Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adra1a |
A |
T |
14: 66,964,981 (GRCm39) |
I324F |
possibly damaging |
Het |
Ago2 |
G |
A |
15: 73,002,746 (GRCm39) |
A162V |
possibly damaging |
Het |
Aox4 |
G |
T |
1: 58,298,211 (GRCm39) |
R1059I |
probably damaging |
Het |
AU021092 |
C |
A |
16: 5,030,483 (GRCm39) |
V304L |
probably damaging |
Het |
Bcs1l |
T |
G |
1: 74,628,775 (GRCm39) |
F20V |
probably damaging |
Het |
Braf |
T |
C |
6: 39,637,801 (GRCm39) |
|
probably benign |
Het |
Cacna1a |
T |
C |
8: 85,296,581 (GRCm39) |
C1200R |
probably damaging |
Het |
Ccdc116 |
T |
A |
16: 16,959,836 (GRCm39) |
R284S |
probably benign |
Het |
Cntnap5a |
T |
G |
1: 116,112,187 (GRCm39) |
|
probably null |
Het |
Col12a1 |
A |
T |
9: 79,521,141 (GRCm39) |
|
probably benign |
Het |
Cpa4 |
T |
A |
6: 30,581,739 (GRCm39) |
Y229N |
probably damaging |
Het |
Fbp1 |
A |
C |
13: 63,022,957 (GRCm39) |
|
probably null |
Het |
Gimap3 |
A |
T |
6: 48,742,172 (GRCm39) |
W253R |
probably benign |
Het |
Gm1330 |
G |
A |
2: 148,832,393 (GRCm39) |
|
probably benign |
Het |
Gm4841 |
A |
G |
18: 60,404,093 (GRCm39) |
|
probably benign |
Het |
Grip1 |
A |
G |
10: 119,814,482 (GRCm39) |
T338A |
probably benign |
Het |
Hmg20b |
A |
T |
10: 81,182,385 (GRCm39) |
|
probably benign |
Het |
Hnrnpdl |
A |
G |
5: 100,185,833 (GRCm39) |
F151L |
probably damaging |
Het |
Klhl30 |
T |
A |
1: 91,281,821 (GRCm39) |
F141I |
probably damaging |
Het |
Lamc3 |
T |
A |
2: 31,810,716 (GRCm39) |
F862Y |
probably benign |
Het |
Lap3 |
T |
C |
5: 45,662,138 (GRCm39) |
C313R |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,363,806 (GRCm39) |
T344A |
possibly damaging |
Het |
Mga |
A |
G |
2: 119,778,251 (GRCm39) |
E2023G |
possibly damaging |
Het |
Mical2 |
A |
T |
7: 111,931,243 (GRCm39) |
K735N |
probably benign |
Het |
Muc15 |
A |
G |
2: 110,562,118 (GRCm39) |
T185A |
probably benign |
Het |
Or12d17 |
T |
C |
17: 37,777,306 (GRCm39) |
C70R |
probably damaging |
Het |
Osbp2 |
T |
C |
11: 3,813,434 (GRCm39) |
K145R |
probably benign |
Het |
Pde1c |
T |
C |
6: 56,158,673 (GRCm39) |
T52A |
probably damaging |
Het |
Pidd1 |
A |
G |
7: 141,019,076 (GRCm39) |
S802P |
possibly damaging |
Het |
Pip5k1c |
C |
A |
10: 81,153,155 (GRCm39) |
|
probably null |
Het |
Prep |
T |
A |
10: 44,991,282 (GRCm39) |
I316N |
probably damaging |
Het |
Prl3d2 |
G |
A |
13: 27,310,014 (GRCm39) |
|
probably null |
Het |
Pygo1 |
A |
T |
9: 72,852,319 (GRCm39) |
I169F |
probably benign |
Het |
Rnf10 |
G |
T |
5: 115,380,725 (GRCm39) |
A716E |
probably benign |
Het |
Rtn4 |
G |
A |
11: 29,656,409 (GRCm39) |
|
probably null |
Het |
Ryr1 |
A |
T |
7: 28,778,199 (GRCm39) |
V2099E |
probably damaging |
Het |
Slc48a1 |
G |
A |
15: 97,687,961 (GRCm39) |
|
probably benign |
Het |
Spag17 |
T |
A |
3: 99,918,110 (GRCm39) |
Y364* |
probably null |
Het |
Syt3 |
A |
T |
7: 44,035,486 (GRCm39) |
D31V |
possibly damaging |
Het |
Tango2 |
G |
T |
16: 18,125,857 (GRCm39) |
P143H |
probably benign |
Het |
Tas2r104 |
A |
G |
6: 131,662,107 (GRCm39) |
S201P |
probably damaging |
Het |
Vmn1r81 |
A |
T |
7: 11,994,374 (GRCm39) |
L78Q |
probably damaging |
Het |
Vmn2r18 |
T |
A |
5: 151,508,072 (GRCm39) |
T351S |
probably benign |
Het |
|
Other mutations in Tas2r107 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02749:Tas2r107
|
APN |
6 |
131,636,917 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02868:Tas2r107
|
APN |
6 |
131,636,249 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02943:Tas2r107
|
APN |
6 |
131,636,369 (GRCm39) |
missense |
probably damaging |
0.99 |
R1564:Tas2r107
|
UTSW |
6 |
131,636,785 (GRCm39) |
missense |
probably damaging |
0.96 |
R1905:Tas2r107
|
UTSW |
6 |
131,636,951 (GRCm39) |
missense |
probably benign |
0.20 |
R1906:Tas2r107
|
UTSW |
6 |
131,636,951 (GRCm39) |
missense |
probably benign |
0.20 |
R1907:Tas2r107
|
UTSW |
6 |
131,636,951 (GRCm39) |
missense |
probably benign |
0.20 |
R2185:Tas2r107
|
UTSW |
6 |
131,636,566 (GRCm39) |
missense |
probably damaging |
0.98 |
R3014:Tas2r107
|
UTSW |
6 |
131,636,972 (GRCm39) |
missense |
probably benign |
0.30 |
R3824:Tas2r107
|
UTSW |
6 |
131,636,293 (GRCm39) |
missense |
probably benign |
0.00 |
R4465:Tas2r107
|
UTSW |
6 |
131,636,972 (GRCm39) |
missense |
probably benign |
0.30 |
R5058:Tas2r107
|
UTSW |
6 |
131,636,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R5646:Tas2r107
|
UTSW |
6 |
131,636,671 (GRCm39) |
missense |
probably benign |
0.02 |
R5975:Tas2r107
|
UTSW |
6 |
131,636,743 (GRCm39) |
missense |
probably benign |
0.02 |
R6008:Tas2r107
|
UTSW |
6 |
131,636,875 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6144:Tas2r107
|
UTSW |
6 |
131,636,966 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6451:Tas2r107
|
UTSW |
6 |
131,636,977 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6662:Tas2r107
|
UTSW |
6 |
131,636,452 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6702:Tas2r107
|
UTSW |
6 |
131,636,347 (GRCm39) |
missense |
probably benign |
0.12 |
R7032:Tas2r107
|
UTSW |
6 |
131,636,153 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7635:Tas2r107
|
UTSW |
6 |
131,636,563 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8303:Tas2r107
|
UTSW |
6 |
131,636,585 (GRCm39) |
missense |
probably benign |
0.00 |
R9156:Tas2r107
|
UTSW |
6 |
131,636,422 (GRCm39) |
missense |
probably benign |
0.01 |
R9497:Tas2r107
|
UTSW |
6 |
131,636,549 (GRCm39) |
missense |
probably benign |
0.02 |
R9789:Tas2r107
|
UTSW |
6 |
131,636,753 (GRCm39) |
missense |
probably damaging |
1.00 |
|