98 |
R4687:Tas2r115
|
UTSW |
6 |
132,714,247 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4948:Tas2r115
|
UTSW |
6 |
132,714,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R5097:Tas2r115
|
UTSW |
6 |
132,714,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R5856:Tas2r115
|
UTSW |
6 |
132,714,501 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6927:Tas2r115
|
UTSW |
6 |
132,714,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R7473:Tas2r115
|
UTSW |
6 |
132,714,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R7688:Tas2r115
|
UTSW |
6 |
132,714,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R8495:Tas2r115
|
UTSW |
6 |
132,714,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R9032:Tas2r115
|
UTSW |
6 |
132,714,327 (GRCm39) |
missense |
probably benign |
0.37 |
R9085:Tas2r115
|
UTSW |
6 |
132,714,327 (GRCm39) |
missense |
probably benign |
0.37 |
R9318:Tas2r115
|
UTSW |
6 |
132,714,472 (GRCm39) |
missense |
probably benign |
0.01 |
R9665:Tas2r115
|
UTSW |
6 |
132,714,390 (GRCm39) |
missense |
probably benign |
0.31 |
R9751:Tas2r115
|
UTSW |
6 |
132,714,918 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1088:Tas2r115
|
UTSW |
6 |
132,714,044 (GRCm39) |
nonsense |
probably null |
|
Z1176:Tas2r115
|
UTSW |
6 |
132,714,819 (GRCm39) |
missense |
probably damaging |
1.00 |
|