Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ache |
A |
G |
5: 137,288,419 (GRCm39) |
|
probably null |
Het |
Aopep |
T |
A |
13: 63,347,334 (GRCm39) |
M631K |
probably damaging |
Het |
Arfgef1 |
T |
C |
1: 10,254,315 (GRCm39) |
D773G |
probably damaging |
Het |
Arhgap45 |
T |
C |
10: 79,863,416 (GRCm39) |
I753T |
probably damaging |
Het |
Cd274 |
T |
A |
19: 29,351,301 (GRCm39) |
|
probably null |
Het |
Cdh16 |
C |
T |
8: 105,345,114 (GRCm39) |
A392T |
possibly damaging |
Het |
Csmd3 |
T |
C |
15: 48,536,927 (GRCm39) |
T92A |
probably damaging |
Het |
Exosc8 |
A |
T |
3: 54,639,419 (GRCm39) |
C129S |
probably benign |
Het |
Fat3 |
T |
G |
9: 15,834,041 (GRCm39) |
I4184L |
probably benign |
Het |
Frem2 |
A |
G |
3: 53,455,199 (GRCm39) |
Y2126H |
probably damaging |
Het |
Fsbp |
T |
C |
4: 11,580,053 (GRCm39) |
M107T |
possibly damaging |
Het |
Gper1 |
A |
G |
5: 139,412,357 (GRCm39) |
Y234C |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,624,777 (GRCm39) |
S1043G |
probably benign |
Het |
Kif2a |
T |
A |
13: 107,123,840 (GRCm39) |
K137N |
probably damaging |
Het |
Mrc2 |
T |
C |
11: 105,239,241 (GRCm39) |
F1332S |
probably damaging |
Het |
Nme8 |
T |
A |
13: 19,844,682 (GRCm39) |
M375L |
possibly damaging |
Het |
Or1e32 |
T |
A |
11: 73,705,176 (GRCm39) |
H244L |
probably damaging |
Het |
Per1 |
T |
C |
11: 68,993,037 (GRCm39) |
L298P |
probably damaging |
Het |
Ppara |
T |
C |
15: 85,682,222 (GRCm39) |
V306A |
probably damaging |
Het |
Rem1 |
G |
A |
2: 152,476,455 (GRCm39) |
V238M |
probably damaging |
Het |
Repin1 |
A |
G |
6: 48,574,768 (GRCm39) |
T566A |
possibly damaging |
Het |
Rhot2 |
T |
A |
17: 26,063,071 (GRCm39) |
D57V |
probably damaging |
Het |
Samd4b |
C |
T |
7: 28,113,435 (GRCm39) |
G177R |
probably damaging |
Het |
Slc5a8 |
C |
A |
10: 88,754,304 (GRCm39) |
P435H |
probably damaging |
Het |
Stpg1 |
G |
A |
4: 135,252,740 (GRCm39) |
A164T |
probably benign |
Het |
Tll2 |
G |
T |
19: 41,084,423 (GRCm39) |
A668D |
possibly damaging |
Het |
Txnl1 |
T |
A |
18: 63,808,539 (GRCm39) |
M180L |
probably benign |
Het |
Vopp1 |
A |
C |
6: 57,766,980 (GRCm39) |
L32R |
probably damaging |
Het |
Wdr95 |
C |
T |
5: 149,505,323 (GRCm39) |
T226I |
possibly damaging |
Het |
Wdr95 |
C |
A |
5: 149,518,829 (GRCm39) |
Q557K |
probably benign |
Het |
|
Other mutations in Polr2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02026:Polr2b
|
APN |
5 |
77,480,099 (GRCm39) |
missense |
probably benign |
|
IGL02069:Polr2b
|
APN |
5 |
77,491,044 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03218:Polr2b
|
APN |
5 |
77,463,764 (GRCm39) |
missense |
probably benign |
0.03 |
R0007:Polr2b
|
UTSW |
5 |
77,488,284 (GRCm39) |
missense |
probably benign |
0.02 |
R0056:Polr2b
|
UTSW |
5 |
77,482,382 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0076:Polr2b
|
UTSW |
5 |
77,474,408 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0099:Polr2b
|
UTSW |
5 |
77,468,797 (GRCm39) |
splice site |
probably benign |
|
R0114:Polr2b
|
UTSW |
5 |
77,491,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R0193:Polr2b
|
UTSW |
5 |
77,467,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R0481:Polr2b
|
UTSW |
5 |
77,479,929 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0607:Polr2b
|
UTSW |
5 |
77,461,006 (GRCm39) |
unclassified |
probably benign |
|
R1597:Polr2b
|
UTSW |
5 |
77,473,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R1674:Polr2b
|
UTSW |
5 |
77,474,470 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1696:Polr2b
|
UTSW |
5 |
77,490,495 (GRCm39) |
missense |
probably benign |
0.12 |
R1704:Polr2b
|
UTSW |
5 |
77,490,407 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1871:Polr2b
|
UTSW |
5 |
77,474,374 (GRCm39) |
splice site |
probably benign |
|
R2114:Polr2b
|
UTSW |
5 |
77,468,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R2137:Polr2b
|
UTSW |
5 |
77,468,193 (GRCm39) |
missense |
probably benign |
0.18 |
R2305:Polr2b
|
UTSW |
5 |
77,468,284 (GRCm39) |
splice site |
probably benign |
|
R3921:Polr2b
|
UTSW |
5 |
77,474,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R4027:Polr2b
|
UTSW |
5 |
77,496,252 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4031:Polr2b
|
UTSW |
5 |
77,496,252 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4526:Polr2b
|
UTSW |
5 |
77,474,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R4750:Polr2b
|
UTSW |
5 |
77,479,886 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4827:Polr2b
|
UTSW |
5 |
77,490,398 (GRCm39) |
missense |
probably benign |
|
R5244:Polr2b
|
UTSW |
5 |
77,490,847 (GRCm39) |
intron |
probably benign |
|
R5360:Polr2b
|
UTSW |
5 |
77,496,993 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5628:Polr2b
|
UTSW |
5 |
77,461,063 (GRCm39) |
missense |
probably damaging |
0.98 |
R5928:Polr2b
|
UTSW |
5 |
77,493,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R6009:Polr2b
|
UTSW |
5 |
77,468,099 (GRCm39) |
missense |
probably benign |
|
R6179:Polr2b
|
UTSW |
5 |
77,468,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R6251:Polr2b
|
UTSW |
5 |
77,496,141 (GRCm39) |
missense |
probably benign |
0.00 |
R7209:Polr2b
|
UTSW |
5 |
77,491,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R7303:Polr2b
|
UTSW |
5 |
77,468,868 (GRCm39) |
missense |
probably benign |
0.04 |
R7328:Polr2b
|
UTSW |
5 |
77,463,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R7345:Polr2b
|
UTSW |
5 |
77,496,966 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7471:Polr2b
|
UTSW |
5 |
77,468,913 (GRCm39) |
nonsense |
probably null |
|
R7581:Polr2b
|
UTSW |
5 |
77,474,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R7697:Polr2b
|
UTSW |
5 |
77,468,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Polr2b
|
UTSW |
5 |
77,488,268 (GRCm39) |
missense |
probably benign |
0.00 |
R7700:Polr2b
|
UTSW |
5 |
77,488,268 (GRCm39) |
missense |
probably benign |
0.00 |
R7956:Polr2b
|
UTSW |
5 |
77,468,092 (GRCm39) |
missense |
probably benign |
0.35 |
R7995:Polr2b
|
UTSW |
5 |
77,473,614 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8015:Polr2b
|
UTSW |
5 |
77,484,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Polr2b
|
UTSW |
5 |
77,468,062 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8318:Polr2b
|
UTSW |
5 |
77,483,576 (GRCm39) |
missense |
probably benign |
0.00 |
R8686:Polr2b
|
UTSW |
5 |
77,483,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R8850:Polr2b
|
UTSW |
5 |
77,463,761 (GRCm39) |
missense |
probably benign |
0.00 |
R9253:Polr2b
|
UTSW |
5 |
77,493,224 (GRCm39) |
missense |
probably benign |
0.16 |
R9275:Polr2b
|
UTSW |
5 |
77,471,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R9278:Polr2b
|
UTSW |
5 |
77,471,485 (GRCm39) |
missense |
probably damaging |
1.00 |
X0054:Polr2b
|
UTSW |
5 |
77,496,152 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1088:Polr2b
|
UTSW |
5 |
77,493,248 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Polr2b
|
UTSW |
5 |
77,490,569 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1176:Polr2b
|
UTSW |
5 |
77,479,818 (GRCm39) |
missense |
probably damaging |
1.00 |
|